Multiresistant Fusarium Pathogens on Plants and Humans: Solutions in (from) the Antifungal Pipeline?

Yaşlı Kadınlarda Üreme Sağlığı

Kokanalı, D., & Engin Üstün, Y. (n.d.) · DergiPark (Istanbul University) · Cited by 170,090 · see citing works

Two new Later Stone Age sites from the Final Pleistocene in the Falémé Valley, eastern Senegal

Ndiaye, M., Lespez, L., Tribolo, C., Rassé, M., Hadjas, I., Davidoux, S., Huysecom, É., & Douze, K. (2024) · Monash University Research Portal (Monash University) · doi:10.3929/ethz-b-000667478 · Cited by 24,015 · see citing works

The Fusarium Laboratory Manual

(2006) · Wiley eBooks · doi:10.1002/9780470278376 · Cited by 4,753 · see citing works

The Top 10 fungal pathogens in molecular plant pathology.

Dean, R., van Kan, J. V., Pretorius, Z., Hammond-Kosack, K., Pietro, A. D., Spanu, P., Rudd, J., Dickman, M., Kahmann, R., Ellis, J., et al. (2012) · Molecular plant pathology · doi:10.1111/j.1364-3703.2011.00783.x · Cited by 4,429 · see citing works

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

Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium

Ma, L., van der Does, H. C., Borkovich, K. A., Coleman, J. J., Daboussi, M., Pietro, A. D., Dufresne, M., Freitag, M., Grabherr, M. G., Henrissat, B., et al. (2010) · Nature · doi:10.1038/nature08850 · Cited by 1,762 · see citing works

Fusarium Infections in Immunocompromised Patients

Nucci, M., & Anaissie, E. J. (2007) · Clinical Microbiology Reviews · doi:10.1128/cmr.00014-07 · Cited by 979 · 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

The Genus Fusarium: A Pictorial Atlas

Gerlach, W. W. P., & Nirenberg, H. I. (1983) · Mycologia · doi:10.2307/3792677 · Cited by 716 · see citing works

Taxonomy, biology, and clinical aspects of Fusarium species

Nelson, P. E., Dignani, M. C., & Anaissie, E. (1994) · Clinical Microbiology Reviews · doi:10.1128/cmr.7.4.479 · Cited by 686 · see citing works

The Evolution of Fungicide Resistance

Lucas, J. A., Hawkins, N. J., & FRAAIJE, B. A. (2014) · Advances in applied microbiology · doi:10.1016/bs.aambs.2014.09.001 · Cited by 652 · see citing works

Efflux-Mediated Antifungal Drug Resistance

Cannon, R. D., Lamping, E., Holmes, A. R., Niimi, K., Baret, P. V., Keniya, M. V., Tanabe, K., Niimi, M., Goffeau, A., & Monk, B. C. (2009) · Clinical Microbiology Reviews · doi:10.1128/cmr.00051-08 · Cited by 608 · see citing works

Azole resistance in Aspergillus fumigatus: a side-effect of environmental fungicide use?

Verweij, P. E., Snelders, E., Kema, G. H., Mellado, E., & Melchers, W. J. (2009) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(09)70265-8 · Cited by 604 · see citing works

Infections due to emerging and uncommon medically important fungal pathogens

Walsh, T. J., Groll, A. H., Hiemenz, J., Fleming, R. V., Roilides, E., & Anaissie, E. J. (2004) · Clinical Microbiology and Infection · doi:10.1111/j.1470-9465.2004.00839.x · Cited by 600 · see citing works

Infection and Drug Resistance

Yokoyama, T., Sasaki, J., Matsumoto, K., et al. (2020) · Infection and Drug Resistance · doi:10.2147/idr · Cited by 583 · see citing works

A multicentre study of antifungal susceptibility patterns among 350 Candida auris isolates (2009–17) in India: role of the ERG11 and FKS1 genes in azole and echinocandin resistance

Chowdhary, A., Prakash, A., Sharma, C., Kordalewska, M., Kumar, A., Sarma, S., Tarai, B., Singh, A., Upadhyaya, G., Upadhyay, S., et al. (2018) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkx480 · Cited by 577 · see citing works

Itraconazole resistance in Aspergillus fumigatus

Denning, D. W., Venkateswarlu, K., Oakley, K. L., Anderson, M. J., Manning, N. J., Stevens, D. A., Warnock, D. W., & Kelly, S. L. (1997) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.41.6.1364 · Cited by 507 · see citing works

A New <i>Aspergillus fumigatus</i> Resistance Mechanism Conferring In Vitro Cross-Resistance to Azole Antifungals Involves a Combination of <i>cyp51A</i> Alterations

Mellado, E., Garcia-Effron, G., Alcázar-Fuoli, L., Melchers, W. J. G., Verweij, P. E., Cuenca-Estrella, M., & Rodríguez-Tudela, J. L. (2007) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01092-06 · Cited by 490 · see citing works

Antimicrobial Agents and Chemotherapy

Billard‐Pomares, T., Clermont, O., Castellanos, M., Magdoud, F., Royer, G., Condamine, B., Fouteau, S., Barbe, V., Roche, D., Cruveiller, S., et al. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac · Cited by 487 · see citing works

Phylogenetic analyses of RPB1 and RPB2 support a middle Cretaceous origin for a clade comprising all agriculturally and medically important fusaria

O'Donnell, K. L., Rooney, A. P., Proctor, R. H., Brown, D. W., McCormick, S. P., Ward, T. J., Frandsen, R. J. N., Lysøe, E., Rehner, S. A., Aoki, T., et al. (2013) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2012.12.004 · Cited by 481 · see citing works

Antifungal resistance: current trends and future strategies to combat

Wiederhold, N. P. (2017) · Infection and Drug Resistance · doi:10.2147/idr.s124918 · Cited by 477 · see citing works

