Search Results - "Razaghian, Anahita"

Tumor Necrosis Factor-α (-308G>A) Gene Polymorphism and Its Association with Asthma and Atopy Status by Razaghian, Anahita, Parvaneh, Nima, Amirzargar, Ali Akbar, Gharagozlou, Mohammad

“…Asthma is one of the most prevalent chronic lung diseases that afflict genetically predisposed individuals. Certain cytokine gene polymorphisms have been…”
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Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector Engagement by Ohishi, Yuta, Ammann, Sandra, Ziaee, Vahid, Strege, Katharina, Groß, Miriam, Amos, Carla Vazquez, Shahrooei, Mohammad, Ashournia, Parisa, Razaghian, Anahita, Griffiths, Gillian M, Ehl, Stephan, Fukuda, Mitsunori, Parvaneh, Nima

“…Griscelli syndrome type 2 (GS-2) is an inborn error of immunity characterized by partial albinism and episodes of hemophagocytic lymphohistiocytosis (HLH). It…”
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Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma by Razaghian, Anahita, Parvaneh, Leila, Delkhah, Mona, Abbasi, Arash, Sadeghirad, Parisa, Shahrooei, Mohammad, Parvaneh, Nima

“…Hemophagocytic lymphohistiocytosis (HLH) disease is a severe immune dysregulation caused by mutations in genes required for lymphocyte cytotoxicity function…”
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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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Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis by Shabani, Mahsima, Razaghian, Anahita, Alimadadi, Hosein, Shiari, Reza, Shahrooei, Mohammad, Parvaneh, Nima

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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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Association between IL-10 (at position -592) and IL-4 (at position -589) genotype polymorphism with atopic and non-atopic asthma in children by Razaghian, Anahita, Parvaneh, Nima, Amirzargar, Ali Akbar, Nirouei, Matineh, Gharagozlou, Mohammad

“…OBJECTIVESAsthma is the most prevalent respiratory disease, caused by chronic bronchial inflammation. Cytokines are known to play an important role in the…”
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Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity by Asgardoon, Mohammad Hossein, Azizi, Gholamreza, Yazdani, Reza, Sohani, Mahsa, Pashangzadeh, Salar, Kalantari, Arash, Shariat, Mansoureh, Shafiei, Alireza, Salami, Fereshte, Jamee, Mahnaz, Rasouli, Seyed Erfan, Mohammadi, Javad, Hassanpour, Gholamreza, Tavakol, Marziyeh, 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, Delavari, Samaneh, Shirmast, Paniz, Babaha, Fateme, Samavat, Ashraf, Mamishi, Setareh, Khazaei, Hossein Ali, Negahdari, Babak, Rezaei, Nima, Abolhassani, Hassan, Aghamohammadi, Asghar

“…Common variable immunodeficiency (CVID) is the most frequent primary immunodeficiency disorder mainly characterized by recurrent bacterial infections besides…”
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Clinical and immunological characteristics of 69 leukocyte adhesion deficiency‐I patients by Fazlollahi, Mohammad Reza, Hamidieh, Amir Ali, Moradi, Leila, Shokouhi Shoormati, Raheleh, Sabetkish, Nastaran, Esmaeili, Behnaz, Badalzadeh, Mohsen, Alizadeh, Zahra, Shamlou, Somayeh, Movahedi, Masoud, Mahloujirad, Maryam, Razaghian, Anahita, Arshi, Saba, Gharagozlou, Mohammad, Kalantari, Arash, Bemanian, Mohammad Hassan, Safari, Mojgan, Heidarzadeh Arani, Marzieh, Nabavi, Mohammad, Parvaneh, Nima, Sadeghi‐Shabestari, Mahnaz, Behfar, Maryam, Behniafard, Nasrin, Sherkat, Roya, Ahmadian Heris, Javad, Shariat, Mansoureh, Radmehr, Roshanak, Houshmand, Massoud, Kazemnejad, Anoshirvan, Molitor, Anne, Carapito, Raphael, Bahram, Seiamak, Pourpak, Zahra, Moin, Mostafa

“…Background In order to support the comprehensive classification of Leukocyte Adhesion Deficiency‐I (LAD‐I) severity by simultaneous screening of CD11a/CD18,…”
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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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Evaluation of respiratory complications in patients with X‐linked and autosomal recessive agammaglobulinemia by Fekrvand, Saba, Yazdani, Reza, Olbrich, Peter, Azizi, Gholamreza, Shirzadi, Rohola, Modaresi, Mohammadreza, Sohani, Mahsa, Delavari, Samaneh, Kalantari, Arash, Shariat, Mansoureh, Shafiei, Alireza, Lu, Na, Hassanpour, Gholamreza, Rahimi Hajiabadi, Maziar, Ashournia, Parisa, Razaghian, Anahita, Asgharyan, Marzieh, Shahraki‐Ghadimi, Zahra, Rouhani, Roja, Hoda Fallah, Fatemeh, Rezaei, Nima, Abolhassani, Hassan, Aghamohammadi, Asghar, Atanaskovic‐Markovic, Marina

“…Background Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently…”
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Sildenafil and Ventriculo-Arterial Coupling in Fontan-Palliated Patients: A Noninvasive Echocardiographic Assessment by Shabanian, Reza, Shahbaznejad, Leila, Razaghian, Anahita, Kiani, Abdolrazagh, Rahimzadeh, Mitra, Seifirad, Soroush, Kocharian, Armen, Gilani, Jami Shakibi, Navabi, Mohammad Ali

“…The fundamental role of pulmonary vascular resistance in the Fontan circulation is obvious. Medications decreasing this resistance may have an impact on the…”
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The Effect of Intensive Phototherapy on Management of Hyperbilirubinemia in Neonates with the Gestational Age of 34 Weeks and More by Maryam Saboute, Ali Mazouri, Nasrin Khalesi, Nasrin Hoseiny Nejad, Anahita Razaghian

“…Background: Neonatal hyperbilirubinemia is one of the most common causes of neonatal morbidity and a global health priority. This study aimed to evaluate the…”
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Erythropoietic protoporphyria and early onset of cholestasis by Khalili, Mani Jeh, Farahmand, Fatemeh, Hirbod-Mobarakeh, Armin, Yousefi, Azizollah, Sotoudeh, Soheila, Monajemzadeh, Maryam, Razaghian, Anahita, Rezaei, Nima

“…Erythropoietic protoporphyria (EPP) is an inherited defect of mitochondrial ferrochelatase. This defect results in accumulation of protoporphyrin in…”
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Bacillus Calmette-Guérin (BCG)-associated hemophagocytic lymphohistiocytosis in the setting of IFN-γR1 deficiency: A diagnostic dilemma by Razaghian, Anahita, Parvaneh, Leila, Delkhah, Mona, Abbasi, Arash, Sadeghirad, Parisa, Shahrooei, Mohammad, Parvaneh, Nima

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Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis by Shabani, Mahsima, Razaghian, Anahita, Alimadadi, Hosein, Shiari, Reza, Shahrooei, Mohammad, Parvaneh, Nima

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