Scedosporium and Lomentospora: an updated overview of underrated opportunists

Hidden Killers: Human Fungal Infections

Brown, G. D., Denning, D. W., Gow, N. A. R., Levitz, S. M., Netea, M. G., & White, T. C. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004404 · Cited by 4,284 · see citing works

Immunity to fungal infections

Romani, L. (2011) · Nature Reviews Immunology · doi:10.1038/nri2939 · Cited by 1,793 · see citing works

Invasive Fungal Infections among Organ Transplant Recipients: Results of the Transplant‐Associated Infection Surveillance Network (TRANSNET)

Pappas, P. G., Alexander, B. D., Andes, D. R., Hadley, S., Kauffman, C. A., Freifeld, A., Anaissie, E. J., Brumble, L. M., Herwaldt, L., Ito, J., et al. (2010) · Clinical Infectious Diseases · doi:10.1086/651262 · Cited by 1,570 · see citing works

International Code of Nomenclature for algae, fungi, and plants (Melbourne Code)

McNeill, J. R., Barrie, F. R., Buck, W., et al. (2012) · Cited by 1,138 · see citing works

An integrated model of the recognition of Candida albicans by the innate immune system

Netea, M. G., Brown, G. D., Kullberg, B. J., & Gow, N. A. R. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1815 · Cited by 946 · see citing works

The antifungal pipeline: a reality check

Perfect, J. R. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.46 · Cited by 866 · see citing works

Infections Caused by <i>Scedosporium</i> spp

Cortez, K. J., Roilides, E., Quiroz-Telles, F., Meletiadis, J., Antachopoulos, C., Knudsen, T., Buchanan, W., Milanovich, J., Sutton, D. A., Fothergill, A., et al. (2008) · Clinical Microbiology Reviews · doi:10.1128/cmr.00039-07 · Cited by 786 · see citing works

Azole Resistance in <i>Aspergillus fumigatus</i> : Can We Retain the Clinical Use of Mold-Active Antifungal Azoles?

Verweij, P. E., Chowdhary, A., Melchers, W. J. G., & Meis, J. F. (2016) · Clinical Infectious Diseases · doi:10.1093/cid/civ885 · Cited by 561 · see citing works

Taurine and Inflammatory Diseases

Marcinkiewicz, J., & Kontny, E. (2014) · Amino Acids · doi:10.1007/s00726-012-1361-4 · Cited by 531 · see citing works

Changing epidemiology of systemic fungal infections

Richardson, M., & Lass-Flörl, C. (2008) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2008.01978.x · Cited by 524 · see citing works

ESCMID and ECMM joint guidelines on diagnosis and management of hyalohyphomycosis: Fusarium spp., Scedosporium spp. and others

Tortorano, A. M., Richardson, M. D., Roilides, E., van Diepeningen, A., Caira, M., Munoz, P., Johnson, E. M., Meletiadis, J., Pana, Z. D., Lackner, M., et al. (2014) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12465 · Cited by 517 · see citing works

Mycotic keratitis: epidemiology, diagnosis and management

Thomas, P. A., & Kaliamurthy, J. (2013) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12126 · Cited by 496 · see citing works

Epidemiology and outcome of invasive fungal infections in solid organ transplant recipients

Neofytos, D., Fishman, J. A., Horn, D., Anaissie, E. J., Chang, C., Olyaei, A. J., Pfaller, M. A., Steinbach, W. J., Webster, K. M., & Marr, K. A. (2010) · Transplant Infectious Disease · doi:10.1111/j.1399-3062.2010.00492.x · Cited by 455 · see citing works

T2 Magnetic Resonance Assay for the Rapid Diagnosis of Candidemia in Whole Blood: A Clinical Trial

Mylonakis, E. E., Clancy, C. J., Ostrosky‐Zeichner, L., Garey, K. W., Alangaden, G. J., Vázquez, J. A., Groeger, J. S., Judson, M. A., Vinagre, Y.-M., Heard, S. O., et al. (2015) · Clinical Infectious Diseases · doi:10.1093/cid/ciu959 · Cited by 446 · see citing works

Harnessing Hsp90 function as a powerful, broadly effective therapeutic strategy for fungal infectious disease

Cowen, L. E., Singh, S. D., Köhler, J. R., Collins, C., Zaas, A. K., Schell, W. A., Aziz, H., Mylonakis, E., Perfect, J. R., Whitesell, L., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813394106 · Cited by 413 · see citing works

The Amsterdam Declaration on Fungal Nomenclature

Hawksworth, D. L., Crous, P. W., Redhead, S. A., Reynolds, D. R., Samson, R. A., Seifert, K. A., Taylor, J. W., Wingfield, M. J., Günyar, Ö. A., Aime, C., et al. (2011) · IMA Fungus · doi:10.5598/imafungus.2011.02.01.14 · Cited by 410 · see citing works

Infections Due to Scedosporium apiospermum and Scedosporium prolificans in Transplant Recipients: Clinical Characteristics and Impact of Antifungal Agent Therapy on Outcome

Husain, S., Munoz, P., Forrest, G. N., Alexander, B. D., Somani, J., Brennan, K., Wagener, M. M., & Singh, N. (2004) · Clinical Infectious Diseases · doi:10.1086/426445 · Cited by 402 · see citing works

Fungal Planet description sheets: 469-557

Crous, P. W., Wingfield, M. J., Burgess, T. I., Hardy, G. E. S. J., Crane, C., Barrett, S., Cano-Lira, J. F., Leroux, J. J., Thangavel, R., Guarro, J., et al. (2016) · Persoonia - Molecular Phylogeny and Evolution of Fungi · doi:10.3767/003158516x694499 · Cited by 398 · see citing works

Chlorination of endogenous amines by isolated neutrophils. Ammonia-dependent bactericidal, cytotoxic, and cytolytic activities of the chloramines.

Grisham, M. B., Jefferson, M. M., Melton, D. F., & Thomas, E. L. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90979-8 · Cited by 396 · see citing works

Invasive Mold Infections in Allogeneic Bone Marrow Transplant Recipients

Baddley, J. W., Stroud, T. P., Salzman, D. E., & Pappas, P. G. (2001) · Clinical Infectious Diseases · doi:10.1086/319985 · Cited by 364 · see citing works

International Society of Human and Animal Mycology (ISHAM)-ITS reference DNA barcoding database—the quality controlled standard tool for routine identification of human and animal pathogenic fungi

Irinyi, L., Serena, C., Garcia‐Hermoso, D., Arabatzis, M., Desnos‐Ollivier, M., Vu, D., Cardinali, G., Arthur, I. H., Normand, A., Giraldo, A., et al. (2015) · Medical Mycology · doi:10.1093/mmy/myv008 · Cited by 333 · see citing works

Occurrence and relevance of filamentous fungi in respiratory secretions of patients with cystic fibrosis--a review.

Pihet, M., Carrère, J., Cimon, B., Chabasse, D., Delhaes, L., Symoens, F., & Bouchara, J. (2009) · Medical Mycology · doi:10.1080/13693780802609604 · Cited by 315 · see citing works

Harnessing calcineurin as a novel anti-infective agent against invasive fungal infections.

