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Cranial Nerve Thinning Distinguishes RFC1‐Related Disorder from Other Late‐Onset Ataxias.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 1, p. 45, doi. 10.1002/mdc3.13930
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- Publication type:
- Article
Spinocerebellar Ataxia Type 6 and Japanese Immigration to Brazil.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 11, p. 1703, doi. 10.1002/mdc3.13888
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- Publication type:
- Article
Juvenile Gerstmann‐Sträussler‐Scheinker Disease Mimicking Anticipation Phenomenon.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 11, p. 1700, doi. 10.1002/mdc3.13878
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- Publication type:
- Article
ATP8A2‐Related Disorder: Beyond Cerebellar Ataxia.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 8, p. 1215, doi. 10.1002/mdc3.13820
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- Publication type:
- Article
Paroxysmal Tonic Upward Gaze: A Clinical Clue for CACNA1A‐Related Disorders.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 8, p. 1225, doi. 10.1002/mdc3.13809
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- Publication type:
- Article
A Woman with Progressive Ataxia and Abnormal Eye Movements.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 3, p. 397, doi. 10.1002/mdc3.13431
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- Publication type:
- Article
Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia‐Like Disorders.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 1, p. 118, doi. 10.1002/mdc3.13110
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- Publication type:
- Article
Postsurgical Myoclonus of the Pectoralis Major.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 6, p. 716, doi. 10.1002/mdc3.12975
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- Publication type:
- Article
POLR3A‐Related Disorder Presenting with Late‐Onset Dystonia and Spastic Paraplegia.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 4, p. 467, doi. 10.1002/mdc3.12945
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- Publication type:
- Article
X‐Linked Adrenoleukodystrophy Mimicking Hereditary Spastic Paraplegia.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 1, p. 109, doi. 10.1002/mdc3.12858
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- Publication type:
- Article
Expanding the Phenotype of Dystonia‐Deafness Syndrome Caused by ACTB Gene Mutation.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 1, p. 86, doi. 10.1002/mdc3.12854
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- Publication type:
- Article
Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia.
- Published in:
- Movement Disorders Clinical Practice, 2018, v. 5, n. 3, p. 330, doi. 10.1002/mdc3.12610
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- Publication type:
- Article
Tractography study in a patient with hemidystonia‐hemiatrophy syndrome.
- Published in:
- 2018
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- Publication type:
- Case Study
Lentiform 'Fork Sign' and Parkinsonism After Acute Myocardial Infarction and Cardiac Failure.
- Published in:
- Movement Disorders Clinical Practice, 2017, v. 4, n. 4, p. 646, doi. 10.1002/mdc3.12482
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- Publication type:
- Article
A Brazilian Football Player Still on the Pitch After 10 Years of Parkinson's Disease with Severe Freezing of Gait.
- Published in:
- Movement Disorders Clinical Practice, 2015, v. 2, n. 1, p. 43, doi. 10.1002/mdc3.12110
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- Publication type:
- Article
Perioral and tongue fasciculations in Kennedy's disease.
- Published in:
- 2018
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- Publication type:
- Case Study
Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-01635-2
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- Publication type:
- Article
Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.
- Published in:
- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2018.01117
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- Publication type:
- Article
SCA23 and prodynorphin: is it time for gene retraction?
- Published in:
- 2016
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- Publication type:
- Letter
Cognition in SCA21 reflects developmental and adult onset cerebellar cognitive affective syndrome.
- Published in:
- 2015
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- Publication type:
- journal article
Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study.
- Published in:
- Neuroradiology, 2021, v. 63, n. 2, p. 217, doi. 10.1007/s00234-020-02528-3
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- Publication type:
- Article
Neuroimaging Features in Congenital Trichomegaly: The Oliver-McFarlane Syndrome.
- Published in:
- Journal of Neuroimaging, 2014, v. 24, n. 4, p. 418, doi. 10.1111/jon.12025
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- Publication type:
- Article
Prevalence and Diagnostic Journey of Friedreich's Ataxia in the State of São Paulo, Brazil.
- Published in:
- Cerebellum, 2024, v. 23, n. 5, p. 1916, doi. 10.1007/s12311-024-01687-w
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- Publication type:
- Article
Correction to: Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Translation, Cross-Cultural Adaptation, and Validation to Brazilian Portuguese of the Cerebellar Cognitive Affective/Schmahmann Syndrome Scale.
- Published in:
- Cerebellum, 2023, v. 22, n. 2, p. 282, doi. 10.1007/s12311-022-01391-7
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- Publication type:
- Article
Spinocerebellar Ataxia Type 5 (SCA5) Mimicking Cerebral Palsy: a Very Early Onset Autosomal Dominant Hereditary Ataxia.
