The Asthma Epidemic

Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys

Asher, M. I., Montefort, S., Björkstén, B., Lai, C. K., Strachan, D. P., Weiland, S. K., & Williams, H. (2006) · The Lancet · doi:10.1016/s0140-6736(06)69283-0 · Cited by 4,223

Occupational Asthma

O’Hollaren, M. T., Bardana, E. J., & Montanaro, A. J. (1991) · Cited by 1,360

Prevalence of Asthma and Atopy in Two Areas of West and East Germany

von Mutius, E., Martinez, F. D., Fritzsch, C., Nicolai, T., Roell, G., & Hh, T. (1994) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.149.2.8306030 · Cited by 897

Changes in asthma prevalence: two surveys 15 years apart.

Burr, M. L., Butland, B. K., King, S., & Vaughan‐Williams, E. (1989) · Archives of Disease in Childhood · doi:10.1136/adc.64.10.1452 · Cited by 859

Perennial allergen sensitisation early in life and chronic asthma in children: a birth cohort study

Illi, S., von Mutius, E., Lau, S., Niggemann, B., Grüber, C., & Wahn, U. (2006) · The Lancet · doi:10.1016/s0140-6736(06)69286-6 · Cited by 720

Early exposure to house-dust mite and cat allergens and development of childhood asthma: a cohort study

Lau, S., Illi, S., Sommerfeld, C., Niggemann, B., Bergmann, R. L., von Mutius, E., & Wahn, U. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02842-7 · Cited by 701

Incidence and prognosis of asthma and wheezing illness from early childhood to age 33 in a national British cohort

Strachan, D. P., Butland, B. K., & ANDERSON, H. R. (1996) · BMJ · doi:10.1136/bmj.312.7040.1195 · Cited by 654

Parental smoking and childhood asthma: longitudinal and case-control studies

Strachan, D. P., & Cook, D. G. (1998) · Thorax · doi:10.1136/thx.53.3.204 · Cited by 597

Increasing prevalence of hay fever and atopy among children in Leipzig, East Germany

von Mutius, E., Weiland, S. K., Fritzsch, C., Duhme, H., & Keil, U. (1998) · The Lancet · doi:10.1016/s0140-6736(97)10100-3 · Cited by 572

Frequency, severity, and duration of rhinovirus infections in asthmatic and non-asthmatic individuals: a longitudinal cohort study

Corne, J. M., Marshall, C., Smith, S. H., Schreiber, J., Sanderson, G., Holgate, S. T., & Johnston, S. L. (2002) · The Lancet · doi:10.1016/s0140-6736(02)07953-9 · Cited by 571

Inverse association between Helicobacter pylori infection and childhood asthma in Greece: a case-control study

Tsigalou, C., Konstantinidis, T. G., Cassimos, D. C., Karvelas, A., Grapsa, A., Tsalkidis, A., Panopoulou, M. I., & Tsakris, A. (2019) · GERMS · doi:10.18683/germs.2019.1174 · Cited by 25

Exposure to traffic-related air pollution and bacterial diversity in the lower respiratory tract of children

Niemeier‐Walsh, C., Ryan, P., Meller, J., Ollberding, N. J., Adhikari, A., & Reponen, T. A. (2021) · PLoS ONE · doi:10.1371/journal.pone.0244341 · Cited by 25

Risk factors for acute asthma in tropical America: a case–control study in the City of Esmeraldas, Ecuador

Ardura‐Garcia, C., Vaca, M. G., Oviedo, G., Sandoval, C. A., Workman, L. J., Schuyler, A. J., Perzanowski, M. S., Platts‐Mills, T. A. E., & Cooper, P. J. (2015) · Pediatric Allergy and Immunology · doi:10.1111/pai.12401 · Cited by 25

Depressive symptoms, risk factors and sleep in asthma: results from a national Israeli health survey

Goral, A., Lipsitz, J. D., Muhsen, K., & Gross, R. (2011) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2011.09.007 · Cited by 26

Predicting Asthma Outcome Using Partial Least Square Regression and Artificial Neural Networks

Chatzimichail, E. A., Paraskakis, E., & Rigas, A. G. (2013) · Advances in Artificial Intelligence · doi:10.1155/2013/435321 · Cited by 25

Anaesthetic management of the child with co-existing pulmonary disease

Lauer, R. E., Vadi, M., & Mason, L. J. (2012) · British Journal of Anaesthesia · doi:10.1093/bja/aes392 · Cited by 25

