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Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation.
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- Movement Disorders, 2006, v. 21, n. 9, p. 1510, doi. 10.1002/mds.21011
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- Publication type:
- Article
Static balance impairment and its change after pallidotomy in Parkinson's disease.
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- Movement Disorders, 2004, v. 19, n. 4, p. 437, doi. 10.1002/mds.10666
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- Publication type:
- Article
Effects of unilateral pallidotomy on voluntary movement, and simple and choice reaction times in Parkinson's disease.
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- Movement Disorders, 2003, v. 18, n. 5, p. 515, doi. 10.1002/mds.10389
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- Publication type:
- Article
Decrease in presynaptic inhibition on heteronymous monosynaptic Ia terminals in patients with Parkinson's disease.
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- 2000
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- Publication type:
- journal article
Markers for Guillain-Barré syndrome with poor prognosis: a multi-center study.
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- Journal of the Peripheral Nervous System, 2017, v. 22, n. 4, p. 433, doi. 10.1111/jns.12234
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- Publication type:
- Article
Pathological, biochemical, and biophysical characteristics of the transthyretin variant Y114H (p.Y134H) explain its very mild clinical phenotype.
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- Journal of the Peripheral Nervous System, 2015, v. 20, n. 4, p. 372, doi. 10.1111/jns.12143
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- Publication type:
- Article
Shinshu Brain Resource Net.
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- Neuropathology, 2016, v. 36, n. 6, p. 600, doi. 10.1111/neup.12304
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- Publication type:
- Article
Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.
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- Neuropathology, 2014, v. 34, n. 3, p. 261, doi. 10.1111/neup.12090
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- Publication type:
- Article
Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).
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- Neuropathology, 2008, v. 28, n. 2, p. 132, doi. 10.1111/j.1440-1789.2007.00864.x
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- Publication type:
- Article
The 31st Neuropathological Meeting of Joh-shin-etsu District 29 October 2005.
- Published in:
- 2006
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- Publication type:
- Other
Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan.
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- Journal of Human Genetics, 2013, v. 58, n. 8, p. 560, doi. 10.1038/jhg.2013.34
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- Publication type:
- Article
Bullous formation in a patient with familial amyloid polyneuropathy type I.
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- International Journal of Dermatology, 2013, v. 52, n. 11, p. 1398, doi. 10.1111/j.1365-4632.2011.05146.x
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- Publication type:
- Article
Peripheral Nerves Regenerated in Familial Amyloid Polyneuropathy after Liver Transplantation.
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- Annals of Internal Medicine, 1997, v. 127, n. 8, p. 618, doi. 10.7326/0003-4819-127-8_Part_1-199710150-00006
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- Publication type:
- Article
Nonparaneoplastic, Nonherpetic Limbic Encephalitis with Severe Episodic Hypothermia: A Case Report.
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- European Neurology, 2005, v. 54, n. 3, p. 170, doi. 10.1159/000089938
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- Publication type:
- Article
Successful Treatment with Alpha-Interferon of a Patient with Chronic Measles Infection of the Brain and Parkinsonism.
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- European Neurology, 2000, v. 44, n. 3, p. 184, doi. 10.1159/000008232
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- Publication type:
- Article
A Case of Pectoral Fasciitis with Spontaneous Remission.
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- European Neurology, 2000, v. 44, n. 2, p. 124, doi. 10.1159/000008212
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- Publication type:
- Article
Clinical Characteristics of Aged Becker Muscular Dystrophy Patients with Onset after 30 Years.
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- European Neurology, 1999, v. 42, n. 3, p. 145, doi. 10.1159/000008089
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- Publication type:
- Article
Prevalence of Dementia ofAlzheimer Type and Apolipoprotein EPhenotypes in Aged Patients withDown’s Syndrome.
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- European Neurology, 1998, v. 39, n. 4, p. 234, doi. 10.1159/000007940
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- Publication type:
- Article
Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan.
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- Neurogenetics, 2010, v. 11, n. 4, p. 409, doi. 10.1007/s10048-010-0245-6
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- Publication type:
- Article
Coexistence of Copper in the Iron-Rich Particles of Aceruloplasminemia Brain.
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- Biological Trace Element Research, 2017, v. 175, n. 1, p. 79, doi. 10.1007/s12011-016-0744-x
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- Publication type:
- Article
A case with rheumatoid arthritis and systemic reactive AA amyloidosis showing rapid regression of amyloid deposition on gastroduodenal mucosa after a combined therapy of corticosteroid and etanercept.
- Published in:
- 2011
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- Publication type:
- Report
Effect of synovial transthyretin amyloid deposition on preoperative symptoms and postoperative recovery of median nerve function among patients with idiopathic carpal tunnel syndrome.
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- Journal of Orthopaedic Science, 2014, v. 19, n. 6, p. 913, doi. 10.1007/s00776-014-0635-y
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- Publication type:
- Article
Polyarteritis nodosa with central nervous system involvement mimicking relapsing-remitting multiple sclerosis.
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- Modern Rheumatology, 2014, v. 24, n. 3, p. 525, doi. 10.3109/14397595.2013.852849
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- Publication type:
- Article
Pneumatosis cystoides intestinalis in neuropsychiatric systemic lupus erythematosus with diabetes mellitus: case report and literature review.
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- Modern Rheumatology, 2011, v. 21, n. 4, p. 415, doi. 10.3109/s10165-010-0407-2
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- Publication type:
- Article
Massive mesenteric edema in a patient with type I hereditary angioedema.
