Search Results - "Molatefi, Rasol"

Impact of SARS-CoV-2 Pandemic on Patients with Primary Immunodeficiency by Delavari, Samaneh, Abolhassani, Hassan, Abolnezhadian, Farhad, Babaha, Fateme, Iranparast, Sara, Ahanchian, Hamid, Moazzen, Nasrin, Nabavi, Mohammad, Arshi, Saba, Fallahpour, Morteza, Bemanian, Mohammad Hassan, Shokri, Sima, Momen, Tooba, Sadeghi-Shabestari, Mahnaz, Molatefi, Rasol, Shirkani, Afshin, Vosughimotlagh, Ahmad, Safarirad, Molood, Sharifzadeh, Meisam, Pashangzadeh, Salar, Salami, Fereshte, Shirmast, Paniz, Rezaei, Arezou, Moeini Shad, Tannaz, Mohraz, Minoo, Rezaei, Nima, Hammarström, Lennart, Yazdani, Reza, Aghamohamamdi, Asghar

“…Although it is estimated that COVID-19 life-threatening conditions may be diagnosed in less than 1:1000 infected individuals below the age of 50, but the real…”
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The interaction of inflammasomes and gut microbiota: novel therapeutic insights by Manshouri, Shirin, Seif, Farhad, Kamali, Monireh, Bahar, Mohammad Ali, Mashayekh, Arshideh, Molatefi, Rasol

“…Inflammasomes are complex platforms for the cleavage and release of inactivated IL-1β and IL-18 cytokines that trigger inflammatory responses against…”
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Juvenile idiopathic recurrent parotitis (JIRP) treated with short course steroids, a case series study and one decade follow up for potential autoimmune disorder by Salehzadeh, Farhad, Molatefi, Rasol, Mardi, Ali, Nahanmoghaddam, Negin

“…Juvenile idiopathic recurrent parotitis (JIRP) in children is a condition characterized with recurrent episodes of idiopathic parotid gland inflammation. Since…”
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Thymus vulgaris ameliorates cough in children with asthma exacerbation: a randomized, triple-blind, placebo-controlled clinical trial by Eskandarpour, Elnaz, Ahadi, Adel, Jazani, Arezoo Moini, Azgomi, Ramin Nasimi Doost, Molatefi, Rasol

“…Asthma is one of the most common chronic respiratory diseases with inflammatory involvement and has a high burden worldwide. This study aimed to determine the…”
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Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes by Mokhtari, Diana, Jahanpanah, Mohammad, Jabbari, Nasim, Azari, Hamed, Davarnia, Sana, Mokaber, Haleh, Arish, Sara, Molatefi, Rasol, Abbasi, Vahid, Davarnia, Behzad

“…Hereditary ataxias are classified by inheritance patterns into autosomal dominant, autosomal recessive, X-linked, and mitochondrial modes of inheritance. A…”
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Clues of HLAs, metabolic SNPs, and epigenetic factors in T cell-mediated drug hypersensitivity reactions by Molatefi, Rasol, Talebi, Sedighe, Samei, Azam, Roshanravan, Neda, Manshouri, Shirin, Hashemi, Baran, Ghobadi Dana, Vahid, Mosharkesh, Erfan, Bahar, Mohammad Ali, Khajoei, Sholeh, Seif, Farhad

