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Experimental Dermatology|July 4, 2020
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosisJanan Mohamad, Arti Nanda, Mor Pavlovsky, et al.
Journal of Psoriasis and Psoriatic Arthritis|September 19, 2024
Scarring Alopecia in Tumor Necrosis Factor-α Antagonists-Induced Scalp PsoriasisAvital Baniel, Alon Peled, Liat Samuelov, et al.
Experimental Dermatology|January 14, 2026
Defective Function of Inhibitor of κB Kinase Subunit Beta Associated With Multiple Immune-Mediated DisordersKiril Malovitski, Noy Keller Rosenthal, Lubna Khair, et al.
The Journal of Investigative Dermatology|April 6, 2020
Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar KeratodermaJanan Mohamad, Ofer Sarig, Liron Malki, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2020
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosisLiron Malki, Ofer Sarig, Nicole Cesarato, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
The Journal of Allergy and Clinical Immunology|September 25, 2018
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitisAlon Peled, Ofer Sarig, Guangping Sun, 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|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
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