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Experimental Dermatology|August 14, 2015
Klippel-Trenaunay syndrome belongs to the PIK3CA-related overgrowth spectrum (PROS)Hassan Vahidnezhad, Leila Youssefian, Jouni Uitto
Frontiers in Oncology|September 19, 2025
Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mappingLeila Youssefian, Trilochan Sahoo, Jia-Chi Wang
The Journal of Investigative Dermatology|August 26, 2018
Research Techniques Made Simple: Genome-Wide Homozygosity/Autozygosity Mapping Is a Powerful Tool for Identifying Candidate Genes in Autosomal Recessive Genetic DiseasesHassan Vahidnezhad, Leila Youssefian, Ali Jazayeri, et al.
Acta Dermato-Venereologica|March 10, 2020
Molecular Genetics of Keratinization Disorders - What's New About IchthyosisJouni Uitto, Leila Youssefian, Amir Hossein Saeidian, et al.
Journal of the American Academy of Dermatology|June 12, 2021
Interpretation of genomic sequence variants in heritable skin diseases: A primer for cliniciansJouni Uitto, Amir Hossein Saeidian, Leila Youssefian, et al.
The Journal of Investigative Dermatology|May 25, 2020
Research Techniques Made Simple: Whole-Transcriptome Sequencing by RNA-Seq for Diagnosis of Monogenic DisordersAmir Hossein Saeidian, Leila Youssefian, Hassan Vahidnezhad, et al.
The Journal of Investigative Dermatology|November 6, 2018
Phenotypic Spectrum of Epidermolysis Bullosa: The Paradigm of Syndromic versus Non-Syndromic Skin Fragility DisordersHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 7, 2016
Molecular pathology of the basement membrane zone in heritable blistering diseases:: The paradigm of epidermolysis bullosaJouni Uitto, Cristina Has, Hassan Vahidnezhad, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|May 3, 2022
Pathomechanisms of epidermolysis bullosa: Beyond structural proteinsNailah Harvey, Leila Youssefian, Amir Hossein Saeidian, et al.
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