Steinbach, W. J., Reedy, J. L., Cramer, R. A., Perfect, J. R., & Heitman, J. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1680 · Cited by 313 · see citing works

The cdr1B efflux transporter is associated with non-cyp51a-mediated itraconazole resistance in Aspergillus fumigatus

Fraczek, M. G., Bromley, M., Buied, A., Moore, C. B., Rajendran, R., Rautemaa‐Richardson, R., Ramage, G., Denning, D. W., & Bowyer, P. (2013) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt075 · Cited by 313 · see citing works

Scedosporium apiospermum: changing clinical spectrum of a therapy-refractory opportunist*

Guarro, J., Kantarcıoğlu, A. S., Horré, R., et al. (2006) · Medical Mycology · doi:10.1080/13693780600752507 · Cited by 301 · see citing works

Molecular Phylogeny of the Pseudallescheria boydii Species Complex: Proposal of Two New Species

Gilgado, F., Cano, J., Gené, J., & Guarro, J. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.10.4930-4942.2005 · Cited by 297 · see citing works

Treatment of Scedosporiosis with Voriconazole: Clinical Experience with 107 Patients

Troke, P. F., Aguirrebengoa, K., Arteaga, C., Ellis, D., Heath, C. H., Lutsar, I., Rovira, M., Nguyen, Q. A., Slavin, M. A., & Chen, W. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01388-07 · Cited by 293 · see citing works

Species-Specific Antifungal Susceptibility Patterns of Scedosporium and Pseudallescheria Species

Lackner, M., de Hoog, S., Verweij, P. E., et al. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05910-11 · Cited by 292 · see citing works

F901318 represents a novel class of antifungal drug that inhibits dihydroorotate dehydrogenase

Oliver, J. D., Sibley, G. E. M., Beckmann, N., Dobb, K. S., Slater, M. J., McEntee, L., du Pré, S., Livermore, J., Bromley, M. J., Wiederhold, N. P., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608304113 · Cited by 289 · see citing works

Antibody immunity and invasive fungal infections

Casadevall, A. (1995) · Infection and Immunity · doi:10.1128/iai.63.11.4211-4218.1995 · Cited by 282 · see citing works

Epidemiology and outcome of Scedosporium prolificans infection, a review of 162 cases

Rodrı́guez-Tudela, J. L., Rodrı́guez-Tudela, J. L., Berenguer, J., et al. (2008) · Medical Mycology · doi:10.1080/13693780802524506 · Cited by 271 · see citing works

Clinical Significance of Scedosporium apiospermum in Patients with Cystic Fibrosis

Cimon, B., Carrère, J., Vinatier, J. F., Chazalette, J. P., Chabasse, D., & Bouchara, J.-P. (2000) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s100960050011 · Cited by 270 · see citing works

Particle-size distributions and seasonal diversity of allergenic and pathogenic fungi in outdoor air

Yamamoto, N., Bibby, K. J., Qian, J., Hospodsky, D., Rismani‐Yazdi, H., Nazaroff, W. W., & Peccia, J. (2012) · The ISME Journal · doi:10.1038/ismej.2012.30 · Cited by 268 · see citing works

In Vitro Drug Interaction Modeling of Combinations of Azoles with Terbinafine against Clinical Scedosporium prolificans Isolates

Meletiadis, J., Mouton, J. W., Meis, J. F. G. M., & Verweij, P. E. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.1.106-117.2003 · Cited by 252 · see citing works

In Vivo Bronchoalveolar Macrophage Defense Against Rhizopus oryzae and Aspergillus fumigatus

Waldorf, A. R., Levitz, S. M., & Diamond, R. D. (1984) · The Journal of Infectious Diseases · doi:10.1093/infdis/150.5.752 · Cited by 247 · see citing works

Airway Inflammation in Cystic Fibrosis

Elizur, A., Cannon, C. L., & Ferkol, T. W. (2008) · CHEST Journal · doi:10.1378/chest.07-1631 · Cited by 238 · see citing works

Molecular and Phenotypic Data Supporting Distinct Species Statuses for Scedosporium apiospermum and Pseudallescheria boydii and the Proposed New Species Scedosporium dehoogii

Gilgado, F., Cano, J., Gené, J., Sutton, D. A., & Guarro, J. (2007) · Journal of Clinical Microbiology · doi:10.1128/jcm.01122-07 · Cited by 226 · see citing works

Adaptive Immunity to Fungi

Wüthrich, M., Deepe, G. S., & Klein, B. S. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-020711-074958 · Cited by 225 · see citing works

Human Antibodies against a Purified Glucosylceramide from Cryptococcus neoformans Inhibit Cell Budding and Fungal Growth

Rodrigues, M. L., Travassos, L. R., de Miranda, K. R., Franzen, A. J., Rozental, S., de Souza, W., Alviano, C. S., & Barreto‐Bergter, E. (2000) · Infection and Immunity · doi:10.1128/iai.68.12.7049-7060.2000 · Cited by 218 · see citing works

Deep Infections Caused by Scedosporium prolificans: A Report on 16 Cases in Spain and a Review of the Literature

Berenguer, J., Rodrı́guez-Tudela, J. L., Richard, C., Alvarez, M., Sanz, M. Á., Gaztelurrutia, L., Ayats, J., & Martı́nez-Suárez, J. V. (1997) · Medicine · doi:10.1097/00005792-199707000-00004 · Cited by 213 · see citing works

Pseudallescheria boydii (Anamorph Scedosporium apiospermum) Infection in Solid Organ Transplant Recipients in a Tertiary Medical Center and Review of the Literature

Castiglioni, B., Sutton, D. A., Rinaldi, M. G., et al. (2002) · Medicine · doi:10.1097/00005792-200209000-00001 · Cited by 212 · see citing works

Activation of neutrophils by recombinant interleukin 6

Borish, L., Rosenbaum, R., Albury, L., & Clark, S. (1989) · Cellular Immunology · doi:10.1016/0008-8749(89)90026-9 · Cited by 211 · see citing works

<i>In Vitro</i> Activity of E1210, a Novel Antifungal, against Clinically Important Yeasts and Molds

Miyazaki, M., Horii, T., Hata, K., Watanabe, N.-A., Nakamoto, K., Tanaka, K., Shirotori, S., Murai, N., Inoue, S., Matsukura, M., et al. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00291-11 · Cited by 200 · see citing works

Successful Control of Disseminated Scedosporium prolificans Infection with a Combination of Voriconazole and Terbinafine

Howden, B. P., Slavin, M. A., Schwarer, A. P., & Mijch, A. M. (2003) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-002-0877-z · Cited by 197 · see citing works

Caspofungin‐Mediated β‐Glucan Unmasking and Enhancement of Human Polymorphonuclear Neutrophil Activity against Aspergillus and Non‐ Aspergillus Hyphae

Lamaris, G. A., Lewis, R. E., Chamilos, G., May, G. S., Safdar, A., Walsh, T. J., RAAD, I. I., & Kontoyiannis, D. P. (2008) · The Journal of Infectious Diseases · doi:10.1086/589305 · Cited by 186 · see citing works

Proposed nomenclature for Pseudallescheria, Scedosporium and related genera

Lackner, M., de Hoog, S., Yang, L., et al. (2014) · Fungal Diversity · doi:10.1007/s13225-014-0295-4 · Cited by 183 · see citing works

Immunoglobulins in Defense, Pathogenesis, and Therapy of Fungal Diseases

Casadevall, A., & Pirofski, L. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.04.004 · Cited by 180 · see citing works

Invasive Fungal Infections in Solid Organ Transplant Recipients

Shoham, S., & Marr, K. A. (2012) · Future Microbiology · doi:10.2217/fmb.12.28 · Cited by 176 · see citing works

Improved Sensitivity for Molecular Detection of Bacterial and Candida Infections in Blood

Bacconi, A., Richmond, G. S., Baroldi, M. A., Laffler, T. G., Blyn, L. B., Carolan, H. E., Frinder, M., TOLENO, D. M., Metzgar, D., Gutierrez, J. R., et al. (2014) · Journal of Clinical Microbiology · doi:10.1128/jcm.00801-14 · Cited by 169 · see citing works

Clinical Features of Human Infection with Scedosporium inflatum

Wood, G., McCormack, J. G., Muir, D. B., et al. (1992) · Clinical Infectious Diseases · doi:10.1093/clinids/14.5.1027 · Cited by 163 · see citing works

Scedosporium Infection in a Tertiary Care Cancer Center: A Review of 25 Cases from 1989-2006

Lamaris, G. A., Chamilos, G., Lewis, R. E., SAFDAR, A. Y. E. S. H. A., RAAD, I. I., & Kontoyiannis, D. P. (2006) · Clinical Infectious Diseases · doi:10.1086/509579 · Cited by 162 · see citing works

T2MR and T2Candida: novel technology for the rapid diagnosis of candidemia and invasive candidiasis

