Hasil Pencarian - Mohsen Badalzadeh

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  1. 1
    In Vitro Analysis of Nine MicroRNAs in CD8+ T Cells of Asthmatic Patients and the Effects of Two FDA-approved Drugs

    In Vitro Analysis of Nine MicroRNAs in CD8+ T Cells of Asthmatic Patients and the Effects of Two FDA-approved Drugs oleh Mohsen Badalzadeh, Marzieh Mazinani, Zahra Pourpak, Hassan Heidarnazhad, Esmaeil Mortaz, Mostafa Moin, Ali Farazmand

    Diterbitkan 2019-08-01
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  2. 2
    A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran

    A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran oleh Shaghayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Fariborz Zandieh, Shamim Khandan, Zahra Pourpak

    Diterbitkan 2016-10-01
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  3. 3
    Molecular Analysis of Four Cases of Chronic Granulomatous Disease Caused by Defects in NCF-2: The Gene Encoding the p67-phox

    Molecular Analysis of Four Cases of Chronic Granulomatous Disease Caused by Defects in NCF-2: The Gene Encoding the p67-phox oleh Mohsen Badalzadeh, Fatemeh Fattahi, Mohammad Reza Fazlollahi, Shaghayegh Tajik, Mohammad Hassan Bemanian, Fatemeh Behmanesh, Massoud Movahedi, Massoud Houshmand, Zahra Pourpak

    Diterbitkan 2012-12-01
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  4. 4
    The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child

    The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child oleh Seyedeh Zalfa Modarresi, Shagayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Marzieh Maddah, Zahra Alizadeh, Mohammad Nabavi, Nasrin Bazargan, Masoud Movahedi, Zahra Pourpak

    Diterbitkan 2023-02-01
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  5. 5
    Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13D

    Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13D oleh 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

    Diterbitkan 2019-10-01
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  6. 6
    Investigating the Variation of TREC/KREC in Combined Immunodeficiencies

    Investigating the Variation of TREC/KREC in Combined Immunodeficiencies oleh 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

    Diterbitkan 2021-08-01
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  7. 7
    Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD

    Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD oleh 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

    Diterbitkan 2019-08-01
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  8. 8
    The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases

    The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases oleh 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

    Diterbitkan 2020-10-01
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