“…Drug hypersensitivities are common reactions due to immunologic responses. They are of utmost importance because they may generate severe and fatal outcomes…”
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Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis by Abolhassani, Hassan, Kiaee, Fatemeh, Tavakol, Marzieh, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Yazdani, Reza, Azizi, Gholamreza, Habibi, Sima, Gharagozlou, Mohammad, Movahedi, Masoud, Hamidieh, Amir Ali, Behniafard, Nasrin, Nabavi, Mohammamd, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Shirkani, Afshin, Amin, Reza, Aleyasin, Soheila, Faridhosseini, Reza, Jabbari-Azad, Farahzad, Mohammadzadeh, Iraj, Ghaffari, Javad, Shafiei, Alireza, Kalantari, Arash, Mansouri, Mahboubeh, Mesdaghi, Mehrnaz, Babaie, Delara, Ahanchian, Hamid, Khoshkhui, Maryam, Soheili, Habib, Eslamian, Mohammad Hossein, Cheraghi, Taher, Dabbaghzadeh, Abbas, Tavassoli, Mahmoud, Kalmarzi, Rasoul Nasiri, Mortazavi, Seyed Hamidreza, Kashef, Sara, Esmaeilzadeh, Hossein, Tafaroji, Javad, Khalili, Abbas, Zandieh, Fariborz, Sadeghi-Shabestari, Mahnaz, Darougar, Sepideh, Behmanesh, Fatemeh, Akbari, Hedayat, Zandkarimi, Mohammadreza, Abolnezhadian, Farhad, Fayezi, Abbas, Moghtaderi, Mojgan, Ahmadiafshar, Akefeh, Shakerian, Behzad, Sajedi, Vahid, Taghvaei, Behrang, Safari, Mojgan, Heidarzadeh, Marzieh, Ghalebaghi, Babak, Fathi, Seyed Mohammad, Darabi, Behzad, Bazregari, Saeed, Bazargan, Nasrin, Fallahpour, Morteza, Khayatzadeh, Alireza, Javahertrash, Naser, Bashardoust, Bahram, Zamani, Mohammadali, Mohsenzadeh, Azam, Ebrahimi, Sarehsadat, Sharafian, Samin, Vosughimotlagh, Ahmad, Tafakoridelbari, Mitra, Rahimi, Maziar, Ashournia, Parisa, Razaghian, Anahita, Rezaei, Arezou, Mamishi, Setareh, Parvaneh, Nima, Rezaei, Nima, Hammarström, Lennart, Aghamohammadi, Asghar

“…Background The number of inherited diseases and the spectrum of clinical manifestations of primary immunodeficiency disorders (PIDs) are ever-expanding…”
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Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency by Abolhassani, Hassan, Chou, Janet, Bainter, Wayne, Platt, Craig D., Tavassoli, Mahmood, Momen, Tooba, Tavakol, Marzieh, Eslamian, Mohammad Hossein, Gharagozlou, Mohammad, Movahedi, Masoud, Ghadami, Mohsen, Hamidieh, Amir Ali, Azizi, Gholamreza, Yazdani, Reza, Afarideh, Mohsen, Ghajar, Alireza, Havaei, Arash, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Cheraghi, Taher, Behniafard, Nasrin, Amin, Reza, Aleyasin, Soheila, Faridhosseini, Reza, Jabbari-Azad, Farahzad, Nabavi, Mohammamd, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Mansouri, Mahboubeh, Mesdaghi, Mehrnaz, Babaie, Delara, Mohammadzadeh, Iraj, Ghaffari, Javad, Shafiei, Alireza, Kalantari, Najmeddin, Ahanchian, Hamid, Khoshkhui, Maryam, Soheili, Habib, Dabbaghzadeh, Abbas, Shirkani, Afshin, Nasiri Kalmarzi, Rasoul, Mortazavi, Seyed Hamidreza, Tafaroji, Javad, Khalili, Abbas, Mohammadi, Javad, Negahdari, Babak, Joghataei, Mohammad-Taghi, al-Ramadi, Basel K., Picard, Capucine, Parvaneh, Nima, Rezaei, Nima, Chatila, Talal A., Massaad, Michel J., Keles, Sevgi, Hammarström, Lennart, Geha, Raif S., Aghamohammadi, Asghar