Generic concepts in Nectriaceae

Lombard, L., van der Merwe, N. A., Groenewald, J. Z., & Crous, P. W. (2015) · Studies in Mycology · doi:10.1016/j.simyco.2014.12.002 · Cited by 462 · see citing works

Current Perspectives on Ophthalmic Mycoses

Thomas, P. A. (2003) · Clinical Microbiology Reviews · doi:10.1128/cmr.16.4.730-797.2003 · Cited by 462 · see citing works

Fusarium: Molecular Diversity and Intrinsic Drug Resistance

Al‐Hatmi, A. M. S., Meis, J. F. G. M., & de Hoog, S. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005464 · Cited by 432 · see citing works

DNA sequence-based identification of Fusarium: Current status and future directions

O'Donnell, K. L., Ward, T. J., Robert, V. A. R. G., Crous, P. W., Geiser, D. M., & Kang, S. (2015) · Phytoparasitica · doi:10.1007/s12600-015-0484-z · Cited by 426 · see citing works

Possible Environmental Origin of Resistance of <i>Aspergillus fumigatus</i> to Medical Triazoles

Snelders, E., Huis in 't Veld, R. A. G., Rijs, A. J. M. M., Kema, G. H. J., Melchers, W. J. G., & Verweij, P. E. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00231-09 · Cited by 423 · see citing works

Fungicide-Driven Evolution and Molecular Basis of Multidrug Resistance in Field Populations of the Grey Mould Fungus Botrytis cinerea

Kretschmer, M., Leroch, M., Mosbach, A., Walker, A. S., Fillinger, S., Mernke, D., Schoonbeek, H., Pradier, J., Leroux, P., Waard, M. A. D., et al. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000696 · Cited by 420 · see citing works

Antifungal Therapy: New Advances in the Understanding and Treatment of Mycosis

Scorzoni, L., de Paula e Silva, A. C. A., Marcos, C. M., Assato, P. A., de Melo, W. C. M. A., de Oliveira, H. C., Costa-Orlandi, C. B., Mendes-Giannini, M. J. S., & Fusco-Almeida, A. M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00036 · Cited by 418 · see citing works

The Case for Adopting the “Species Complex” Nomenclature for the Etiologic Agents of Cryptococcosis

Kwon-Chung, K. J., Bennett, J. E., Wickes, B. L., Meyer, W., Cuomo, C. A., Wollenburg, K. R., Bicanic, T. A., Castañeda, E., Chang, Y. C., Chen, J., et al. (2017) · mSphere · doi:10.1128/msphere.00357-16 · Cited by 401 · see citing works

Members of theFusarium solaniSpecies Complex That Cause Infections in Both Humans and Plants Are Common in the Environment

Zhang, N., O'Donnell, K. L., Sutton, D. A., Nalim, F. A., Summerbell, R. C., Padhye, A. A., & Geiser, D. M. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.00120-06 · Cited by 386 · see citing works

Emergence of Azole-Resistant Aspergillus fumigatus Strains due to Agricultural Azole Use Creates an Increasing Threat to Human Health

Chowdhary, A., Kathuria, S., Xu, J., & Meis, J. F. G. M. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003633 · Cited by 383 · see citing works

Amplification of an Esterase Gene Is Responsible for Insecticide Resistance in a California Culex Mosquito

Mouchès, C., Pasteur, N., Bergé, J. B., Hyrien, O., Michel Raymond, A., Vincent, B. R. D. S., de Silvestri, M., & Georghiou, G. P. (1986) · Science · doi:10.1126/science.3755546 · Cited by 350 · see citing works

The Mycotic Ulcer Treatment Trial

Prajna, N. V., Krishnan, T., Mascarenhas, J., Rajaraman, R., Lalitha, P., Srinivasan, M., Raghavan, A., Oldenburg, C. E., Ray, K. J., Zegans, M. E., et al. (2012) · JAMA Ophthalmology · doi:10.1001/jamaophthalmol.2013.1497 · Cited by 348 · see citing works

Clinical implications of globally emerging azole resistance in Aspergillus fumigatus

Meis, J. F. G. M., Chowdhary, A., Rhodes, J. L., Fisher, M. C., & Verweij, P. E. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0460 · Cited by 310 · see citing works

One Fungus, One Name: Defining the Genus Fusarium in a Scientifically Robust Way That Preserves Longstanding Use

Geiser, D. M., Aoki, T., Bacon, C. W., Baker, S., Bhattacharyya, M. K., Brandt, M. E., Brown, D. W., Burgess, L. W., Chulze, S., Coleman, J. J., et al. (2013) · Phytopathology · doi:10.1094/phyto-07-12-0150-le · Cited by 307 · 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

<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

Fusarium oxysporum as a Multihost Model for the Genetic Dissection of Fungal Virulence in Plants and Mammals

Ortoneda, M., Guarro, J., Madrid, M. P., Caracuel, Z., Roncero, M. I. G., Mayayo, E., & Pietro, A. D. (2004) · Infection and Immunity · doi:10.1128/iai.72.3.1760-1766.2004 · Cited by 199 · see citing works

New Horizons in Antifungal Therapy

Pianalto, K. M., & Alspaugh, J. A. (2016) · Journal of Fungi · doi:10.3390/jof2040026 · Cited by 195 · see citing works

Molecular mechanisms of pathogenicity: how do pathogenic microorganisms develop cross-kingdom host jumps?

van Baarlen, P., van Belkum, A., Summerbell, R. C., Crous, P. W., & Thomma, B. P. H. J. (2007) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2007.00065.x · Cited by 194 · see citing works

Back to the roots: a reappraisal of Neocosmospora

Sandoval‐Denis, M., Lombard, L., & Crous, P. W. (2019) · Persoonia - Molecular Phylogeny and Evolution of Fungi · doi:10.3767/persoonia.2019.43.04 · Cited by 180 · see citing works

Heteroresistance to Fluconazole in <i>Cryptococcus neoformans</i> Is Intrinsic and Associated with Virulence

