Found: 37
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The Parkinson's disease e-diary: Developing a clinical and research tool for the digital age.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Altered gut microbiome and metabolome in patients with multiple system atrophy.
- Published in:
- 2018
- By:
- Publication type:
- letter
LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/867321
- By:
- Publication type:
- Article
OFF-Period Purposeless Groaning in Parkinsonism.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
A Systematic Review and Meta-Analysis Protocol for Qualitative and Quantitative Appraisals of Faecal Markers for Intestinal Permeability and Intestinal Inflammation in Older Adults.
- Published in:
- Malaysian Journal of Medicine & Health Sciences, 2023, v. 19, p. 79
- By:
- Publication type:
- Article
Happiness at the end of life: A qualitative study.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Gut Microbial Ecosystem in Parkinson Disease: New Clinicobiological Insights from Multi‐Omics.
- Published in:
- Annals of Neurology, 2021, v. 89, n. 3, p. 546, doi. 10.1002/ana.25982
- By:
- Publication type:
- Article
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 1, p. 14, doi. 10.1002/mdc3.13903
- By:
- Publication type:
- Article
Toward e‐Scales: Digital Administration of the International Parkinson and Movement Disorder Society Rating Scales.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 2, p. 208, doi. 10.1002/mdc3.13135
- By:
- Publication type:
- Article
Methylmalonic Aciduria: A Treatable Disorder of Which Adult Neurologists Need to Be Aware.
- Published in:
- Movement Disorders Clinical Practice, 2016, v. 3, n. 1, p. 104, doi. 10.1002/mdc3.12237
- By:
- Publication type:
- Article
Rapid-Onset Dystonia-Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation.
- Published in:
- Movement Disorders Clinical Practice, 2015, v. 2, n. 1, p. 74, doi. 10.1002/mdc3.12122
- By:
- Publication type:
- Article
Expanding the DARS phenotype: Late-adult onset myelopathy and leukoencephalopathy.
- Published in:
- Neurology Asia, 2023, v. 28, n. 1, p. 185, doi. 10.54029/2023vkd
- By:
- Publication type:
- Article
Expanding the DARS phenotype: Late-adult onset myelopathy and leukoencephalopathy.
- Published in:
- Neurology Asia, 2023, v. 28, n. 1, p. 185, doi. 10.54029/2023vkd
- By:
- Publication type:
- Article
Rare homozygous PRKN exon 7 duplication in a Ibanese patient from Northwestern Borneo with young onset Parkinson's disease.
- Published in:
- Neurology Asia, 2022, v. 27, n. 2, p. 515, doi. 10.54029/2022frs
- By:
- Publication type:
- Article
Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters.
- Published in:
- Neurology Asia, 2021, v. 26, n. 1, p. 167
- By:
- Publication type:
- Article
Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation.
- Published in:
- Neurology Asia, 2021, v. 26, n. 1, p. 161
- By:
- Publication type:
- Article
Neurological melioidosis in East Malaysia: Case series and review of the literature.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Primary angiitis of the central nervous system with myelopathy as initial clinical presentation.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features.
- Published in:
- Journal of Neural Transmission, 2022, v. 129, n. 1, p. 37, doi. 10.1007/s00702-021-02421-0
- By:
- Publication type:
- Article
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters.
- Published in:
- Neurodegenerative Diseases, 2020, v. 20, n. 1, p. 39, doi. 10.1159/000508131
- By:
- Publication type:
- Article
PARK16 is associated with PD in the Malaysian population.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 839, doi. 10.1002/ajmg.b.32454
- By:
- Publication type:
- Article
Parkinson's disease and the gastrointestinal microbiome.
- Published in:
- Journal of Neurology, 2020, v. 267, n. 9, p. 2507, doi. 10.1007/s00415-019-09320-1
- By:
- Publication type:
- Article
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00526-9
- By:
- Publication type:
- Article
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 10, p. 4203, doi. 10.1007/s10072-021-05056-x
- By:
- Publication type:
- Article
Understanding patients' and caregivers' perspectives and educational needs in Parkinson's disease: a multi-ethnic Asian study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Probiotics for Parkinson's disease: Current evidence and future directions.
- Published in:
- JGH Open, 2021, v. 5, n. 4, p. 414, doi. 10.1002/jgh3.12450
- By:
- Publication type:
- Article
Management of dysphagia and gastroparesis in Parkinson's disease in real-world clinical practice - Balancing pharmacological and non-pharmacological approaches.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.979826
- By:
- Publication type:
- Article
Helicobacter pylori Eradication in Parkinson's Disease: A Randomized Placebo‐Controlled Trial.
- Published in:
- Movement Disorders, 2020, v. 35, n. 12, p. 2250, doi. 10.1002/mds.28248
- By:
- Publication type:
- Article
Brief Clinical Rating Scales Should Not Be Overlooked.
- Published in:
- 2020
- By:
- Publication type:
- letter
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00560-7
- By:
- Publication type:
- Article
The Association Between Bullous Pemphigoid and Neurological Disorders in A Selected Malaysian Population.
- Published in:
- Medical Journal of Malaysia, 2015, v. 70, n. 2, p. 81
- By:
- Publication type:
- Article
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case–control association study for Parkinson's disease.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 11, p. N.PAG, doi. 10.1002/mgg3.604
- By:
- Publication type:
- Article
Osmotic Demyelination Syndrome With Evolving Movement Disorders.
- Published in:
- JAMA Neurology, 2018, v. 75, n. 7, p. 888, doi. 10.1001/jamaneurol.2018.0983
- By:
- Publication type:
- Article
Levodopa and Parkinson Disease-Myths Revisited.
- Published in:
- JAMA Neurology, 2017, v. 74, n. 10, p. 1270, doi. 10.1001/jamaneurol.2017.2560
- By:
- Publication type:
- Article
Augmentation of Autoantibodies by Helicobacter pylori in Parkinson’s Disease Patients May Be Linked to Greater Severity.
- Published in:
- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153725
- By:
- Publication type:
- Article
Correction: R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138600
- By:
- Publication type:
- Article
R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0135470
- By:
- Publication type:
- Article