Found: 8
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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
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- Article
P1‐610: ADVANCE CARE PLANNING (ACP) OUTCOMES IN PATIENTS WITH DEMENTIA.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P573, doi. 10.1016/j.jalz.2018.06.623
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- Article
A Phenomenological Investigation Into the Meaning of Food in Palliative Care Patients With Anorexia.
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- American Journal of Hospice & Palliative Medicine, 2023, v. 40, n. 11, p. 1190, doi. 10.1177/10499091221148141
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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
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
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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- Article