Artikel dengan mandat akses publik - Huw R MorrisPelajari lebih lanjut
KeseluruhanMRCParkinson's UKNIHNIHRWellcomeMichael J Fox FoundationAlzheimers's UKMotor Neurone Disease Association, UKASAPEuropean CommissionBMBFDFGSwedish Research CouncilDoDUK Research & InnovationESRCGovernment of SpainBrain Research, UKRannisCIHRParkinson's Foundation, USAHelmholtzCanada First Research Excellence FundNHMRCCancer Research UKEPSRCGovernment of ItalyTelethonKnut and Alice Wallenberg FoundationNWOBBSRCFondazione CariploANRSNSFFWOFRQSVolkswagen FoundationINSERMDMTMultiple Sclerosis Society, UKZonMwRCNVAACLHHMIFWFARCNSERCNSFCFCTFORTEVersus Arthritis, UKBHFNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKWorldwide Cancer Research, UKNRFNMRCRWJFVinnova, SwedenGovernment of Argentina
Tidak tersedia di mana pun: 13
Systematic Review and UK‐Based Study of PARK2 (parkin), PINK1, PARK7 (DJ‐1) and LRRK2 in early‐onset Parkinson's disease
LL Kilarski, JP Pearson, V Newsway, E Majounie, MDW Knipe, ...
Movement Disorders 27 (12), 1522-1529, 2012
Mandat: Parkinson's UK
The motor phenotype of Parkinson's disease in relation to age at onset
MM Wickremaratchi, MDW Knipe, BSD Sastry, E Morgan, A Jones, ...
Movement Disorders 26 (3), 457-463, 2011
Mandat: Parkinson's UK
The pathogenesis of Parkinson's disease
HR Morris, MG Spillantini, CM Sue, CH Williams-Gray
The Lancet 403 (10423), 293-304, 2024
Mandat: UK Medical Research Council, National Institute for Health Research, UK …
A comparison of clinical and objective measures of freezing of gait in Parkinson's disease
TR Morris, C Cho, V Dilda, JM Shine, SL Naismith, SJG Lewis, ST Moore
Parkinsonism & related disorders 18 (5), 572-577, 2012
Mandat: US National Institutes of Health
Recent advances in Parkinson’s disease genetics
S Lubbe, HR Morris
Journal of neurology 261, 259-266, 2014
Mandat: UK Medical Research Council, Parkinson's UK
Parkinson's disease: chameleons and mimics
K Ali, HR Morris
Practical neurology 15 (1), 14-25, 2015
Mandat: UK Medical Research Council, Parkinson's UK
Quality of life in young‐compared with late‐onset Parkinson's disease
MDW Knipe, MM Wickremaratchi, E Wyatt‐Haines, HR Morris, ...
Movement Disorders 26 (11), 2011-2018, 2011
Mandat: Parkinson's UK
Recent advances in the genetics of the ALS-FTLD complex
HR Morris, AJ Waite, NM Williams, JW Neal, DJ Blake
Current neurology and neuroscience reports 12, 243-250, 2012
Mandat: Motor Neurone Disease Association, UK, Parkinson's UK
Defining neurodegeneration on G uam by targeted genomic sequencing
JC Steele, I Guella, C Szu‐Tu, MK Lin, C Thompson, DM Evans, ...
Annals of neurology 77 (3), 458-468, 2015
Mandat: Canadian Institutes of Health Research, UK Medical Research Council
Psychiatric disorders, myoclonus dystonia, and the epsilon‐sarcoglycan gene: a systematic review
KJ Peall, AJ Waite, DJ Blake, MJ Owen, HR Morris
Movement disorders 26 (10), 1939-1942, 2011
Mandat: Motor Neurone Disease Association, UK, Parkinson's UK, Government of Spain
Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome
MM Wickremaratchi, E Majounie, HR Morris, NM Williams, H Lewis, ...
Movement disorders: official journal of the Movement Disorder Society 24 (1 …, 2009
Mandat: US National Institutes of Health
Motor Complications in Parkinson's Disease: Results from 3343 Patients Followed for up to 12 Years
SE Gandhi, T Zerenner, A Nodehi, MA Lawton, V Marshall, F Al‐Hajraf, ...
Movement Disorders Clinical Practice, 2024
Mandat: UK Medical Research Council, National Institute for Health Research, UK …
Making neurogenetics a global endeavour
HR Morris
Brain 143 (7), 1970-1973, 2020
Mandat: UK Medical Research Council, Parkinson's UK
Tersedia di suatu tempat: 224
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron, 2011
Mandat: US National Institutes of Health, German Research Foundation
Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria
GU Höglinger, G Respondek, M Stamelou, C Kurz, KA Josephs, AE Lang, ...
Movement disorders 32 (6), 853-864, 2017
Mandat: US National Institutes of Health, German Research Foundation, Alzheimers's …
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
Mandat: US National Institutes of Health, UK Medical Research Council, Parkinson's …
Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study
A Varatharaj, N Thomas, MA Ellul, NWS Davies, TA Pollak, EL Tenorio, ...
The Lancet Psychiatry 7 (10), 875-882, 2020
Mandat: Motor Neurone Disease Association, UK, UK Medical Research Council, National …
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Mandat: US National Institutes of Health, Swedish Research Council, Alzheimers's UK …
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
Mandat: US National Institutes of Health, German Research Foundation, Motor Neurone …
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
MA Nalls, V Plagnol, DG Hernandez, M Sharma, UM Sheerin, M Saad, ...
Lancet 377 (9766), 641, 2011
Mandat: US National Institutes of Health, Parkinson's UK
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