Search Results - "Zandieh, Fariborz"

Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations by Saghafi, Shiva, Zandieh, Fariborz, Fazlollahi, Mohammad Reza, Glocker, Cristina, Frede, Natalie, Buchta, Mary, Yang, Linlin, Mahmoudi, Amir Hossein, Houshmand, Massoud, Pourpak, Zahra, Grimbacher, Bodo, Moin, Mostafa

“…Early diagnosis of primary immunodeficiencies is crucial for timely treatment and preventing unwanted complications. Next-generation sequencing (NGS) and…”
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Clinical and immunological features of 65 Iranian patients with common variable immunodeficiency by Aghamohammadi, Asghar, Farhoudi, Abolhasan, Moin, Mostafa, Rezaei, Nima, Kouhi, Ali, Pourpak, Zahra, Yaseri, Nima, Movahedi, Masoud, Gharagozlou, Mohammad, Zandieh, Fariborz, Yazadni, Fereshteh, Arshi, Saba, Mohammadzadeh, Iraj, Ghazi, Bahram Mirsaeid, Mahmoudi, Maryam, Tahaei, Seyedamir, Isaeian, Anna

“…Common variable immunodeficiency (CVID) is a primary immunodeficiency disease characterized by hypogammaglobulinemia and recurrent bacterial infections. The…”
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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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Update on Hyper IgE syndrome (HIES) by Javad Ghaffari, Hamid Ahanchian, Fariborz Zandieh

“…Hyper IgE Syndrome (HIES) is a rare primary immunodeficiency disease. Most of HIES cases are sporadic. HIES type AD is caused by mutation in signal transducer…”
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Papillon Lefevre Syndrome and Footprints of Mycobacterium Tuberculosis by Zandieh, Fariborz, Ghazi, Bahram Mirsaed, Izadi, Anahita, Gharegozlu, Mohammad, Aghajani, Motahareh, Sheikh, Mahdi

“…Papillon-Lefevre syndrome (PLS) is a very rare genetic syndrome, and fewer than 500 cases have been reported in the world. Patients exhibit typical cutaneous…”
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Reiter's syndrome in a patient with polyarthritis and nail involvement by Zandieh, Fariborz, Loghmani, Mojgan

“…An 8-year old boy with polyarthritis and nail involvement is presented in this report. Nail involvement in Reiter's syndrome is a rare condition that may…”
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A survey on Sensitivity and Specificity of "Serum Total IgE" and "Nasal Eosinophil Count" in Diagnosis of Allergic Rhinitis and the Relationship between the Tests and Clinical Manifestation Severity by Nezamo'din Berjis, Fariborz Zandieh, Ehsan علایی Alaei Tabatabaei, Mojtaba Akbari

“…Background: Allergic rhinitis, one of the rhinitis syndromes, is associated with a symptom complex characterized by paroxysms of sneezing, rhinorrhea, nasal…”
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Does the reaction size of skin prick test associated with the allergic rhinitis symptom severity? by Madani, Sedigheh, Zandieh, Fariborz, Ahmadi, Maryam, Parvizi, Maryam, Rezaei, Nima

“…Skin prick test (SPT) has the best positive predictive value to diagnose respiratory atopic diseases, including allergic rhinitis (AR), but the association of…”
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Oral Wheat Immunotherapy: Long-Term Follow-Up in Children with Wheat Anaphylaxis by Babaie, Delara, Ebisawa, Motohiro, Soheili, Habib, Ghasemi, Ramin, Zandieh, Fariborz, Sahragard, Mitra, Seifi, Hamideh, Fallahi, Mazdak, Khoshmirsafa, Majid, Darougar, Sepideh, Mesdaghi, Mehrnaz

“…There has been substantial increase in food allergies in recent decades. The management of severe food allergy often includes strict avoidance and medical…”
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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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Objective score of atopic dermatitis and prebiotic in infant (382.8) by Ghanei, Nila, Siassi, Fereydoun, Zandieh, Fariborz

“…Background: Atopic dermatitis (AD) is a prevalent medical condition in infants aging from 6 months to 12 years old. Due to changes in life style, the…”
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The Vocal Fold Dysfunction Questionnaire: Validity and Reliability of the Persian Version by Ghaemi, Hamide, Khoddami, Seyyedeh Maryam, Soleymani, Zahra, Zandieh, Fariborz, Jalaie, Shohreh, Ahanchian, Hamid, Khadivi, Ehsan