Pyrogenic activity of air to characterize bioaerosol exposure in public buildings: a pilot study

Bernasconi, C., Rodolfi, M., Picco, A. M., Grisoli, P., Dacarro, C., & Rembges, D. (2010) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2010.02831.x · Cited by 25

Asthma and risk of non-respiratory tract infection: a population-based case–control study

Bang, D. W., Yang, H. J., Ryoo, E., Al‐Hasan, M. N., Lahr, B. D., Baddour, L. M., Yawn, B. P., & Juhn, Y. J. (2013) · BMJ Open · doi:10.1136/bmjopen-2013-003857 · Cited by 25

p-STAT6, PU.1, and NF-κB are involved in allergen-induced late-phase airway inflammation in asthma patients

Hoppenot, D., Malakauskas, K., Lavinskienė, S., & Sakalauskas, R. (2015) · BMC Pulmonary Medicine · doi:10.1186/s12890-015-0119-7 · Cited by 25

Health care access, concentrated poverty, and pediatric asthma hospital care use in California's San Joaquin Valley: A multilevel approach

Alcala, E., Cisneros, R., & Capitman, J. A. (2017) · Journal of Asthma · doi:10.1080/02770903.2017.1409234 · Cited by 25

IL‑27 suppresses airway inflammation, hyperresponsiveness and remodeling via the STAT1 and STAT3 pathways in mice with allergic asthma

Lu, D., Lu, J., Ji, X., Ji, Y., Zhang, Z., Peng, H., Sun, F., & Zhang, W. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4622 · Cited by 25

Modifiable exposures to air pollutants related to asthma phenotypes in the first year of life in children of the EDEN mother-child cohort study

The EDEN Mother-Child Cohort Study Group, Zhou, C., Baïz, N., Zhang, T., Banerjee, S., & Annesi‐Maesano, I. (2013) · BMC Public Health · doi:10.1186/1471-2458-13-506 · Cited by 25

Extreme temperatures exacerbated oxidative stress and airway inflammation in a mouse model of allergic asthma

Lu, C., Wang, F., Qiao, Z., Deng, M., Liu, Q., & Yang, X. (2023) · Allergy · doi:10.1111/all.15883 · Cited by 24

Eosinophil: A central player in modulating pathological complexity in asthma

Pritam, P., Manna, S., Sahu, A., Swain, S. S., Ramchandani, S., Bissoyi, S., Panda, M. K., Sing, Y. D., Mohanta, Y. K., Behera, R. K., et al. (2021) · Allergologia et Immunopathologia · doi:10.15586/aei.v49i2.50 · Cited by 26

Perinatal programming of murine immune responses by polyunsaturated fatty acids

van Vlies, N., Hogenkamp, A., Fear, A. L., van Esch, B. C. A. M., Oosting, A., van de Heijning, B., van der Beek, E. M., Calder, P. C., & Garssen, J. (2010) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s204017441000067x · Cited by 24

The association between paracetamol use and asthma: causation or coincidence?

Weatherall, M., Ioannides, S. J., Braithwaite, I. E., & Beasley, R. W. (2014) · Clinical & Experimental Allergy · doi:10.1111/cea.12410 · Cited by 24

Oral Administration of Heat-Inactivated Lactobacillus plantarum K37 Modulated Airway Hyperresponsiveness in Ovalbumin-Sensitized BALB/c Mice

Liu, Y.-W., Liao, T.-W., Chen, Y., Chiang, Y.-C., & Tsai, Y.-C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100105 · Cited by 24

Thirty-Year Survey on Airborne Pollen Concentrations in Genoa, Italy: Relationship with Sensitizations, Meteorological Data, and Air Pollution

Negrini, A. C., Negrini, S. M., Giunta, V., Quaglini, S., & Ciprandi, G. (2011) · American Journal of Rhinology and Allergy · doi:10.2500/ajra.2011.25.3729 · Cited by 24

30-year trends in asthma and the trends in relation to hospitalization and mortality

Pelkonen, M. K., Notkola, I.-L. K., Laatikainen, T. K., & Jousilahti, P. (2018) · Respiratory Medicine · doi:10.1016/j.rmed.2018.07.012 · Cited by 24

Neonatal Urine Metabolic Profiling and Development of Childhood Asthma

Chawes, B., Giordano, G., Pirillo, P., Rago, D., Rasmussen, M. A., Stokholm, J., Bønnelykke, K., Bisgaard, H. F., & Baraldi, E. (2019) · Metabolites · doi:10.3390/metabo9090185 · Cited by 25

