Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Masoud Ghahvechi"'
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:
Mahmoud Reza Ashrafi, Ali Zare Dehnavi, Ali Reza Tavasoli, Morteza Heidari, Masoud Ghahvechi Akbari, Ali Reza Ronagh, Mohammad Ghafouri, Nejat Mahdieh, Pouria Mohammadi, Zahra Rezaei
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background Giant axonal neuropathy (GAN) is a progressive childhood hereditary polyneuropathy that affects both the peripheral and central nervous systems. Disease‐causing variants in the gigaxonin gene (GAN) cause autosomal recessive gian
Externí odkaz:
https://doaj.org/article/1a582d12e3c2419fa5e52d2b3a69a7bc
Autor:
Reza Shervin Badv, Sara Memarian, Masoud Ghahvechi, Hossein Farshad Moghaddam, Maryam Saidi, Reihaneh Mohsenipour, Parisa Rahmani, Bahram Yarali, Mojtaba Gorji, Behdad Gharib
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 4, Iss 12, Pp 35-38 (2018)
Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of
Externí odkaz:
https://doaj.org/article/fb28ad3022b04b1db09af02ae2d97dbe
Akademický článek
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Autor:
Ashrafi, Mahmoud Reza, Mohammadi, Pouria, Tavasoli, Ali Reza, Heidari, Morteza, Hosseinpour, Sareh, Rasulinejad, Maryam, Rohani, Mohammad, Akbari, Masoud Ghahvechi, Malamiri, Reza Azizi, Badv, Reza Shervin, Fathi, Davood, Dehnavi, Ali Zare, Savad, Shahram, Rabbani, Ali, Synofzik, Matthis, Mahdieh, Nejat, Rezaei, Zahra
Publikováno v:
Cerebellum; Aug2023, Vol. 22 Issue 4, p640-650, 11p
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b25958ae7efb771e60fc969cfd5cc0aa
https://doi.org/10.1007/s12311-022-01430-3
https://doi.org/10.1007/s12311-022-01430-3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Parisa Rahmani, Sara Memarian, Behdad Gharib, Maryam Saidi, Mojtaba Gorji, Bahram Yarali, Reihaneh Mohsenipour, Reza Shervin Badv, Masoud Ghahvechi, Hossein Farshad Moghaddam
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 4, Iss 12, Pp 35-38 (2018)
Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::993e11c77c5de47041c75521165ee525
https://doi.org/10.29252/nirp.cjns.4.12.35
https://doi.org/10.29252/nirp.cjns.4.12.35