Sionov, E., Chang, Y. C., Garraffo, H. M., & Kwon-Chung, K. J. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00295-09 · Cited by 179 · see citing works

Characterization of the sterol 14α‐demethylases of Fusarium graminearum identifies a novel genus‐specific CYP 51 function

Fan, J., Urban, M., Parker, J. E., Brewer, H. C., Kelly, S. L., Hammond-Kosack, K. E., FRAAIJE, B. A., Liu, X., & Cools, H. J. (2013) · New Phytologist · doi:10.1111/nph.12193 · Cited by 175 · see citing works

Parallels in Fungal Pathogenesis on Plant and Animal Hosts

Sexton, A., & Howlett, B. J. (2006) · Eukaryotic Cell · doi:10.1128/ec.00277-06 · Cited by 173 · see citing works

Phylogenetic relationships among members of the Fusarium solani species complex in human infections and the descriptions of F. keratoplasticum sp. nov. and F. petroliphilum stat. nov.

Short, D. P. G., O'Donnell, K. L., Thrane, U., Nielsen, K. F., Zhang, N., Juba, J. H., & Geiser, D. M. (2013) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2013.01.004 · Cited by 164 · 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

Exchange of core chromosomes and horizontal transfer of lineage‐specific chromosomes in Fusarium oxysporum

Vlaardingerbroek, I., Beerens, B., Rose, L., Fokkens, L., Cornelissen, B. J. C., & Rep, M. (2016) · Environmental Microbiology · doi:10.1111/1462-2920.13281 · Cited by 135 · see citing works

Genes encoding multiple drug resistance-like proteins in Aspergillus fumigatus and Aspergillus flavus

Tobin, M. B., Peery, R. B., & Skatrud, P. L. (1997) · Gene · doi:10.1016/s0378-1119(97)00281-3 · Cited by 129 · see citing works

Current antifungal treatment of fusariosis

Al‐Hatmi, A. M. S., Bonifáz, A., Ranque, S., de Hoog, S., Verweij, P. E., & Meis, J. F. G. M. (2017) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2017.06.017 · Cited by 123 · see citing works

New species from the Fusarium solani species complex derived from perithecia and soil in the Old World tropics

Nalim, F. A., Samuels, G. J., Wijesundera, R. L. C., & Geiser, D. M. (2011) · Mycologia · doi:10.3852/10-307 · Cited by 118 · see citing works

Three Fusarium oxysporum mitogen‐activated protein kinases (MAPKs) have distinct and complementary roles in stress adaptation and cross‐kingdom pathogenicity

Segorbe, D., Pietro, A. D., Pérez‐Nadales, E., & Turrà, D. (2016) · Molecular Plant Pathology · doi:10.1111/mpp.12446 · Cited by 116 · see citing works

Epitypification of Fusisporium ( Fusarium ) solani and its assignment to a common phylogenetic species in the Fusarium solani species complex

Schroers, H., Samuels, G. J., Zhang, N., Short, D. P. G., Juba, J. H., & Geiser, D. M. (2016) · Mycologia · doi:10.3852/15-255 · Cited by 112 · see citing works

In Vitro and In Vivo Antifungal Activities of T-2307, a Novel Arylamidine

Mitsuyama, J., Nomura, N., Hashimoto, K., Yamada, E., Nishikawa, H., Kaeriyama, M., Kimura, A., Todo, Y., & Narita, H. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01159-07 · Cited by 111 · see citing works

Profile of isavuconazole and its potential in the treatment of severe invasive fungal infections

Pasqualotto, A. C., & Falci, D. R. (2013) · Infection and Drug Resistance · doi:10.2147/idr.s51340 · Cited by 110 · see citing works

The Membrane Mucin Msb2 Regulates Invasive Growth and Plant Infection in Fusarium oxysporum

Pérez‐Nadales, E., & Pietro, A. D. (2011) · The Plant Cell · doi:10.1105/tpc.110.075093 · Cited by 110 · see citing works

Development of a novel multiplex DNA microarray for Fusarium graminearum and analysis of azole fungicide responses

Becher, R., Weihmann, F., Deising, H. B., & Wirsel, S. G. R. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-52 · Cited by 110 · see citing works

Crossover fungal pathogens: The biology and pathogenesis of fungi capable of crossing kingdoms to infect plants and humans

Gauthier, G. M., & Keller, N. P. (2013) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2013.08.016 · Cited by 107 · see citing works

Specific antifungal susceptibility profiles of opportunists in the Fusarium fujikuroi complex

Al‐Hatmi, A. M. S., van Diepeningen, A. D., Curfs-Breuker, I., de Hoog, S., & Meis, J. F. G. M. (2014) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dku505 · Cited by 107 · see citing works

Antifungal Activities of SCY-078 (MK-3118) and Standard Antifungal Agents against Clinical Non-Aspergillus Mold Isolates

Lamoth, F., & Alexander, B. D. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00234-15 · Cited by 100 · see citing works

Activity of MK-3118, a new oral glucan synthase inhibitor, tested against Candida spp. by two international methods (CLSI and EUCAST)

Pfaller, M. A., Messer, S. A., Motyl, M. R., Jones, R. N., & Castanheira, M. (2012) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dks466 · Cited by 99 · see citing works

T-2307 Causes Collapse of Mitochondrial Membrane Potential in Yeast

Shibata, T., Takahashi, T., Yamada, E., Kimura, A., Nishikawa, H., Hayakawa, H., Nomura, N., & Mitsuyama, J. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05954-11 · Cited by 99 · 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

Fungi between extremotolerance and opportunistic pathogenicity on humans

Gostinčar, C., Zajc, J., Lenassi, M., Plemenitaš, A., de Hoog, S., Al‐Hatmi, A. M. S., & Gunde‐Cimerman, N. (2018) · Fungal Diversity · doi:10.1007/s13225-018-0414-8 · Cited by 97 · see citing works