Pfaller, M. A., Wolk, D. M., & Lowery, T. J. (2015) · Future Microbiology · doi:10.2217/fmb.15.111 · Cited by 157 · see citing works

An α-Glucan of Pseudallescheria boydii Is Involved in Fungal Phagocytosis and Toll-like Receptor Activation

Bittencourt, V. C. B., Figueiredo, R. T., da Silva, R. B., Mourão‐Sá, D., Fernández, P. L., Sassaki, G. L., Mulloy, B., Bozza, M. T., & Barreto‐Bergter, E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m511417200 · Cited by 154 · see citing works

Regulation of neutrophil migration and superoxide production by recombinant tumor necrosis factors-alpha and -beta: comparison to recombinant interferon-gamma and interleukin-1 alpha

Figari, I., Mori, N., & Palladino, M. J. (1987) · Blood · doi:10.1182/blood.v70.4.979.979 · Cited by 150 · see citing works

Efficacy of oral E1210, a new broad-spectrum antifungal with a novel mechanism of action, in murine models of candidiasis, aspergillosis, and fusariosis

Hata, K., Horii, T., Miyazaki, M., Watanabe, N.-A., Okubo, M., Sonoda, J., Nakamoto, K., Tanaka, K., Shirotori, S., Murai, N., et al. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00366-11 · Cited by 149 · see citing works

Activity of MGCD290, a Hos2 Histone Deacetylase Inhibitor, in Combination with Azole Antifungals against Opportunistic Fungal Pathogens

Pfaller, M. A., Messer, S. A., Georgopapadakou, N., Martell, L. A., Besterman, J. M., & Diekema, D. J. (2009) · Journal of Clinical Microbiology · doi:10.1128/jcm.00618-09 · Cited by 143 · see citing works

Differences in beta-glucan levels in culture supernatants of a variety of fungi

Odabaşı, Z., Paetznick, V. L., Rodriguez, J. R., Chen, E., McGinnis, M. R., & Ostrosky‐Zeichner, L. (2006) · Medical Mycology · doi:10.1080/13693780500474327 · Cited by 143 · see citing works

Antifungal Activity Of Elutriated Human Monocytes Against Aspergillus Fumigatus Hyphae: Enhancement By Granulocyte-Macrophage Colonystimulating Factor And Interferon-a

Roilides, E., Holmes, A., Blake, C., Venzon, D. J., Pizzo, P. A., & Walsh, T. J. (1994) · The Journal of Infectious Diseases · doi:10.1093/infdis/170.4.894 · Cited by 137 · see citing works

Interaction of phagocytes with filamentous fungi

Brakhage, A. A., Bruns, S., Thywißen, A., Zipfel, P. F., & Behnsen, J. (2010) · Current Opinion in Microbiology · doi:10.1016/j.mib.2010.04.009 · Cited by 136 · see citing works

Ecology of Pseudallescheria and Scedosporium species in human-dominated and natural environments and their distribution in clinical samples.

Kaltseis, J., Rainer, J., & de Hoog, G. (2009) · Medical Mycology · doi:10.1080/13693780802585317 · Cited by 136 · see citing works

Subcutaneous mycoses

Queiroz‐Telles, F., McGinnis, M. R., Salkin, I. F., & Graybill, J. R. (2003) · Infectious Disease Clinics of North America · doi:10.1016/s0891-5520(02)00066-1 · Cited by 136 · see citing works

Biodiversity, evolution and adaptation of fungi in extreme environments

Selbmann, L., Egidi, E., Isola, D., Onofri, S., Zucconi, L., de Hoog, S., Chinaglia, S., Testa, L., Tosi, S., Balestrazzi, A., et al. (2012) · Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology · doi:10.1080/11263504.2012.753134 · Cited by 134 · see citing works

Pulmonary defense mechanisms against opportunistic fungal pathogens.

Waldorf, A. R. (1989) · PubMed · Cited by 132 · see citing works

N-chlorotaurine, a natural antiseptic with outstanding tolerability

Gottardi, W., & Nagl, M. (2010) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkp466 · Cited by 131 · see citing works

Invasive Pulmonary Infection Due to Scedosporium apiospermum in Two Children with Chronic Granulomatous Disease

Jabado, N., Casanova, J., Haddad, É., Dulieu, F., Fournet, J., Dupont, B., Fischer, A., Hennequin, C., & Blanche, S. (1998) · Clinical Infectious Diseases · doi:10.1086/515015 · Cited by 128 · see citing works

Population-based surveillance for scedosporiosis in Australia: epidemiology, disease manifestations and emergence of Scedosporium aurantiacum infection

Heath, C. H., Slavin, M. A., Sorrell, T. C., Handke, R., Harun, A. B., Phillips, M. R., Nguyen, Q. A., Delhaès, L., Ellis, D., Meyer, W., et al. (2009) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2009.02802.x · Cited by 123 · see citing works

Characteristics and consequences of airway colonization by filamentous fungi in 201 adult patients with cystic fibrosis in France

Paugam, A., Baixench, M.-T., Demazes-Dufeu, N., Burgel, P.-R., Sauter, E., Kanaan, R., Dusser, D., Dupouy-Camet, J., & Hubert, D. (2010) · Medical Mycology · doi:10.3109/13693786.2010.503665 · Cited by 123 · see citing works

Scedosporium apiospermum infection after near‐drowning

Katragkou, A., Dotis, J., Kotsiou, M., Tamiolaki, M., & Roilides, E. (2007) · Mycoses · doi:10.1111/j.1439-0507.2007.01388.x · Cited by 118 · see citing works

Disseminated Infection and Colonization by Scedosporium prolificans: A Review of 18 Cases, 1990-1999

Idígoras, P., Pérez‐Trallero, E., Piñeiro, L. D., et al. (2001) · Clinical Infectious Diseases · doi:10.1086/320521 · Cited by 117 · see citing works

Ecology and physiology of the emerging opportunistic fungi Pseudallescheria boydii and Scedosporium prolificans

de Hoog, S., Marvin-Sikkema, F. D., Lahpoor, G. A., et al. (1994) · Mycoses · doi:10.1111/j.1439-0507.1994.tb00780.x · Cited by 113 · see citing works

Central Nervous System Infection Caused by Pseudallescheria boydii: Case Report and Review

Berenguer, J., Díaz-Mediavilla, J., Urra, D. G., et al. (1989) · Clinical Infectious Diseases · doi:10.1093/clinids/11.6.890 · Cited by 110 · see citing works

Epidemiology of Invasive Mold Infections in Lung Transplant Recipients

Doligalski, C. T., Benedict, K., Cleveland, A. A., Park, B., Derado, G., Pappas, P. G., Baddley, J. W., Zaas, D., Harris, M., & Alexander, B. D. (2014) · American Journal of Transplantation · doi:10.1111/ajt.12691 · Cited by 109 · see citing works

In Vitro Interaction of Terbinafine with Itraconazole against Clinical Isolates of Scedosporium prolificans

Meletiadis, J., Mouton, J. W., Rodrı́guez-Tudela, J. L., Meis, J. F. G. M., & Verweij, P. E. (2000) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.44.2.470-472.2000 · Cited by 109 · see citing works

Many facets of mammalian lanosterol 14α-demethylase from the evolutionarily conserved cytochrome P450 family CYP51

Debeljak, N., Fink, M., & Rozman, D. (2003) · Archives of Biochemistry and Biophysics · doi:10.1016/s0003-9861(02)00418-6 · Cited by 103 · see citing works

Scedosporium prolificans Osteomyelitis in an Immunocompetent Child Treated with Voriconazole and Caspofungin, as Well as Locally Applied Polyhexamethylene Biguanide

Steinbach, W. J., Schell, W. A., Miller, J. L., et al. (2003) · Journal of Clinical Microbiology · doi:10.1128/jcm.41.8.3981-3985.2003 · Cited by 102 · see citing works

Scedosporium apiospermum (Pseudoallescheria boydii) Infection in Lung Transplant Recipients

Sahi, H., Avery, R. K., Minai, O. A., Hall, G. S., Mehta, A. C., Raina, P., & Budev, M. M. (2007) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2007.01.011 · Cited by 100 · see citing works

