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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.
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.
Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran.
Nourizadeh M, Shakerian L, Borte S, Fazlollahi M, Badalzadeh M, Houshmand M, Alizadeh Z, Dalili H, Rashidi-Nezhad A, Kazemnejad A, Moin M, Hammarström L, Pourpak Z. Nourizadeh M, et al. Among authors: houshmand m. Scand J Immunol. 2018 Aug;88(2):e12699. doi: 10.1111/sji.12699. Scand J Immunol. 2018. PMID: 29943473 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.
The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases.
Modarresi SZ, Sabetkish N, Badalzadeh M, Tajik S, Esmaeili B, Fazlollahi MR, Houshmand M, Gharehdaghi J, Niroomanesh S, Rahimi Sherbaf F, Alizadeh Z, Khodayari Namini N, Maddah M, Pourpak Z, Moin M. Modarresi SZ, et al. Among authors: houshmand m. Iran J Allergy Asthma Immunol. 2020 Oct 18;19(5):478-483. doi: 10.18502/ijaai.v19i5.4463. Iran J Allergy Asthma Immunol. 2020. PMID: 33463115 Free article.
222 results