Youssefian L - Search Results

1

First report of COL7A1 mutations in two patients with recessive dystrophic epidermolysis bullosa from Peru.

Saeidian AH, Youssefian L, Rosales-Solis GM, Vahidnezhad H, Atanasova VS, Uitto J, South AP, Salas-Alanis JC. Saeidian AH, et al. Among authors: youssefian l. Clin Exp Dermatol. 2018 Aug;43(6):719-722. doi: 10.1111/ced.13400. Epub 2018 Feb 9. Clin Exp Dermatol. 2018. PMID: 29427316 No abstract available.

2

Expanding mutation landscape and phenotypic spectrum of autosomal recessive congenital ichthyosis.

Uitto J, Youssefian L, Vahidnezhad H. Uitto J, et al. Among authors: youssefian l. Br J Dermatol. 2017 Aug;177(2):342-343. doi: 10.1111/bjd.15689. Br J Dermatol. 2017. PMID: 28833017 No abstract available.

3

Seven novel COL7A1 mutations identified in patients with recessive dystrophic epidermolysis bullosa from Mexico.

Saeidian AH, Youssefian L, Moreno Trevino MG, Fortuna G, Vahidnezhad H, Atanasova VS, Uitto J, Salas-Alanis JC, South AP. Saeidian AH, et al. Among authors: youssefian l. Clin Exp Dermatol. 2018 Jul;43(5):579-584. doi: 10.1111/ced.13407. Epub 2018 Feb 23. Clin Exp Dermatol. 2018. PMID: 29473190

4

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. Clin Exp Dermatol. 2022 Aug;47(8):1561-1566. doi: 10.1111/ced.15217. Epub 2022 Jun 23. Clin Exp Dermatol. 2022. PMID: 35396755

5

Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene.

Vahidnezhad H, Ziaee V, Youssefian L, Li Q, Sotoudeh S, Uitto J. Vahidnezhad H, et al. Among authors: youssefian l. Clin Exp Dermatol. 2015 Aug;40(6):636-9. doi: 10.1111/ced.12616. Epub 2015 Mar 7. Clin Exp Dermatol. 2015. PMID: 25754064

6

Erythrokeratoderma: a manifestation associated with multiple types of ichthyoses with different gene defects.

Youssefian L, Touati A, Vahidnezhad H, Saeidian AH, Sotoudeh S, Zeinali S, Uitto J. Youssefian L, et al. Br J Dermatol. 2018 Mar;178(3):e219-e221. doi: 10.1111/bjd.16053. Epub 2018 Jan 22. Br J Dermatol. 2018. PMID: 29023646 No abstract available.

7

Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation.

Abdollahimajd F, Rajabi F, Shahidi-Dadras M, Saket S, Youssefian L, Vahidnezhad H, Uitto J. Abdollahimajd F, et al. Among authors: youssefian l. Br J Dermatol. 2019 Sep;181(3):584-586. doi: 10.1111/bjd.17276. Epub 2018 Dec 2. Br J Dermatol. 2019. PMID: 30307612

8

Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis.

Simpson JK, Martinez-Queipo M, Onoufriadis A, Tso S, Glass E, Liu L, Higashino T, Scott W, Tierney C, Simpson MA, Desomchoke R, Youssefian L, SaeIdian AH, Vahidnezhad H, Bisquera A, Ravenscroft J, Moss C, O'Toole EA, Burrows N, Leech S, Jones EA, Lim D, Ilchyshyn A, Goldstraw N, Cork MJ, Darne S, Uitto J, Martinez AE, Mellerio JE, McGrath JA. Simpson JK, et al. Among authors: youssefian l. Br J Dermatol. 2020 Mar;182(3):729-737. doi: 10.1111/bjd.18211. Epub 2019 Aug 26. Br J Dermatol. 2020. PMID: 31168818

9

Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP.

Youssefian L, Khodavaisy S, Khosravi-Bachehmir F, Park JS, Saeidian AH, Mahmoudi H, Saffarian Z, Naraghi ZS, Kamyab-Hesari K, Zeinali S, Vahidnezhad H, Uitto J. Youssefian L, et al. J Eur Acad Dermatol Venereol. 2022 Mar;36(3):472-479. doi: 10.1111/jdv.17856. Epub 2021 Dec 29. J Eur Acad Dermatol Venereol. 2022. PMID: 34863005 Review.

10

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: youssefian l. 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.

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