“…Combined immunodeficiencies (CIDs) are diseases of defective adaptive immunity with diverse clinical phenotypes. Although CIDs are more prevalent in the Middle…”
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Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients by Momtazmanesh, Sara, Rayzan, Elham, Zoghi, Samaneh, Shahkarami, Sepideh, Molatefi, Rasol, Mohammadzadeh, Iraj, Ghaffari, Javad, Mahmoudi, Hamidreza, Dmytrus, Jasmin, Segarra-Roca, Anna, Somekh, Ido, Witzel, Maximilian, Hauck, Fabian, Boztug, Kaan, Klein, Christoph, Rezaei, Nima

“…Dedicator of Cytokinesis 8 (DOCK8) deficiency, the most frequent cause of autosomal recessive hyper immunoglobulin (Ig)E syndrome, is a rare combined…”
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Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity by Azizi, Gholamreza, Tavakol, Marzieh, Yazdani, Reza, Delavari, Samaneh, Moeini Shad, Tannaz, Rasouli, Seyed Erfan, Jamee, Mahnaz, Pashangzadeh, Salar, Kalantari, Arash, Shariat, Mansoureh, Shafiei, Alireza, Mohammadi, Javad, Hassanpour, Gholamreza, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Behniafard, Nasrin, Nabavi, Mohammad, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Shirkani, Afshin, Alyasin, Soheila, Jabbari‐Azad, Farahzad, Ghaffari, Javad, Mesdaghi, Mehrnaz, Ahanchian, Hamid, Khoshkhui, Maryam, Eslamian, Mohammad Hossein, Cheraghi, Taher, Dabbaghzadeh, Abbas, Nasiri Kalmarzi, Rasoul, Esmaeilzadeh, Hossein, Tafaroji, Javad, Khalili, Abbas, Sadeghi‐Shabestari, Mahnaz, Darougar, Sepideh, Moghtaderi, Mojgan, Ahmadiafshar, Akefeh, Shakerian, Behzad, Heidarzadeh, Marzieh, Ghalebaghi, Babak, Fathi, Seyed Mohammad, Darabi, Behzad, Fallahpour, Morteza, Mohsenzadeh, Azam, Ebrahimi, Sarehsadat, Sharafian, Samin, Vosughimotlagh, Ahmad, Tafakoridelbari, Mitra, Rahimi Haji‐Abadi, Maziyar, Ashournia, Parisa, Razaghian, Anahita, Rezaei, Arezou, Salami, Fereshte, Shirmast, Paniz, Bazargan, Nasrin, Mamishi, Setareh, Khazaei, Hossein Ali, Negahdari, Babak, Shokri, Sima, Nabavizadeh, Seyed Hesamedin, Bazregari, Saeed, Ghasemi, Ramin, Bayat, Shiva, Eshaghi, Hamid, Rezaei, Nima, Abolhassani, Hassan, Aghamohammadi, Asghar, Atanaskovic‐Markovic, Marina

