Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Reza, Shervin Badv"'
Autor:
Reza Shervin Badv, Fakhreddin Shariatmadari, Shiva Bayat, Sara Memarian, Samaneh Esteghamat Hanzae, Hossein Yousefimanesh
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-4 (2024)
Abstract Background Progressive myoclonic epilepsy is a clinically and genetically heterogeneous group of diseases characterized by myoclonic seizures, drug-resistant epilepsy and neurodevelopmental regression. The disease is attributed to mutations
Externí odkaz:
https://doaj.org/article/650803acae5549468827c4b99f9dd443
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:
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:
Morteza Zarrabi, Masood Ghahvechi Akbari, Man Amanat, Anahita Majmaa, Ali Reza Moaiedi, Hadi Montazerlotfelahi, Masoumeh Nouri, Amir Ali Hamidieh, Reza Shervin Badv, Hossein Karimi, Ali Rabbani, Ali Mohebbi, Shahram Rahimi-Dehgolan, Rosa Rahimi, Ensieh Dehghan, Massoud Vosough, Saeed Abroun, Farhad Mahvelati Shamsabadi, Ali Reza Tavasoli, Houman Alizadeh, Neda Pak, Gholam Reza Zamani, Mahmoud Mohammadi, Mohsen Javadzadeh, Mohammad Ghofrani, Seyed Hossein Hassanpour, Morteza Heidari, Mohammad Mehdi Taghdiri, Mohamad Javad Mohseni, Zahra Noparast, Safdar Masoomi, Mehrdad Goudarzi, Masood Mohamadpour, Razieh Shodjaee, Solaleh Samimi, Monireh Mohammad, Mona Gholami, Nahid Vafaei, Leyli Koochakzadeh, Amir Valizadeh, Reza Azizi Malamiri, Mahmoud Reza Ashrafi
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Introduction The current multi-center, randomized, double-blind study was conducted among children with cerebral palsy (CP) to assess the safety and efficacy of umbilical cord blood mononuclear cell (UCB-MNC). We performed the diffusion tens
Externí odkaz:
https://doaj.org/article/6f139e136d1f4fa284713638f9f33fef
Autor:
Maryam Sotoudeh Anvari, Hamed Vasei, Hossein Najmabadi, Reza Shervin Badv, Akram Golipour, Samira Mohammadi-Yeganeh, Saeede Salehi, Mahmood Mohamadi, Hamidreza Goodarzynejad, Seyed Javad Mowla
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene which can lead to a loss or shortage of the FMR1 protein. This protein interacts with specific miRNAs and can cause a range of neurological disorders. Therefore, miRNAs could
Externí odkaz:
https://doaj.org/article/6e3da80d43c44ec9a30becd6734c8572
Autor:
Tina Eshaghian, Bahareh Rabbani, Reza Shervin Badv, Sahar Mikaeeli, Behdad Gharib, Stanley Iyadurai
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100553- (2023)
Externí odkaz:
https://doaj.org/article/58798953cb874275a9103a0b9a58b38a
Autor:
Elham Pourbakhtyaran, Morteza Heidari, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Gholamreza Zamani, Ali Reza Tavasoli, Zahra Rezaei, Setareh Mamishi, Elmira Haji Esmaeil Memar, Seyyed Mohammad Mahdi Hosseiny, Homa Ghabeli, Roya Haghighi, Mahmoud Reza Ashrafi
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract We reported an association between SARS‐CoV‐2 infection and Guillain–Barre syndrome (GBS). From 37 patients with GBS, previous SARS‐CoV‐2 clinical clues, including fever, cough, and diarrhea, were recorded in 18 patients. Among the
Externí odkaz:
https://doaj.org/article/885d23d3f3394b2eaded5d0665d3dfd8
Autor:
Man Amanat, Anahita Majmaa, Morteza Zarrabi, Masoumeh Nouri, Masood Ghahvechi Akbari, Ali Reza Moaiedi, Omid Ghaemi, Fatemeh Zamani, Sharif Najafi, Reza Shervin Badv, Massoud Vosough, Amir Ali Hamidieh, Mona Salehi, Hadi Montazerlotfelahi, Ali Reza Tavasoli, Morteza Heidari, Hossein Mohebi, Ali Fatemi, Amir Garakani, Mahmoud Reza Ashrafi
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-15 (2021)
Abstract Background This study assessed the safety and efficacy of intrathecal injection of umbilical cord tissue mesenchymal stem cells (UCT-MSC) in individuals with cerebral palsy (CP). The diffusion tensor imaging (DTI) was performed to evaluate t
Externí odkaz:
https://doaj.org/article/7d747857d7d1432cb2cee6e8f2e59e73
Publikováno v:
Behavioral Sciences, Vol 13, Iss 3, p 208 (2023)
There is growing evidence that prevalence rates of autism spectrum disorder (ASD) are increasing. A number of factors appear to contribute to this increase, including excessive screen time. Screen time seems to be linked to the severity of the sympto
Externí odkaz:
https://doaj.org/article/d3c7684014dc4948831434af84abfe5c