Advanced filters
In Vitro Analysis of Nine MicroRNAs in CD8+ T Cells of Asthmatic Patients and the Effects of Two FDA-approved Drugs
Mohsen Badalzadeh, Marzieh Mazinani, Zahra Pourpak, Hassan Heidarnazhad, Esmaeil Mortaz, Mostafa Moin, Ali Farazmand
Published: 2019-08-17
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
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
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
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
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
Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD
Marzieh Maddah, Mohammad Reza Fazlollahi, Reza Shiari, Farhad Shahram, Setareh Mamishi, Delara Babaie, Maryam Monajemzadeh, Soheila Sotudeh, Amir Ali Hamidieh, Mohsen Badalzadeh, Shaghayegh Tajik, Leila Sedighipour, Zahra Pourpak
Published: 2019-08-17
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
1 - 9 of 9 items