Scedosporium prolificans brain abscess in a patient with chronic granulomatous disease: Successful combination therapy with voriconazole and terbinafine

Bhat, S. V., Paterson, D. L., Rinaldi, M. G., & Veldkamp, P. J. (2006) · Scandinavian Journal of Infectious Diseases · doi:10.1080/00365540600786564 · Cited by 100 · see citing works

Activities of E1210 and Comparator Agents Tested by CLSI and EUCAST Broth Microdilution Methods against Fusarium and Scedosporium Species Identified Using Molecular Methods

Castanheira, M., Duncanson, F. P., Diekema, D. J., Guarro, J., Jones, R. N., & Pfaller, M. A. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05414-11 · Cited by 98 · see citing works

Nosocomial outbreak caused by Scedosporium prolificans (inflatum): four fatal cases in leukemic patients

Alvarez, M., Ponga, B. L., Rayón, C., et al. (1995) · Journal of Clinical Microbiology · doi:10.1128/jcm.33.12.3290-3295.1995 · Cited by 97 · see citing works

Insights into fungal communities in composts revealed by 454-pyrosequencing: implications for human health and safety

de Gannes, V., Eudoxie, G. D., & Hickey, W. J. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00164 · Cited by 96 · see citing works

Clinical associations and prevalence ofScedosporiumspp. in Australian cystic fibrosis patients: identification of novel risk factors?

Blyth, C. C., Middleton, P. G., Harun, A. B., Sorrell, T. C., Meyer, W., & Chen, S. C.-A. (2010) · Medical Mycology · doi:10.3109/13693786.2010.500627 · Cited by 96 · see citing works

N -Chloramines, a Promising Class of Well-Tolerated Topical Anti-Infectives

Gottardi, W., Debabov, D. V., & Nagl, M. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02132-12 · Cited by 94 · see citing works

Genotyping Study of Scedosporium apiospermum Isolates from Patients with Cystic Fibrosis

Defontaine, A., Zouhair, R., Cimon, B., Carrère, J., Bailly, É., Symoens, F., Diouri, M., Hallet, J. N., & Bouchara, J. (2002) · Journal of Clinical Microbiology · doi:10.1128/jcm.40.6.2108-2114.2002 · Cited by 94 · see citing works

Interrogation of Related Clinical Pan-Azole-Resistant Aspergillus fumigatus Strains: G138C, Y431C, and G434C Single Nucleotide Polymorphisms incyp51A, Upregulation ofcyp51A, and Integration and Activation of TransposonAtf1in thecyp51APromoter

Albarrag, A., Anderson, M. J., Howard, S. J., Robson, G., Warn, P. A., Sanglard, D., & Denning, D. W. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00517-11 · Cited by 94 · see citing works

The fungal Achilles’ heel: targeting Hsp90 to cripple fungal pathogens

Cowen, L. E. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.03.005 · Cited by 93 · see citing works

Atypical Infections in Tsunami Survivors

Garzoni, C., Emonet, S., Legout, L., Benedict, R., Hoffmeyer, P. J., Bernard, L., & Garbino, J. (2005) · Emerging infectious diseases · doi:10.3201/eid1110.050715 · Cited by 93 · see citing works

Infection withScedosporium apiospermumandS.prolificans, Australia

Cooley, L., Spelman, D., Thursky, K., & Slavin, M. A. (2007) · Emerging infectious diseases · doi:10.3201/eid1308.060576 · Cited by 92 · see citing works

New Fks Hot Spot for Acquired Echinocandin Resistance in Saccharomyces cerevisiae and Its Contribution to Intrinsic Resistance of Scedosporium Species

Johnson, M. E., Katiyar, S. K., & Edlind, T. D. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01811-10 · Cited by 91 · see citing works

Structure and biological functions of fungal cerebrosides

Barreto‐Bergter, E., Pinto, M. R., & Rodrigues, M. L. (2004) · Anais da Academia Brasileira de Ciências · doi:10.1590/s0001-37652004000100007 · Cited by 91 · see citing works

A 33 kDa serine proteinase from Scedosporium apiospermum

Larcher, G., Cimon, B., Symoens, F., Tronchin, G., Chabasse, D., & Bouchara, J. (1996) · Biochemical Journal · doi:10.1042/bj3150119 · Cited by 90 · see citing works

Characterization of glucosylceramides in Pseudallescheria boydii and their involvement in fungal differentiation

Pinto, M. R., Rodrigues, M. L., Travassos, L. R., et al. (2002) · Glycobiology · doi:10.1093/glycob/12.4.251 · Cited by 88 · see citing works

Fungal epidemiology and diversity in cystic fibrosis patients over a 5-year period in a national reference center

Ziesing, S., Suerbaum, S., & Sedlacek, L. (2016) · Medical Mycology · doi:10.1093/mmy/myw035 · Cited by 88 · see citing works

Abundance of Pseudallescheria/Scedosporium species in the Australian urban environment suggests a possible source for scedosporiosis including the colonization of airways in cystic fibrosis

Harun, A. B., Gilgado, F., Chen, S. C. ‐., et al. (2010) · Medical Mycology · doi:10.3109/13693786.2010.515254 · Cited by 87 · see citing works

Detection of Occult Scedosporium Species in Respiratory Tract Specimens from Patients with Cystic Fibrosis by Use of Selective Media

Blyth, C. C., Harun, A. B., Middleton, P. G., et al. (2009) · Journal of Clinical Microbiology · doi:10.1128/jcm.01470-09 · Cited by 86 · see citing works

Dihydroorotate dehydrogenase inhibitor F901318 has potent in vitro activity against Scedosporium species and Lomentospora prolificans

Wiederhold, N. P., Law, D., & Birch, M. (2017) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkx065 · Cited by 85 · see citing works

Cure of orthopaedic infection with Scedosporium prolificans, using voriconazole plus terbinafine, without the need for radical surgery

Gosbell, I. B., Toumasatos, V., Yong, J., Kuo, R.-S., Ellis, D., & Perrie, R. C. (2003) · Mycoses (Berlin) · doi:10.1046/j.1439-0507.2003.00878.x · Cited by 85 · see citing works

Prevalence of Scedosporium species and Lomentospora prolificans in patients with cystic fibrosis in a multicenter trial by use of a selective medium

Sedlacek, L., Graf, B., Schwarz, C., Albert, F., Peter, S., Würstl, B., Wagner, S., Klotz, M., Becker, A., Haase, G., et al. (2015) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2014.12.014 · Cited by 85 · see citing works

Toll-like receptors (TLR2 and TLR4) recognize polysaccharides of Pseudallescheria boydii cell wall

Figueiredo, R. T., Bittencourt, V. C. B., Lopes, L. C. L., Sassaki, G. L., & Barreto‐Bergter, E. (2012) · Carbohydrate Research · doi:10.1016/j.carres.2012.02.028 · Cited by 85 · see citing works

In Vitro Activities of 35 Double Combinations of Antifungal Agents against Scedosporium apiospermum and Scedosporium prolificans

Cuenca‐Estrella, M., Alastruey‐Izquierdo, A., Alcázar‐Fuoli, L., Bernal‐Martínez, L., Gómez‐López, A., Buitrago, M. J., Mellado, E., & Rodrı́guez-Tudela, J. L. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01160-07 · Cited by 85 · see citing works

Molecular Typing of AustralianScedosporiumIsolates Showing Genetic Variability and NumerousS. aurantiacum

Delhaès, L., Harun, A. B., Chen, S. C. ‐., Nguyen, Q. A., Slavin, M. A., Heath, C. H., Maszewska, K., Halliday, C. L., Robert, V., Sorrell, T. C., et al. (2008) · Emerging infectious diseases · doi:10.3201/eid1402.070920 · Cited by 84 · see citing works

Disseminated Scedosporium / Pseudallescheria Infection after Double-Lung Transplantation in Patients with Cystic Fibrosis

