Search Results - "Badalzadeh, Mohsen"

A New Patient with Inherited TYK2 Deficiency by Sarrafzadeh, Shokouh Azam, Mahloojirad, Maryam, Casanova, Jean-Laurent, Badalzadeh, Mohsen, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Pourpak, Zahra, Nourizadeh, Maryam, Moin, Mostafa

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A fludarabine and melphalan reduced-intensity conditioning regimen for HSCT in fifteen chronic granulomatous disease patients and a literature review by Vaezi, Mohammad, Souri, Maryam, Setarehdan, Seyed Amin, Hamidieh, Amir Ali, Fazlollahi, Mohammad Reza, Pourpak, Zahra, Badalzadeh, Mohsen, Tajik, Shaghayegh, Mahdaviani, Seyed Alireza, Alimoghaddam, Kamran, Ghavamzadeh, Ardeshir

“…Chronic granulomatous disease (CGD) is a life-threatening immunodeficiency condition. To date, hematopoietic stem cell transplantation (HSCT) is the only…”
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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 by Modarresi, Seyedeh Zalfa, Tajik, Shagayegh, Badalzadeh, Mohsen, Fazlollahi, Mohammad Reza, Houshmand, Massoud, Maddah, Marzieh, Alizadeh, Zahra, Nabavi, Mohammad, Bazargan, Nasrin, Movahedi, Masoud, Pourpak, Zahra

“…Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder more common in autosomal recessive (AR) than X-linked in Iran. This study aimed…”
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In Vitro Analysis of Nine MicroRNAs in CD8+ T Cells of Asthmatic Patients and the Effects of Two FDA-approved Drugs by Badalzadeh, Mohsen, Mazinani, Marzieh, Pourpak, Zahra, Heidarnazhad, Hassan, Mortaz, Esmaeil, Moin, Mostafa, Farazmand, Ali

“…In this study, we first tried to determine whether the expression level of 9 miRNAs in the peripheral blood CD8+ T cells of asthmatic patients varies from that…”
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Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD by Maddah, Marzieh, Fazlollahi, Mohammad Reza, Shiari, Reza, Shahram, Farhad, Mamishi, Setareh, Babaie, Delara, Monajemzadeh, Maryam, Sotudeh, Soheila, Hamidieh, Amir Ali, Badalzadeh, Mohsen, Tajik, Shaghayegh, Sedighipour, Leila, Pourpak, Zahra

“…Chronic granulomatous disease (CGD) is a rare genetic disorder of neutrophil activity, resulting in increased rate of recurrent infections with…”
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The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases by Modarresi, Seyedeh Zalfa, Sabetkish, Nastaran, Badalzadeh, Mohsen, Tajik, Shaghayegh, Esmaeili, Behnaz, Fazlollahi, Mohammad Reza, Houshmand, Massoud, Gharehdaghi, Jaber, Niroomanesh, Shirin, Sherbaf, Fatemeh Rahimi, Alizadeh, Zahra, Khodayari Namini, Nazanin, Maddah, Marzieh, Pourpak, Zahra, Moin, Mostafa

“…This study aims to investigate the role of prenatal diagnosis (PND) in Iranian couples with a previous history of primary immunodeficiency disorders (PIDD) in…”
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Investigating the Variation of TREC/KREC in Combined Immunodeficiencies by Shakerian, Leila, Nourizadeh, Maryam, Badalzadeh, Mohsen, Fazlollahi, Mohammad Reza, Shokouhi Shoormasti, Raheleh, Saghafi, Shiva, Esmaeili, Behnaz, Alizadeh, Zahra, Borte, Stephan, Houshmand, Massoud, Hammarström, Lennart, Pourpak, Zahra

“…T-cell receptor excision circles (TREC)/Kappa-deleting recombination excision circles (KREC) assay has been recently recognized for detecting patients with…”
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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 by Vahidi, Maryam, Badalzadeh, Mohsen, Jannesar, Masoomeh, Mazinani, Marzieh, Fazlollahi, Mohammad Reza, Khodayari Namini, Nazanin, Houshmand, Massoud, Hamidieh, Amir Ali, Moradi, Leila, Pourpak, Zahra, Moin, Mostafa

“…Familial haemophagocytic lymphohistiocytosis (FHL) is a rare disorder of immune dysregulation. FHL inherited in an autosomal recessive pattern is classified…”
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A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran by Tajik, Shaghayegh, Badalzadeh, Mohsen, Fazlollahi, Mohammad Reza, Houshmand, Massoud, Zandieh, Fariborz, Khandan, Shamim, Pourpak, Zahra

“…Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder due to a genetic defect in one of the components of nicotinamide adenine…”
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Identification of a 53 kDa protein, as a new high molecular weight allergen from Fraxinusexcelsior (Ash) pollen by Sharif Shoushtari, Maryam, Majd, Ahmad, Assarehzadegan, Mohammad-Ali, Fanuel, Songwe, Moin, Mostafa, Nejadsattari, Taher, Shoormasti, Raheleh Shokouhi, Badalzadeh, Mohsen, Tajik, Shaghayegh, Fazlollahi, Mohammad Reza, Tayebi, Behnoosh, Pourpak, Zahra, Kardar, Gholam Ali

“…Summary Background Fraxinus excelsior (Ash) is a common tree and is important cause of winter–spring pollinosis in many temperate regions in the world. In this…”
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Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: the gene encoding the p67-phox by Badalzadeh, Mohsen, Fattahi, Fatemeh, Fazlollahi, Mohammad Reza, Tajik, Shaghayegh, Bemanian, Mohammad Hassan, Behmanesh, Fatemeh, Movahedi, Massoud, Houshmand, Massoud, Pourpak, Zahra

