Artiklar med krav på offentlig åtkomst - Carolyn SueLäs mer
TotaltNHMRCNIHMRCMichael J Fox FoundationDFGMedical Research Future Fund, AustraliaWellcomeNIHRARCASAPParkinson's UKParkinson's Foundation, USAFWONRFDoDAcademy of FinlandGovernment of SpainHHMICIHRBBSRCCancer Research UKEuropean CommissionBMBFSNSFUSEDVAAHAFWFNSFCHelmholtzTelethonVersus Arthritis, UKBHFMotor Neurone Disease Association, UKNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKWorldwide Cancer Research, UKZonMwFNRDoris Duke Charitable FoundationJules Thorn Trust, UK
Inte tillgängliga någonstans: 19
The pathogenesis of Parkinson's disease
HR Morris, MG Spillantini, CM Sue, CH Williams-Gray
The Lancet 403 (10423), 293-304, 2024
Krav: UK Medical Research Council, National Institute for Health Research, UK …
The role of ATP13A2 in Parkinson's disease: clinical phenotypes and molecular mechanisms
JS Park, NF Blair, CM Sue
Movement Disorders 30 (6), 770-779, 2015
Krav: National Health and Medical Research Council, Australia
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
A Grünewald, B Arns, P Seibler, A Rakovic, A Münchau, A Ramirez, ...
Neurobiology of aging 33 (8), 1843. e1-1843. e7, 2012
Krav: German Research Foundation
Pathogenic effects of novel mutations in the P‐type ATPase ATP13A2 (PARK9) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism
JS Park, P Mehta, AA Cooper, D Veivers, A Heimbach, B Stiller, ...
Human mutation 32 (8), 956-964, 2011
Krav: 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
Krav: US National Institutes of Health
Olfactory impairment in older adults is associated with poorer diet quality over 5 years
B Gopinath, J Russell, CM Sue, VM Flood, G Burlutsky, P Mitchell
European journal of nutrition 55, 1081-1087, 2016
Krav: National Health and Medical Research Council, Australia
POLG mutations in Australian patients with mitochondrial disease
P Woodbridge, C Liang, RL Davis, H Vandebona, CM Sue
Internal medicine journal 43 (2), 150-156, 2013
Krav: National Health and Medical Research Council, Australia
The gut microbiota: a novel therapeutic target in Parkinson's disease?
M Lubomski, RL Davis, CM Sue
Parkinsonism & related disorders 66, 265-266, 2019
Krav: National Health and Medical Research Council, Australia
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
Krav: National Health and Medical Research Council, Australia
Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models
JS Park, B Koentjoro, RL Davis, CM Sue
Parkinsonism & related disorders 27, 67-73, 2016
Krav: National Health and Medical Research Council, Australia
Phenotypic variability of parkin mutations in single kindred
B Koentjoro, JS Park, AD Ha, CM Sue
Movement disorders 27 (10), 1299-1303, 2012
Krav: National Health and Medical Research Council, Australia, Government of Spain
SPAST mutations in Australian patients with hereditary spastic paraplegia
H Vandebona, NP Kerr, C Liang, CM Sue
Internal medicine journal 42 (12), 1342-1347, 2012
Krav: National Health and Medical Research Council, Australia
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
Krav: 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
Krav: National Health and Medical Research Council, Australia
A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family
KE Ahmad, RL Davis, CM Sue
Journal of neurology 262, 2323-2328, 2015
Krav: National Health and Medical Research Council, Australia
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
Krav: National Health and Medical Research Council, Australia, Research Foundation …
Hereditary parkinsonism-associated genetic variations in PARK9 locus Lead to functional impairment of ATPase type 13A2
C M. Sue, JS Park
Current Protein and Peptide Science 18 (7), 725-732, 2017
Krav: National Health and Medical Research Council, Australia
Strong predictive algorithm of pathogenesis-based biomarkers improves Parkinson’s disease diagnosis
DKY Chan, N Braidy, RF Chen, YH Xu, S Bentley, M Lubomski, RL Davis, ...
Molecular Neurobiology, 1-10, 2022
Krav: 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
Krav: National Health and Medical Research Council, Australia
Tillgängliga någonstans: 100
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
Krav: Swiss National Science Foundation, US National Institutes of Health, US …
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