Morio, F., Horeau-Langlard, D., Gay‐Andrieu, F., Talarmin, J., Haloun, A., Treilhaud, M., Despins, P., Jossic, F., Nourry, L., Danner‐Boucher, I., et al. (2010) · Journal of Clinical Microbiology · doi:10.1128/jcm.01840-09 · Cited by 82 · see citing works

Mycetoma in the United States: A Review and Report of Seven Additional Cases

Green, W. O., & Adams, T. E. (1964) · American Journal of Clinical Pathology · doi:10.1093/ajcp/42.1.75 · Cited by 82 · see citing works

An Antifungal Combination Matrix Identifies a Rich Pool of Adjuvant Molecules that Enhance Drug Activity against Diverse Fungal Pathogens

Robbins, N., Spitzer, M., Yu, T., Cerone, R. P., Averette, A. K., Bahn, Y.-S., Heitman, J., Sheppard, D. C., Tyers, M., & Wright, G. D. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.018 · Cited by 78 · see citing works

Susceptibility and Diversity in the Therapy-Refractory Genus Scedosporium

Lackner, M., Hagen, F., Meis, J. F. G. M., van den Ende, A. H. G. G., Vu, D., Robert, V., Fritz, J., Moussa, T. A. A., & de Hoog, S. (2014) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.03211-14 · Cited by 77 · see citing works

Antifungal Th Immunity: Growing up in Family

Borghi, M., Renga, G., Puccetti, M., Oikonomou, V., Palmieri, M., Galosi, C., Bartoli, A., & Romani, L. R. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00506 · Cited by 76 · see citing works

Pseudallescheria/Scedosporiumcomplex species identification by matrix-assisted laser desorption ionization time-of-flight mass spectrometry

Coulibaly, O., Marinach, C., Cassagne, C., Piarroux, R., Mazier, D., & Ranque, S. (2011) · Medical Mycology · doi:10.3109/13693786.2011.555424 · Cited by 76 · see citing works

The anti- Aspergillus drug pipeline: Is the glass half full or empty?: Table 1.

Osherov, N., & Kontoyiannis, D. P. (2016) · Medical Mycology · doi:10.1093/mmy/myw060 · Cited by 75 · see citing works

Characterization of microbial siderophores by mass spectrometry

Pluháček, T., Lemr, K., Ghosh, D., Milde, D., Novák, J., & Havlíček, V. (2016) · Mass Spectrometry Reviews · doi:10.1002/mas.21461 · Cited by 74 · see citing works

Degradation of hydrocarbons in crude oil by the ascomycetePseudallescheria boydii(Microascaceae)

April, T. M., Abbott, S. P., Foght, J. M., et al. (1998) · Canadian Journal of Microbiology · doi:10.1139/w97-152 · Cited by 72 · see citing works

Distinct patterns of inflammation in the airway lumen and bronchial mucosa of children with cystic fibrosis

Regamey, N., Tsartsali, L., Hilliard, T. N., Fuchs, O., Tan, H., Zhu, J., Qiu, Y., Alton, E. W. F. W., Jeffery, P. K., Bush, A., et al. (2011) · Thorax · doi:10.1136/thoraxjnl-2011-200585 · Cited by 72 · see citing works

In vitro activity of miltefosine as a single agent and in combination with voriconazole or posaconazole against uncommon filamentous fungal pathogens

Biswas, C., Sorrell, T. C., Djordjevic, J. T., et al. (2013) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt282 · Cited by 70 · see citing works

Chlorine covers on living bacteria: the initial step in antimicrobial action of active chlorine compounds

Gottardi, W., & Nagl, M. (2005) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dki054 · Cited by 70 · see citing works

Efficacy of a selective isolation procedure for members of the Pseudallescheria boydii complex

Rainer, J., Kaltseis, J., de Hoog, S., et al. (2007) · Antonie van Leeuwenhoek · doi:10.1007/s10482-007-9206-y · Cited by 69 · see citing works

Fungal adaptation to the mammalian host: it is a new world, after all

Cooney, N. M., & Klein, B. S. (2008) · Current Opinion in Microbiology · doi:10.1016/j.mib.2008.09.018 · Cited by 68 · see citing works

Inteferon gamma and granulocyte–macrophage colony-stimulating factor augment the antifungal activity of human polymorphonuclear leukocytes againstScedosporiumspp.: comparison withAspergillusspp.

Gil‐Lamaignere, C., Winn, R. M., Simitsopoulou, M., Maloukou, A., Walsh, T. J., & Roilides, E. (2004) · Medical Mycology · doi:10.1080/13693780412331271072 · Cited by 68 · see citing works

The ‘species complex’ issue in clinically relevant fungi: A case study in Scedosporium apiospermum

Chen, M., Zeng, J., de Hoog, S., Stielow, J. B., van den Ende, A. H. G. G., Liao, W., & Lackner, M. (2015) · Fungal Biology · doi:10.1016/j.funbio.2015.09.003 · Cited by 68 · see citing works

In vitro activity of a Hos2 deacetylase inhibitor, MGCD290, in combination with echinocandins against echinocandin-resistant Candida species

Pfaller, M. A., Rhomberg, P. R., Messer, S. A., & Castanheira, M. (2015) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2014.11.008 · Cited by 67 · see citing works

Epidemiology, clinical manifestations, and outcomes of S cedosporium infections among solid organ transplant recipients

Johnson, L. S., Shields, R. K., & Clancy, C. J. (2014) · Transplant Infectious Disease · doi:10.1111/tid.12244 · Cited by 67 · see citing works

Azole-Resistant Invasive Aspergillosis: Relationship to Agriculture

Stensvold, C. R., Jørgensen, L. N., & Arendrup, M. C. (2012) · Current Fungal Infection Reports · doi:10.1007/s12281-012-0097-7 · Cited by 67 · see citing works

A review of GermanScedosporium prolificanscases from 1993 to 2007

Tintelnot, K., Just‐Nübling, G., Horré, R., et al. (2009) · Medical Mycology · doi:10.1080/13693780802627440 · Cited by 66 · see citing works

A peptidorhamnomannan from the mycelium of Pseudallescheria boydii is a potential diagnostic antigen of this emerging human pathogen

Pinto, M. R., Mulloy, B., Haido, R. M. T., et al. (2001) · Microbiology · doi:10.1099/00221287-147-6-1499 · Cited by 65 · see citing works

Structural Analysis of Natural Products

Přichystal, J., Schug, K. A., Lemr, K., et al. (2016) · Analytical Chemistry · doi:10.1021/acs.analchem.6b02386 · Cited by 64 · see citing works

Human‐impacted areas of F rance are environmental reservoirs of the P seudallescheria boydii / S cedosporium apiospermum species complex

Rougeron, A., Schuliar, G., Leto, J., Sitterlé, E., Landry, D., Bougnoux, M., Kobi, A., Bouchara, J., & Giraud, S. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12472 · Cited by 61 · see citing works

Cytokine responses and regulation of interferon-gamma release by human mononuclear cells toAspergillus fumigatusand other filamentous fungi

Warris, A., Netea, M. G., Verweij, P. E., Gaustad, P., Kullberg, B. J., Weemaes, C. M. R., & Abrahamsen, T. G. (2005) · Medical Mycology · doi:10.1080/13693780500088333 · Cited by 61 · see citing works

Involvement of peptidorhamnomannan in the interaction of Pseudallescheria boydii and HEp2 cells

Pinto, M. R., de Sá, A. C. M., Limongi, C. L., Rozental, S., dos Santos, A. L. S., & Barreto‐Bergter, E. (2004) · Microbes and Infection · doi:10.1016/j.micinf.2004.07.006 · Cited by 60 · see citing works

Molecular identification of Mucorales in human tissues: contribution of PCR electrospray-ionization mass spectrometry

Alanio, A., Garcia‐Hermoso, D., Mercier‐Delarue, S., Lanternier, F., Gits‐Muselli, M., Ménotti, J., Denis, B., Bergeron, A., Legrand, M. M., Lortholary, O., et al. (2015) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2015.01.017 · Cited by 60 · see citing works

Lethal brain abscess due to the fungusScedosporium apiospermum(teleomorphPseudallescheria boydii) after a near-drowning incident: case report and review of the literature

