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Biomarker-driven phenotyping in Parkinson's disease: A translational missing link in disease-modifying clinical trials.
- Published in:
- 2017
- By:
- Publication type:
- journal article
PLA2G6 mutations and Parkinsonism: Long-term follow-up of clinical features and neuropathology.
- Published in:
- 2016
- By:
- Publication type:
- letter
The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia.
- Published in:
- Movement Disorders, 2011, v. 26, n. 3, p. 549, doi. 10.1002/mds.23551
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- Publication type:
- Article
Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification.
- Published in:
- Movement Disorders, 2007, v. 22, n. 12, p. 1708, doi. 10.1002/mds.21370
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- Publication type:
- Article
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
- Published in:
- Movement Disorders, 2004, v. 19, n. 6, p. 649, doi. 10.1002/mds.20097
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- Publication type:
- Article
Spongiform encephalopathy mimicking corticobasal degeneration.
- Published in:
- Movement Disorders, 2002, v. 17, n. 3, p. 606, doi. 10.1002/mds.10166
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- Publication type:
- Article
Young-onset Parkinson's disease: A clinical pathologic description of two siblings.
- Published in:
- Movement Disorders, 2000, v. 15, n. 4, p. 744, doi. 10.1002/1531-8257(200007)15:4<744::AID-MDS1026>3.0.CO;2-#
- By:
- Publication type:
- Article
Relationship of retinotopic ordering of axons in the optic pathway to the formation of visual maps in central targets.
- Published in:
- Journal of Comparative Neurology, 1991, v. 307, n. 3, p. 393, doi. 10.1002/cne.903070305
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- Publication type:
- Article
Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 637, doi. 10.1093/hmg/ddt450
- By:
- Publication type:
- Article
Clinical Impact of <sup>123</sup>I-Ioflupane SPECT (DaTscan) in a Movement Disorder Center.
- Published in:
- Neurodegenerative Diseases, 2016, v. 17, n. 1, p. 38, doi. 10.1159/000447561
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- Publication type:
- Article
Efficacy of Deep Brain Stimulation in a Patient with Genetically Confirmed Chorea-Acanthocytosis.
- Published in:
- Case Reports in Neurology, 2019, v. 11, n. 2, p. 199, doi. 10.1159/000500951
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- Publication type:
- Article
Parkinson Disease in Twins.
- Published in:
- JAMA: Journal of the American Medical Association, 1999, v. 282, n. 14, p. 1328, doi. 10.1001/jama.282.14.1328
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- Publication type:
- Article
No Sex Differences in Use of Dopaminergic Medication in Early Parkinson Disease in the US and Canada - Baseline Findings of a Multicenter Trial.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0112287
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- Publication type:
- Article
Pgc-1α Overexpression Downregulates Pitx3 and Increases Susceptibility to MPTP Toxicity Associated with Decreased Bdnf.
- Published in:
- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0048925
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- Publication type:
- Article
Oral N-Acetyl-Cysteine Attenuates Loss of Dopaminergic Terminals in α-Synuclein Overexpressing Mice.
- Published in:
- PLoS ONE, 2010, v. 5, n. 8, p. 1, doi. 10.1371/journal.pone.0012333
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- Publication type:
- Article
Inverse probability weighted Cox regression for doubly truncated data.
- Published in:
- Biometrics, 2018, v. 74, n. 2, p. 481, doi. 10.1111/biom.12771
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- Publication type:
- Article
Do SomaticMitochondrial DNAMutations Contribute to Parkinson's Disease?
- Published in:
- Parkinson's Disease (20420080), 2011, p. 1, doi. 10.4061/2011/659694
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- Publication type:
- Article
Mitochondrial DNA mutations in Parkinson's disease brain.
- Published in:
- 2017
- By:
- Publication type:
- Letter to the Editor
Efficacy of Nilotinib in Patients With Moderately Advanced Parkinson Disease: A Randomized Clinical Trial.
- Published in:
- JAMA Neurology, 2021, v. 78, n. 3, p. 312, doi. 10.1001/jamaneurol.2020.4725
- By:
- Publication type:
- Article
Targeting energy metabolism via the mitochondrial pyruvate carrier as a novel approach to attenuate neurodegeneration.
- Published in:
- Molecular Neurodegeneration, 2018, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13024-018-0260-x
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- Publication type:
- Article
Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease.
- Published in:
- BMC Medical Genetics, 2011, v. 12, n. 1, p. 69, doi. 10.1186/1471-2350-12-69
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- Publication type:
- Article
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 53, doi. 10.1186/1471-2350-11-53
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- Publication type:
- Article
High-throughput mutational analysis of TOR1A in primary dystonia.
- Published in:
- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-24
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- Publication type:
- Article
An Autopsy Series of Seven Cases of VPS13A Disease (Chorea‐Acanthocytosis).
- Published in:
- Movement Disorders, 2023, v. 38, n. 12, p. 2163, doi. 10.1002/mds.29589
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- Publication type:
- Article
Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea‐Acanthocytosis.
- Published in:
- Movement Disorders, 2023, v. 38, n. 8, p. 1535, doi. 10.1002/mds.29445
- By:
- Publication type:
- Article
A New Approach to the Development of Disease-Modifying Therapies for PD.
- Published in:
- 2021
- By:
- Publication type:
- letter
The Relationship Between Olfactory Dysfunction and Constipation in Early Parkinson's Disease.
- Published in:
- Movement Disorders, 2021, v. 36, n. 3, p. 781, doi. 10.1002/mds.28483
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- Publication type:
- Article
Altered muscle electrical tissue properties in a mouse model of premature aging.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids.
- Published in:
- Muscle & Nerve, 2009, v. 40, n. 3, p. 381, doi. 10.1002/mus.21355
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- Publication type:
- Article
Reply.
- Published in:
- Annals of Neurology, 2012, v. 72, n. 5, p. 823, doi. 10.1002/ana.23739
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- Publication type:
- Article
Somatic mitochondrial DNA mutations in early parkinson and incidental lewy body disease.
- Published in:
- Annals of Neurology, 2012, v. 71, n. 6, p. 850, doi. 10.1002/ana.23568
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- Publication type:
- Article
Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2.
- Published in:
- Annals of Neurology, 2012, v. 71, n. 3, p. 370, doi. 10.1002/ana.22687
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- Publication type:
- Article
Do mtDNA deletions drive premature aging in mtDNA mutator mice?
- Published in:
- Aging Cell, 2009, v. 8, n. 4, p. 502, doi. 10.1111/j.1474-9726.2009.00484.x
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- Publication type:
- Article
Association of Cumulative Lead Exposure with Parkinson's Disease.
- Published in:
- Environmental Health Perspectives, 2010, v. 118, n. 11, p. 1609, doi. 10.1289/ehp.1002339
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- Publication type:
- Article