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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.Experimental Dermatology|March 3, 2012
Calcitonin gene-related peptide (CGRP) may award relative protection from interferon-γ-induced collapse of human hair follicle immune privilegeMichael Kinori, Marta Bertolini, Wolfgang Funk, et al.Pediatric Dermatology|March 26, 2018
Fractional ablative carbon dioxide laser followed by topical sodium stibogluconate application: A treatment option for pediatric cutaneous leishmaniasisYuval Hilerowicz, Amir Koren, Jacob Mashiah, et al.European Journal of Endocrinology|March 17, 2010
ANE syndrome caused by mutated RBM28 gene: a novel etiology of combined pituitary hormone deficiencyRonen Spiegel, Stavit A Shalev, Amin Adawi, et al.Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|January 14, 2020
Laser pretreatment for the attenuation of planned surgical scars: A randomized self-controlled hemi-scar pilot studyOr Friedman, Dina Gofstein, Ehud Arad, et al.Pediatrics|December 7, 2018
Use of Social Psychology to Improve Adherence to National Bronchiolitis GuidelinesEli Sprecher, Grace Chi, Al Ozonoff, et al.Acta Dermato-Venereologica|March 21, 2022
Segmental Pigmentation Disorder: Clinical Manifestations and Epidemiological Features in 144 patients, a Retrospective Case-control StudyMeital Oren-Shabtai, Aryeh Metzker, Dan Ben Amitai, et al.Journal of the American Academy of Dermatology|January 20, 2010
Disadhesion of epidermal keratinocytes: a histologic clue to palmoplantar keratodermas caused by DSG1 mutationsReuven Bergman, Dov Hershkovitz, Dana Fuchs, et al.Clinical Lymphoma, Myeloma & Leukemia|November 24, 2022
T-Cell Monoclonality in the Blood and the Skin Correlates With Poor Response to Treatment in Mycosis FungoidesShamir Geller, Shira F Tel-Dan, Irit Solar, et al.Biochimica Et Biophysica Acta|November 4, 2008
GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activityIlana Chefetz, Kimitoshi Kohno, Hiroto Izumi, et al.Pageof 29