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International Journal of Dermatology|January 12, 2017
Assessment of the effectiveness of topical propranolol 4% gel for infantile hemangiomasJacob Mashiah, Ana Kutz, Smail Hadj Rabia, et al.Journal of Molecular Medicine (Berlin, Germany)|December 16, 2004
Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disordersYaacov Frishberg, Orit Topaz, Reuven Bergman, et al.Acta Dermato-Venereologica|April 8, 2022
Relationship Between Pemphigus Vulgaris Severity and PCR-positive Herpes Simplex VirusSharon Baum, Itai Atar, Dan Coster, et al.The Journal of Pediatrics|November 13, 2022
A Mixed-Methods Assessment of Coronavirus Disease of 2019-Era Telehealth Acute Care Visits in the Medical HomeEli Sprecher, Kathleen Conroy, Jennifer Krupa, et al.European Journal of Dermatology : EJD|August 25, 2010
Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expressionBettina Burger, Dov Hershkovitz, Margarita Indelman, et al.The Journal of Investigative Dermatology|August 28, 2009
Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosisJanna Nousbeck, Ofer Sarig, Nili Avidan, et al.Stem Cell Research|October 23, 2013
Angiomodulin is required for cardiogenesis of embryonic stem cells and is maintained by a feedback loop network of p63 and Activin-AZohar Wolchinsky, Shoham Shivtiel, Evelyn Nathalie Kouwenhoven, et al.Pediatric Dermatology|May 19, 2025
Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two PatientsFiona Haxho, Richard M Haber, Janan Mohamad, et al.Journal of Voice : Official Journal of the Voice Foundation|February 15, 2021
Laryngeal Pemphigoid Evolution and Response to TreatmentShira Barmatz, Avital Baniel, Ron Eremenko, et al.American Journal of Human Genetics|August 9, 2011
A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphiaJanna Nousbeck, Bettina Burger, Dana Fuchs-Telem, et al.Pageof 29