Biblio

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2024
Hozhabrpour A, Mojbafan M, Palizban F, Vahidnezhad F, Talebi S, Amani M, Garshasbi M, Naghavi A, Khalesi R, Mansouri P, et al. DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity. DNA Repair (Amst). 2024;136:103633.
2023
Hosseinpour S, Razmara E, Heidari M, Rezaei Z, Ashrafi MReza, Dehnavi AZare, Kameli R, Bereshneh AHosseini, Vahidnezhad H, Azizimalamiri R, et al. A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies. Brain Dev. 2023.
2022
Youssefian L, Naji M, Park JS, Rajabi F, Abdollahimajd F, Mahmoudi H, Kamyab-Hesari K, Ghalamkarpour F, Zabihi M, Teimoorian M, et al. Ichthyosis follicularis syndromes in patients with germline mutations in GJB2. Clin Exp Dermatol. 2022.
Pourani MReza, Vahidnezhad H, Mansouri P, Youssefian L, Rakhshan A, Hajimoradi B, Abdollahimajd F, Uitto J. Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series. Dermatol Ther. 2022:e15515.
Saeidian AHossein, Youssefian L, Huang CY, Palizban F, Naji M, Saffarian Z, Mahmoudi H, Goodarzi A, Sotoudeh S, Vahidnezhad F, et al. Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions. JCI Insight. 2022.
2018
Vahidnezhad H, Youssefian L, Saeidian AHossein, Touati A, Pajouhanfar S, Baghdadi T, Shadmehri AAhmadi, Giunta C, Kraenzlin M, Syx D, et al. Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency. Matrix Biol. 2018.