The role of innate immunity in asthma development and protection: Lessons from the environment

Pivniouk, V. I., Gimenes-Júnior, J. A., Honeker, L. K., & Vercelli, D. (2019) · Clinical & Experimental Allergy · doi:10.1111/cea.13508 · Cited by 24

Horizontes en la neumología española: algunas reflexiones

Villena, V., & Álvarez-Sala, J. L. (2007) · Archivos de Bronconeumología · doi:10.1157/13110883 · Cited by 24

Functional polymorphisms of GSTA1 and GSTO2 genes associated with asthma in Italian children

Piacentini, S., Verrotti, A., Polimanti, R. A., Giannini, C., Saccucci, P., Manfellotto, D., & Fuciarelli, M. (2011) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.2011.774 · Cited by 23

Synthesis and Incorporation into Cyclic Peptides of Tolan Amino Acids and Their Hydrogenated Congeners: Construction of an Array of A–B-loop Mimetics of the Cε3 Domain of Human IgE

Offermann, D. A., McKendrick, J. E., Sejberg, J. J. P., Mo, B., Holdom, M. D., Helm, B. A., Leatherbarrow, R. J., Beavil, A. J., Sutton, B. J., & Spivey, A. C. (2012) · The Journal of Organic Chemistry · doi:10.1021/jo202604q · Cited by 23

Nationwide Survey on the Prevalence of Allergic Diseases according to Region and Age

Seong, H. U., Cho, S. D., Park, S.-Y., Yang, J. M., Lim, D. H., Kim, J. H., & Son, B. K. (2012) · Pediatric Allergy and Respiratory Disease · doi:10.7581/pard.2012.22.3.224 · Cited by 23

Effects of maternal geohelminth infections on allergy in early childhood

Cooper, P. J., Chico, M. E., Amorim, L. D. A. F., Sandoval, C. A., Vaca, M. G., Strina, A., Campos, A. C. P., Rodrigues, L. C., Barreto, M. L., & Strachan, D. P. (2015) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.07.044 · Cited by 24

Asthma in farm children is more determined by genetic polymorphisms and in non‐farm children by environmental factors

Krautenbacher, N., Kabesch, M., Horak, E., Braun‐Fahrländer, C., Genuneit, J., Boznański, A., von Mutius, E., Theis, F. J., Fuchs, C., Ege, M. J., et al. (2020) · Pediatric Allergy and Immunology · doi:10.1111/pai.13385 · Cited by 23

Effectiveness of Sublingual Immunotherapy in the Treatment of HDM-Induced Nasobronchial Allergies: A 3-Year Randomized Case-Control Study From Kashmir

Baba, S. M., Rasool, R., Gull, A., Qureshi, T. A., Beigh, A. H., Qadri, Q., & Shah, Z. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.723814 · Cited by 23

Increasing Prevalence of Allergic Disease and Its Impact on Current Practice

Edwards-Salmon, S. E., Padmanabhan, S. L., Kuruvilla, M. E., & Levy, J. M. (2022) · Current Otorhinolaryngology Reports · doi:10.1007/s40136-022-00406-5 · Cited by 27

A “hydroxyl radicals standard” for evaluating the efficacy of anti-asthma drugs by using a two-photon NIR optical sensor

Yue, L., Li, G., Chen, Z., Dai, L., Huang, H., Li, H., & Lin, W. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.139019 · Cited by 23

Sphingosine-1-Phosphate Aggravates Antigen-Induced Airway Inflammation in Mice

Chiba, Y., Suzuki, K., Kurihara, E., Uechi, M., Sakai, H., & Misawa, M. (2010) · The Open Respiratory Medicine Journal · doi:10.2174/1874306401004010082 · Cited by 23

Tolerizing allergic responses in the lung

Lloyd, C. M., & Murdoch, J. R. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.19 · Cited by 23

Feeding Bottles Usage and the Prevalence of Childhood Allergy and Asthma

Hsu, N., Wu, P.-C., Bornehag, C., Sundell, J., & Su, H.-J. J. (2012) · Clinical and Developmental Immunology · doi:10.1155/2012/158248 · Cited by 23

Endogenous γ-Aminobutyric Acid Modulates Tonic Guinea Pig Airway Tone and Propofol-induced Airway Smooth Muscle Relaxation

Gallos, G., Gleason, N. R., Virag, L., Zhang, Y., Mizuta, K., Whittington, R. A., & Emala, C. W. (2009) · Anesthesiology · doi:10.1097/aln.0b013e31819c44e1 · Cited by 23

