Found: 50
Select item for more details and to access through your institution.
Efficacy and Safety of Elobixibat in Parkinson's Disease with Chronic Constipation: CONST‐PD Study.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 4, p. 352, doi. 10.1002/mdc3.13972
- By:
- Publication type:
- Article
Investigation of 22q11.2 Deletion in Japanese Early‐Onset Parkinsonism.
- Published in:
- Movement Disorders, 2024, v. 39, n. 3, p. 626, doi. 10.1002/mds.29692
- By:
- Publication type:
- Article
Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
- Published in:
- Movement Disorders, 2023, v. 38, n. 12, p. 2249, doi. 10.1002/mds.29610
- By:
- Publication type:
- Article
Radiation-induced Brain Calcification Leads to L-dopa-resistant Parkinsonism and Cerebellar Ataxia.
- Published in:
- Internal Medicine, 2022, v. 61, n. 24, p. 3723, doi. 10.2169/internalmedicine.8400-21
- By:
- Publication type:
- Article
α‐Synuclein V15A Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid‐Binding Property.
- Published in:
- Movement Disorders, 2022, v. 37, n. 10, p. 2075, doi. 10.1002/mds.29162
- By:
- Publication type:
- Article
Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00367-y
- By:
- Publication type:
- Article
Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration.
- Published in:
- Brain: A Journal of Neurology, 2022, v. 145, n. 8, p. 2769, doi. 10.1093/brain/awac091
- By:
- Publication type:
- Article
Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population Studies.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.764917
- By:
- Publication type:
- Article
Deep Brain Stimulation for a Patient with Familial Parkinson's Disease Harboring CHCHD2 p.T61I.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 3, p. 407, doi. 10.1002/mdc3.13428
- By:
- Publication type:
- Article
Improvement in the Symptoms and VEGF Levels after Resection of an Extrame Dullary Spinal Tumor and Additional Chemotherapy in a Patient with Multiple Myeloma Complicated with POEMS Syndrome.
- Published in:
- Internal Medicine, 2021, v. 60, n. 22, p. 3625, doi. 10.2169/internalmedicine.6929-20
- By:
- Publication type:
- Article
A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson's Disease Affects LRRK2 Protein Levels.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3708, doi. 10.3390/ijms22073708
- By:
- Publication type:
- Article
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
- Published in:
- 2020
- By:
- Publication type:
- journal article
The absence of orthostatic heart rate increase is associated with cognitive impairment in Parkinson's disease.
- Published in:
- PLoS ONE, 2020, v. 15, n. 10, p. 1, doi. 10.1371/journal.pone.0240491
- By:
- Publication type:
- Article
Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.576465
- By:
- Publication type:
- Article
Unclassified four-repeat tauopathy associated with familial parkinsonism and progressive respiratory failure.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01025-1
- By:
- Publication type:
- Article
Variants in saposin D domain of prosaposin gene linked to Parkinson's disease.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Mutations in CHCHD2 cause α-synuclein aggregation.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 23, p. 3895, doi. 10.1093/hmg/ddz241
- By:
- Publication type:
- Article
Arylsulfatase A, a genetic modifier of Parkinson's disease, is an α-synuclein chaperone.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Painful legs and moving toes syndrome evaluated through brain single photon emission computed tomography: a case series.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 3, p. 717, doi. 10.1007/s00415-019-09194-3
- By:
- Publication type:
- Article
Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0617-y
- By:
- Publication type:
- Article
GCH1 mutations in dopa-responsive dystonia and Parkinson’s disease.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 8, p. 1860, doi. 10.1007/s00415-018-8930-8
- By:
- Publication type:
- Article
COQ2 variants in Parkinson’s disease and multiple system atrophy.
- Published in:
- Journal of Neural Transmission, 2018, v. 125, n. 6, p. 937, doi. 10.1007/s00702-018-1885-1
- By:
- Publication type:
- Article
Genetic association between RAGE polymorphisms and Alzheimer's disease and Lewy body dementias in a Japanese cohort: a case-control study.
- Published in:
- 2017
- By:
- Publication type:
- journal article
DNAJC12 and dopa-responsive nonprogressive parkinsonism.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Psychometric assessment of the Japanese version of the Revised Fibromyalgia Impact Questionnaire: reliability and validity.
- Published in:
- International Journal of Rheumatic Diseases, 2017, v. 20, n. 9, p. 1088, doi. 10.1111/1756-185X.12574
- By:
- Publication type:
- Article
Paraneoplastic neuromyotonia due to lung carcinoma and invisible muscle cramps evaluated using ultrasonography.
- Published in:
- 2017
- By:
- Publication type:
- Letter
High prevalence of anti- TSH receptor antibody in fibromyalgia syndrome.
- Published in:
- International Journal of Rheumatic Diseases, 2017, v. 20, n. 6, p. 685, doi. 10.1111/1756-185X.12964
- By:
- Publication type:
- Article
Case of Morvan syndrome with anti-Ma2/Ta antibodies.