In Vitro and In Vivo Antimalarial Activities of T-2307, a Novel Arylamidine

Kimura, A., Nishikawa, H., Nomura, N., Mitsuyama, J., Fukumoto, S., Inoue, N., & Kawazu, S. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.05856-11 · Cited by 93 · see citing works

ASP2397: a novel antifungal agent produced by Acremonium persicinum MF-347833

Nakamura, I., Yoshimura, S., Masaki, T., Takase, S., Ohsumi, K., Hashimoto, M., Furukawa, S., & Fujie, A. (2016) · The Journal of Antibiotics · doi:10.1038/ja.2016.107 · Cited by 85 · see citing works

The Celecoxib Derivative AR-12 Has Broad-Spectrum Antifungal Activity <i>In Vitro</i> and Improves the Activity of Fluconazole in a Murine Model of Cryptococcosis

Koselny, K., Green, J., DiDone, L., Halterman, J. P., Fothergill, A. W., Wiederhold, N. P., Patterson, T. F., Cushion, M. T., Rappelye, C., Wellington, M., et al. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01061-16 · Cited by 83 · see citing works

Newer topical treatments in skin and nail dermatophyte infections

Dogra, S., Sahni, K., & Singh, S. (2018) · Indian Dermatology Online Journal · doi:10.4103/idoj.idoj_281_17 · Cited by 81 · see citing works

The ‘forma specialis’ issue in Fusarium: A case study in Fusarium solani f. sp. pisi

Šišić, A., Baćanović-Šišić, J., Al‐Hatmi, A. M. S., Karlovský, P., Ahmed, S. A., Maier, W., de Hoog, S., & Finckh, M. R. (2018) · Scientific Reports · doi:10.1038/s41598-018-19779-z · Cited by 80 · see citing works

Natamycin in the treatment of fungal keratitis: a systematic review and Meta-analysis.

Qiu, S., Zhao, G., Lin, J., Wang, X., Hu, L., Du, Z.-D., Wang, Q., & Zhu, C.-C. (2015) · PubMed Central · doi:10.3980/j.issn.2222-3959.2015.03.29 · Cited by 78 · see citing works

Spectrum ofFusariuminfections in tropical dermatology evidenced by multilocus sequencing typing diagnostics

van Diepeningen, A. D., Feng, P., Ahmed, S. A., Sudhadham, M., Bunyaratavej, S., & de Hoog, S. (2014) · Mycoses · doi:10.1111/myc.12273 · Cited by 77 · 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

Molecular Characterization and Antifungal Susceptibility of Clinical Fusarium Species From Brazil

Herkert, P. F., Al‐Hatmi, A. M. S., Salvador, G. L. D. O., Muro, M. D., Pinheiro, R. L., Nucci, M., Queiroz‐Telles, F., de Hoog, S., & Meis, J. F. G. M. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00737 · Cited by 76 · see citing works

EUCAST Determination of Olorofim (F901318) Susceptibility of Mold Species, Method Validation, and MICs

Jørgensen, K. M., Astvad, K. M. T., Hare, R. K., & Arendrup, M. C. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00487-18 · Cited by 75 · see citing works

Superficial skin lesions positive for Fusarium are associated with subsequent development of invasive fusariosis

Varon, A. G., Nouér, S. A., Barreiros, G., Trope, B. M., Magalhães, F., Akiti, T., Garnica, M. M., & Nucci, M. (2013) · Journal of Infection · doi:10.1016/j.jinf.2013.08.011 · Cited by 70 · see citing works

Reversible fluconazole resistance in Candida albicans: a potential in vitro model

Calvet, H. M., Yeaman, M. R., & Filler, S. G. (1997) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.41.3.535 · Cited by 68 · see citing works

Role for Fks1 in the Intrinsic Echinocandin Resistance of Fusarium solani as Evidenced by Hybrid Expression in Saccharomyces cerevisiae

Katiyar, S. K., & Edlind, T. D. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00020-09 · 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

In vitrocombinations of natamycin with voriconazole, itraconazole and micafungin against clinicalFusariumstrains causing keratitis: Table 1.

Al‐Hatmi, A. M. S., Meletiadis, J., Curfs-Breuker, I., Bonifáz, A., Meis, J. F. G. M., & de Hoog, S. (2015) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkv421 · Cited by 67 · see citing works

Galleria mellonella as model host for the trans-kingdom pathogen Fusarium oxysporum

Navarro‐Velasco, G. Y., Prados‐Rosales, R., Ortiz‐Urquiza, A., Quesada‐Moraga, E., & Pietro, A. D. (2011) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2011.08.004 · Cited by 65 · see citing works

Antitumor/Antifungal Celecoxib Derivative AR-12 is a Non-Nucleoside Inhibitor of the ANL-Family Adenylating Enzyme Acetyl CoA Synthetase

Koselny, K., Green, J., Favazzo, L. J., Glazier, V. E., DiDone, L., Ransford, S. T., & Krysan, D. J. (2016) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.5b00134 · Cited by 60 · see citing works

Emergence of azole resistant Aspergillus fumigatus and One Health: time to implement environmental stewardship

Chowdhary, A., & Meis, J. F. G. M. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14055 · Cited by 59 · see citing works

Fusarium allergic fungal sinusitis

Wickern, G. M. (1993) · Journal of Allergy and Clinical Immunology · doi:10.1016/0091-6749(93)90087-v · Cited by 51 · see citing works

Airborne transmission of invasive fusariosis in patients with hematologic malignancies

Moretti, M. L., Busso-Lopes, A. F., Tararam, C. A., Moraes, R., Muraosa, Y., Mikami, Y., Gonoi, T., Taguchi, H., Lyra, L., Reichert‐Lima, F., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0196426 · Cited by 50 · see citing works

Efficacy of Luliconazole Against Broad-Range Filamentous Fungi Including Fusarium solani Species Complex Causing Fungal Keratitis