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- Modern Rheumatology, 2005, v. 15, n. 5, p. 361, doi. 10.3109/s10165-005-0416-8
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- Publication type:
- Article
A Long-Term Observation on the Possible Adverse Effects in Japanese Adolescent Girls after Human Papillomavirus Vaccination.
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- Vaccines, 2021, v. 9, n. 8, p. 856, doi. 10.3390/vaccines9080856
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- Publication type:
- Article
ULTRASTRUCTURAL FINDINGS OF RECTAL AND SKIN BIOPSIES IN ADULT G<sub>M1</sub>-GANGLIOSIDOSIS.
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- Pathology International, 1986, v. 36, n. 12, p. 1823, doi. 10.1111/j.1440-1827.1986.tb02246.x
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- Publication type:
- Article
Cerebral hemorrhage in Fabry's disease.
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- Journal of Human Genetics, 2010, v. 55, n. 4, p. 259, doi. 10.1038/jhg.2010.18
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- Publication type:
- Article
A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2).
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- Journal of Human Genetics, 2009, v. 54, n. 12, p. 746, doi. 10.1038/jhg.2009.104
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- Publication type:
- Article
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene.
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- Journal of Human Genetics, 2009, v. 54, n. 2, p. 127, doi. 10.1038/jhg.2008.8
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- Publication type:
- Article
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 675, doi. 10.1007/s10038-007-0170-1
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- Publication type:
- Article
A Japanese case of SCA14 with the Gly128Asp mutation.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1118, doi. 10.1007/s10038-006-0063-8
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- Publication type:
- Article
A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.
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- Journal of Human Genetics, 2006, v. 51, n. 5, p. 461, doi. 10.1007/s10038-006-0385-6
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- Publication type:
- Article
Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families.
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- Journal of Human Genetics, 2004, v. 49, n. 11, p. 610, doi. 10.1007/s10038-004-0196-6
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- Publication type:
- Article
Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers.
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- Human Molecular Genetics, 2011, v. 20, n. 9, p. 1787, doi. 10.1093/hmg/ddr062
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- Publication type:
- Article
Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial.
- Published in:
- 2013
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- Publication type:
- journal article
Size variance of motor evoked potential at initiation of voluntary contraction in palsy of conversion disorder.
- Published in:
- Psychiatry & Clinical Neurosciences, 2008, v. 62, n. 3, p. 286, doi. 10.1111/j.1440-1819.2008.01795.x
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- Publication type:
- Article
Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia.
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- Acta Neuropathologica, 2002, v. 104, n. 2, p. 209, doi. 10.1007/s00401-002-0531-y
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- Publication type:
- Article
Survey of epidemiology, clinical picture and current treatments for elderly-onset (≥ 65 years) patients with myasthenia gravis in Nagano Prefecture, Japan.
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- Neurology & Clinical Neuroscience, 2017, v. 5, n. 4, p. 107, doi. 10.1111/ncn3.12129
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- Publication type:
- Article
Living donor liver transplantation using a graft with periportal fibrosis.
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- Hepatology Research, 2015, v. 45, n. 12, p. 1248, doi. 10.1111/hepr.12490
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- Publication type:
- Article
Patient with adult-onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma: Indication for liver transplantation.
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- Hepatology Research, 2013, v. 43, n. 5, p. 563, doi. 10.1111/j.1872-034X.2012.01098.x
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- Publication type:
- Article
First two cases of adult-onset type II citrullinemia successfully treated by deceased-donor liver transplantation in Japan.
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- Hepatology Research, 2012, v. 42, n. 9, p. 934, doi. 10.1111/j.1872-034X.2012.00992.x
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- Publication type:
- Article
Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate–glutamate carrier
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- Hepatology Research, 2005, v. 33, n. 2, p. 181, doi. 10.1016/j.hepres.2005.09.031
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- Publication type:
- Article
Sporadic hereditary diffuse leukoencephalopathy with axonal spheroids showing numerous lesions with restricted diffusivity caused by a novel splice site mutation in the CSF1R gene.
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- Clinical & Experimental Neuroimmunology, 2013, v. 4, p. 76, doi. 10.1111/cen3.12076
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- Publication type:
- Article
Hypertrophic neuritis due to chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): a postmortem pathological study.
- Published in:
- 1996
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- Publication type:
- journal article
Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia.
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- Muscle & Nerve, 1995, v. 18, n. 11, p. 1321, doi. 10.1002/mus.880181115
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- Publication type:
- Article
Familial amyloid polyneuropathy in Taiwan: Identification of transthyretin variant (Leu<sup>55</sup> → Pro).
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- Muscle & Nerve, 1994, v. 17, n. 6, p. 637, doi. 10.1002/mus.880170611
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- Publication type:
- Article
Molecular analysis of the duchenne muscular dystrophy gene in patients with becker muscular dystrophy presenting with dilated cardiomyopathy.
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- Muscle & Nerve, 1993, v. 16, n. 11, p. 1161, doi. 10.1002/mus.880161104
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- Publication type:
- Article
Peripheral nerve pathological findings in familial amyloid polyneuropathy: A correlative study of proximal sciatic nerve and sural nerve lesions.
- Published in:
- Annals of Neurology, 1989, v. 25, n. 4, p. 340, doi. 10.1002/ana.410250405
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- Publication type:
- Article
Presurgical Factors Affecting Patient Satisfaction with Pallidal Surgery in Parkinson’s Disease.
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- Stereotactic & Functional Neurosurgery, 2006, v. 84, n. 1, p. 24, doi. 10.1159/000093719
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- Publication type:
- Article