Rhinoconjunctivitis prevalence and associated factors in school children aged 6–7 and 13–14 years old in Bogota, Colombia

Augusto Peñaranda, S., Aristizábal, G., García, E., Vásquez, C., & Rodríguez‐Martínez, C. E. (2012) · International Journal of Pediatric Otorhinolaryngology · doi:10.1016/j.ijporl.2012.01.010 · Cited by 23

A case-control study of body mass index and asthma in Asian children

Henkin, S., Brugge, D., Bermudez, O. I., & Gao, X. (2008) · Annals of Allergy Asthma & Immunology · doi:10.1016/s1081-1206(10)60469-3 · Cited by 23

Beta‐2 receptor agonist exposure in the uterus associated with subsequent risk of childhood asthma

Ogawa, K., Tanaka, S., Yang, L., Arata, N., Sago, H., Yamamoto‐Hanada, K., Narita, M., & Ohya, Y. (2017) · Pediatric Allergy and Immunology · doi:10.1111/pai.12805 · Cited by 23

Retrospective analysis of aeroallergen’s sensitization patterns in Edmonton, Canada

Ahmed, H., Ospina, M. B., Sideri, K., & Vliagoftis, H. (2019) · Allergy Asthma and Clinical Immunology · doi:10.1186/s13223-019-0320-y · Cited by 23

Racial/Ethnic‐Specific Differences in the Effects of Inhaled Corticosteroid Use on Bronchodilator Response in Patients With Asthma

Samedy-Bates, L.-A., Oh, S. S., Nuckton, T. J., Elhawary, J. R., White, M. J., Elliot, T., Zeiger, A. M., Eng, C. S., Salazar, S., LeNoir, M. A., et al. (2019) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.1555 · Cited by 23

Interleukin-4 upregulates RhoA protein via an activation of STAT6 in cultured human bronchial smooth muscle cells

Chiba, Y., Todoroki, M., & Misawa, M. (2009) · Pharmacological Research · doi:10.1016/j.phrs.2009.10.003 · Cited by 23

Aspirin‐intolerant asthma in the population: prevalence and important determinants

Eriksson, J. G., Ekerljung, L., Bossios, A., Bjerg, A., Wennergren, G., Rönmark, E., Torén, K., Lötvall, J. O., & Lundbäck, B. (2014) · Clinical & Experimental Allergy · doi:10.1111/cea.12359 · Cited by 23

S100A12 and the Airway Smooth Muscle: Beyond Inflammation and Constriction

Camoretti-Mercado, B., & Karrar, E. E. (2012) · Journal of Allergy & Therapy · doi:10.4172/2155-6121.s1-007 · Cited by 22

Duration of day care attendance during infancy predicts asthma at the age of seven: the Cincinnati Childhood Allergy and Air Pollution Study

Cheng, G., Smith, A. M., Levin, L., Epstein, T., Ryan, P., LeMasters, G. K., Hershey, G. K. K., Reponen, T. A., Villareal, M., Lockey, J. E., et al. (2014) · Clinical & Experimental Allergy · doi:10.1111/cea.12397 · Cited by 22

Parasitic worms and allergies in childhood: Insights from population studies 2008–2013

Amoah, A. S., Boakye, D. A., van Ree, R., & Yazdanbakhsh, M. (2013) · Pediatric Allergy and Immunology · doi:10.1111/pai.12174 · Cited by 23

Reconciling Hygiene and Cleanliness: A New Perspective from Human Microbiome

Gupta, V., Kumar, R., Sood, U., & Singhvi, N. (2019) · Indian Journal of Microbiology · doi:10.1007/s12088-019-00839-5 · Cited by 23

Relevance of Early Introduction of Cow’s Milk Proteins for Prevention of Cow’s Milk Allergy

Ulfman, L. H., Tsuang, A. J., Sprikkelman, A. B., Goh, A., & van Neerven, R. J. J. (2022) · Nutrients · doi:10.3390/nu14132659 · Cited by 22

Prevalence, Management, and Risk Factors of Asthma Among School-Age Children in Yogyakarta, Indonesia

Triasih, R., Setyowireni, D., Nurani, N., & Setyati, A. (2023) · Journal of Asthma and Allergy · doi:10.2147/jaa.s392733 · Cited by 22

Asthma and allergic diseases: Cross talk of immune system and environmental factors

Beerweiler, C., Masanetz, R. K., & Schaub, B. (2023) · European Journal of Immunology · doi:10.1002/eji.202249981 · Cited by 27

