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Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13D.
Vahidi M, Badalzadeh M, Jannesar M, Mazinani M, Fazlollahi MR, Khodayari Namini N, Houshmand M, Hamidieh AA, Moradi L, Pourpak Z, Moin M. Vahidi M, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2019 Oct 23;18(5):487-492. doi: 10.18502/ijaai.v18i5.1911. Iran J Allergy Asthma Immunol. 2019. PMID: 32245292 Free article.
Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).
Alizadeh Z, Fazlollahi MR, Houshmand M, Maddah M, Chavoshzadeh Z, Hamidieh AA, Shamsian BS, Eshghi P, Bolandghamat Pour S, Sadaaie Jahromi H, Mansouri M, Movahedi M, Nayebpour M, Pourpak Z, Moin M. Alizadeh Z, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2013 Mar;12(1):86-92. Iran J Allergy Asthma Immunol. 2013. PMID: 23454784 Free article.
Three novel mutations in Iranian patients with Tay-Sachs disease.
Jamali S, Eskandari N, Aryani O, Salehpour S, Zaman T, Kamalidehghan B, Houshmand M. Jamali S, et al. Among authors: houshmand m. Iran Biomed J. 2014;18(2):114-9. doi: 10.6091/ibj.1137.2013. Iran Biomed J. 2014. PMID: 24518553 Free PMC article.
DOCK8 deficiency in six Iranian patients.
Saghafi S, Pourpak Z, Nussbaumer F, Fazlollahi MR, Houshmand M, Hamidieh AA, Bemanian MH, Nabavi M, Parvaneh N, Grimbacher B, Moin M, Glocker C. Saghafi S, et al. Among authors: houshmand m. Clin Case Rep. 2016 May 17;4(6):593-600. doi: 10.1002/ccr3.574. eCollection 2016 Jun. Clin Case Rep. 2016. PMID: 27398204 Free PMC article.
226 results