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C3 Glomerulonephritis With Multiple Mutations in Complement Factor H.
Dalili N, Behnam B, Vali F, Parvin M, Torbati P, Rasaii N, Samadian F, Ahmadpoor P. Dalili N, et al. Iran J Kidney Dis. 2018 Nov;12(6):376-381. Iran J Kidney Dis. 2018. PMID: 30595568
An ABCD1 Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree.
Mehrpour M, Gohari F, Dizaji MZ, Ahani A, Malicdan MC, Behnam B. Mehrpour M, et al. J Mol Genet Med. 2016 Jun;10(2):222. doi: 10.4172/1747-0862.1000222. Epub 2016 Jun 19. J Mol Genet Med. 2016. PMID: 27489563 Free PMC article.
CTNS molecular genetics profile in a Persian nephropathic cystinosis population.
Ghazi F, Hosseini R, Akouchekian M, Teimourian S, Ataei Kachoei Z, Otukesh H, Gahl WA, Behnam B. Ghazi F, et al. Nefrologia. 2017 May-Jun;37(3):301-310. doi: 10.1016/j.nefro.2016.11.024. Epub 2017 Feb 24. Nefrologia. 2017. PMID: 28238446 English, Spanish.
First Report of Familial Juvenile Hyperuricemic Nephropathy (FJHN) in Iran Caused By a Novel De Novo Mutation (E197X) in UMOD.
Malakoutian T, Amouzegar A, Vali F, Asgari M, Behnam B. Malakoutian T, et al. J Mol Genet Med. 2016 Jun;10(2):218. doi: 10.4172/1747-0862.1000218. Epub 2016 May 29. J Mol Genet Med. 2016. PMID: 27489562 Free PMC article.
First report of inherited thyroxine-binding globulin deficiency in Iran caused by a known de novo mutation in SERPINA7.
Soheilipour F, Fazilaty H, Jesmi F, Gahl WA, Behnam B. Soheilipour F, et al. Mol Genet Metab Rep. 2016 Jun 11;8:13-6. doi: 10.1016/j.ymgmr.2016.06.001. eCollection 2016 Sep. Mol Genet Metab Rep. 2016. PMID: 27331012 Free PMC article.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Braun DA, et al. Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14. Nat Genet. 2017. PMID: 28805828 Free PMC article.
Genetics and genomic medicine in Iran.
Behnam B, Zakeri M. Behnam B, et al. Mol Genet Genomic Med. 2019 Feb;7(2):e00606. doi: 10.1002/mgg3.606. Mol Genet Genomic Med. 2019. PMID: 30816028 Free PMC article.
Alteration of spermatogenesis following spermatogonial stem cells transplantation in testicular torsion-detorsion mice.
Azizollahi S, Aflatoonian R, Sadighi Gilani MA, Behnam B, Tajik N, Asghari-Jafarabadi M, Asgari HR, Koruji M. Azizollahi S, et al. J Assist Reprod Genet. 2016 Jun;33(6):771-81. doi: 10.1007/s10815-016-0708-2. Epub 2016 Apr 6. J Assist Reprod Genet. 2016. PMID: 27052833 Free PMC article.
Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.
Ahani A, Akbari MT, Saliminejad K, Behnam B, Akhondi MM, Vosoogh P, Ghassemi F, Naseripour M, Bahoush G, Khorshid HR. Ahani A, et al. Mol Vis. 2013;19:454-62. Epub 2013 Feb 22. Mol Vis. 2013. PMID: 23441118 Free PMC article.
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