Climate change and the epithelial barrier theory in allergic diseases: A One Health approach to a green environment

Pawankar, R., & Akdiş, C. A. (2023) · Allergy · doi:10.1111/all.15885 · Cited by 23

The Novel 10-Item Asthma Prediction Tool: External Validation in the German MAS Birth Cohort

Grabenhenrich, L., Reich, A., Fischer, F. H., Zepp, F., Förster, J., Schuster, A., Bauer, C., Bergmann, R. L., Bergmann, K. E., Wahn, U., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115852 · Cited by 22

Diverging trends of chronic bronchitis and smoking habits between 1998 and 2010

Accordini, S., Corsico, A. G., Cerveri, I., Antonicelli, L., Attena, F., Bono, R., Casali, L., Ferrari, M., Fois, A. G., Marchetti, P., et al. (2013) · Respiratory Research · doi:10.1186/1465-9921-14-16 · Cited by 22

Lack of association between GSTM1, GSTP1, and GSTT1 gene polymorphisms and asthma in adult patients from Rome, central Italy.

Piacentini, S., Polimanti, R. A., Moscatelli, B., Re, M. A., Manfellotto, D., & Fuciarelli, M. (2012) · PubMed · Cited by 22

The indirect effect of fine particulate matter on health through individuals’ life-style

Novi, C. D. (2013) · The Journal of Socio-Economics · doi:10.1016/j.socec.2013.02.002 · Cited by 22

The triumph of the null hypothesis: epidemiology in an age of change

Maziak, W. (2008) · International Journal of Epidemiology · doi:10.1093/ije/dyn268 · Cited by 23

Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma

Yao, Y., Zeng, Q., Deng, X.-Q., Tang, G., Guo, J.-B., Sun, Y., Ru, K., Rizzo, A. N., Shi, J., & Fu, Q. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144106 · Cited by 22

Potential health risk of allergenic pollen with climate change associated spreading capacity: Ragweed and olive sensitization in two German federal states

Höflich, C., Balakirski, G., Hajdu, Z., Baron, J. M., Kaiser, L., Czaja, K., Merk, H. F., Gerdsen, S., Straßen, U., Baş, M., et al. (2016) · International Journal of Hygiene and Environmental Health · doi:10.1016/j.ijheh.2016.01.007 · Cited by 22

Evaluation of tetrabromobisphenol A effects on human glucocorticoid and androgen receptors: A comparison of results from human- with yeast-based in vitro assays

Beck, K. R., Sommer, T. J., Schuster, D., & Odermatt, A. (2016) · Toxicology · doi:10.1016/j.tox.2016.09.014 · Cited by 22

Systemic and mucosal pre-administration of recombinantHelicobacter pylorineutrophil-activating protein prevents ovalbumin-induced allergic asthma in mice

Zhou, S., Huang, Y., Liang, B., Dong, H., Yao, S., Chen, Y., Xie, Y., Long, Y., Gong, S., & Zhou, Z. (2017) · FEMS Microbiology Letters · doi:10.1093/femsle/fnw288 · Cited by 22

Prevention of Asthma Exacerbation in a Mouse Model by Simultaneous Inhibition of NF-κB and STAT6 Activation Using a Chimeric Decoy Strategy

Miyake, T., Miyake, T., Sakaguchi, M., Nankai, H., Nakazawa, T., & Morishita, R. (2017) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2017.12.005 · Cited by 22

Exposure to polycyclic aromatic hydrocarbons, vitamin D, and lung function in children with asthma

Han, Y., Rosser, F. J., Forno, E., & Celedon, J. C. (2018) · Pediatric Pulmonology · doi:10.1002/ppul.24084 · Cited by 22

Hyperbilirubinemia, Phototherapy, and Childhood Asthma

Kuzniewicz, M. W., Niki, H., Walsh, E. M., McCulloch, C. E., & Newman, T. B. (2018) · PEDIATRICS · doi:10.1542/peds.2018-0662 · Cited by 22

Bronchial asthma

Liccardi, G., Salzillo, A., Sofia, M., D’Amato, M., & D’Amato, G. (2011) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0b013e32834e7b2e · Cited by 22

Angiotensin II induces hyperresponsiveness of bronchial smooth muscle via an activation of p42/44 ERK in rats

Sakai, H., Nishizawa, Y., Nishimura, A., Chiba, Y., Goto, K., Hanazaki, M., & Misawa, M. (2010) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-010-0844-y · Cited by 22

An imbalance in C/EBPs and increased mitochondrial activity in asthmatic airway smooth muscle cells: novel targets in asthma therapy?

