Search Results - "Alizadeh, Hooman"

Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemia by AGHAMOHAMMADI, Asghar, ALLAHVERDI, Abdolreza, ABOLHASSANI, Hassan, MOAZZAMI, Kasra, ALIZADEH, Hooman, GHARAGOZLOU, Mohammad, KALANTARI, Najmoddin, SAJEDI, Vahid, SHAFIEI, Alireza, PARVANEH, Nima, MOHAMMADPOUR, Masoud, KARIMI, Nasser, SADAGHIANI, Mohammad Salehi, REZAEI, Nima

“…ABSTRACT Background and objective:  Pulmonary disease is the most common complication in patients with common variable immunodeficiency (CVID) or X‐linked…”
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Estrogen-Only–Producing Adrenal Mass As An Overlooked Etiology Of Isosexual Precocious Puberty In Girls: A Case Report And Literature Review by Haghshenas, Zahra, Mollaian, Mansour, Alizadeh, Hooman, Alehossein, Mehdi, Harsini, Sara, Zoham, Mojdeh Habibi

“…Objective: An estrogen-only–producing adrenal tumor is a rare etiology of isosexual precocious puberty (PP) in girls.Methods: We describe a 2.5-year-old girl…”
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First Description of Factors Influencing the Outcome of Developmental Dysplasia of the Hip in Children’s Medical Center by Mehdizadeh, Mehrzad, Babakhan Kondori, Nasir, Zandifar, Afrooz, Alizadeh, Hooman

“…Background: There are several factors may have an impact on the prognosis of developmental dysplasia of the hip (DDH). They may change the outcome and…”
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High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry by Ashrafi, Mahmoudreza, Kameli, Reyhaneh, Hosseinpour, Sareh, Razmara, Ehsan, Zamani, Zahra, Rezaei, Zahra, Mashayekhi, Raziyeh, Pak, Neda, Barzegar, Mohammad, Azizimalamiri, Reza, Kashani, Morteza Rezvani, Khosroshahi, Nahideh, Rasulinezhad, Maryam, Heidari, Morteza, Amanat, Man, Abdi, Alireza, Mohammadi, Bahram, Mohammadi, Mahmoud, Zamani, Gholam Reza, Badv, Reza Shervin, Omrani, Abdolmajid, Nikbakht, Sedigheh, Bereshneh, Ali Hosseini, Movahedinia, Mojtaba, Moghaddam, Hossein Farshad, Ardakani, Hossein Shojaaldini, Akbari, Masood Ghahvechi, Tousi, Mehran Beiraghi, Shahi, Mohammad Vafaee, Hosseini, Firouzeh, Amouzadeh, Masoud Hassanvand, Hosseini, Seyed Ahmad, Nikkhah, Ali, Khajeh, Ali, Alizadeh, Hooman, Yarali, Bahram, Rohani, Mohammad, Karimi, Parviz, Elahi, Hadi Montazer Lotf, Hosseiny, Seyyed Mohamad Mahdi, Sadeghzadeh, Masoumeh Sadat, Mohebbi, Hossein, Moghadam, Maryam Hosseini, Aryan, Hajar, Vahidnezhad, Hassan, Soveizi, Mahdieh, Rabbani, Bahareh, Rabbani, Ali, Mahdieh, Nejat, Garshasbi, Masoud, Tavasoli, Ali Reza

“…Leukodystrophies (LDs) are a heterogeneous group of progressive neurological disorders and characterized by primary involvement of white matter of the central…”
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Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry by Ashrafi, Mahmoudreza, Kameli, Reyhaneh, Hosseinpour, Sareh, Razmara, Ehsan, Zamani, Zahra, Rezaei, Zahra, Mashayekhi, Raziyeh, Pak, Neda, Barzegar, Mohammad, Azizimalamiri, Reza, Kashani, Morteza Rezvani, Khosroshahi, Nahideh, Rasulinezhad, Maryam, Heidari, Morteza, Amanat, Man, Abdi, Alireza, Mohammadi, Bahram, Mohammadi, Mahmoud, Zamani, Gholam Reza, Badv, Reza Shervin, Omrani, Abdolmajid, Nikbakht, Sedigheh, Bereshneh, Ali Hosseini, Movahedinia, Mojtaba, Moghaddam, Hossein Farshad, Ardakani, Hossein Shojaaldini, Akbari, Masood Ghahvechi, Tousi, Mehran Beiraghi, Shahi, Mohammad Vafaee, Hosseini, Firouzeh, Amouzadeh, Masoud Hassanvand, Hosseini, Seyed Ahmad, Nikkhah, Ali, Khajeh, Ali, Alizadeh, Hooman, Yarali, Bahram, Rohani, Mohammad, Karimi, Parviz, Elahi, Hadi Montazer Lotf, Hosseiny, Seyyed Mohamad Mahdi, Sadeghzadeh, Masoumeh Sadat, Mohebbi, Hossein, Moghadam, Maryam Hosseini, Aryan, Hajar, Vahidnezhad, Hassan, Soveizi, Mahdieh, Rabbani, Bahareh, Rabbani, Ali, Mahdieh, Nejat, Garshasbi, Masoud, Tavasoli, Ali Reza

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Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from Iran by Ashrafi, Mahmoud-Reza, Tavasoli, Alireza, Aryani, Omid, Alizadeh, Hooman, Houshmand, Massoud

“…Alexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants and children and usually results in death within ten years after onset…”
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Pelizaeus-merzbacher disease: the first genetically approved case report from iran by Ashrafi, Mahmoud-Reza, Mohammadi, Mahmoud, Alizadeh, Hooman, Nikkhah, Ali

“…Classic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein expression first described clinically in 1885. This disease is…”
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Echocardiographic abnormalities and their correlation with bronchiectasis score in primary antibody deficiencies by Zeinaloo, Ali Akbar, Aghamohammadi, Asghar, Shabanian, Reza, Salavati, Ali, Abdollahzade, Sina, Rezaei, Nima, Alizadeh, Hooman, Zanjani, Keyhan Sayadpour, Kiani, Abdolrazagh

“…BACKGROUNDPrimary antibody deficiencies are characterized by defective antibody production and recurrent infections. Patients usually present with recurrent…”
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Pelizaeus-merzbacher disease: the first genetically approved case report from iran by Ashrafi, Mahmoud-Reza, Mohammadi, Mahmoud, Alizadeh, Hooman, Nikkhah, Ali

“…BACKGROUNDClassic Pelizaeus-Merzbacher disease is a rare x-linked disorder of proteolipid protein expression first described clinically in 1885. This disease…”
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Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from Iran by Ashrafi, Mahmoud-Reza, Tavasoli, Alireza, Aryani, Omid, Alizadeh, Hooman, Houshmand, Massoud

“…BACKGROUNDAlexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants and children and usually results in death within ten years…”
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Involvement of basolateral amygdala GABAA receptors in the effect of dexamethasone on memory in rats by Khajehpour, Lotfollah, Alizadeh-Makvandi, Acieh, Kesmati, Mahnaz, Eshagh-Harooni, Hooman

“…In this study we investigated whether GABAA receptors of the basolateral amygdala （BLA） interact with the effect of dexamethasone on the retrieval stage of…”
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