“…The aim of this study was to develop, validate, and assess the reliability of the Persian version of Vocal Cord Dysfunction Questionnaire (VCDQP). The study…”
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Primary Immunodeficiency Disorders in Iran: Update and New Insights from the Third Report of the National Registry by Aghamohammadi, Asghar, Mohammadinejad, Payam, Abolhassani, Hassan, Mirminachi, Babak, Movahedi, Masoud, Gharagozlou, Mohammad, Parvaneh, Nima, Zeiaee, Vaheid, Mirsaeed-Ghazi, Bahram, Chavoushzadeh, Zahra, Mahdaviani, Alireza, Mansouri, Mahboubeh, Yousefzadegan, Sedigheh, Sharifi, Bahareh, Zandieh, Fariborz, Hedayat, Ehsan, Nadjafi, Ali, Sherkat, Roya, Shakerian, Behzad, Sadeghi-Shabestari, Mahnaz, Farid Hosseini, Reza, Jabbari-Azad, Farahzad, Ahanchian, Hamid, Behmanesh, Fatemeh, Zandkarimi, Mohammadreza, Shirkani, Afshin, Cheraghi, Taher, Fayezi, Abbas, Mohammadzadeh, Iraj, Amin, Reza, Aleyasin, Soheila, Moghtaderi, Mojgan, Ghaffari, Javad, Arshi, Saba, Javahertrash, Naser, Nabavi, Mohammad, Bemanian, Mohammad Hassan, Shafiei, Alireza, Kalantari, Najmedin, Ahmadiafshar, Akefeh, Khazaei, Hossein Ali, Atarod, Lida, Rezaei, Nima

“…Background Primary immunodeficiency disorders (PID) are a group of heterogeneous disorders mainly characterized by severe and recurrent infections and…”
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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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Inheritance Pattern and Clinical Aspects of 93 Iranian Patients with Chronic Granulomatous Disease by Fattahi, Fatemeh, Badalzadeh, Mohsen, Sedighipour, Leyla, Movahedi, Masoud, Fazlollahi, Mohammad Reza, Mansouri, Seyed Davood, Khotaei, Ghamar Taj, Bemanian, Mohammad Hassan, Behmanesh, Fatemeh, Hamidieh, Amir Ali, Bazargan, Nasrin, Mamishi, Setareh, Zandieh, Fariborz, Chavoshzadeh, Zahra, Mohammadzadeh, Iraj, Mahdaviani, Seyed Alireza, Tabatabaei, Seyed Ahmad, Kalantari, Najmeddin, Tajik, Shaghayegh, Maddah, Marzieh, Pourpak, Zahra, Moin, Mostafa

“…Background Chronic granulomatous disease (CGD) is a rare immunodeficiency due to a genetic defect in one of the NADPH-oxidase components. We studied CGD…”
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Gastrointestinal manifestations in patients with common variable immunodeficiency by KHODADAD, Ahmad, AGHAMOHAMMADI, Asghar, ABDOLLAHZADE, Sina, SALAVATI, Ali, KOUHI, Ali, TALEBPOUR, Bahram, NASSER EBRAHIMI DARYANI, PARVANEH, Nima, REZAEI, Nima, MAHJOOB, Fatemeh, BASHASHATI, Mohammad, MOVAHEDI, Masoud, MOHAMMAD REZA FAZLOLLAHI, ZANDIEH, Fariborz, ROOHI, Zahra

“…This study focuses on endoscopic and pathologic alterations of gastrointestinal (GI) disorders of Iranian patients with common variable immunodeficiency…”
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Validation of Persian Version of PedsQL™ 4.0™ Generic Core Scales in Toddlers and Children by Gheissari, Alaleh, Farajzadegan, Ziba, Heidary, Maryam, Salehi, Fatemeh, Masaeli, Ali, Mazrooei, Amin, Varni, James W, Fallah, Zahra, Zandieh, Fariborz

“…To evaluate the reliability, validity and feasibility of the Persian version of the Pediatric Quality of Life inventory (PedsQL™ 4.0™ 4.0) Generic Core Scales…”
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Papillon Lefevre Syndrome and footsteps of mycobacterium tuberculosis by Zandieh, Fariborz, Mirsaed Ghazi, Bahram, Izadi, Anahita, Gharegozlu, Mohammad, Aghajani, Motahareh, Sheikh, Mahdi

“…Papillon Lefevre Syndrome ( PLS ) is a very rare genetic syndrome that only less than 500 cases have reported in the world. Patients have a typical cutaneous…”
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Update on Hyper IgE syndrome (HIES) by Javad Ghaffari, Hamid Ahanchian, Fariborz Zandieh

“…Hyper IgE Syndrome (HIES) is a rare primary immunodeficiency disease. Most of HIES cases are sporadic. Autosomal dominant HIES is caused by mutation in signal…”
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Clinical and laboratory findings in Iranian patients with leukocyte adhesion deficiency (study of 15 cases) by Movahedi, Masoud, Entezari, Neda, Pourpak, Zahra, Mamishi, Setareh, Chavoshzadeh, Zahra, Gharagozlou, Mohammad, Mir-Saeeid-Ghazi, Bahram, Fazlollahi, Mohammad-Reza, Zandieh, Fariborz, Bemanian, Mohammad-Hasan, Farhoudi, Aboulhasan, Aghamohammadi, Asghar

“…Leukocyte adhesion deficiency type I (LAD I) is a rare, inherited, autosomal recessive, immunodeficiency disease caused by the combined loss of expression on…”
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