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Painless legs and moving toes from parasagittal meningioma.
- Published in:
- Movement Disorders, 2012, v. 27, n. 4, p. 586, doi. 10.1002/mds.24887
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- Publication type:
- Article
Estimation of skeletal muscle energy metabolism in Machado-Joseph disease using (31)P-MR spectroscopy.
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- 2011
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- Publication type:
- journal article
Estimation of skeletal muscle energy metabolism in Machado-Joseph disease using.
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- Movement Disorders, 2011, v. 26, n. 1, p. 165, doi. 10.1002/mds.23335
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- Publication type:
- Article
Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 Genes.
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- Movement Disorders, 2008, v. 23, n. 8, p. 1161, doi. 10.1002/mds.22046
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- Publication type:
- Article
G protein-coupled receptor 26 immunoreactivity in intranuclear inclusions associated with polyglutamine and intranuclear inclusion body diseases.
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- Neuropathology, 2016, v. 36, n. 1, p. 50, doi. 10.1111/neup.12237
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- Publication type:
- Article
Localization of nuclear receptor subfamily 4, group A, member 3 ( NR4A3) in Lewy body disease and multiple system atrophy.
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- Neuropathology, 2015, v. 35, n. 6, p. 503, doi. 10.1111/neup.12210
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- Publication type:
- Article
Isopentenyl diphosphate isomerase, a cholesterol synthesizing enzyme, is localized in Lewy bodies.
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- Neuropathology, 2015, v. 35, n. 5, p. 432, doi. 10.1111/neup.12204
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- Publication type:
- Article
Accumulation of the sigma-1 receptor is common to neuronal nuclear inclusions in various neurodegenerative diseases.
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- Neuropathology, 2014, v. 34, n. 2, p. 148, doi. 10.1111/neup.12080
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- Publication type:
- Article
ALS-associated protein FIG4 is localized in Pick and Lewy bodies, and also neuronal nuclear inclusions, in polyglutamine and intranuclear inclusion body diseases.
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- Neuropathology, 2014, v. 34, n. 1, p. 19, doi. 10.1111/neup.12056
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- Publication type:
- Article
Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease.
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- Neuropathology, 2013, v. 33, n. 6, p. 637, doi. 10.1111/neup.12050
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- Publication type:
- Article
Degeneration of the inferior olive in spinocerebellar ataxia 6 may depend on disease duration: Report of two autopsy cases and statistical analysis of autopsy cases reported to date.
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- Neuropathology, 2005, v. 25, n. 2, p. 125, doi. 10.1111/j.1440-1789.2005.00596.x
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- Publication type:
- Article
The implications of genetic studies on the pathogenesis of Alzheimer's disease.
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- Neuropathology, 1998, v. 18, n. 1, p. 103, doi. 10.1111/j.1440-1789.1998.tb00086.x
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- Publication type:
- Article
Idiopathic Hypoglossal Nerve Laceration Detected by High-Resolution Three-Dimensional Constructive Interference in Steady State Magnetic Resonance Imaging.
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- Journal of Neuroimaging, 2011, v. 21, n. 2, p. e177, doi. 10.1111/j.1552-6569.2010.00498.x
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- Publication type:
- Article
Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 848, doi. 10.1007/s10038-007-0182-x
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- Publication type:
- Article
Four mutations of the spastin gene in Japanese families with spastic paraplegia.
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- Journal of Human Genetics, 2006, v. 51, n. 8, p. 711, doi. 10.1007/s10038-006-0412-7
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- Publication type:
- Article
Pathological study of subacute autoimmune encephalopathy with anti-AQP4 antibodies in a pregnant woman.
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- Multiple Sclerosis Journal, 2012, v. 18, n. 5, p. 683, doi. 10.1177/1352458511422928
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- Publication type:
- Article
Identification of plasma microRNA expression changes in multiple system atrophy and Parkinson's disease.
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- Molecular Brain, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13041-019-0471-2
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- Publication type:
- Article
Serum carnitine and disabling fatigue in multiple sclerosis.
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- Psychiatry & Clinical Neurosciences, 1996, v. 50, n. 6, p. 323, doi. 10.1111/j.1440-1819.1996.tb00573.x
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- Publication type:
- Article
Proteasome inhibition induces selective motor neuron death in organotypic slice cultures.
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- Journal of Neuroscience Research, 2005, v. 82, n. 4, p. 443, doi. 10.1002/jnr.20665
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- Publication type:
- Article
Ubiquilin immunoreactivity in cytoplasmic and nuclear inclusions in synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease.
- Published in:
- 2012
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- Publication type:
- Letter
The carboxy-terminal fragment of α<sub>1A</sub> calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.
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- Acta Neuropathologica, 2010, v. 119, n. 4, p. 447, doi. 10.1007/s00401-009-0630-0
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- Publication type:
- Article
Pseudodystonia in sarcoid myopathy.
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- Neurology & Clinical Neuroscience, 2017, v. 5, n. 1, p. 34, doi. 10.1111/ncn3.12093
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- Publication type:
- Article
Spinocerebellar ataxia type 14 family with a novel PRKCG mutation.
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- Neurology & Clinical Neuroscience, 2016, v. 4, n. 5, p. 199, doi. 10.1111/ncn3.12070
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- Publication type:
- Article
Frontotemporal dementia and progressive supranuclear palsy-like syndrome with a novel TARDBP mutation.
