Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Sareh, Hosseinpour"'
Autor:
Nejat Mahdieh, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinejad, Ali Zare Dehnavi, Masoud Ghahvechi Akbari, Reza Shervin Badv, Elahe Vafaei, Ali Mohebbi, Pouria Mohammadi, Seyyed Mohammad Mahdi Hosseiny, Reza Azizimalamiri, Ali Nikkhah, Elham Pourbakhtyaran, Mohammad Rohani, Narges Khanbanha, Sedigheh Nikbakht, Mojtaba Movahedinia, Parviz Karimi, Homa Ghabeli, Seyed Ahmad Hosseini, Fatemeh Sadat Rashidi, Masoud Garshasbi, Morteza Rezvani Kashani, Noor M. Ghiasvand, Stephan Zuchner, Matthis Synofzik, Mahmoud Reza Ashrafi
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-18 (2024)
Abstract Background To investigate the genetics of early-onset progressive cerebellar ataxia in Iran, we conducted a study at the Children’s Medical Center (CMC), the primary referral center for pediatric disorders in the country, over a three-year
Externí odkaz:
https://doaj.org/article/73901f9896264335a878fdd5b263980b
Autor:
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background Phospholipase-associated neurodegeneration (PLAN) caused by mutations in the PLA2G6 gene is a rare neurodegenerative disorder that presents with four sub-groups. Infantile neuroaxonal dystrophy (INAD) and PLA2G6-related dystonia-p
Externí odkaz:
https://doaj.org/article/33b08d5b1a9846ac9b6a4cfa26acdbbd
Autor:
Gholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Sareh Hosseinpour, Roya Haghighi, Elham Pourbakhtyaran, Nahid Khosroshahi, Morteza Heidari
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Objectives This study aimed to analyze the health-related quality of life (HRQoL) of patients with spinal muscular atrophy (SMA) based on the type of SMA, demographic and clinical features and compare HRQoL of these patients with a matched h
Externí odkaz:
https://doaj.org/article/4590cd086b444024a85813ef44d486f1
Autor:
Gholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Mahmoud Mohammadi, Reza Shervin Badv, Ali Reza Tavasoli, Masood Ghahvechi Akbari, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Morteza Heidari
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy in the pediatric population. The manifestations of this disease include progressive muscle weakness, gait dysfunction, and motor impairment, leading to a loss
Externí odkaz:
https://doaj.org/article/46d808fb5a5f461bb7a8856d26dabd27
Autor:
Hadi Sorkhi, Mohamadreza esmaeilidooki, Maryam Nikpour, Mohsen Mohammadi, Ali Mohammadpour-Mir, Masood Kiani, Sanaz Mehrabani, Sahar Sadr Moharerpour, Morteza Alijanpour, Kazem Babazadeh, Hassan Mahmoodi-Nesheli, Mohamadreza Tabatabaie, Ahmad Tamaddoni, Mohammadreza Salehiomran, Paiam Payandeh, Iraj Mohammadzadeh, Sareh Hosseinpour
Publikováno v:
Caspian Journal of Internal Medicine, Vol 13, Iss Covid 19 Supplement 2, Pp 193-198 (2022)
Background: The New coronavirus (SARS COV-2) can cause acute respiratory disease and also multiorgan dysfunction. There is insufficient data about kidney involvement in children. So, this study was done on children with COVID-19 to evaluate nephrolog
Externí odkaz:
https://doaj.org/article/fa2ad6e4c7494e7285c6dc125703a3ce
Autor:
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/1a7e2a9cd0cb490ba3fb6216410a703b
Autor:
Mahmoud Reza Ashrafi, Elham Pourbakhtyaran, Mohammad Rohani, Bita Shalbafan, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinezhad, Zahra Rezaei, Ali Zare Dehnavi, Seyyed Mohammad Mahdi Hosseiny, Roya Haghighi, Homa Ghabeli, Morteza Heidari
Publikováno v:
Clinical Case Reports, Vol 10, Iss 4, Pp n/a-n/a (2022)
Abstract Autosomal recessive cerebellar ataxias are a group of heterogeneous early‐onset progressive disorders that some of them are treatable. We performed a 4‐year follow‐up for 25 patients who had treatable ataxia. According to our study, pa
Externí odkaz:
https://doaj.org/article/d669e88a76874f04803a1c12ee0f33ce
Autor:
Vahid Mansouri, Morteza Heidari, Maryam Bemanalizadeh, Reza Azizimalamiri, Shahriar Nafissi, Masood Ghahvechi Akbari, Mohammad Barzegar, Ali Reza Moayedi, Reza Shervin Badv, Mahmood Mohamadi, Ali Reza Tavasoli, Susan Amirsalari, Ali Khajeh, Soroor Inaloo, Farzad Fatehi, Sareh Hosseinpour, Meisam Babaei, Seyed Ahmad Hosseini, Seyyed Mohammad Mahdi Hosseiny, Afshin Fayyazi, Firoozeh Hosseini, Mehran Beiraghi Toosi, Nahid Khosroshahi, Homa Ghabeli, Habibeh Nejad Biglari, Simin Khayatzadeh Kakhki, Seyed Hossein Mirlohi, Elham Bidabadi, Bahram Mohammadi, Abdolmajid Omrani, Mostafa Sedighi, Mohammad Vafaee-Shahi, Maryam Rasulinezhad, Seyyed Mohamad Hoseini, Mojtaba Movahedinia, Zahra Rezaei, Parviz Karimi, Hossein Farshadmoghadam, Saeed Anvari, Omid Yaghini, Jafar Nasiri, Gholamreza Zamani, Mahmoud Reza Ashrafi
Publikováno v:
Journal of Neuromuscular Diseases. 10:211-225
Background: Insufficient amounts of survival motor neuron protein is leading to one of the most disabling neuromuscular diseases, spinal muscular atrophy (SMA). Before the current study, the detailed characteristics of Iranian patients with SMA had n
Autor:
Ali Reza Tavasoli, Ali Zare Dehnavi, Maryam Bemanalizadeh, Mohammad Kahani, Mohammad Rohani, Mehran Beriraghi Toosi, Mahmoud Reza Ashrafi, Morteza Heidari, Man Amanat, Sareh Hosseinpour
Publikováno v:
Sunday, April 23.
Autor:
Mahmoud Reza Ashrafi, Pouria Mohammadi, Ali Reza Tavasoli, Morteza Heidari, Sareh Hosseinpour, Maryam Rasulinejad, Mohammad Rohani, Masoud Ghahvechi Akbari, Reza Azizi Malamiri, Reza Shervin Badv, Davood Fathi, Ali Zare Dehnavi, Shahram Savad, Ali Rabbani, Matthis Synofzik, Nejat Mahdieh, Zahra Rezaei
Publikováno v:
The Cerebellum 22(4), 640-650 (2023). doi:10.1007/s12311-022-01430-3
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS) is now increasingly identified from all countries over the world, possibly rendering it one of the most common autosomal recessive ataxias. Here, we selected patients harboring SACS v