“…Background The inborn errors of immunity (IEIs) are a group of heterogeneous disorders mainly characterized by severe and recurrent infections besides other…”
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Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort by Yazdani, Reza, Abolhassani, Hassan, Kiaee, Fatemeh, Habibi, Sima, Azizi, Gholamreza, Tavakol, Marzieh, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Gharagozlou, Mohammad, Movahedi, Masoud, Hamidieh, Amir Ali, Behniafard, Nasrin, Nabavi, Mohammamd, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Shirkani, Afshin, Amin, Reza, Aleyasin, Soheila, Faridhosseini, Reza, Jabbari-Azad, Farahzad, Mohammadzadeh, Iraj, Ghaffari, Javad, Shafiei, Alireza, Kalantari, Arash, Mansouri, Mahboubeh, Mesdaghi, Mehrnaz, Babaie, Delara, Ahanchian, Hamid, Khoshkhui, Maryam, Soheili, Habib, Eslamian, Mohammad Hossein, Cheraghi, Taher, Dabbaghzadeh, Abbas, Tavassoli, Mahmoud, Kalmarzi, Rasoul Nasiri, Mortazavi, Seyed Hamidreza, Kashef, Sara, Esmaeilzadeh, Hossein, Tafaroji, Javad, Khalili, Abbas, Zandieh, Fariborz, Sadeghi-Shabestari, Mahnaz, Darougar, Sepideh, Behmanesh, Fatemeh, Akbari, Hedayat, Zandkarimi, Mohammadreza, Abolnezhadian, Farhad, Fayezi, Abbas, Moghtaderi, Mojgan, Ahmadiafshar, Akefeh, Shakerian, Behzad, Sajedi, Vahid, Taghvaei, Behrang, Safari, Mojgan, Heidarzadeh, Marzieh, Ghalebaghi, Babak, Fathi, Seyed Mohammad, Darabi, Behzad, Bazregari, Saeed, Bazargan, Nasrin, Fallahpour, Morteza, Khayatzadeh, Alireza, Javahertrash, Naser, Bashardoust, Bahram, Zamani, Mohammadali, Mohsenzadeh, Azam, Ebrahimi, Sarehsadat, Sharafian, Samin, Vosughimotlagh, Ahmad, Tafakoridelbari, Mitra, Rahim, Maziar, Ashournia, Parisa, Razaghian, Anahita, Rezaei, Arezou, Samavat, Ashraf, Mamishi, Setareh, Khazaei, Hossein Ali, Mohammadi, Javad, Negahdari, Babak, Parvaneh, Nima, Rezaei, Nima, Lougaris, Vassilios, Giliani, Silvia, Plebani, Alessandro, Ochs, Hans D., Hammarström, Lennart, Aghamohammadi, Asghar

“…Predominantly antibody deficiencies (PADs) are the most common primary immunodeficiencies, characterized by hypogammaglobulinemia and inability to generate…”
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Adverse reactions in a large cohort of patients with inborn errors of immunity receiving intravenous immunoglobulin by Esmaeilzadeh, Hossein, Askarisarvestani, Aida, Hosseini, Nazanin, Samimi, Sahar, Shafiei, Alireza, Mahdaviani, Seyed Alireza, Eslami, Narges, Chavoshzadeh, Zahra, Fallahi, Mazdak, Khakbazanfard, Nasrin, Shabestari, Mahnaz Sadeghi, Aleyasin, Soheila, Nabavizadeh, Seyed Hesamedin, Cheraghi, Taher, Kalantari, Arash, Ahmadiafshar, Akefeh, Safari, Mojgan, Eslamian, Mohammad Hossein, Molatefi, Rasol, Shirkani, Afshin, Heidarzadeh Arani, Marzieh, Tavakol, Marzieh, Bemanian, Mohammad Hassan, Arshi, Saba, Nabavi, Mohammad, Shokri, Sima, Shahhosseini, Babak, Mortazavi, Negar, Nakhaei, Pooria, Nazari, Farzad, Fallahpour, Morteza, Ahanchian, Hamid, Moazzen, Nasrin, Khoshkhui, Maryam, Motlagh, Ahmad Vosughi, Aghamohammadi, Asghar, Abolhassani, Hassan, Yazdani, Reza, Rezaei, Nima

“…Intravenous immunoglobulins (IVIg) are the major treatment in inborn errors of immunity (IEI) disorders; However, IVIg infusions show some adverse effects. We…”
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Phenotyping and follow up of forty-seven Iranian patients with common variable immunodeficiency by Arshi, Saba, Nabavi, Mohammad, Bemanian, Mohammad Hasan, Shakeri, Ramin, Taghvaei, Behrang, Ghalebaghi, Babak, Babaie, Delara, Bahrami, Ahmad, Fallahpour, Morteza, Esmaeilzadeh, Hossein, Rekabi, Mahsa, Amadian, Javad, Eslami, Narjes, Shokri, Sima, Jalali, Farhad, Akbarpour, Nadieh, Molatefi, Rasol, Rezaei, Nima

“…Common variable immune deficiency (CVID) is a heterogeneous syndrome with a wide variety of signs and symptoms. This study describes the phenotyping and…”
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