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A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran
Shaghayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Fariborz Zandieh, Shamim Khandan, Zahra Pourpak
Published: 2016-10-31
IL7R and RAG1/2 Genes Mutations/Polymorphisms in Patients SCID
Sepideh Safaei, Zahra Pourpak, Mostafa Moin, Massoud Houshmand
Molecular Analysis of Four Cases of Chronic Granulomatous Disease Caused by Defects in NCF-2: The Gene Encoding the p67-phox
Mohsen Badalzadeh, Fatemeh Fattahi, Mohammad Reza Fazlollahi, Shaghayegh Tajik, Mohammad Hassan Bemanian, Fatemeh Behmanesh, Massoud Movahedi, Massoud Houshmand, Zahra Pourpak
Different Pattern of Gene Mutations in Iranian Patients with Severe Congenital Neutropenia (Including 2 New Mutations)
Zahra Alizadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Marzieh Maddah, Zahra Chavoshzadeh, Amir Ali Hamidieh, Bibi Shahin Shamsian, Payman Eshghi, Samaneh Bolandghamat Pour, Hoda Sadaaie Jahromi, Mahboobeh Mansouri, Masoud Movahedi, Mohsen Nayebpour, Zahra Pourpak, Mostafa Moin
Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations
Shiva Saghafi, Fariborz Zandieh, Mohammad Reza Fazlollahi, Cristina Glocker, Natalie Frede, Mary Buchta, Linlin Yang, Amir Hossein Mahmoudi, Massoud Houshmand, Zahra Pourpak, Bodo Grimbacher, Mostafa Moin
Published: 2022-06-18
Investigating the Variation of TREC/KREC in Combined Immunodeficiencies
Leila Shakerian, Maryam Nourizadeh, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Raheleh Shokouhi Shoormasti, Shiva Saghafi, Behnaz Esmaeili, Zahra Alizadeh, Stephan Borte, Massoud Houshmand, Lennart Hammarström, Zahra Pourpak
Published: 2021-08-07
The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases
Seyedeh Zalfa Modarresi, Nastaran Sabetkish, Mohsen Badalzadeh, Shaghayegh Tajik, Behnaz Esmaeili, Mohammad Reza Fazlollahi, Massoud Houshmand, Jaber Gharehdaghi, Shirin Niroomanesh, Fatemeh Rahimi Sherbaf, Zahra Alizadeh, Nazanin Khodayari Namini, Marzieh Maddah, Zahra Pourpak, Mostafa Moin
Published: 2020-10-18
Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13D
Maryam Vahidi, Mohsen Badalzadeh, Masoomeh Jannesar, Marzieh Mazinani, Mohammad Reza Fazlollahi, Nazanin Khodayari Namini, Massoud Houshmand, Amir Ali Hamidieh, Leila Moradi, Zahra Pourpak, Mostafa Moin
Published: 2019-10-23
Clinical Characterization and Mutation Analysis of 13 Iranian Ataxia Telangiectasia Patients: Introducing Two Novel Mutations
Mohsen Badalzadeh, Maryam Soleimani Bavani, Zahra Alizadeh, Milad Mirmoghtadaei, Leila Shakerian, Seiamak Bahram, Anne Molitor, Raphael Carapito, Leila Moradi, Anahita Razaghian, Raheleh Assari, Masoud Movahedi, Mansoureh Shariat, Massoud Houshmand, Laleh Habibi, Amir Ali Hamidieh, Mahmoud Reza Ashrafi, Zahra Pourpak
Published: 2025-03-10
The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child
Seyedeh Zalfa Modarresi, Shagayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Marzieh Maddah, Zahra Alizadeh, Mohammad Nabavi, Nasrin Bazargan, Masoud Movahedi, Zahra Pourpak
Published: 2023-02-20
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