Found: 12
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Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case report.
- Published in:
- BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03846-2
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- Article
Mind the Gap: LRRK2 Phenotypes in the Clinic vs. in Patient Cells.
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- Cells (2073-4409), 2021, v. 10, n. 5, p. 981, doi. 10.3390/cells10050981
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- Article
Overexpression of Wild-Type Human Alpha-Synuclein Causes Metabolism Abnormalities in Thy1-aSYN Transgenic Mice.
- Published in:
- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00321
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- Article
LRRK2 detection in human biofluids: potential use as a Parkinson's disease biomarker?
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- Biochemical Society Transactions, 2017, v. 45, n. 1, p. 207, doi. 10.1042/BST20160334
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- Article
Centrosomal cohesion deficits as cellular biomarker in lymphoblastoid cell lines from LRRK2 Parkinson's disease patients.
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- Biochemical Journal, 2019, v. 476, n. 19, p. 2797, doi. 10.1042/BCJ20190315
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- Article
Alterations in the LRRK2-Rab pathway in urinary extracellular vesicles as Parkinson's disease and pharmacodynamic biomarkers.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00445-9
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- Article
Transcriptomic signatures of brain regional vulnerability to Parkinson's disease.
- Published in:
- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0804-9
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- Article
Reply to: "Further Evidence of Cerebellar Cognitive Affective/Schmahmann Syndrome in RFC1‐Related Syndrome".
- Published in:
- Movement Disorders, 2024, v. 39, n. 7, p. 1248, doi. 10.1002/mds.29886
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- Article
Cognitive Impairment Is Part of the Phenotype of Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (CANVAS).
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- Movement Disorders, 2024, v. 39, n. 5, p. 892, doi. 10.1002/mds.29750
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- Article
Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson′s Disease.
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- Movement Disorders, 2022, v. 37, n. 8, p. 1761, doi. 10.1002/mds.29124
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- Article
SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.
- Published in:
- Human Mutation, 2011, v. 32, n. 4, p. E2079, doi. 10.1002/humu.21459
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- Publication type:
- Article
Alterations in the LRRK2-Rab pathway in urinary extracellular vesicles as Parkinson's disease and pharmacodynamic biomarkers.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00445-9
- By:
- Publication type:
- Article