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- Neurology & Clinical Neuroscience, 2016, v. 4, n. 2, p. 76, doi. 10.1111/ncn3.12041
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- Publication type:
- Article
Variants associated with Gaucher disease in multiple system atrophy.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 4, p. 417, doi. 10.1002/acn3.185
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- Publication type:
- Article
Analysis of microRNA from archived formalin-fixed paraffin-embedded specimens of amyotrophic lateral sclerosis.
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- Acta Neuropathologica Communications, 2014, v. 2, n. 1, p. 1, doi. 10.1186/s40478-014-0173-z
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- Publication type:
- Article
Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies.
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- Genes to Cells, 1999, v. 4, n. 12, p. 743, doi. 10.1046/j.1365-2443.1999.00294.x
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- Publication type:
- Article
A common disease haplotype segregating in spinocerebellar ataxia 2 (SCA2) pedigrees of diverse ethnic origin.
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- European Journal of Human Genetics, 1999, v. 7, n. 7, p. 841, doi. 10.1038/sj.ejhg.5200372
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- Publication type:
- Article
Genomic copy number variation analysis in multiple system atrophy.
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- Molecular Brain, 2017, v. 10, p. 1, doi. 10.1186/s13041-017-0335-6
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- Publication type:
- Article
Identification of plasma microRNAs as a biomarker of sporadic Amyotrophic Lateral Sclerosis.
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- Molecular Brain, 2015, v. 8, p. 1, doi. 10.1186/s13041-015-0161-7
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- Publication type:
- Article
Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy.
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- Molecular Brain, 2011, v. 4, n. 1, p. 24, doi. 10.1186/1756-6606-4-24
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- Publication type:
- Article
Regional distribution of amino acid transmitters in postmortem brains of presenile and senile dementia of Alzheimer type.
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- Annals of Neurology, 1986, v. 19, n. 3, p. 263, doi. 10.1002/ana.410190307
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- Publication type:
- Article
Gerstmann-Sträussler-Scheinker's disease.
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- Annals of Neurology, 1983, v. 14, n. 2, p. 216, doi. 10.1002/ana.410140208
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- Publication type:
- Article
Epilepsia partialis continua following metrizamide cisternography.
- Published in:
- 1981
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- Publication type:
- case study
3D neuromelanin-sensitive magnetic resonance imaging with semi-automated volume measurement of the substantia nigra pars compacta for diagnosis of Parkinson's disease.
- Published in:
- Neuroradiology, 2013, v. 55, n. 6, p. 719, doi. 10.1007/s00234-013-1171-8
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- Publication type:
- Article
Usefulness of C-methionine-positron emission tomography for the diagnosis of progressive multifocal leukoencephalopathy.
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- Journal of Neurology, 2014, v. 261, n. 12, p. 2314, doi. 10.1007/s00415-014-7500-y
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- Publication type:
- Article
Identification of anti-Sez6l2 antibody in a patient with cerebellar ataxia and retinopathy.
- Published in:
- 2014
- By:
- Publication type:
- Letter
Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people.
- Published in:
- Journal of Neurology, 2012, v. 259, n. 9, p. 1913, doi. 10.1007/s00415-012-6439-0
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- Publication type:
- Article
The Responsiveness of Triaxial Accelerometer Measurement of Gait Ataxia Is Higher than That of the Scale for the Assessment and Rating of Ataxia in the Early Stages of Spinocerebellar Degeneration.
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- Cerebellum, 2019, v. 18, n. 4, p. 721, doi. 10.1007/s12311-019-01025-5
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- Publication type:
- Article
Comparison of Different Symptom Assessment Scales for Multiple System Atrophy.
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- Cerebellum, 2016, v. 15, n. 2, p. 190, doi. 10.1007/s12311-015-0686-4
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- Publication type:
- Article
Epidemiology of Multiple System Atrophy in Hokkaido, the Northernmost Island of Japan.
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- Cerebellum, 2015, v. 14, n. 6, p. 682, doi. 10.1007/s12311-015-0668-6
- By:
- Publication type:
- Article
Treatment of cerebellar ataxia with 5‐HT1A agonist.
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- Cerebellum, 2005, v. 4, n. 3, p. 211, doi. 10.1080/14734220500222318
- By:
- Publication type:
- Article
A Retrospective Epidemiological Study of Tick-Borne Encephalitis Virus in Patients with Neurological Disorders in Hokkaido, Japan.
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- Microorganisms, 2020, v. 8, n. 11, p. 1672, doi. 10.3390/microorganisms8111672
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- Publication type:
- Article
Clinical factors affecting evoked magnetic fields in patients with Parkinson's disease.
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- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0232808
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- Publication type:
- Article
Circulating miRNome profiling in Moyamoya disease-discordant monozygotic twins and endothelial microRNA expression analysis using iPS cell line.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0385-3
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- Publication type:
- Article
A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.
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- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/s13023-014-0118-4
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- Publication type:
- Article
A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Hyperintense putaminal rim at 1.5 T: prevalence in normal subjects and distinguishing features from multiple system atrophy.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Hyperintense putaminal rim at 1.5 T: prevalence in normal subjects and distinguishing features from multiple system atrophy.
- Published in:
- BMC Neurology, 2012, v. 12, n. 1, p. 39, doi. 10.1186/1471-2377-12-39
- By:
- Publication type:
- Article
AMBRA1, a novel α-synuclein-binding protein, is implicated in the pathogenesis of multiple system atrophy.
- Published in:
- Brain Pathology, 2018, v. 28, n. 1, p. 28, doi. 10.1111/bpa.12461
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- Publication type:
- Article