Todokoro, D., Suzuki, T., Tamura, T., Makimura, K., Yamaguchi, H., Inagaki, K., & Akiyama, H. (2018) · Cornea · doi:10.1097/ico.0000000000001812 · Cited by 49 · see citing works

Keratitis by Fusarium temperatum, a novel opportunist

Al‐Hatmi, A. M. S., Bonifáz, A., de Hoog, S., Vázquez-Maya, L., García-Carmona, K., Meis, J. F. G. M., & van Diepeningen, A. D. (2014) · BMC Infectious Diseases · doi:10.1186/s12879-014-0588-y · Cited by 45 · see citing works

Fungicide-driven alterations in azole-resistantAspergillus fumigatusare related to vegetable crops in Colombia, South America

Álvarez, C., Lavergne, R., Hagen, F., Morio, F., Meis, J. F. G. M., & Pape, P. L. (2019) · Mycologia · doi:10.1080/00275514.2018.1557796 · Cited by 45 · see citing works

Isavuconazole for treatment of invasive fungal diseases caused by more than one fungal species

Marty, F. M., Cornely, O. A., Mullane, K. M., Ostrosky‐Zeichner, L., Maher, R., Croos‐Dabrera, R., Lu, Q., Lademacher, C., Oren, I., Schmitt-Hoffmann, A.-H., et al. (2018) · Mycoses · doi:10.1111/myc.12777 · Cited by 38 · see citing works

Fusarium spp. is able to grow and invade healthy human nails as a single source of nutrients

Galletti, J., Negri, M., Grassi, F. L., Kioshima, É. S., & Svidzinski, T. I. E. (2015) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-015-2410-1 · Cited by 37 · see citing works

In Vitro Activity of Chlorhexidine Compared with Seven Antifungal Agents against 98 Fusarium Isolates Recovered from Fungal Keratitis Patients

dos Santos, C. O., Kolwijck, E., van der Lee, H. A., Tehupeiory-Kooreman, M. C., Al‐Hatmi, A. M. S., Matayan, E., Burton, M. J., Eggink, C. A., & Verweij, P. E. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02669-18 · Cited by 35 · see citing works

Natamycin in the treatment of fungal keratitis : a systematic review and Meta-analysis

Sheng, S., Qiu, Gui-Qiu, Zhao, Jing, Lin, L., Xue, Wang, Li-Ting, Hu, et al. (2015) · Acta Scientiarum Naturalium Universitatis Sunyatseni · Cited by 35 · see citing works

Efficacy of Liposomal Amphotericin B in Treatment of Systemic Murine Fusariosis

Ortoneda, M., Capilla, J., Pastor, F., Pujol, I., & Guarro, J. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.7.2273-2275.2002 · Cited by 32 · see citing works

Fusarium solani species complex isolates conspecific with Fusarium solani f. sp. cucurbitae race 2 from naturally infected human and plant tissue and environmental sources are equally virulent on plants, grow at 37°C and are interfertile

Mehl, H. L., & Epstein, L. (2007) · Environmental Microbiology · doi:10.1111/j.1462-2920.2007.01333.x · Cited by 32 · see citing works

Potent Activities of Luliconazole, Lanoconazole, and Eight Comparators against Molecularly Characterized Fusarium Species

Abastabar, M., Al‐Hatmi, A. M. S., Moghaddam, M. V., de Hoog, S., Haghani, I., Âghili, S. R., Shokohi, T., Hedayati, M. T., Ghazvini, R. D., Kachuei, R., et al. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00009-18 · Cited by 32 · see citing works

Grundlagen einer Monographie der Gattung Fusarium (Link).

Appel, O., & Wollenweber, H. (1913) · OpenAgrar · Cited by 32 · see citing works

Murine Model for Fusarium oxysporum Invasive Fusariosis Reveals Organ-Specific Structures for Dissemination and Long-Term Persistence

Schäfer, K., Pietro, A. D., Gow, N. A. R., & MacCallum, D. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089920 · Cited by 27 · see citing works

An Assessment of In Vitro Antifungal Activities of Efinaconazole and Itraconazole against Common Non-Dermatophyte Fungi Causing Onychomycosis

Tupaki‐Sreepurna, A., Jishnu, B. T., Thanneru, V., Sharma, S., Gopi, A., Sundaram, M., & Kindo, A. J. (2017) · Journal of Fungi · doi:10.3390/jof3020020 · Cited by 27 · see citing works

Outcomes of patients with invasive fusariosis who undergo further immunosuppressive treatments, is there a role for secondary prophylaxis?

Nucci, M., Shoham, S., Abdala, E., Hamerschlak, N., Rico, J. C., Forghieri, F., Nouér, S. A., Cappellano, P., Solza, C., Gonzaga, Y. B. D. M., et al. (2019) · Mycoses · doi:10.1111/myc.12901 · Cited by 23 · see citing works

Fusarium volatile, a new potential pathogen from a human respiratory sample

Al‐Hatmi, A. M. S., Sandoval‐Denis, M., Nabet, C., Ahmed, S. A., Demar, M., Normand, A., & de Hoog, S. (2019) · Fungal Systematics and Evolution · doi:10.3114/fuse.2019.04.09 · Cited by 17 · see citing works

Mycotic Keratitis Caused by Fusarium solani sensu stricto (FSSC5): A Case Series

Boral, H., van Diepeningen, A., Erdem, E., Yağmur, M., de Hoog, S., İlkit, M., Meis, J. F. G. M., & Al‐Hatmi, A. M. S. (2018) · Mycopathologia · doi:10.1007/s11046-018-0280-7 · Cited by 16 · see citing works

Natamycin and Voriconazole Exhibit Synergistic Interactions with Nonantifungal Ophthalmic Agents against Fusarium Species Ocular Isolates

Rees, C. A., Bao, R., Zegans, M. E., & Cramer, R. A. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02505-18 · Cited by 15 · see citing works

In Vitro Efficacy of Chlorhexidine and a riboflavin/UVA Combination on Fungal Agents of Keratitis

Kunt, Z., Yağmur, M., Kandemir, H., Harbiyeli, I., Erdem, E., Kalkancı, A., de Hoog, S., & İlkit, M. (2019) · Current Eye Research · doi:10.1080/02713683.2019.1652916 · Cited by 8 · see citing works

The Fusaria; their description, injurious effects, and control.

