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گزیدهای از مقالات
- Hassanlou M, Abiri M, Zeinali S. Prenatal diagnosis of citrullinemia type 1; seven families with c.1168G > A mutation of Argininosuccinate synthetase 1 gene in Southwest Iran: A case series. Int J Reprod Biomed. 2023 Jan 9;20(12):1047-1050.
- Damavandi N, Soleymaniniya A, Bahrami Zadegan S, Samiee Aref MH, Zeinali S. Development of a genetic risk score for obesity predisposition evaluation. Mol Genet Genomics. 2022 Nov;297(6):1495-1503.
- Nodehi H, Faranoush M, Arshi S, Nabavi M, Bemanian MH, Shokri S, Saghafi MR, Fallah MS, Fallahpour M. Neonatal Onset of Hemophagocytic Lymphohistiocytosis Due to Prenatal Varicella-Zoster Infection in a Neonate with Griscelli Syndrome Type 2. Iran J Allergy Asthma Immunol. 2022 Aug 12;21(4):488-493.
- Keshvar Y, Sabeghi S, Sharifi Z, Fatemi KS, Fouladi P, Younesi Khah S, Rahiminejad F, Joudaki A, Amini M, Bagherian H, Ghaffari Novin M, Movahedin M, Mojbafan M, Zeinali S. A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran. BMC Pregnancy Childbirth. 2022 Apr 15;22(1):330.
- Shahab-Movahed Z, Majd A, Siasi Torbati E, Zeinali S. Distal Renal Tubular Acidosis in an Iranian Patient with Hereditary Spherocytosis. Iran Biomed J. 2021 Sep 1;25(5):359-67.
- Asgari T, Naji M, Mansouri P, Mahmoudi H, Zabihi M, Youssefian L, Mahdavi M, Naraghi ZS, Zeinali S, Vahidnezhad H, Uitto J. Keratitis-ichthyosis-deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation. Dermatol Ther. 2020 Nov;33(6):e14493.
- Vahidnezhad H, Youssefian L, Saeidian AH, Mansoori B, Jazayeri A, Azizpour A, Hesari KK, Yousefi M, Zeinali S, Jouanguy E, Casanova JL, Uitto J. A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis. J Invest Dermatol. 2019 May;139(5):1195-1198.
- Sharifi Z, Rahiminejad F, Joudaki A, Bandehi AS, Farahzadi H, Keshvar Y, Golnabi F, Naderi S, Yazdani R, Shafaat M, Ghadami S, Abiri M, Zeinali S. Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases. Sci Rep. 2019 May 15;9(1):7452.
- Youssefian L, Vahidnezhad H, Mahmoudi H, Saeidian AH, Daneshpazhooh M, Kamyab Hesari K, Zeinali S, de Jong SJ, Orth G, Blanchet-Bardon C, Jouanguy E, Casanova JL, Uitto J. Epidermodysplasia Verruciformis: Genetic Heterogeneity and EVER1 and EVER2 Mutations Revealed by Genome-Wide Analysis. J Invest Dermatol. 2019 Jan;139(1):241-244.