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Israel Journal of Health Policy Research|October 21, 2022
The role of models in the covid-19 pandemicDavid M Steinberg, Ran D Balicer, Yoav Benjamini, et al.
Acta Dermato-Venereologica|April 5, 2024
Identification of Risk Factors for Gliptin-associated Bullous Pemphigoid among Diabetic PatientsDana Shalmon, Efrat Bar-Ilan, Alon Peled, et al.
The Journal of Experimental Medicine|February 20, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotypeShir Bergson, Ofer Sarig, Moshe Giladi, et al.
The Journal of Investigative Dermatology|November 26, 2002
A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophyMargarita Indelman, Reuven Bergman, Raziel Lurie, et al.
The Journal of Investigative Dermatology|March 18, 2011
The Samd9L gene: transcriptional regulation and tissue-specific expression in mouse developmentQiujie Jiang, Benjamin Quaynor, Alex Sun, et al.
The British Journal of Dermatology|May 20, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Yarden Feller, et al.
Journal of Psoriasis and Psoriatic Arthritis|September 19, 2024
Acute Respiratory Distress Syndrome in a Carrier of an Interleukin-36 Receptor Antagonist Mutation With Generalized Pustular PsoriasisAvital Baniel, Efrat Bar-Ilan, Yuval Hilerowicz, et al.
Archives of Dermatology|March 19, 2008
Defective lamellar granule secretion in arthrogryposis, renal dysfunction, and cholestasis syndrome caused by a mutation in VPS33BDov Hershkovitz, Hannah Mandel, Akemi Ishida-Yamamoto, et al.
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