Roth, M., & Black, J. L. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00188.x · Cited by 22

Why parents cross for children's health care: Transnational cultural capital in the United States–Mexico border region

Grineski, S. E. (2011) · Social Theory & Health · doi:10.1057/sth.2011.7 · Cited by 21

Genetics of Complex Airway Disease

Cookson, W., & Moffatt, M. F. (2011) · Proceedings of the American Thoracic Society · doi:10.1513/pats.201101-003ms · Cited by 21

Induction of Bronchial Tolerance After 1 Cycle of Monophosphoryl-A-Adjuvanted Specific Immunotherapy in Children With Grass Pollen Allergies

Rosewich, M., Girod, K., Zielen, S., Schubert, R., & Schulze, J. (2016) · Allergy Asthma and Immunology Research · doi:10.4168/aair.2016.8.3.257 · Cited by 21

A Multi-Omics Approach Reveals New Signatures in Obese Allergic Asthmatic Children

Llorente, M. A. G., Martínez‐Cañavate, A., Chueca, N., Rico-Prados, M. C., Romero, R., Anguita‐Ruiz, A., Aguilera, C. M., Gil‐Campos, M., Mesa, M. D., Khakimov, B., et al. (2020) · Biomedicines · doi:10.3390/biomedicines8090359 · Cited by 20

Prostaglandin I2 signaling licenses Treg suppressive function and prevents pathogenic reprogramming

Norlander, A. E., Bloodworth, M. H., Toki, S., Zhang, J., Zhou, W., Boyd, K. L., Polosukhin, V. V., Cephus, J.-Y., Ceneviva, Z. J., Gandhi, V. D., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci140690 · Cited by 21

Use of Eco-Friendly UV-C LEDs for Indoor Environment Sanitization: A Narrative Review

Palma, F., Baldelli, G., Schiavano, G. F., Amagliani, G., Aliano, M. P., & Brandi, G. (2022) · Atmosphere · doi:10.3390/atmos13091411 · Cited by 25

Regulatory T-cells in asthma

Harb, H., & Chatila, T. A. (2023) · Current Opinion in Allergy and Clinical Immunology · doi:10.1097/aci.0000000000000887 · Cited by 21

Do We Need Worms to Promote Immune Health?

Weinstock, J. V. (2014) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-014-8458-3 · Cited by 21

The September Epidemic of Asthma in Israel

Scheuerman, O., Meyerovitch, J., Marcus, N., Hoffer, V., Batt, E., & Garty, B. (2009) · Journal of Asthma · doi:10.1080/02770900902963102 · Cited by 21

Determinants of house dust, endotoxin, andβ-(1→3)- D -glucan in homes of Danish children

Holst, G. J., Høst, A., Doekes, G., Meyer, H. W., Madsen, A. M., & Sigsgaard, T. (2014) · Indoor Air · doi:10.1111/ina.12143 · Cited by 21

Residential exposure to motor vehicle emissions and the risk of wheezing among 7-8 year-old schoolchildren: a city-wide cross-sectional study in Nicosia, Cyprus

Middleton, N., Yiallouros, P. K., Nicolaou, N. C., Kleanthous, S., Pipis, S., Zeniou, M., Demokritou, P., & Koutrakis, P. (2010) · Environmental Health · doi:10.1186/1476-069x-9-28 · Cited by 21

Increased Risk of Asthma in Children with ADHD: Role of Prematurity and Maternal Stress during Pregnancy.

Grizenko, N., Osmanlliu, E., Fortier, M., & Joober, R. (2015) · Europe PMC (PubMed Central) · Cited by 21

Validation of Strasbourg environmental exposure chamber (EEC) ALYATEC® in mite allergic subjects with asthma

Khayath, N., Doyen, V., Gherasim, A., Radu, C., Choual, I., Beck, N., Jacob, A., Schoettel, F., Vecellio, L., Domis, N., et al. (2020) · Journal of Asthma · doi:10.1080/02770903.2018.1563902 · Cited by 21

Yeast Fermentate Prebiotic Ameliorates Allergic Asthma, Associating with Inhibiting Inflammation and Reducing Oxidative Stress Level through Suppressing Autophagy

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Effect of airborne Alternaria conidia, ozone exposure, PM10 and weather on emergency visits for asthma in school-age children in Kolkata city, India

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