受强制性开放获取政策约束的文章 - mohammad rohani了解详情
无法在其他位置公开访问的文章：7 篇
Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families
M Pashaei, A Davarzani, R Hajati, B Zamani, S Nafissi, F Larti, Y Nilipour, ...
Journal of neurogenetics 35 (2), 84-94, 2021
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council
CAPN1 and hereditary spastic paraplegia: a novel variant in an Iranian family and overview of the genotype-phenotype correlation
MM Rahimi Bidgoli, L Javanparast, M Rohani, H Najmabadi, B Zamani, ...
International Journal of Neuroscience 131 (10), 962-974, 2021
强制性开放获取政策： UK Medical Research Council
NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variants
Z Sadr, A Ghasemi, M Rohani, A Alavi
Neuromuscular Disorders 33 (4), 295-301, 2023
强制性开放获取政策： US National Institutes of Health
Coexistence of deep brain stimulators and cardiac implantable electronic devices: A systematic review of safety
FH Akhoundi, MF Contarino, A Fasano, J Vaidyanathan, M Ziaee, ...
Parkinsonism & Related Disorders 88, 129-135, 2021
强制性开放获取政策： Michael J Fox Foundation
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry
M Ashrafi, R Kameli, S Hosseinpour, E Razmara, Z Zamani, Z Rezaei, ...
neurogenetics 24 (4), 279-289, 2023
强制性开放获取政策： UK Medical Research Council
Neurodegeneration with Brain Iron Accumulation Disorders and Retinal Neurovascular Structure
E Amini, M Rohani, A Fasano, Z Azad, S Miri, SAH Habibi, M Emamikhah, ...
Movement Disorders 39 (2), 411-423, 2024
强制性开放获取政策： UK Medical Research Council
Olfactory status in neurodegeneration with brain iron accumulation disorders
E Amini, M Rohani, M Jalessi, Z Azad, F Valzania, F Cavallieri, M Farhadi, ...
Neurological Sciences 45 (2), 647-654, 2024
强制性开放获取政策： UK Medical Research Council
可在其他位置公开访问的文章：12 篇
Mutation in ADORA1 identified as likely cause of early‐onset parkinsonism and cognitive dysfunction
E Jaberi, M Rohani, GA Shahidi, S Nafissi, E Arefian, M Soleimani, ...
Movement Disorders 31 (7), 1004-1011, 2016
强制性开放获取政策： US National Institutes of Health
PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation
MA Dezfouli, A Alavi, M Rohani, M Rezvani, T Nekuie, B Klotzle, ...
Movement Disorders 28 (2), 228-231, 2013
强制性开放获取政策： Parkinson's UK
Clinical spectrum in multiple families with primary COQ10 deficiency
SS Hashemi, D Zare‐Abdollahi, MK Bakhshandeh, A Vafaee, ...
American Journal of Medical Genetics Part A 185 (2), 440-452, 2021
强制性开放获取政策： UK Medical Research Council
Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations
M Khani, H Shamshiri, F Fatehi, M Rohani, B Haghi Ashtiani, ...
Molecular Genetics & Genomic Medicine 8 (7), e1240, 2020
强制性开放获取政策： UK Medical Research Council
Anticipation can be more common in hereditary spastic paraplegia with SPAST mutations than it appears
SS Hashemi, R Hajati, A Davarzani, M Rohani, F DanaeeFard, ...
Canadian Journal of Neurological Sciences 49 (5), 651-661, 2022
强制性开放获取政策： UK Medical Research Council
BVVL/FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes
M Khani, H Shamshiri, H Taheri, J Hardy, JT Bras, S Carmona, ...
Neurobiology of Aging 99, 102. e1-102. e10, 2021
强制性开放获取政策： UK Medical Research Council
Clinical and molecular findings of autosomal recessive spastic ataxia of Charlevoix Saguenay: an Iranian case series expanding the genetic and neuroimaging spectra
MR Ashrafi, P Mohammadi, AR Tavasoli, M Heidari, S Hosseinpour, ...
The Cerebellum 22 (4), 640-650, 2023
强制性开放获取政策： German Research Foundation, UK Medical Research Council
Late‐Onset Mitochondrial Membrane Protein–Associated Neurodegeneration With Extensive Brain Iron Deposition
A Alavi, M Mokhtari, R Hajati, A Davarzani, A Fasano, AE Lang, M Rohani
Movement Disorders Clinical Practice 7 (1), 120, 2019
强制性开放获取政策： UK Medical Research Council
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
AZ Dehnavi, M Bemanalizadeh, SM Kahani, MR Ashrafi, M Rohani, ...
Orphanet journal of rare diseases 18 (1), 177, 2023
强制性开放获取政策： UK Medical Research Council
Whole-genome study of a multigenerational family with essential tremor
M Zhang, M Rohani, MM Haghighi, C Sato, E Rogaeva, A Fasano
Canadian Journal of Neurological Sciences 49 (3), 381-386, 2022
强制性开放获取政策： 国家自然科学基金委员会
Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study
MR Ashrafi, E Pourbakhtyaran, M Rohani, B Shalbafan, AR Tavasoli, ...
Clinical Case Reports 10 (4), e05777, 2022
强制性开放获取政策： UK Medical Research Council
Estimation of Ambulation and Survival in Neurodegeneration with Brain Iron Accumulation Disorders
E Amini, M Rohani, AE Lang, Z Azad, SAH Habibi, A Alavi, G Shahidi, ...
Movement Disorders Clinical Practice 11 (1), 53-62, 2024
强制性开放获取政策： UK Medical Research Council
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