“…Chronic granulomatous disease (CGD), a rare inherited primary immunodeficiency disorder, is caused by mutation in any one of the genes encoding components of…”
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Determining reference ranges for lymphocyte proliferation responses to phytohemagglutinin and Bacillus Calmette–Guérin in Iranian children by Nourizadeh, Maryam, Sarrafzadeh, Shokouh Azam, Shoormasti, Raheleh Shokouhi, Fazlollahi, Mohammad Reza, Saghafi, Shiva, Badalzadeh, Mohsen, Mirmoghtadaei, Milad, Pourpak, Zahra

“…To establish reference ranges (RRs) for stimulation index of T cell proliferation triggered by phytohemagglutinin (PHA-SI) and Bacillus Calmette–Guérin…”
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Increased Expression Level of Human Blood Clotting Factor VIII Using NS0 Cell Line as a Host Cells by Zarei, Mahboobeh, Ferdosi-Shahandashti, Elaheh, Badalzadeh, Mohsen, Kardar, Gholam Ali

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Purine Nucleoside Phosphorylase Deficiency in Two Unrelated Patients with Autoimmune Hemolytic Anemia and Eosinophilia: Two Novel Mutations by Alizadeh, Zahra, Badalzadeh, Mohsen, Heydarlou, Hanieh, Shakerian, Leila, Mahlooji Rad, Maryam, Zandieh, Fariborz, Fazlollahi, Mohammad Reza

“…Two Iranian patients with purine nucleoside phosphorylase (PNP) deficiency are described in terms of their clinical and molecular evaluations. PNP deficiency…”
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Early diagnosis of immunodeficient patients with partial albinism: The role of hair study and peripheral blood smear by Tajik, Shaghayegh, Fazlollahi, Mohammad Reza, Alizadeh, Zahra, Badalzadeh, Mohsen, Houshmand, Massoud, Razaghian, Anahita, Bahram, Seiamak, Molitor, Anne, Carapito, Raphael, Shariat, Mansoureh, Hamidieh, Amir Ali, Behniafard, Nasrin, Abdolkarimi, Babak, Rostami, Tahereh, Moin, Mostafa, Pourpak, Zahra

“…Primary immunodeficiency diseases (inborn errors of immunity) with partial albinism are a group of autosomal recessive syndromes including Chediak Higashi…”
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Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient by Tajik, Shaghayegh, Badalzadeh, Mohsen, Houshmand, Massoud, Alizadeh, Zahra, Moradi, Leila, Hamidieh, Amir Ali, Shafiei, Alireza, Heris, Javad Ahmadiani, Bahram, Seiamak, Molitor, Anne, Carapito, Raphael, Moin, Mostafa, Fazlollahi, Mohammad Reza, Pourpak, Zahra

“…Griscelli syndrome type 2 (GS2) is an autosomal recessive immunodeficiency characterized by hair hypopigmentation, recurrent fever, hepatosplenomegaly and…”
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Clinical, immunological and molecular findings of 8 patients with typical and atypical severe combined immunodeficiency: identification of 7 novel mutations by whole exome sequencing by Alizadeh, Zahra, Fazlollahi, Mohammad Reza, Mazinani, Marzieh, Badalzadeh, Mohsen, Heydarlou, Hanieh, Carapito, Raphael, Molitor, Anne, de Oteyza, Andrés Caballero Garcia, Proietti, Michele, Bavani, Maryam Soleimani, Shariat, Mansoureh, Fallahpour, Morteza, Movahedi, Masoud, Moradi, Leila, Grimbacher, Bodo, Bahram, Seiamak, Pourpak, Zahra

“…Severe combined immunodeficiency (SCID) is one of the severe inborn errors of the immune system associated with life-threatening infections. Variations in SCID…”
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Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease by Sarrafzadeh, Shokouh Azam, Nourizadeh, Maryam, Mahloojirad, Maryam, Fazlollahi, Mohammad Reza, Shokouhi Shoormasti, Raheleh, Badalzadeh, Mohsen, Deswarte, Caroline, Casanova, Jean-Laurent, Pourpak, Zahra, Bustamante, Jacinta, Moin, Mostafa

“…Purpose Mendelian susceptibility to mycobacterial disease (MSMD) is a rare primary immunodeficiency, triggered by non-tuberculous mycobacteria or Bacillus…”
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Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran by Nourizadeh, Maryam, Shakerian, Leila, Borte, Stephan, Fazlollahi, Mohammadreza, Badalzadeh, Mohsen, Houshmand, Massoud, Alizadeh, Zahra, Dalili, Hossein, Rashidi‐Nezhad, Ali, Kazemnejad, Anoshirvan, Moin, Mostafa, Hammarström, Lennart, Pourpak, Zahra

“…T‐cell receptor excision circles (TRECs) and κ‐deleting recombination excision circles (KRECs) are recently used for detection of T or B cell lymphopenia in…”
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Genetic and molecular findings of 38 Iranian patients with chronic granulomatous disease caused by p47‐phox defect by Tajik, Shaghayegh, Badalzadeh, Mohsen, Fazlollahi, Mohammad Reza, Houshmand, Massoud, Bazargan, Nasrin, Movahedi, Masoud, Mahlouji Rad, Maryam, Mahdaviani, Seyed Alireza, Mamishi, Setareh, Khotaei, Ghamar Taj, Mansouri, Davood, Zandieh, Fariborz, Pourpak, Zahra

“…One of the components of NADPH oxidase is p47‐phox, encoded by NCF1 gene. This study aims to find new genetic changes and clinical features in 38 Iranian…”
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