Showing results (151-160 of 166) with videos related to
Sort By:
Pageof 17
Nature Communications|January 23, 2015
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility lociRegina C Betz, Lynn Petukhova, Stephan Ripke, et al.American Journal of Human Genetics|November 22, 2016
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair SyndromeF Buket Ü Basmanav, Laura Cau, Aylar Tafazzoli, et al.HNO|January 27, 2021
[Effects of the SARS-CoV‑2 pandemic on the otolaryngology university hospitals in the field of research, student teaching and specialist training]T Stöver, S Dazert, S K Plontke, et al.Allergy|February 2, 2026
The Unmet Need of Olfactory Testing in Inflammatory Disorders of the Upper Airways-An EAACI Position PaperL Klimek, J Mullol, Th Hummel, et al.Laryngo- Rhino- Otologie|August 9, 2020
[Effects of the SARS-CoV-2 pandemic on the otorhinolaryngology university hospitals in the field of medical care]T Stöver, S Dazert, T K Hoffmann, et al.Journal of the American Academy of Dermatology|March 14, 2020
The Alopecia Areata Consensus of Experts (ACE) study: Results of an international expert opinion on treatments for alopecia areataNekma Meah, Dmitri Wall, Katherine York, et al.Journal of the American Academy of Dermatology|September 14, 2020
The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expert opinion on diagnosis and laboratory evaluation for alopecia areataNekma Meah, Dmitri Wall, Katherine York, et al.JAMA Dermatology|August 31, 2022
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 IndividualsF Buket Basmanav, Nicole Cesarato, Sheetal Kumar, et al.Nature Genetics|January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYaran Wen, Yang Liu, Yiming Xu, et al.Nature Genetics|February 11, 2022
GestaltMatcher facilitates rare disease matching using facial phenotype descriptorsTzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, et al.Pageof 17