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Page 1
Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages.
Vahidnezhad H, Youssefian L, Zeinali S, Saeidian AH, Sotoudeh S, Mozafari N, Abiri M, Kajbafzadeh AM, Barzegar M, Ertel A, Fortina P, Uitto J. Vahidnezhad H, et al. Among authors: kajbafzadeh am. J Invest Dermatol. 2017 Mar;137(3):660-669. doi: 10.1016/j.jid.2016.10.023. Epub 2016 Oct 27. J Invest Dermatol. 2017. PMID: 27899325 Free article.
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: kajbafzadeh am. 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.
Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.
Vahidnezhad H, Youssefian L, Saeidian AH, Mahmoudi H, Touati A, Abiri M, Kajbafzadeh AM, Aristodemou S, Liu L, McGrath JA, Ertel A, Londin E, Kariminejad A, Zeinali S, Fortina P, Uitto J. Vahidnezhad H, et al. Among authors: kajbafzadeh am. Matrix Biol. 2018 Mar;66:22-33. doi: 10.1016/j.matbio.2017.11.003. Epub 2017 Nov 11. Matrix Biol. 2018. PMID: 29138120
Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.
Sobhani M, Amin Tabatabaiefar M, Ghafouri-Fard S, Rajab A, Mozafarpour S, Nasrniya S, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Among authors: kajbafzadeh am. Endocrine. 2019 Nov;66(2):185-191. doi: 10.1007/s12020-019-02004-w. Epub 2019 Jul 16. Endocrine. 2019. PMID: 31313226
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
Reutter H, Rüschendorf F, Mattheisen M, Draaken M, Bartels E, Hübner N, Hoffmann P, Payabvash S, Saar K, Nöthen MM, Kajbafzadeh AM, Ludwig M. Reutter H, et al. Among authors: kajbafzadeh am. Birth Defects Res A Clin Mol Teratol. 2010 Sep;88(9):757-61. doi: 10.1002/bdra.20701. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20672349
Mutation analysis of androgen receptor gene: multiple uses for a single test.
Shojaei A, Behjati F, Ebrahimzadeh-Vesal R, Razzaghy-Azar M, Derakhshandeh-Peykar P, Izadi P, Kajbafzadeh AM, Dowlatih MA, Karami F, Tavakkoly-Bazzaz J. Shojaei A, et al. Among authors: kajbafzadeh am. Gene. 2014 Dec 1;552(2):234-8. doi: 10.1016/j.gene.2014.09.038. Epub 2014 Sep 18. Gene. 2014. PMID: 25241384
338 results