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Ichthyosis follicularis syndromes in patients with mutations in GJB2.
Youssefian L, Naji M, Park JS, Rajabi F, Abdollahimajd F, Mahmoudi H, Kamyab-Hesari K, Ghalamkarpour F, Zabihi M, Teimoorian M, Youssefian L, Zeinali S, Vahidnezhad H, Uitto J. Youssefian L, et al. Among authors: zeinali s. Clin Exp Dermatol. 2022 Aug;47(8):1561-1566. doi: 10.1111/ced.15217. Epub 2022 Jun 23. Clin Exp Dermatol. 2022. PMID: 35396755
The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.
Youssefian L, Vahidnezhad H, Barzegar M, Li Q, Sotoudeh S, Yazdanfar A, Ehsani AH, Kajbafzadeh AM, Mozafari N, Ebrahimi Daryani N, Agha-Hosseini F, Zeinali S, Uitto J. Youssefian L, et al. Among authors: zeinali s. J Invest Dermatol. 2015 May;135(5):1447-1450. doi: 10.1038/jid.2015.9. Epub 2015 Jan 19. J Invest Dermatol. 2015. PMID: 25599393 Free article. No abstract available.
Phenotypic heterogeneity in PIK3CA-related overgrowth spectrum.
Vahidnezhad H, Youssefian L, Baghdadi T, Sotoudeh S, Tavassoli A, Zeinali S, Afsharaalam S, Uitto J. Vahidnezhad H, et al. Among authors: zeinali s. Br J Dermatol. 2016 Oct;175(4):810-4. doi: 10.1111/bjd.14618. Epub 2016 Jul 27. Br J Dermatol. 2016. PMID: 27037860 No abstract available.
KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family.
Vahidnezhad H, Youssefian L, Saeidian AH, Mozafari N, Barzegar M, Sotoudeh S, Daneshpazhooh M, Isaian A, Zeinali S, Uitto J. Vahidnezhad H, et al. Among authors: zeinali s. J Invest Dermatol. 2016 Sep;136(9):1897-1901. doi: 10.1016/j.jid.2016.05.106. Epub 2016 Jun 7. J Invest Dermatol. 2016. PMID: 27283507 Free article. No abstract available.
261 results