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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|May 3, 2022
Pathomechanisms of epidermolysis bullosa: Beyond structural proteinsNailah Harvey, Leila Youssefian, Amir Hossein Saeidian, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|April 9, 2018
Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zoneCristina Has, Alexander Nyström, Amir Hossein Saeidian, et al.
Orphanet Journal of Rare Diseases|December 7, 2017
A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndromeLeila Youssefian, Andrew Touati, Amir Hossein Saeidian, et al.
Experimental Dermatology|April 30, 2020
The matriptase-prostasin proteolytic cascade in dermatologic diseasesAndrew Touati, Amir Hossein Saeidian, Leila Youssefian, et al.
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