Buzina, W., Feierl, G., Haas, D., et al. (2006) · Medical Mycology · doi:10.1080/13693780600654588 · Cited by 58 · see citing works

Antifungal Triazoles and Polymorphonuclear Leukocytes Synergize To Cause Increased Hyphal Damage toScedosporium prolificansandScedosporium apiospermum

Gil‐Lamaignere, C., Roilides, E., Mosquera, J., et al. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.7.2234-2237.2002 · Cited by 58 · see citing works

Update in Cystic Fibrosis 2005

Accurso, F. J. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.2601006 · Cited by 56 · see citing works

Distribution of the different species of thePseudallescheria boydii/Scedosporium apiospermumcomplex in French patients with cystic fibrosis

Zouhair, R., Rougeron, A., Razafimandimby, B., Kobi, A., Bouchara, J., & Giraud, S. (2013) · Medical Mycology · doi:10.3109/13693786.2013.770606 · Cited by 56 · see citing works

Liposomal amphotericin B and granulocyte colony-stimulating factor therapy in a murine model of invasive infection by Scedosporium prolificans

Ortoneda, M. (2002) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/49.3.525 · Cited by 55 · see citing works

Bone and joint infection after traumatic implantation of Scedosporium prolificans treated with voriconazole and surgery

Studahl, M., Backteman, T., Stålhammar, F., et al. (2003) · Acta Paediatrica · doi:10.1111/j.1651-2227.2003.tb00636.x · Cited by 53 · see citing works

Performance of Matrix-Assisted Laser Desorption Ionization−Time of Flight Mass Spectrometry for Identification of Aspergillus, Scedosporium, and Fusarium spp. in the Australian Clinical Setting

Sleiman, S., Halliday, C. L., Chapman, B., et al. (2016) · Journal of Clinical Microbiology · doi:10.1128/jcm.00906-16 · Cited by 53 · see citing works

Blocking Hsp70 Enhances the Efficiency of Amphotericin B Treatment against Resistant Aspergillus terreus Strains

Blatzer, M., Blum, G., Jukic, E., Posch, W., Gruber, P., Nagl, M., Binder, U., Maurer, E., Sarg, B., Lindner, H. H., et al. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05164-14 · Cited by 52 · see citing works

Successful Treatment of Disseminated Scedosporium Infection in 2 Lung Transplant Recipients: Review of the Literature and Recommendations for Management

Musk, M., Chambers, D. C., Chin, W., Murray, R., & Gabbay, E. (2006) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2006.06.002 · Cited by 52 · see citing works

Detection, Identification, and Distribution of Fungi in Bronchoalveolar Lavage Specimens by Use of Multilocus PCR Coupled with Electrospray Ionization/Mass Spectrometry

Shin, J. H., Ranken, R., Sefers, S. E., et al. (2012) · Journal of Clinical Microbiology · doi:10.1128/jcm.01907-12 · Cited by 52 · see citing works

Effects of Double and Triple Combinations of Antifungal Drugs in a Murine Model of Disseminated Infection by Scedosporium prolificans

Rodríguez, M. M., Calvo, E., Serena, C., et al. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01477-08 · Cited by 52 · see citing works

Scedosporium aurantiacum brain abscess after near-drowning in a survivor of a tsunami in Japan

Nakamura, Y., Suzuki, N., Nakajima, Y., et al. (2013) · Respiratory Investigation · doi:10.1016/j.resinv.2013.07.001 · Cited by 52 · see citing works

Control, immunoregulation, and expression of innate pulmonary host defenses againstAspergillus fumigatus

Walsh, T. J., Roilides, E., Cortez, K. J., Kottilil, S., Bailey, J., & Lyman, C. A. (2005) · Medical Mycology · doi:10.1080/13693780500064672 · Cited by 51 · see citing works

Multilocus sequence typing of Scedosporium apiospermum and Pseudallescheria boydii isolates from cystic fibrosis patients

Bernhardt, A., Sedlacek, L., Wagner, S., et al. (2013) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2013.05.007 · Cited by 51 · see citing works

Successful control of Scedosporium prolificans septic arthritis and probable osteomyelitis without radical surgery in a long‐term renal transplant recipient

Li, J. Y. Z., Yong, T. Y., Grove, D. I., et al. (2007) · Transplant Infectious Disease · doi:10.1111/j.1399-3062.2007.00240.x · Cited by 51 · see citing works

Matrix-assisted laser desorption ionization-time of flight mass spectrometry for fast and accurate identification of Pseudallescheria/ Scedosporium species

Sitterlé, E., Giraud, S., Leto, J., Bouchara, J. ‐., Rougeron, A., Morio, F., Dauphin, B., Angebault, C., Quesne, G., Béretti, J., et al. (2014) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12574 · Cited by 50 · see citing works

Amphotericin B lipid complex exerts additive antifungal activity in combination with polymorphonuclear leucocytes against Scedosporium prolificans and Scedosporium apiospermum

Gil‐Lamaignere, C. (2002) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkf198 · Cited by 50 · see citing works

Osteoarticular Infections Caused by Non-Aspergillus Filamentous Fungi in Adult and Pediatric Patients

Taj‐Aldeen, S. J., Rammaert, B., Gamaletsou, M. N., et al. (2015) · Medicine · doi:10.1097/md.0000000000002078 · Cited by 50 · see citing works

Pseudallescheria boydii releases metallopeptidases capable of cleaving several proteinaceous compounds

Silva, B. A., Pinto, M. R., Soares, R. M. A., Barreto‐Bergter, E., & dos Santos, A. L. S. (2006) · Research in Microbiology · doi:10.1016/j.resmic.2005.11.010 · Cited by 49 · see citing works

Glucosylceramides in Colletotrichum gloeosporioides are involved in the differentiation of conidia into mycelial cells

da Silva, A. F. C., Rodrigues, M. L., Farias, S. E., de Almeida, I. C., Pinto, M. R., & Barreto‐Bergter, E. (2004) · FEBS Letters · doi:10.1016/s0014-5793(04)00156-5 · Cited by 49 · see citing works

Fatal Scedosporiosis in Multiple Solid Organ Allografts Transmitted From a Nearly-Drowned Donor

Kim, S., Kim, S., Ha, Y. E., et al. (2015) · American Journal of Transplantation · doi:10.1111/ajt.13008 · Cited by 48 · see citing works

Case Reports. Infection due to Scedosporium apiospermum in renal transplant recipients: a report of two cases and literature review of central nervous system and cutaneous infections by Pseudallescheria boydii/Sc. apiospermum

Montejo, M., Muñiz, M., Zárraga, S., Aguirrebengoa, K., Amenábar, J., López-Soria, L., & González, R. (2002) · Mycoses (Berlin) · doi:10.1046/j.1439-0507.2002.00790.x · Cited by 48 · see citing works

Infection and colonisation due to Scedosporium in Northern Spain. An in vitro antifungal susceptibility and molecular epidemiology study of 60 isolates

Lackner, M., Rezusta, A., Villuendas, M. C., et al. (2011) · Mycoses · doi:10.1111/j.1439-0507.2011.02110.x · Cited by 48 · see citing works

In Vitro Synergistic Interaction between Amphotericin B and Micafungin against Scedosporium spp

Yustes, C., & Guarro, J. (2005) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.8.3498-3500.2005 · Cited by 48 · see citing works

Scedosporium prolificans: an emerging pathogen in France?

