Items where Author is "Abiri, M."

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Number of items: 13.

Article

Eghbali, M. and Fatemi, K.S. and Salehpour, S. and Abiri, M. and Saei, H. and Talebi, S. and Olyaei, N.A. and Yassaee, V.R. and Modarressi, M.H. (2021) Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi�Bickel Syndrome. Frontiers in Genetics, 11.

Eghbali, M. and Abiri, M. and Talebi, S. and Noroozi, Z. and Shakiba, M. and Rostami, P. and Alimadadi, H. and Najafi, M. and Yazarlou, F. and Rabbani, A. and Modarressi, M.H. (2020) Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b). Orphanet Journal of Rare Diseases, 15 (1).

Sharifi, Z. and Rahiminejad, F. and Joudaki, A. and Bandehi, A.S. and Farahzadi, H. and Keshvar, Y. and Golnabi, F. and Naderi, S. and Yazdani, R. and Shafaat, M. and Ghadami, S. and Abiri, M. and Zeinali, S. (2019) 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. Scientific Reports, 9 (1).

Abiri, M. and Saei, H. and Eghbali, M. and Karamzadeh, R. and Shirzadeh, T. and Sharifi, Z. and Zeinali, S. (2019) Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations. Metabolic Brain Disease.

Zafarghandi Motlagh, F. and Fallah, M.S. and Bagherian, H. and Shirzadeh, T. and Ghasri, S. and Dabbagh, S. and Jamali, M. and Salehi, Z. and Abiri, M. and Zeinali, S. (2019) Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; Reporting novel and recurrent mutations. Orphanet Journal of Rare Diseases, 14 (1).

Zafarghandi Motlagh, F. and Fallah, M.S. and Bagherian, H. and Shirzadeh, T. and Ghasri, S. and Dabbagh, S. and Jamali, M. and Salehi, Z. and Abiri, M. and Zeinali, S. (2019) Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; Reporting novel and recurrent mutations. Orphanet Journal of Rare Diseases, 14 (1).

Shafaat, M. and Alaee, M.R. and Rahmanifar, A. and Setoodeh, A. and Razzaghy-Azar, M. and Bagherian, H. and Bagheri, S.D. and Zafarghandi Motlagh, F. and Hashemi, M. and Abiri, M. and Zeinali, S. (2018) Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort. Metabolic Brain Disease, 33 (5). pp. 1689-1697.

Bahrami Zadegan, S. and Dabbagh Bagheri, S. and Joudaki, A. and Samiee Aref, M.H. and Saeidian, A.H. and Abiri, M. and Zeinali, S. (2018) Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility. Andrologia, 50 (4).

Bahrami Zadegan, S. and Dabbagh Bagheri, S. and Joudaki, A. and Samiee Aref, M.H. and Saeidian, A.H. and Abiri, M. and Zeinali, S. (2018) Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility. Andrologia, 50 (4).

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Zeinali, S. and Touati, A. and Abiri, M. and Sotoudeh, S. and Norouz-zadeh, S. and Amirinezhad, N. and Mozafari, N. and Daneshpazhooh, M. and Mahmoudi, H. and Hamid, M. and Bradfield, J.P. and Kim, C.E. and Hakonarson, H. and Uitto, J. (2018) Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Experimental Dermatology.

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Zeinali, S. and Touati, A. and Abiri, M. and Sotoudeh, S. and Norouz-zadeh, S. and Amirinezhad, N. and Mozafari, N. and Daneshpazhooh, M. and Mahmoudi, H. and Hamid, M. and Bradfield, J.P. and Kim, C.E. and Hakonarson, H. and Uitto, J. (2018) Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Experimental Dermatology.

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Mahmoudi, H. and Touati, A. and Abiri, M. and Kajbafzadeh, A.-M. and Aristodemou, S. and Liu, L. and McGrath, J.A. and Ertel, A. and Londin, E. and Kariminejad, A. and Zeinali, S. and Fortina, P. and Uitto, J. (2018) Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biology, 66. pp. 22-33.

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Mahmoudi, H. and Touati, A. and Abiri, M. and Kajbafzadeh, A.-M. and Aristodemou, S. and Liu, L. and McGrath, J.A. and Ertel, A. and Londin, E. and Kariminejad, A. and Zeinali, S. and Fortina, P. and Uitto, J. (2018) Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biology, 66. pp. 22-33.

This list was generated on Mon Apr 12 11:09:57 2021 +0430.