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Journal of Human Genetics|March 11, 2006
Hyperphosphatemic familial tumoral calcinosis caused by a mutation in GALNT3 in a European kindredPolina Specktor, John G Cooper, Margarita Indelman, 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 American Journal of Dermatopathology|January 26, 2017
Epidermolytic Ichthyosis Sine EpidermolysisMarina Eskin-Schwartz, Marianna Drozhdina, Ofer Sarig, et al.Pediatric Dermatology|May 17, 2018
Risk factors for ocular complications in periocular infantile hemangiomasLiat Samuelov, Michael Kinori, Karen Rychlik, et al.Acta Orthopaedica|March 21, 2009
Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndromeFaysal Gok, Ilana Chefetz, Margarita Indelman, et al.Archives of Dermatology|May 18, 2005
Diffuse nonepidermolytic palmoplantar keratoderma caused by a recurrent nonsense mutation in DSG1Hannah Keren, Reuven Bergman, Mordechai Mizrachi, et al.Ocular Immunology and Inflammation|November 3, 2017
Anterior Scleritis Associated with Pemphigus VulgarisTal Zeeli, Efrat Bar-Ilan, Zohar Habot-Wilner, et al.Journal of Asthma and Allergy|August 30, 2021
Role of Patch Testing in Chronic Spontaneous UrticariaJonathan Bar, Sari Godlewicz, Arieh Ingber, et al.International Journal of Dermatology|April 11, 2016
Papillon-Lefèvre syndrome: report of six patients and identification of a novel mutationBurak Tekin, Deniz Yucelten, Filippo Beleggia, et al.Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]|April 2, 2021
Pulse-Dye Laser Followed by Betamethasone-Calcipotriol and Fractional Ablative CO2-Laser-Assisted Delivery for Nail PsoriasisWaseem Shehadeh, Hagit Matz, Eran Ellenbogen, et al.Pageof 28