Grenouillet, F., Botterel, F., Crouzet, J., Larosa, F., Hicheri, Y., Forel, J., Hélias, P., Ranque, S., & Delhaes, L. (2009) · Medical Mycology · doi:10.1080/13693780802454761 · Cited by 47 · see citing works

Petriellidium boydiiInfection of the Sphenoid Sinus

Bryan, C. S., DiSalvo, A. F., Kaufman, L., et al. (1980) · American Journal of Clinical Pathology · doi:10.1093/ajcp/74.6.846 · Cited by 47 · see citing works

Selective Isolation of Pseudallescheria and Scedosporium Species from Respiratory Tract Specimens of Cystic Fibrosis Patients

Horré, R., Marklein, G., Siekmeier, R., et al. (2008) · Respiration · doi:10.1159/000167419 · Cited by 47 · see citing works

Cutaneous Scedosporium apiospermum Infection in an Immunocompromised Patient and a Review of the Literature

Uenotsuchi, T., Moroi, Y., Urabe, K., et al. (2005) · Acta Dermato Venereologica · doi:10.1080/00015550410024553 · Cited by 47 · see citing works

Optimizing Outcomes in Immunocompromised Hosts: Understanding the Role of Immunotherapy in Invasive Fungal Diseases

Ravikumar, S., Win, M. S., & Chai, L. Y. A. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01322 · Cited by 46 · see citing works

CycloBranch: De Novo Sequencing of Nonribosomal Peptides from Accurate Product Ion Mass Spectra

Novák, J., Lemr, K., Schug, K. A., et al. (2015) · Journal of the American Society for Mass Spectrometry · doi:10.1007/s13361-015-1211-1 · Cited by 45 · see citing works

Breakthrough Scedosporium prolificans infection while receiving voriconazole prophylaxis in an allogeneic stem cell transplant recipient

Tong, S. Y. C., Peleg, A. Y., Yoong, J., Handke, R., Szer, J., & Slavin, M. A. (2007) · Transplant Infectious Disease · doi:10.1111/j.1399-3062.2007.00203.x · Cited by 44 · see citing works

Tracking the Emerging Human Pathogen Pseudallescheria boydii by Using Highly Specific Monoclonal Antibodies

Thornton, C. (2009) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00061-09 · Cited by 44 · see citing works

Interaction of granulocyte colony-stimulating factor and high doses of liposomal amphotericin B in the treatment of systemic murine scedosporiosis

Ortoneda, M., Capilla, J., Pastor, F. J., et al. (2004) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2004.07.011 · Cited by 43 · see citing works

Development and Validation of a Multiplex PCR for Detection of Scedosporium spp. in Respiratory Tract Specimens from Patients with Cystic Fibrosis

Harun, A. B., Blyth, C. C., Gilgado, F., et al. (2011) · Journal of Clinical Microbiology · doi:10.1128/jcm.01810-10 · Cited by 43 · see citing works

Scedosporiosis in patients with acute leukemia: a retrospective multicenter report

Caira, M., Girmenia, C., Valentini, C. G., Sanguinetti, M., Bonini, A., Rossi, G., Fianchi, L., Leone, G. G. M., & Pagano, L. (2007) · Haematologica · doi:10.3324/haematol.11740 · Cited by 42 · see citing works

Comparison of the virulence of Scedosporium prolificans strains from different origins in a murine model.

Ortoneda, M., Pastor, F., Mayayo, E., & Guarro, J. (2002) · Journal of Medical Microbiology · doi:10.1099/0022-1317-51-11-924 · Cited by 42 · see citing works

Virulence Studies ofScedosporiumandFusariumSpecies inDrosophila melanogaster

Lamaris, G. A., Chamilos, G., Lewis, R. E., et al. (2007) · The Journal of Infectious Diseases · doi:10.1086/523765 · Cited by 41 · see citing works

TLR4 Recognizes Pseudallescheria boydii Conidia and Purified Rhamnomannans

Figueiredo, R. T., Fernández, P. L., Dutra, F. F., González, Y., Lopes, L. C. L., Bittencourt, V. C. B., Sassaki, G. L., Barreto‐Bergter, E., & Bozza, M. T. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.181255 · Cited by 41 · see citing works

Characterization of Scedosporium apiospermum Glucosylceramides and Their Involvement in Fungal Development and Macrophage Functions

Rollin‐Pinheiro, R., Liporagi-Lopes, L. C., de Meirelles, J. V., de Souza, L. M., & Barreto‐Bergter, E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098149 · Cited by 41 · see citing works

Clinical characteristics and epidemiology of pulmonary pseudallescheriasis

Kantarcıoğlu, A. S., de Hoog, G. S., & Guarro, J. (2011) · Revista Iberoamericana de Micología · doi:10.1016/j.riam.2011.04.002 · Cited by 39 · see citing works

Antifungal Activities of Posaconazole and Granulocyte-Macrophage Colony-Stimulating Factor Ex Vivo and in Mice with Disseminated Infection Due to Scedosporium prolificans

Simitsopoulou, M., Gil‐Lamaignere, C., Avramidis, N., et al. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.10.3801-3805.2004 · Cited by 39 · see citing works

A study of the growth of Pseudallescheria boydii isolates from sewage sludge and clinical sources on tributyrin, rapeseed oil, biodiesel oil and diesel oil.

Janda, K., Ulfig, K., Cano, J., et al. (2008) · PubMed · Cited by 39 · see citing works

Hydroxamate siderophores of Scedosporium apiospermum

Bertrand, S., Larcher, G., Landreau, A., Richomme, P., Duval, O., & Bouchara, J. (2009) · BioMetals · doi:10.1007/s10534-009-9253-0 · Cited by 37 · see citing works

Broad-Spectrum Biosensor Capable of Detecting and Identifying Diverse Bacterial and Candida Species in Blood

Metzgar, D., Frinder, M., Lovari, R., et al. (2013) · Journal of Clinical Microbiology · doi:10.1128/jcm.00966-13 · Cited by 37 · see citing works

Re‐identification of clinical isolates of the Pseudallescheria boydii‐complex involved in near‐drowning

Tintelnot, K., Wagner, N., Seibold, M., et al. (2008) · Mycoses · doi:10.1111/j.1439-0507.2008.01579.x · Cited by 37 · see citing works

Pathobiology of Lomentospora prolificans : could this species serve as a model of primary antifungal resistance?

Pellón, A., Ramirez‐Garcia, A., Buldain, I., Antoran, A., Martin–Souto, L., Rementerı́a, A., & Hernando, F. L. (2017) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2017.06.009 · Cited by 37 · see citing works

Cell Wall Modifications during Conidial Maturation of the Human Pathogenic Fungus Pseudallescheria boydii

Ghamrawi, S., Rénier, G., Saulnier, P., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100290 · Cited by 36 · see citing works

Glycoconjugates and polysaccharides from the Scedosporium/Pseudallescheria boydii complex: structural characterisation, involvement in cell differentiation, cell recognition and virulence

Lopes, L. C. L., Xisto, M. I. D. D. S., Bittencourt, V. C. B., et al. (2011) · Mycoses · doi:10.1111/j.1439-0507.2011.02105.x · Cited by 35 · see citing works

Effects of interleukin-15 on antifungal responses of human polymorphonuclear leukocytes against Fusarium spp. and Scedosporium spp.

Winn, R. M., Gil‐Lamaignere, C., Roilides, E., Simitsopoulou, M., Lyman, C. A., Maloukou, A., & Walsh, T. J. (2005) · Cytokine · doi:10.1016/j.cyto.2004.07.016 · Cited by 35 · see citing works

Breakthrough Disseminated Scedosporium prolificans Infection in a Patient with Relapsed Leukaemia on Prolonged Voriconazole Followed by Posaconazole Prophylaxis

Ananda-Rajah, M. R., Grigg, A., & Slavin, M. A. (2008) · Mycopathologia · doi:10.1007/s11046-008-9131-2 · Cited by 35 · see citing works

Phenotypic Profiling of Scedosporium aurantiacum, an Opportunistic Pathogen Colonizing Human Lungs

Kaur, J., Duan, S. Y., Vaas, L. A. I., Penesyan, A., Meyer, W., Paulsen, I. T., & Nevalainen, H. K. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0122354 · Cited by 34 · see citing works

Infections due to Pseudallescheria/Scedosporium species in patients with advanced HIV disease — a diagnostic and therapeutic challenge

Tammer, I., Tintelnot, K., Braun-Dullaeus, R. C., et al. (2011) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2011.03.004 · Cited by 34 · see citing works

Endocytosis of<i>Candida albicans</i>by vascular endothelial cells is associated with tyrosine phosphorylation of specific host cell proteins