- Published in:
- Clinical & Experimental Neuroimmunology, 2016, v. 7, n. 4, p. 369, doi. 10.1111/cen3.12325
- By:
- Publication type:
- Article
[11C]PBB3 PET VISUALIZES TAU AGGREGATES IN PATIENTS WITH FTDP-17 MAPT GENE MUTATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P135, doi. 10.1016/j.jalz.2016.06.217
- By:
- Publication type:
- Article
Fibromyalgia syndrome and cognitive dysfunction in elderly: a case series.
- Published in:
- International Journal of Rheumatic Diseases, 2016, v. 19, n. 1, p. 21, doi. 10.1111/1756-185X.12734
- By:
- Publication type:
- Article
The E3 ligase synoviolin controls body weight and mitochondrial biogenesis through negative regulation of PGC-1β.
- Published in:
- EMBO Journal, 2015, v. 34, n. 8, p. 1042, doi. 10.15252/embj.201489897
- By:
- Publication type:
- Article
ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout.
- Published in:
- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 3, p. 302, doi. 10.1002/acn3.167
- By:
- Publication type:
- Article
Quantitative evaluation of electroconvulsive therapy for Parkinson's disease with refractory psychiatric symptoms.
- Published in:
- Journal of Neural Transmission, 2014, v. 121, n. 11, p. 1405, doi. 10.1007/s00702-014-1212-4
- By:
- Publication type:
- Article
An Epidemiologic Internet Survey of Fibromyalgia and Chronic Pain in Japan.
- Published in:
- Arthritis Care & Research, 2014, v. 66, n. 7, p. 1093, doi. 10.1002/acr.22277
- By:
- Publication type:
- Article
Vulnerability to traumatic stress in fibromyalgia patients: 19 month follow-up after the great East Japan disaster.
- Published in:
- Arthritis Research & Therapy, 2013, v. 15, n. 5, p. 1, doi. 10.1186/ar4310
- By:
- Publication type:
- Article
The Japanese version of the modified ACR Preliminary Diagnostic Criteria for Fibromyalgia and the Fibromyalgia Symptom Scale: reliability and validity.
- Published in:
- Modern Rheumatology, 2013, v. 23, n. 5, p. 846, doi. 10.3109/s10165-012-0759-x
- By:
- Publication type:
- Article
Acute transient freezing of gait in a patient with posterior reversible encephalopathy syndrome.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Acute transient freezing of gait in a patient with posterior reversible encephalopathy syndrome.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Longitudinally Extensive Transverse Myelitis with Intramedullary Metastasis of Small-Cell Lung Carcinoma: An Autopsy Case Report.
- Published in:
- Case Reports in Neurological Medicine, 2013, p. 1, doi. 10.1155/2013/305670
- By:
- Publication type:
- Article
The Japanese version of the 2010 American College of Rheumatology Preliminary Diagnostic Criteria for Fibromyalgia and the Fibromyalgia Symptom Scale: reliability and validity.
- Published in:
- Modern Rheumatology, 2012, v. 22, n. 1, p. 40, doi. 10.3109/s10165-011-0462-3
- By:
- Publication type:
- Article
LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors.
- Published in:
- Molecular Neurodegeneration, 2012, v. 7, n. 1, p. 25, doi. 10.1186/1750-1326-7-25
- By:
- Publication type:
- Article
Methotrexate leukoencephalopathy mimics acute progressive stroke.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Expanding the clinical phenotype of SNCA duplication carriers.
- Published in:
- Movement Disorders, 2009, v. 24, n. 12, p. 1811, doi. 10.1002/mds.22682
- By:
- Publication type:
- Article
Genetic Association between SORL1 Polymorphisms and Alzheimer’s Disease in a Japanese Population.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 2, p. 161, doi. 10.1159/000149821
- By:
- Publication type:
- Article
Familial Parkinsonism with digenic parkin and PINK1 mutations.
- Published in:
- Movement Disorders, 2008, v. 23, n. 10, p. 1461, doi. 10.1002/mds.22143
- By:
- Publication type:
- Article
Genomic investigation of α-synuclein multiplication and parkinsonism.
- Published in:
- Annals of Neurology, 2008, v. 63, n. 6, p. 743, doi. 10.1002/ana.21380
- By:
- Publication type:
- Article
Prognosis of Parkinson's disease: Time to stage III, IV, V, and to motor fluctuations.
- Published in:
- Movement Disorders, 2006, v. 21, n. 9, p. 1384, doi. 10.1002/mds.20993
- By:
- Publication type:
- Article
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease.
- Published in:
- Annals of Neurology, 2006, v. 59, n. 2, p. 298
- By:
- Publication type:
- Article
An Autopsy Case of Schilder’s Variant of Multiple Sclerosis (Schilder’s Disease).
- Published in:
- European Neurology, 2006, v. 55, n. 2, p. 103, doi. 10.1159/000092785
- By:
- Publication type:
- Article