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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: khodayari namini n. 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: khodayari namini n. 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.