Belanger, P. H., Johnston, D. A., Fratti, R. A., Zhang, M., & G. Filler, S. (2002) · Cellular Microbiology · doi:10.1046/j.1462-5822.2002.00232.x · Cited by 34 · see citing works

Human phagocytic cell responses toScedosporium prolificans

Gil‐Lamaignere, C., Maloukou, A., Rodríguez-Tudela, J. L., et al. (2001) · Medical Mycology · doi:10.1080/mmy.39.2.169.175 · Cited by 33 · see citing works

Scedosporium apiospermum in chronic granulomatous disease treated with an HLA matched bone marrow transplant: Figure 1

Gompels, M. M., Bethune, C. A., Jackson, G., et al. (2002) · Journal of Clinical Pathology · doi:10.1136/jcp.55.10.784 · Cited by 33 · see citing works

Molecular identification tools for sibling species ofScedosporiumandPseudallescheria

Lackner, M., Klaassen, C. H. W., Meis, J. F. G. M., et al. (2012) · Medical Mycology · doi:10.3109/13693786.2011.618939 · Cited by 33 · see citing works

Molecular cloning and biochemical characterization of a Cu,Zn-superoxide dismutase from Scedosporium apiospermum

de Lima, O. C., Larcher, G., Vandeputte, P., Lebouil, A., Chabasse, D., Simoneau, P., & Bouchara, J. (2007) · Microbes and Infection · doi:10.1016/j.micinf.2007.01.027 · Cited by 32 · see citing works

Unique histological characteristics of Scedosporium that could aid in its identification

Kimura, M., Maenishi, O., Ito, H., & Ohkusu, K. (2010) · Pathology international (Print) · doi:10.1111/j.1440-1827.2009.02491.x · Cited by 32 · see citing works

Targeted Disruption of Melanin Biosynthesis Genes in the Human Pathogenic Fungus Lomentospora prolificans and Its Consequences for Pathogen Survival

Al-laaeiby, A. I. E., Kershaw, M. J., Penn, T. J., & Thornton, C. R. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17040444 · Cited by 32 · see citing works

Nebulized voriconazole in infections with Scedosporium apiospermum — Case report and review of the literature

Holle, J., Leichsenring, M. L., & Meissner, P. E. (2013) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2013.10.014 · Cited by 31 · see citing works

Frequency of fungi in respiratory samples from Turkish cystic fibrosis patients

Güngör, Ö., Tamay, Z., Güler, N., & Erturan, Z. (2012) · Mycoses · doi:10.1111/j.1439-0507.2012.02221.x · Cited by 31 · see citing works

Fatal Mycotic Aneurysms Due to Scedosporium and Pseudallescheria Infection

Ong, A., Blyth, C. C., Bency, R., et al. (2011) · Journal of Clinical Microbiology · doi:10.1128/jcm.02615-10 · Cited by 31 · see citing works

The relationship between the acid and alkaline phosphatase activity and the adherence of clinical isolates of Candida parapsilosis to human buccal epithelial cells

Fernanado, P. H. R., Panagoda, G. J., & Samaranayake, L. P. (1999) · Apmis · doi:10.1111/j.1699-0463.1999.tb01507.x · Cited by 30 · see citing works

Bactericidal and Fungicidal Activity of N -Chlorotaurine Is Enhanced in Cystic Fibrosis Sputum Medium

Gruber, M., Moser, I., Nagl, M., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02527-16 · Cited by 30 · see citing works

AS-183, a novel inhibitor of acyl-CoA: Cholesterol acyltranseferase produced by Scedosporium sp. SPC-15549.

Kuroda, K., Yoshida, M., Uosaki, Y., et al. (1993) · The Journal of Antibiotics · doi:10.7164/antibiotics.46.1196 · Cited by 29 · see citing works

O-Glycosylation in Cell Wall Proteins in Scedosporium prolificans Is Critical for Phagocytosis and Inflammatory Cytokines Production by Macrophages

Xisto, M. I. D. D. S., Bittencourt, V. C. B., Liporagi-Lopes, L. C., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0123189 · Cited by 29 · see citing works

Infective endocarditis caused by Scedosporium prolificans infection in a patient with acute myeloid leukemia undergoing induction chemotherapy

Ochi, Y., Hiramoto, N., Takegawa, H., et al. (2015) · International Journal of Hematology · doi:10.1007/s12185-015-1752-x · Cited by 28 · see citing works

S cedosporium prolificans pericarditis and mycotic aortic aneurysm in a lung transplant recipient receiving voriconazole prophylaxis

Sayah, D. M., Schwartz, B. S., Kukreja, J., et al. (2013) · Transplant Infectious Disease · doi:10.1111/tid.12056 · Cited by 28 · see citing works

Infective endocarditis and meningitis due to Scedosporium prolificans in a renal transplant recipient

Uno, K., Kasahara, K., Kutsuna, S., et al. (2013) · Journal of Infection and Chemotherapy · doi:10.1016/j.jiac.2013.09.006 · Cited by 27 · see citing works

Purification and Characterization of a Mycelial Catalase from Scedosporium boydii, a Useful Tool for Specific Antibody Detection in Patients with Cystic Fibrosis

Mina, S., Marot-Leblond, A., Cimon, B., et al. (2014) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00482-14 · Cited by 27 · see citing works

Does a triple combination have better activity than double combinations against multiresistant fungi? Experimental in vitro evaluation

Martín‐Vicente, A., Guarro, J., & Capilla, J. (2017) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2016.12.015 · Cited by 27 · see citing works

Mycelial forms of Pseudallescheria boydii present ectophosphatase activities

Kiffer-Moreira, T., Pinheiro, A. A. S., Pinto, M. R., Esteves, F. F., Souto-Padrón, T. C. B. S., Barreto‐Bergter, E., & Meyer‐Fernandes, J. R. (2007) · Archives of Microbiology · doi:10.1007/s00203-007-0232-y · Cited by 26 · see citing works

Scedosporium apiospermum EUMYCETOMA SUCCESSFULLY TREATED WITH ORAL VORICONAZOLE: REPORT OF A CASE AND REVIEW OF THE BRAZILIAN REPORTS ON SCEDOSPORIOSIS

Oliveira, F. D. M., Unis, G., a, B. H., & Severo, L. C. (2013) · Revista do Instituto de Medicina Tropical de São Paulo · doi:10.1590/s0036-46652013000200010 · Cited by 26 · see citing works

Performance evaluation of multiplex PCR including Aspergillus—not so simple!: Table 1.

Alanio, A., & Bretagne, S. (2016) · Medical Mycology · doi:10.1093/mmy/myw080 · Cited by 26 · see citing works

Investigational Agents for the Treatment of Resistant Yeasts and Molds

Seiler, G. T., & Ostrosky-Zeichner, L. (2021) · Current Fungal Infection Reports · doi:10.1007/s12281-021-00419-5 · Cited by 32 · see citing works

Impaired Colonization Defence of the Oropharynx

JOHANSON, W. G. (1989) · Update in intensive care and emergency medicine · doi:10.1007/978-3-642-83752-4_7 · Cited by 3 · see citing works

Microbiological factors affecting the colonization of tomato roots byRalstonia solanacearumYU1Rif43lux

Toyota, K., Kimura, M., & Kinoshita, T. (2000) · Soil Science & Plant Nutrition · doi:10.1080/00380768.2000.10409129 · Cited by 14 · see citing works

The Influence of Climate Factor on Betula albo-sinensis's Colonization and Colonization Intensity by AMF

Li, W. (2005) · Sichuan linye ke-ji

Co-colonization with multiple different species of multidrug-resistant gram-negative bacteria

Snyder, G. M., O’Fallon, E., & D’Agata, E. M. C. (2011) · American Journal of Infection Control · doi:10.1016/j.ajic.2010.09.012 · Cited by 30 · see citing works

Environmental and genetic effects on the formation of ectomycorrhizal and arbuscular mycorrhizal associations in cottonwoods

Gehring, C. A., Mueller, R., & Whitham, T. G. (2006) · Oecologia · doi:10.1007/s00442-006-0437-9 · Cited by 153 · see citing works