Wollenweber, H. W., & Recking, O. A. (1935) · Cited by 6 · see citing works

Outcomes in Patients with Invasive Mold Disease Caused by Fusarium or Scedosporium spp. Treated with Isavuconazole: Experience from the VITAL and SECURE Trials

Cornely, O. A., Ostrosky-Zeichner, L., Rahav, G., Maher, R., Zeiher, B. G., Lee, M., & Perfect, J. R. (2015) · Kölner Universitäts PublikationsServer (Universität zu Köln) · Cited by 6 · see citing works

Azole resistance is related to overexpression of the CYP51 gene in Mycosphaerella fijiensis

Díaz-Trujillo, C., da Cunha, V. C., Chong, P., Kema, G. H. J., Arango-Isaza, R., Guzman, M. S., Stergiopoulos, I., & WIT, P. J. G. M. D. (2011) · Socio-Environmental Systems Modeling · Cited by 1 · see citing works

Review of the Novel Investigational Antifungal Olorofim

Wiederhold, N. P. (2020) · Journal of Fungi · doi:10.3390/jof6030122 · Cited by 155 · see citing works

Microbial diversity in soils suppressive to Fusarium diseases

Todorović, I., Moënne-Loccoz, Y., Raičević, V., Jovičić-Petrović, J., & Muller, D. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1228749 · Cited by 105 · see citing works

FUSARIUM-ID v.3.0: An Updated, Downloadable Resource for Fusarium Species Identification

Torres-Cruz, T. J., Whitaker, B. K., Proctor, R. H., Broders, K. D., Laraba, I., Kim, H.-S., Brown, D. W., O’Donnell, K., Estrada-Rodríguez, T. L., Lee, Y.-H., et al. (2021) · Plant Disease · doi:10.1094/pdis-09-21-2105-sr · Cited by 112 · see citing works

No to Neocosmospora : Phylogenomic and Practical Reasons for Continued Inclusion of the Fusarium solani Species Complex in the Genus Fusarium

O'Donnell, K. L., Al‐Hatmi, A. M. S., Aoki, T., Brankovics, B., Cano, J., Coleman, J. J., de Hoog, S., Pietro, A. D., Frandsen, R. J. N., Geiser, D. M., et al. (2020) · mSphere · doi:10.1128/msphere.00810-20 · Cited by 111 · see citing works

A One Health Perspective to Recognize Fusarium as Important in Clinical Practice

Saenz, V., Álvarez, C., Pape, P. L., Restrepo, S., Guarro, J., & Ramírez, A. M. C. (2020) · Journal of Fungi · doi:10.3390/jof6040235 · Cited by 79 · see citing works

Ten decadal advances in fungal biology leading towards human well-being

Mapook, A., Hyde, K. D., Hassan, K., Kemkuignou, B. M., Čmoková, A., Surup, F., Kuhnert, E., Paomephan, P., Cheng, T., de Hoog, S., et al. (2022) · Fungal Diversity · doi:10.1007/s13225-022-00510-3 · Cited by 72 · see citing works

Fungicide resistance in Fusarium species: exploring environmental impacts and sustainable management strategies

Naqvi, S. A. H., Farhan, M., Ahmad, M., Kiran, R., Shahbaz, M., Abbas, A., Hakim, F., Shabbir, M., Tan, Y. S., & Sathiya Seelan, J. S. (2025) · Archives of Microbiology · doi:10.1007/s00203-024-04219-6 · Cited by 61 · see citing works

Review of the novel antifungal drug olorofim (F901318)

Vanbiervliet, Y., Nieuwenhuyse, T. V., Aerts, R., Lagrou, K., Spriet, I., & Maertens, J. A. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-10143-3 · Cited by 46 · see citing works

Dry root rot disease, an emerging threat to citrus industry worldwide under climate change: A review

Ezrari, S., Radouane, N., Tahiri, A., Housni, Z. E., Mokrını, F., Özer, G., Lazraq, A., Belabess, Z., Amiri, S., & Lahlali, R. (2021) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2021.101753 · Cited by 41 · 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

Emerging Diagnostics and Therapeutics for Invasive Fungal Infections

Friedman, D. Z. P., & Schwartz, I. S. (2023) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2023.05.001 · Cited by 23 · see citing works

Crossover between the control of fungal pathogens in medicine and the wider environment, and the threat of antifungal resistance

Gisi, U. (2021) · Plant Pathology · doi:10.1111/ppa.13429 · Cited by 18 · see citing works

Microplastics affect soil-plant system: Implications for rhizosphere biology and fitness of sage (Salvia officinalis L.)

Ranauda, M. A., Zuzolo, D., Maisto, M., Tartaglia, M., Scarano, P., Prigioniero, A., Sciarrillo, R., & Guarino, C. (2024) · Environmental Pollution · doi:10.1016/j.envpol.2024.123656 · Cited by 17 · see citing works

Assessment of Genetic Diversity and the Population Structure of Species from the Fusarium fujikuroi Species Complex Causing Fusarium Stalk Rot of Maize

Jambhulkar, P. P., Bajpai, R., Harish, J., Tripathy, P. S., Rout, A. K., Varun, P., Behera, B. K., Lakshman, D. K., & Mallikarjuna, N. (2024) · Journal of Fungi · doi:10.3390/jof10080574 · Cited by 17 · see citing works

Silent invaders: the hidden threat of asymptomatic phytobiomes to forest biosecurity

Tanney, J. B., Kemler, M., Vivas, M., Wingfield, M. J., & Slippers, B. (2025) · New Phytologist · doi:10.1111/nph.70209 · Cited by 16 · see citing works

Fungal Genomics in Respiratory Medicine: What, How and When?

