Houshmand M - Search Results

1

First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations.

Jalalirad M, Houshmand M, Mirfakhraie R, Goharbari MH, Mirzajani F. Jalalirad M, et al. Among authors: houshmand m. J Trop Pediatr. 2004 Dec;50(6):359-61. doi: 10.1093/tropej/50.6.359. J Trop Pediatr. 2004. PMID: 15537723

2

The first study of galactose-1-phosphate uridyl transferase mutations in Iranian galactosemia patients.

Mirzajani F, Mirfakhraie R, Nabati F, Tabatabaei NN, Talachian E, Houshmand M. Mirzajani F, et al. Among authors: houshmand m. Clin Biochem. 2006 Jul;39(7):697-9. doi: 10.1016/j.clinbiochem.2006.04.020. Clin Biochem. 2006. PMID: 16765930

3

The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.

Safinejad K, Darbouy M, Kalantar SM, Zeinali S, Mirfakhraie R, Yadegar L, Houshmand M. Safinejad K, et al. Among authors: houshmand m. J Assist Reprod Genet. 2011 Nov;28(11):1087-90. doi: 10.1007/s10815-011-9632-7. Epub 2011 Oct 6. J Assist Reprod Genet. 2011. PMID: 21976147 Free PMC article.

4

BAK, BAX, and NBK/BIK proapoptotic gene alterations in Iranian patients with ataxia telangiectasia.

Isaian A, Bogdanova NV, Houshmand M, Movahadi M, Aghamohammadi A, Rezaei N, Atarod L, Sadeghi-Shabestari M, Tonekaboni SH, Chavoshzadeh Z, Hassani SM, Mirfakhrai R, Cheraghi T, Kalantari N, Ataei M, Dork-Bousset T, Sanati MH. Isaian A, et al. Among authors: houshmand m. J Clin Immunol. 2010 Jan;30(1):132-7. doi: 10.1007/s10875-009-9340-6. Epub 2009 Nov 7. J Clin Immunol. 2010. PMID: 19898928

5

Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.

Safaei S, Fazlollahi MR, Houshmand M, Hamidieh AA, Bemanian MH, Alavi S, Mousavi F, Pourpak Z, Moin M. Safaei S, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2012 Dec;11(4):345-8. Iran J Allergy Asthma Immunol. 2012. PMID: 23264413 Free article.

6

Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene.

Houshmand M, Mahmoudi T, Panahi MS, Seyedena Y, Saber S, Ataei M. Houshmand M, et al. Braz J Med Biol Res. 2006 Jun;39(6):725-30. doi: 10.1590/s0100-879x2006000600004. Epub 2006 Jun 2. Braz J Med Biol Res. 2006. PMID: 16751977 Free article.

7

Novel mutations of CHST6 in Iranian patients with macular corneal dystrophy.

Birgani SA, Salehi Z, Houshmand M, Mohamadi MJ, Promehr LA, Mozafarzadeh Z. Birgani SA, et al. Among authors: houshmand m. Mol Vis. 2009;15:373-7. Epub 2009 Feb 18. Mol Vis. 2009. PMID: 19223992 Free PMC article.

8

Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations).

Nabilou S, Pak F, Alizadeh Z, Fazlollahi MR, Houshmand M, Ayazi M, Mohammadzadeh I, Bemanian MH, Fayezi A, Nabavi M, Saghafi S, Mohammadian S, Kokhaei P, Moin M, Pourpak Z. Nabilou S, et al. Among authors: houshmand m. Immunol Invest. 2022 Jan;51(1):170-181. doi: 10.1080/08820139.2020.1817068. Epub 2020 Sep 8. Immunol Invest. 2022. PMID: 32896191

9

Genetic Analysis of Patients with Two Different Types of Hyper IgM Syndrome.

Alizadeh Z, Mazinani M, Houshmand M, Shakerian L, Nourizadeh M, Pourpak Z, Fazlollahi MR. Alizadeh Z, et al. Among authors: houshmand m. Immunol Invest. 2018 Oct;47(7):745-753. doi: 10.1080/08820139.2018.1493052. Epub 2018 Aug 6. Immunol Invest. 2018. PMID: 30081731

10

Novel Mutations in Sandhoff Disease: A Molecular Analysis among Iranian Cohort of Infantile Patients.

Aryan H, Aryani O, Banihashemi K, Zaman T, Houshmand M. Aryan H, et al. Among authors: houshmand m. Iran J Public Health. 2012;41(3):112-8. Epub 2012 Mar 31. Iran J Public Health. 2012. PMID: 23113155 Free PMC article.

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