Search Results - "Nafisi, Shahriar"

Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias by Safaei, Sepideh, Houshmand, Massoud, Banoei, Mohammad Mehdi, Panahi, Mehdi Shafa Shariat, Nafisi, Shahriar, Parivar, Kazem, Rostami, Maryam, Shariati, Parvin

“…The spinocerebellar ataxias (SCA) comprise a heterogeneous group of severe late-onset neurodegenerative diseases that are promoted by the expansion of a…”
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Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia by Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Nafisi, Shahriar, Soltanzadeh, Akbar, Alkandari, Fawziah M

“…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…”
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Genotype–Phenotype Correlations in Iranian Myotonic Dystrophy Type I Patients by Kimia Kahrizi, Neda Moradin, Mojtaba Azimian, Bahareh Shojasaffar, Kaveh Alavi, Shahriar Nafisi, Mandana Hasanzad, Seyed Mohammad Ebrahim Moosavi, Azadeh Shirazian, Hossein Najmabadi

“…Objectives: Myotonic Dystrophy type I (DM1) is a dominantly inherited disorder with a multisystemic pattern affecting skeletal muscle, heart, eye, endocrine…”
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Vestibular evoked myogenic potential for diagnoses of multiple sclerosis: is it beneficial? by Harirchian, Mohammad Hossein, Karimi, Narges, Nafisi, Shahriar, Akrami, Shahram, Ghanbarian, Davod, Gharibzadeh, Shahriar

“…To determine the sensitivity of the vestibular evoked myogenic potential (VEMP) in multiple sclerosis (MS) patients as well as its relation to clinical signs…”
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Antigliadin antibody in sporadic adult ataxia by Hamidian, Yaser, Togha, Mansoureh, Nafisi, Shahriar, Dowlatshahi, Shahab, Jahromi, Soodeh Razeghi, Moghadam, Nahid Beladi, Namazi, Navid, Tajik, Parvin, Majed, Masoud, Aloosh, Mahdi

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