受强制性开放获取政策约束的文章 - Kishore Raj Kumar了解详情
无法在其他位置公开访问的文章：17 篇
Genetics of Parkinson disease and other movement disorders
KR Kumar, K Lohmann, C Klein
Current opinion in neurology 25 (4), 466-474, 2012
强制性开放获取政策： National Health and Medical Research Council, Australia, German Research …
Genetics of Parkinson's disease
KR Kumar, A Djarmati-Westenberger, A Grünewald
Seminars in neurology 31 (05), 433-440, 2011
强制性开放获取政策： German Research Foundation
Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: novel clinical and genetic findings
KR Kumar, M Needham, K Mina, M Davis, J Brewer, C Staples, K Ng, ...
Neuromuscular Disorders 20 (5), 330-334, 2010
强制性开放获取政策： US National Institutes of Health
High degree of genetic heterogeneity for hereditary cerebellar ataxias in Australia
C Kang, C Liang, KE Ahmad, Y Gu, SF Siow, JG Colebatch, S Whyte, ...
The Cerebellum 18, 137-146, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia
Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings
FF Jia, AP Drew, GA Nicholson, A Corbett, KR Kumar
Neuromuscular Disorders 31 (11), 1101-1112, 2021
强制性开放获取政策： Michael J Fox Foundation, Aligning Science Across Parksinson's, USA
A novel homozygous mutation in the FUCA1 gene highlighting fucosidosis as a cause of dystonia: Case report and literature review
G Wali, GM Wali, CM Sue, KR Kumar
Neuropediatrics 50 (04), 248-252, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia, Medical Research …
Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation–a neurophysiological study using excitability techniques
KR Kumar, CM Sue, D Burke, K Ng
Clinical neurophysiology 123 (7), 1454-1459, 2012
强制性开放获取政策： National Health and Medical Research Council, Australia
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy
BR Grosz, I Stevanovski, S Negri, M Ellis, S Barnes, S Reddel, S Vucic, ...
Journal of the Peripheral Nervous System 27 (2), 120-126, 2022
强制性开放获取政策： National Health and Medical Research Council, Australia, UK Medical Research …
Mutations in TUBB4A and spastic paraplegia
KR Kumar, F Vulinovic, K Lohmann, JS Park, S Schaake, CM Sue, C Klein
Movement Disorders 30 (13), 1857-1858, 2015
强制性开放获取政策： National Health and Medical Research Council, Australia, Research Foundation …
Clinical characteristics and diagnostic clues to Neurometabolic causes of dystonia
CS Phua, KR Kumar, S Levy
Journal of the Neurological Sciences 419, 117167, 2020
强制性开放获取政策： Michael J Fox Foundation, Aligning Science Across Parksinson's, USA
Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)
EM Martin, Y Zhu, CM Kraan, KR Kumar, DE Godler, M Field
Journal of medical genetics 59 (7), 706-709, 2022
强制性开放获取政策： National Health and Medical Research Council, Australia, Michael J Fox …
GNAL Mutations and Dystonia—Reply
KR Kumar, KA Martemyanov, K Lohmann
JAMA neurology 71 (8), 1053-1054, 2014
强制性开放获取政策： German Research Foundation, European Commission
Reduced facial nerve hyperexcitability from contralateral cerebral stroke in hemifacial spasm
KR Kumar, K Ng
Movement disorders 25 (9), 1310-1312, 2010
强制性开放获取政策： US National Institutes of Health, Chief Scientist Office, Scottish Executive
A recurrent missense variant in ITPR3 causes demyelinating Charcot-Marie-Tooth with variable severity
D Beijer, MF Dohrn, A Rebelo, MC Danzi, BR Grosz, M Ellis, KR Kumar, ...
Brain 148 (1), 227-237, 2025
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
The Next, Next-Generation of Sequencing, Promising to Boost Research and Clinical Practice
KR Kumar, MJ Cowley, RL Davis
Seminars in Thrombosis and Hemostasis, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia, Michael J Fox …
Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's disease
K Raj Kumar
Movement Disorders 30 (12), 1620-1620, 2015
强制性开放获取政策： National Health and Medical Research Council, Australia
Axonal excitability during ischemia in MELAS
K Ng, KR Kumar, C Sue, D Burke
Muscle & Nerve 47 (5), 762-765, 2013
强制性开放获取政策： National Health and Medical Research Council, Australia
可在其他位置公开访问的文章：72 篇
New insights into the complex role of mitochondria in Parkinson’s disease
A Grünewald, KR Kumar, CM Sue
Progress in neurobiology 177, 73-93, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia, German Research …
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
K Lohmann, RA Wilcox, S Winkler, A Ramirez, A Rakovic, JS Park, B Arns, ...
Annals of neurology 73 (4), 537-545, 2013
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14
H Rafehi, J Read, DJ Szmulewicz, KC Davies, P Snell, LG Fearnley, ...
The American Journal of Human Genetics 110 (1), 105-119, 2023
强制性开放获取政策： National Health and Medical Research Council, Australia, German Research …
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