Brackin, A. P., Hemmings, S., Fisher, M. C., & Rhodes, J. L. (2021) · Mycopathologia · doi:10.1007/s11046-021-00573-x · Cited by 15 · see citing works

Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review

de Queiroz, J. C. E., Leite, J. R. S. A., & Vasconcelos, A. G. (2023) · Antibiotics · doi:10.3390/antibiotics12030427 · Cited by 15 · see citing works

Discovery of a Novel Lineage Burkholderia cepacia ST 1870 Endophytically Isolated from Medicinal Polygala paniculata Which Shows Potent In Vitro Antileishmanial and Antimicrobial Effects

Cruz, F. D. P. N., de Paula, A. F., Nogueira, C. T., de Andrade, P. H. M., Borges, L. M., Lacava, P. T., Camargo, I. L. B. D. C., Aníbal, F. D. F., & de Sousa, C. P. (2021) · International Journal of Microbiology · doi:10.1155/2021/6618559 · Cited by 14 · see citing works

In Vitro Antifungal Susceptibility Profile of Miltefosine against a Collection of Azole and Echinocandins Resistant Fusarium Strains

Nosratabadi, M., Akhtari, J., Faeli, L., Haghani, I., Âghili, S. R., Shokohi, T., Hedayati, M. T., Zarrinfar, H., Mohammadi, R., Najafzadeh, M. J., et al. (2022) · Journal of Fungi · doi:10.3390/jof8070709 · Cited by 14 · see citing works

Biofilm Formation in Clinical Isolates of Fusarium

Zhang, R., Wiederhold, N. P., Calderone, R., & Li, D. (2024) · Journal of Fungi · doi:10.3390/jof10110766 · Cited by 11 · see citing works

Climate change: shifting boundaries of fungal disease in Europe and beyond

Bottery, M. J., Sedik, S., Schwartz, I. S., Hoenigl, M., & van Rhijn, N. (2025) · Thorax · doi:10.1136/thorax-2024-222168 · Cited by 13 · see citing works

Phylogenetic Analysis of Clinically Relevant Fusarium Species in Iran

Najafzadeh, M. J., Dolatabadi, S., de Hoog, S., Esfahani, M. K., Haghani, I., Âghili, S. R., Ghazvini, R. D., Rezaei‐Matehkolaei, A., Abastabar, M., & Al‐Hatmi, A. M. S. (2020) · Mycopathologia · doi:10.1007/s11046-020-00460-x · Cited by 11 · see citing works

Fusariosis: an update on therapeutic options for management

Yazidi, L. S. A., & Al‐Hatmi, A. M. S. (2021) · Expert Opinion on Orphan Drugs · doi:10.1080/21678707.2021.1904394 · Cited by 9 · see citing works

Species Diversity in the Fusarium solani (Neocosmospora) Complex and Their Pathogenicity for Plants and Humans

Соколова, Г. Д., Budynkov, N. I., Евгеньевна, Ц. Е., & Glinushkin, A. P. (2022) · Doklady Biological Sciences · doi:10.1134/s0012496622060217 · Cited by 7 · see citing works

The Ecological Strategy Determines the Response of Fungi to Stress: A Study of the 2,4‐diacetylphloroglucinol Activity Against Aspergillus and Fusarium Species

Stepanov, A. A., Shulaev, N. А., & Vasilchenko, A. S. (2024) · Journal of Basic Microbiology · doi:10.1002/jobm.202400334 · Cited by 7 · see citing works

Response in barley roots during interaction with Bacillus subtilis and Fusarium graminearum

Reyna, M., Macor, E. P., Vilchez, A. C., & Villasuso, A. L. (2022) · Biological Control · doi:10.1016/j.biocontrol.2022.105128 · Cited by 7 · see citing works

In vitro antifungal susceptibility profile of Iranian Fusarium isolates: Emphasising on the potent inhibitory effect of efinaconazole compared to other drugs

Nosratabadi, M., Faeli, L., Haghani, I., Mohammadi, R., Khodavaisy, S., Kachuei, R., Katiraee, F., Âghili, S. R., Shokohi, T., Hedayati, M. T., et al. (2022) · Mycoses · doi:10.1111/myc.13550 · Cited by 6 · see citing works

The Multifaceted Menace of Fusarium as a Plant, Animal, and Human Pathogen

Abeysinghe, K. C., Madhushan, A., Ismail, A. M., Ilyukhin, E., & Maharachchikumbura, S. S. N. (2026) · Biology · doi:10.3390/biology15060453 · Cited by 5 · see citing works

Endophthalmitis as the initial manifestation of invasive fusariosis in an allogeneic stem cell transplant patient: A case report

Kao, A. S., Cramer‐Bour, C., Kupsky, W. J., & Soubani, A. O. (2023) · Medical Mycology Case Reports · doi:10.1016/j.mmcr.2023.02.004 · Cited by 5 · see citing works

Antifungal activity of a novel synthetic polymer M451 against phytopathogens

Tetz, V., Kardava, K. M., Krasnov, K. A., Vecherkovskaya, M. F., & Tetz, G. V. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1176428 · Cited by 5 · see citing works

Essential oils of thyme ( Thymus vulgaris ) and oregano ( Origanum vulgare ) as an alternative for the control of pesticide‐resistant Fusarium spp . in quinoa seeds

Fonseca-Guerra, I. R., Posada, A. M. V., Rozo, M. E. B., & Pineda, M. E. B. (2024) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.13993 · Cited by 3 · see citing works

Diethyl 2-((aryl(alkyl)amino)methylene)malonates: Unreported Mycelial Growth Inhibitors against Fusarium oxysporum

Cely-Veloza, W., Quiroga, D., & Coy-Barrera, E. D. (2023) · Molbank · doi:10.3390/m1630 · Cited by 2 · see citing works

Evaluation of antifungal potentials of Albizia kalkora extract as a natural fungicide: In vitro and computational studies

Hassan, A., Zaib, S., & Anjum, T. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107561 · Cited by 2 · see citing works

Fusarium spp. causing invasive disease in humans: A case series from north India

Gourav, S., Mishra, H., Xess, I., Bhalla, A. S., Chandola, S., Gupta, S., Appasami, K. P., Shukla, B. D., Bakhshi, S., Manhas, A., et al. (2024) · Medical Mycology · doi:10.1093/mmy/myae111 · Cited by 2 · see citing works

Medical Fusarium: novel species or uncertain identifications?

