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Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient.
Tajik S, Badalzadeh M, Houshmand M, Alizadeh Z, Moradi L, Hamidieh AA, Shafiei A, Heris JA, Bahram S, Molitor A, Carapito R, Moin M, Fazlollahi MR, Pourpak Z. Tajik S, et al. Among authors: houshmand m. Scand J Immunol. 2023 May;97(5):e13264. doi: 10.1111/sji.13264. Epub 2023 Mar 21. Scand J Immunol. 2023. PMID: 37368332 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.
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.
A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran.
Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Zandieh F, Khandan S, Pourpak Z. Tajik S, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2016 Oct;15(5):426-429. Iran J Allergy Asthma Immunol. 2016. PMID: 27917630 Free article.
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.
Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations.
Saghafi S, Zandieh F, Fazlollahi MR, Glocker C, Frede N, Buchta M, Yang L, Mahmoudi AH, Houshmand M, Pourpak Z, Grimbacher B, Moin M. Saghafi S, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2022 Jun 18;21(3):355-363. doi: 10.18502/ijaai.v21i3.9809. Iran J Allergy Asthma Immunol. 2022. PMID: 35822685 Free article.
The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child.
Modarresi SZ, Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Maddah M, Alizadeh Z, Nabavi M, Bazargan N, Movahedi M, Pourpak Z. Modarresi SZ, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2023 Feb 20;22(1):119-123. doi: 10.18502/ijaai.v22i1.12014. Iran J Allergy Asthma Immunol. 2023. PMID: 37002626 Free article.
225 results