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Dermatologic Therapy|October 8, 2020
Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutationElham Behrangi, Afsaneh Sadeghzadeh-Bazargan, Sepehr Khosravi, et al.
BMC Medical Genetics|May 27, 2018
The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case seriesLeila Youssefian, Hassan Vahidnezhad, Andrew Touati, et al.
Dermatologic Therapy|April 14, 2022
Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case seriesMohammad Reza Pourani, Hassan Vahidnezhad, Parvin Mansouri, et al.
Journal of the American Academy of Dermatology|August 13, 2022
Inherited ichthyosis as a paradigm of rare skin disorders: Genomic medicine, pathogenesis, and managementJason S Park, Amir Hossein Saeidian, Leila Youssefian, et al.
The Journal of Investigative Dermatology|January 10, 2021
Knockdown of SDR9C7 Impairs Epidermal Barrier FunctionLeila Youssefian, Fatemeh Niaziorimi, Amir Hossein Saeidian, et al.
International Journal of Immunogenetics|February 18, 2020
Association of MTHFR C677T polymorphism with elevated homocysteine level and disease development in vitiligoArash Bagheri Hamidi, Nastaran Namazi, Mahsa Mohammad Amoli, et al.
Pediatric Dermatology|March 19, 2022
Evaluation of neurodevelopmental symptoms in 10 cases of neonatal ichthyosis and sclerosing cholangitis syndromeDeborah Salik, Smail Hadj-Rabia, Daniel Hohl, et al.
Human Mutation|January 14, 2020
Genomics-based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathicaHassan Vahidnezhad, Leila Youssefian, Soheila Sotoudeh, et al.
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