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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
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- Article
Rapid-Onset Dystonia-Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation.
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- Movement Disorders Clinical Practice, 2015, v. 2, n. 1, p. 74, doi. 10.1002/mdc3.12122
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- Article
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.
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- Neurological Sciences, 2021, v. 42, n. 10, p. 4203, doi. 10.1007/s10072-021-05056-x
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- Article
Identification of the genomic mutation in Epha4<sup> rb-2J/rb-2J</sup> mice.
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- Genome, 2016, v. 59, n. 7, p. 439, doi. 10.1139/gen-2015-0142
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- Article
PARK16 is associated with PD in the Malaysian population.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 839, doi. 10.1002/ajmg.b.32454
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- Article
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.
- Published in:
- PLoS ONE, 2023, v. 18, n. 10, p. 1, doi. 10.1371/journal.pone.0292180
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- Article
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPH.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.868000
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- Article
Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic kadazandusun family.
- Published in:
- 2016
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- Publication type:
- journal article
X-linked Charcot-Marie-Tooth disease predominates in a cohort of multiethnic Malaysian patients.
- Published in:
- Muscle & Nerve, 2014, v. 49, n. 2, p. 198, doi. 10.1002/mus.23892
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- Article
A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia A.
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- Muscle & Nerve, 2012, v. 46, n. 3, p. 454, doi. 10.1002/mus.23346
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- Article
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters.
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- Neurodegenerative Diseases, 2020, v. 20, n. 1, p. 39, doi. 10.1159/000508131
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- Article
Editorial: Genetic and molecular diversity in Parkinson’s disease.
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- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.1094914
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- Article
Association of LRRK2 Haplotype With Age at Onset in Parkinson Disease.
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- JAMA Neurology, 2018, v. 75, n. 1, p. 127, doi. 10.1001/jamaneurol.2017.3363
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- Article
A Perspective on the Role of microRNA-128 Regulation in Mental and Behavioral Disorders.
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- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00465
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- Article
A mixed method study on the impact of living with spinal muscular atrophy in Malaysia from patients' and caregivers' perspectives.
- Published in:
- 2022
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- Publication type:
- journal article
Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans.
- Published in:
- Scientifica, 2017, p. 1, doi. 10.1155/2017/5364827
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- Article
Rare homozygous PRKN exon 7 duplication in a Ibanese patient from Northwestern Borneo with young onset Parkinson's disease.
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- Neurology Asia, 2022, v. 27, n. 2, p. 515, doi. 10.54029/2022frs
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- Article
Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters.
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- Neurology Asia, 2021, v. 26, n. 1, p. 167
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- Article
Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation.
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- Neurology Asia, 2021, v. 26, n. 1, p. 161
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- Article
Using global team science to identify genetic parkinson's disease worldwide.
- Published in:
- 2019
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- Publication type:
- Editorial
Signaling across the synapse: a role for Wnt and Dishevelled in presynaptic assembly and neurotransmitter release.
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- Journal of Cell Biology, 2006, v. 174, n. 1, p. 127, doi. 10.1083/jcb.200511054
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- 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.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 11, p. N.PAG, doi. 10.1002/mgg3.604
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- Publication type:
- Article
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 2, p. 143, doi. 10.1002/mgg3.126
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- Article
Genome-wide association study of Parkinson's disease in East Asians.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 1, p. 226, doi. 10.1093/hmg/ddw379
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- Publication type:
- Article
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.
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- Human Molecular Genetics, 2014, v. 23, n. 14, p. 3891, doi. 10.1093/hmg/ddu086
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- Publication type:
- Article
Missense Mutation of Brain Derived Neurotrophic Factor (BDNF) Alters Neurocognitive Performance in Patients with Mild Traumatic Brain Injury: A Longitudinal Study.
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- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0158838
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- Article
Deregulation of microRNAs in blood and skeletal muscles of myotonic dystrophy type 1 patients.
- Published in:
- 2017
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- Publication type:
- journal article
Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia.
- Published in:
- Movement Disorders, 2024, v. 39, n. 10, p. 1829, doi. 10.1002/mds.29932
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- Publication type:
- Article
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.
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- Movement Disorders, 2022, v. 37, n. 8, p. 1593, doi. 10.1002/mds.29126
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- Publication type:
- Article
COVID‐19 pandemic: Lessons learned for undergraduate research training.
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- Biochemistry & Molecular Biology Education, 2022, v. 50, n. 5, p. 476, doi. 10.1002/bmb.21665
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- Publication type:
- Article
Cranial neural tube defect after trimethoprim exposure.
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- BMC Research Notes, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13104-018-3593-1
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- Publication type:
- Article
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features.
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- Journal of Neural Transmission, 2022, v. 129, n. 1, p. 37, doi. 10.1007/s00702-021-02421-0
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- Publication type:
- Article
Maternal intake of dietary virgin coconut oil modifies essential fatty acids and causes low body weight and spiky fur in mice.
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- BMC Complementary & Alternative Medicine, 2017, v. 17, p. 1, doi. 10.1186/s12906-017-1600-z
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- Publication type:
- Article
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family.
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- Neurogenetics, 2019, v. 20, n. 3, p. 117, doi. 10.1007/s10048-019-00576-3
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- Article
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies.
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- Neurogenetics, 2014, v. 15, n. 4, p. 229, doi. 10.1007/s10048-014-0414-0
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- Article
LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population.
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- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/867321
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- Article