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Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 6, p. 992, doi. 10.1002/mdc3.13740
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- Article
Hereditary Spastic Paraplegia 7 Presenting as Multifocal Dystonia with Prominent Cranio‐Cervical Involvement.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 6, p. 966, doi. 10.1002/mdc3.13257
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- Article
Paraneoplastic Neurological Syndromes and Glutamic Acid Decarboxylase Antibodies.
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- JAMA Dermatology, 2015, v. 151, n. 8, p. 874, doi. 10.1001/jamaneurol.2015.0749
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- Article
Neurologic complications in herpes simplex encephalitis: clinical, immunological and genetic studies.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4306, doi. 10.1093/brain/awad238
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- Article
Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on Biomarkers.
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- Cerebellum, 2024, v. 23, n. 3, p. 881, doi. 10.1007/s12311-023-01561-1
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- Article
Consensus Recommendations for Clinical Outcome Assessments and Registry Development in Ataxias: Ataxia Global Initiative (AGI) Working Group Expert Guidance.
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- Cerebellum, 2024, v. 23, n. 3, p. 924, doi. 10.1007/s12311-023-01547-z
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- Publication type:
- Article
Standards of NGS Data Sharing and Analysis in Ataxias: Recommendations by the NGS Working Group of the Ataxia Global Initiative.
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- Cerebellum, 2024, v. 23, n. 2, p. 391, doi. 10.1007/s12311-023-01537-1
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- Article
Mesial temporal sclerosis as a complication of hematologic cancer.
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- 2009
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- Publication type:
- Letter
Clinical and Immunological Features of Opsoclonus-Myoclonus Syndrome in the Era of Neuronal Cell Surface Antibodies.
- Published in:
- JAMA Neurology, 2016, v. 73, n. 4, p. 417, doi. 10.1001/jamaneurol.2015.4607
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- Article
Paraneoplastic Neurological Syndromes and Glutamic Acid Decarboxylase Antibodies.
- Published in:
- JAMA Neurology, 2015, v. 72, n. 8, p. 874, doi. 10.1001/jamaneurol.2015.0749
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- Publication type:
- Article
Cerebellar Ataxia and Glutamic Acid Decarboxylase Antibodies Immunologic Profile and Long-term Effect of Immunotherapy.
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- JAMA Neurology, 2014, v. 71, n. 8, p. 1009, doi. 10.1001/jamaneurol.2014.1011
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- Article
Late-onset vascular complications of radiotherapy for primary brain tumors: a case–control and cross-sectional analysis.
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- Journal of Cancer Survivorship, 2024, v. 18, n. 1, p. 59, doi. 10.1007/s11764-023-01350-z
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- Publication type:
- Article
Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy.
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- Brain: A Journal of Neurology, 2008, v. 131, n. 11, p. 3051, doi. 10.1093/brain/awn228
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- Article
Spectrum of neurological syndromes associated with glutamic acid decarboxylase antibodies: diagnostic clues for this association.
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- Brain: A Journal of Neurology, 2008, v. 131, n. 10, p. 2553, doi. 10.1093/brain/awn183
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- Publication type:
- Article
Increased Velocity Storage in Subjects with Meniere's Disease.
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- Journal of International Advanced Otology, 2016, v. 12, n. 1, p. 87, doi. 10.5152/iao.2016.1947
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- Article
Primary lateral sclerosis and hereditary spastic paraplegia in sporadic patients. An important distinction in descriptive studies.
- Published in:
- 2016
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- Publication type:
- Letter
Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia.
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- Annals of Neurology, 2011, v. 69, n. 2, p. 303, doi. 10.1002/ana.22297
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- Article
AMPA receptor antibodies in limbic encephalitis alter synaptic receptor location.
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- Annals of Neurology, 2009, v. 65, n. 4, p. 424, doi. 10.1002/ana.21589
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- Article
Carbonic anhydrase–related protein VIII: Autoantigen in paraneoplastic cerebellar degeneration.
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- Annals of Neurology, 2004, v. 56, n. 4, p. 575, doi. 10.1002/ana.20238
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- Article
Autoantigen diversity in the opsoclonus-myoclonus syndrome.
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- Annals of Neurology, 2003, v. 53, n. 3, p. 347
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- Publication type:
- Article
The MAZ protein is an autoantigen of Hodgkin's disease and paraneoplastic cerebellar dysfunction.
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- Annals of Neurology, 2003, v. 53, n. 1, p. 123
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- Publication type:
- Article
A study of the phenotypic variability and disease progression in Laing myopathy through the evaluation of muscle imaging.
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- European Journal of Neurology, 2021, v. 28, n. 4, p. 1356, doi. 10.1111/ene.14630
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- Article
STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8.
- Published in:
- Movement Disorders, 2024, v. 39, n. 9, p. 1641, doi. 10.1002/mds.29910
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- Publication type:
- Article
Co-occurrence of myasthenia gravis with Parkinson's disease: A not to be missed diagnosis.
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- Geriatrics & Gerontology International, 2016, v. 16, n. 4, p. 528, doi. 10.1111/ggi.12558
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- Publication type:
- Article
Atypical periodic alternating nystagmus responding to high-dose intravenous immunoglobulins: a case report.
- Published in:
- 2017
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- Publication type:
- journal article
Isolated hemidystonia associated with NMDA receptor antibodies.
- Published in:
- Movement Disorders, 2011, v. 26, n. 2, p. 351, doi. 10.1002/mds.23315
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- Publication type:
- Article
Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease.
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- Journal of the Peripheral Nervous System, 2010, v. 15, n. 4, p. 334, doi. 10.1111/j.1529-8027.2010.00286.x
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- Publication type:
- Article