Search Results - "Ashrafi, Mahmoudreza"

The Relationship Between Emotional Content and Phonological Processing in Persian Speaking Children Who Stutter: A Study by Event-related Potential by Salehi, Sousan, Khatoonabadi, Ahmad Reza, Ashrafi, Mahmoudreza, Mohammadkhani, Ghasem, Maroufizadeh, Saman

“…Introduction: Emotion can contribute to the severity of stuttering, although the underlying mechanism is unknown. Event-related Potential (ERP) could be very…”
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COVID-19: A New Horizon in Congenital Heart Diseases by Aghaei Moghadam, Ehsan, Mohammadzadeh, Shabnam, Sattarzadeh Badkoubeh, Roya, Ghamari, Azin, Rabbani, Ali, Mohebbi, Ali, Zeinaloo, Aliakbar, Ashrafi, Mahmoudreza, Kamran, Niyoosha, Masoominasab, Paniz, Mahmoudi, Zahra, Zamani Mehryan, Asma, Mirzaaghayan, Mohammad Reza

“…Previous studies have demonstrated that both children and adult patients with a history of congenital heart disease (CHD) are at high risk for coronavirus…”
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Safety and efficacy of levetiracetam and carbamazepine monotherapy in the management of pediatric focal epilepsy: a randomized clinical trial by Montazerlotfelahi, Hadi, Haj Mohamad Ebrahim Ketabforoush, Arsh, Tavakol, Marzieh, Ashrafi, Mahmoudreza, Dehghani, Mahdieh, Mostafavi, Keihan, Mardi, Shayan, Tajfirooz, Sanaz

“…Due to the limited number of studies in children with focal epilepsy and the importance of choosing the most suitable drug to control seizures in children, the…”
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Novel disease-causing variants in a cohort of Iranian patients with metachromatic leukodystrophy and in silico analysis of their pathogenicity by Mahdieh, Nejat, Sharifi, Ameneh, Rabbani, Ali, Ashrafi, Mahmoudreza, Tavasoli, Ali Reza, Badv, Reza Shervin, Bonkowsky, Joshua L., Rabbani, Bahareh

“…•ARSA gene variants in metachromatic leukodystrophy in an Iranian population.•The structural and stability analyses of the missense variants predict different…”
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SZT2 mutation in a boy with intellectual disability, seizures and autistic features by Kariminejad, Ariana, Yazdan, Hilda, Rahimian, Elham, Kalhor, Zahra, Fattahi, Zohreh, Zonooz, Mehrshid Faraji, Najmabadi, Hossein, Ashrafi, Mahmoudreza

“…The seizure threshold 2 (SZT2) gene has been shown to confer a low seizure threshold and may enhance epileptogenesis in mice. However, its biological function…”
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A Comparative Study of EEG and aEEG in Seizure Diagnosis in Infants Admitted to the NICU by Movahedi Moghadam, Elahe, Taghipour, Yalda, Shervin Badv, Reza, Kadivar, Maliheh, Sangsari, Raziyeh, Saeedi, Maryam, Ashrafi, Mahmoud Reza

“…Seizure is a common sign in neonates hospitalized in the neonatal intensive care units (NICU) that may lead to morbidity and mortality. Most neonatal seizures…”
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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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Neurological Involvements in COVID-19: A hospital-based study by Montazerlotfelahi, Hadi, Norouzi, Mahsa, Askarimoghaddam, ough, Hashemnejad, Mohammad Amin, Sarabi, Niusha Bastan, Qorbani, Mostafa, Dehghani, Mahdieh, Ashrafi, Mahmoudreza, Mostafavi, Keihan, Ketabforoush, Arsh Haj Mohamad Ebrahim, Nikkhah, Ali

“…Objectives The SARS-CoV-2 pandemic is the most challenging crisis in the contemporary world. Besides severe pulmonary involvement, the disease also has several…”
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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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A Novel Mutation in Aspartoacylase Gene; Canavan Disease by Ashrafi, Mahmoudreza, Tavasoli, Alireza, Katibeh, Pegah, Aryani, Omid, Vafaee-Shahi, Mohammad

“…Objective Canavan disease (CD) is a type of vacuolating leukodystrophy with autosomal recessive inheritance. Aspartoacylase deficiency results in decrease of…”
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Effect of anti-epileptic drugs on serum immunoglobulin levels in children by Ashrafi, Mahmoudreza, Hosseini, Seyed Ahmad, Abolmaali, Sarah, Biglari, Mohammad, Azizi, Reza, Farghadan, Maryam, Samadian, Azam, Saghafi, Shiva, Mombeini, Hoda, Saladjegheh, Narges, Rezaei, Nima, Aghamohammadi, Asghar

“…Epilepsy is one of the most frequent neurological disorders. Despite the advances and improvements in treatment of seizure disorders, immunologic alterations…”
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A Novel Mutation in Aspartoacylase Gene; Canavan Disease by Ashrafi, Mahmoudreza, Tavasoli, Alireza, Katibeh, Pegah, Aryani, Omid, Vafaee-Shahi, Mohammad

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