Showing results (361-370 of 489) with videos related to
Sort By:
Pageof 49
American Journal of Medical Genetics. Part A|January 29, 2011
Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with NeutropeniaCarol Clericuzio, Karine Harutyunyan, Weidong Jin, et al.The Journal of Investigative Dermatology|July 1, 2006
Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitisAileen Sandilands, Gráinne M O'Regan, Haihui Liao, et al.The New England Journal of Medicine|March 15, 2023
Two Phase 3 Trials of Lebrikizumab for Moderate-to-Severe Atopic DermatitisJonathan I Silverberg, Emma Guttman-Yassky, Diamant Thaçi, et al.The Journal of Infectious Diseases|September 10, 2003
An outbreak of trichinellosis due to consumption of bear meat infected with Trichinella nativa, in 2 northern Saskatchewan communitiesRoberta S Schellenberg, Ben J K Tan, James D Irvine, et al.Circulation|December 8, 1998
Identification of a novel genetic locus for familial cardiac myxomas and Carney complexM Casey, C Mah, A D Merliss, et al.The British Journal of Dermatology|October 15, 2013
Development of mycosis fungoides after bone marrow transplantation for chronic myeloid leukaemia: transmission from an allogeneic donorC M R Fahy, A Fortune, F Quinn, et al.The British Journal of Dermatology|May 25, 2026
Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disordersKunlun Lv, Karina M Forde, Amanda T Moon, et al.Allergy|March 3, 2025
Integrated Efficacy and Safety Analysis of Abrocitinib in Adolescents With Moderate-to-Severe Atopic DermatitisAmy S Paller, Lawrence F Eichenfield, Alan D Irvine, et al.The Journal of Allergy and Clinical Immunology|April 9, 2008
Filaggrin mutations, atopic eczema, hay fever, and asthma in childrenStephan Weidinger, Maureen O'Sullivan, Thomas Illig, et al.The Journal of Investigative Dermatology|October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotypeB P Korge, H Hamm, C S Jury, et al.Pageof 49