Song, Y., Hu, S., de Hoog, S., Liu, X., Meng, X., Xue, R., van Diepeningen, A. D., Fokkens, L., Li, R., & Gao, S. (2023) · Mycosphere · doi:10.5943/mycosphere/14/1/27 · Cited by 2 · see citing works

Bioremediation for Global Environmental Conservation [Working Title]

Shiomi, N., Zambare, V., & Din, M. F. M. (2023) · Environmental sciences · doi:10.5772/intechopen.107789 · Cited by 2 · see citing works

Antifungal and fungicide susceptibility of clinical, animal, and environmental Fusarium and Neocosmospora species from Colombia: a one-health approach

Saenz, V., Lizcano-Salas, A. F., Pape, P. L., & Ramírez, A. M. C. (2025) · Scientific Reports · doi:10.1038/s41598-025-32234-0 · Cited by 1 · see citing works

Aromatic Plants: Alternatives for Management of Crop Pathogens and Ideal Candidates for Phytoremediation of Contaminated Land

Banda, M. F., Munyengabe, A., & Augustyn, W. A. (2023) · Environmental sciences · doi:10.5772/intechopen.112214 · Cited by 1 · see citing works

In vitro antifungal activity of biosynthesized selenium nanoparticles using plant extracts and six comparators against clinical Fusarium strains.

Nosratabadi, M., Ebrahimzadeh, M. A., Alizadeh, S. R., Haghani, I., Faeli, L., Barough, R. E., Al‐Hatmi, A. M. S., & Abastabar, M. (2023) · PubMed Central · doi:10.22034/cmm.2024.345189.1504 · Cited by 1 · see citing works

The use of selenium nanoparticles from Bacillus licheniformis AD70 to enhance cucumber defense genes against Fusarium root and stem rot disease and increase antifungal activity, antioxidant stability, and fruit yield

Husnain, L. A., Almutairi, H. H., Khalil, F. M. A., Alamoudi, S. A., Alshaharni, M. O., Ahmed, A. F., Omar, B. A., Elakkad, H. A., Attia, S., & Nader, M. M. (2025) · Journal of Plant Pathology · doi:10.1007/s42161-025-01932-z · Cited by 1 · see citing works

Control of malting barley Fusarium head blight by bioagents

Gazdík, Z., Vymětal, T., Koprna, R., Lojková, L., & Cerkal, R. (2023) · Kvasny Prumysl · doi:10.18832/kp2023.69.747 · Cited by 1 · see citing works

Etiologic Structure of Fungi Isolated in Children with Oncohematological Diseases in Removed Central Venous Catheters and Assessment of the Role of Fungal Pathogens in the Development of Catheter-Associated Infections of Bloodstream

Черновецкий, М. А., & Кондаурова, С. Л. (2022) · Лабораторная диагностика Восточная Европа · doi:10.34883/pi.2022.11.4.004

Identification and antifungal sensitivity of Fusarium species isolated from piscine hosts

Khangembam, V., Thakuria, D., Tandel, R., Pant, V., Pandey, N., & Pandey, P. (2024) · Diseases of Aquatic Organisms · doi:10.3354/dao03809

Antifungal activity of AR-12 and its derivatives against clinically relevant fusarium solani isolates in keratitis

Ma, Y., Han, L., Wang, Y., Jiang, S., & Gao, X. (2026) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2026.109516

Emerging Antifungal Resistance in Ocular Infections

de Oliveira, H. C., Tabuse, A. M., Höfling-Lima, A. L., & Rodrigues, A. M. (2026) · Springer eBooks · doi:10.1007/978-3-032-19923-2_3

Atividade de ZnO e NiO obtidos pelo método de coprecipitação química frente a bactérias e fungos filamentosos

Santos, P. R. D. O., das Neves, M. R. M., & de Brito, D. F. (2026) · Research Society and Development · doi:10.33448/rsd-v15i7.51459

A Multifactorial Azole Response in Clinically Relevant Fusarium Species Complexes

Barião, P. H. G., Tonani, L., Alves, A. R., de Almeida, O. G. G., Santos, C., & Kress, M. R. V. Z. (2026) · Mycoses · doi:10.1111/myc.70220

Current antifungal treatment of fusariosis

Al‐Hatmi, A. M. S., Bonifáz, A., Ranque, S., de Hoog, S., Verweij, P. E., & Meis, J. F. G. M. (2017) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2017.06.017 · Cited by 123 · see citing works

Fusariosis: an update on therapeutic options for management

Yazidi, L. S. A., & Al‐Hatmi, A. M. S. (2021) · Expert Opinion on Orphan Drugs · doi:10.1080/21678707.2021.1904394 · Cited by 9 · see citing works

Fusariosis: Taxonomy and treatment

Josep, G. (2015) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2015.02.002

Human fusariosis: An emerging infection that is difficult to treat

Batista, B. G., de Chaves, M. A., Reginatto, P., Saraiva, O. J., & Fuentefría, A. M. (2020) · Revista da Sociedade Brasileira de Medicina Tropical · doi:10.1590/0037-8682-0013-2020 · Cited by 143 · see citing works

Opportunistic fusarial infections in humans

Guarro, J., & Gené, J. (1995) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/bf01690988 · Cited by 200 · see citing works