- Published in:
- 2023
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- Publication type:
- Case Study
A Diagnostic Approach to Spastic ataxia Syndromes.
- Published in:
- Cerebellum, 2022, v. 21, n. 6, p. 1073, doi. 10.1007/s12311-021-01345-5
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- Publication type:
- Article
Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient.
- Published in:
- 2022
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- Publication type:
- Case Study
Gluten Ataxia: an Overestimated Condition?
- Published in:
- Cerebellum, 2022, v. 21, n. 4, p. 617, doi. 10.1007/s12311-021-01269-0
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- Publication type:
- Article
The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach.
- Published in:
- Cerebellum, 2022, v. 21, n. 3, p. 497, doi. 10.1007/s12311-021-01275-2
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- Publication type:
- Article
Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective.
- Published in:
- Cerebellum, 2022, v. 21, n. 1, p. 49, doi. 10.1007/s12311-021-01268-1
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- Publication type:
- Article
A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7.
- Published in:
- Cerebellum, 2021, v. 20, n. 3, p. 384, doi. 10.1007/s12311-020-01215-6
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- Publication type:
- Article
Beyond the Typical Syndrome: Understanding Non-motor Features in Niemann-Pick Type C Disease.
- Published in:
- Cerebellum, 2020, v. 19, n. 5, p. 722, doi. 10.1007/s12311-020-01156-0
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- Publication type:
- Article
Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach.
- Published in:
- Cerebellum, 2019, v. 18, n. 6, p. 1011, doi. 10.1007/s12311-019-01042-4
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- Publication type:
- Article
Cognitive and Psychiatric Evaluation in SYNE1 Ataxia.
- Published in:
- Cerebellum, 2019, v. 18, n. 4, p. 731, doi. 10.1007/s12311-019-01033-5
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- Publication type:
- Article
Selective Forces Related to Spinocerebellar Ataxia Type 2.
- Published in:
- Cerebellum, 2019, v. 18, n. 2, p. 188, doi. 10.1007/s12311-018-0977-7
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- Publication type:
- Article
Correction to: Selective Forces Related to Spinocerebellar Ataxia Type 2.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Clinical and molecular evaluation of 13 Brazilian patients with Gomez-López-Hernández syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 4, p. 1047, doi. 10.1002/ajmg.a.62059
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- Publication type:
- Article
Structural signature of classical versus late-onset friedreich's ataxia by Multimodality brain M RI.
- Published in:
- Human Brain Mapping, 2017, v. 38, n. 8, p. 4157, doi. 10.1002/hbm.23655
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- Publication type:
- Article
Sleep Disorders in Hereditary Ataxias.
- Published in:
- Current Neurology & Neuroscience Reports, 2019, v. 19, n. 8, p. N.PAG, doi. 10.1007/s11910-019-0968-1
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- Publication type:
- Article
Movement Disorders in Metabolic Disorders.
- Published in:
- Current Neurology & Neuroscience Reports, 2019, v. 19, n. 2, p. 1, doi. 10.1007/s11910-019-0921-3
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- Publication type:
- Article
The progression rate of spinocerebellar ataxia type 2 changes with stage of disease.
- Published in:
- 2018
- By:
- Publication type:
- journal article
What General Neurologists Should Know about Autoinflammatory Syndromes?
- Published in:
- Brain Sciences (2076-3425), 2023, v. 13, n. 9, p. 1351, doi. 10.3390/brainsci13091351
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- Publication type:
- Article
Movement Disorders in Prionopathies: A Systematic Review.
- Published in:
- Tremor & Other Hyperkinetic Movements, 2019, p. 1, doi. 10.7916/tohm.v0.712
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- Publication type:
- Article
Arm Levitation as Initial Manifestation of Creutzfeldt-Jakob Disease: Case Report and Review of the Literature.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
An Unusual Fundus Finding in a Teenage Girl.
- Published in:
- JAMA Neurology, 2018, v. 75, n. 12, p. 1566, doi. 10.1001/jamaneurol.2018.3108
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- Publication type:
- Article
Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01219
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- Publication type:
- Article
Reconstructing the History of Machado-Joseph Disease.
- Published in:
- European Neurology, 2020, v. 83, n. 1, p. 99, doi. 10.1159/000507191
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- Publication type:
- Article
The cerebellum in Parkinson's disease and parkinsonism in cerebellar disorders.
- Published in:
- 2013
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- Publication type:
- Journal Article
The cerebellum in Parkinson’s disease and parkinsonism in cerebellar disorders.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 9, p. e248, doi. 10.1093/brain/awt089
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- Publication type:
- Article