Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shahriar Nafisi"'
Autor:
Kimia Kahrizi, Neda Moradin, Mojtaba Azimian, Bahareh Shojasaffar, Kaveh Alavi, Shahriar Nafisi, Mandana Hasanzad, Seyed Mohammad Ebrahim Moosavi, Azadeh Shirazian, Hossein Najmabadi
Publikováno v:
Iranian Rehabilitation Journal, Vol 8, Iss 1, Pp 8-12 (2010)
Objectives: Myotonic Dystrophy type I (DM1) is a dominantly inherited disorder with a multisystemic pattern affecting skeletal muscle, heart, eye, endocrine and central nervous system. DM1 is associated with the expansion and instability of CTG repea
Externí odkaz:
https://doaj.org/article/b5ac67cd38984dc78e0552172e8d9ec9
Publikováno v:
Majallah-i taḥqīqāt-i ̒ulūm-i pizishkī-i Zāhidān, Vol 15, Iss 7, Pp 26-30 (2013)
Background: Huntington disease (HD) is a dominantly inherited, neurodegenerative disease characterized by choreiform movement disturbances and dementia. The onset age of this disease is varied but usually is between the ages 40-50. Huntington's disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::1d85397aa985b90486c0869fd38ebb14
http://www.zjrms.ir/browse.php?a_id=1250&sid=1&slc_lang=en
http://www.zjrms.ir/browse.php?a_id=1250&sid=1&slc_lang=en
Autor:
Kazem Parivar, Parvin Shariati, Sepideh Safaei, Mehdi Shafa Shariat Panahi, Shahriar Nafisi, Maryam Rostami, Mohammad Mehdi Banoei, Massoud Houshmand
Publikováno v:
Neurodegenerative Diseases. 6:16-22
Background: The spinocerebellar ataxias (SCA) comprise a heterogeneous group of severe late-onset neurodegenerative diseases that are promoted by the expansion of a tandem-arrayed DNA sequence that modifies the primary structure of the protein. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a14838df735cadd1b7947363e918979
https://doi.org/10.1159/000170885
https://doi.org/10.1159/000170885
Autor:
Mohammad Hossein, Harirchian, Narges, Karimi, Shahriar, Nafisi, Shahram, Akrami, Davod, Ghanbarian, Shahriar, Gharibzadeh
Publikováno v:
Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina. 10(2)
To determine the sensitivity of the vestibular evoked myogenic potential (VEMP) in multiple sclerosis (MS) patients as well as its relation to clinical signs and symptoms, course of the disease and other evoked potentials.This case-control study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::028abfb15796b84c12ac232ff9e888ef
https://pubmed.ncbi.nlm.nih.gov/23892852
https://pubmed.ncbi.nlm.nih.gov/23892852
Autor:
Yaser, Hamidian, Mansoureh, Togha, Shahriar, Nafisi, Shahab, Dowlatshahi, Soodeh Razeghi, Jahromi, Nahid Beladi, Moghadam, Navid, Namazi, Parvin, Tajik, Masoud, Majed, Mahdi, Aloosh
Publikováno v:
Iranian Journal of Neurology
Background The most common neurologic manifestation of gluten sensitivity is ataxia, which accounts for up to 40% of idiopathic sporadic ataxia. Timing of diagnosis of gluten ataxia is vital as it is one of the very few treatable causes of sporadic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea9784e0f42f0fc32d3a7e62234ff372
https://pubmed.ncbi.nlm.nih.gov/24250853
https://pubmed.ncbi.nlm.nih.gov/24250853
Autor:
Sepideh, Safaei, Massoud, Houshmand, Mohammad Mehdi, Banoei, Mehdi Shafa Shariat, Panahi, Shahriar, Nafisi, Kazem, Parivar, Maryam, Rostami, Parvin, Shariati
Publikováno v:
Neuro-degenerative diseases. 6(1-2)
The spinocerebellar ataxias (SCA) comprise a heterogeneous group of severe late-onset neurodegenerative diseases that are promoted by the expansion of a tandem-arrayed DNA sequence that modifies the primary structure of the protein.Genomic DNA of 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b42f809d0193a493f43040f19dbdb30
https://pubmed.ncbi.nlm.nih.gov/19066432
https://pubmed.ncbi.nlm.nih.gov/19066432
Autor:
Akbar Soltanzadeh, Massoud Houshmand, Mehdi Shafa Shariat Panahi, Shahriar Nafisi, Fawziah M. Alkandari
Publikováno v:
Scopus-Elsevier
Friedreich's Ataxia (FA) is the commonest genetic cause of ataxia and is associated with the expansion of a GAA repeat in intron 1 of the frataxin gene. Iron accumulation in the mitochondria of patients with FA would result in hypersensitivity to oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad8fa189524a848e813c5870dce6dbfa
http://www.scopus.com/inward/record.url?eid=2-s2.0-33747170625&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33747170625&partnerID=MN8TOARS
