Works matching DE "CEREBELLAR ataxia"
Results: 1978
Ataxia cerebelosa: caso clínico.
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- Religación: Revista de Ciencias Sociales y Humanidades, 2024, v. 9, n. 42, p. 1, doi. 10.46652/rgn.v9i42.1296
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- Article
Effects of Low-Frequency Deep Brain Stimulation in Bilateral Zona Incerta for a Patient With Tremor and Cerebellar Ataxia.
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- Tremor & Other Hyperkinetic Movements, 2024, v. 14, n. 1, p. 1, doi. 10.5334/tohm.925
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- Article
Horizontal Pendular Nystagmus and Ataxia Secondary to Severe Hypomagnesemia.
- Published in:
- 2024
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- Publication type:
- Case Study
L-2 hydroxyglutaric aciduria: report of a Mexican-Mayan patient with the mutation c.569C>T and response to vitamin supplements and levocarnitine.
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- 2024
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- Publication type:
- Case Study
Resolution of Wing-Beating Tremor and Magnetic Resonance Imaging Lesions in Wilson's Disease Following Penicillamine.
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- Tremor & Other Hyperkinetic Movements, 2024, v. 14, n. 1, p. 1, doi. 10.5334/tohm.857
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- Article
ALCOHOL RELATED CEREBELLAR DEGENERATION: A CASE REPORT.
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- 2024
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- Case Study
Toxic encephalopathy, vision loss, and memory disorder caused by acute acrylamide exposure.
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- Journal of Occupational & Environmental Hygiene, 2024, v. 21, n. 3, p. 152, doi. 10.1080/15459624.2024.2305135
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- Article
Angelman syndrome as a rare anaesthetic problem.
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- 2004
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- Publication type:
- Letter
Síndrome de Gómez-López-Hernández (displasia cerebelo-trigéminodérmica). Informe de un caso.
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- Acta Pediatrica de Mexico, 2011, v. 32, n. 5, p. 292
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- Article
R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update.
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- 2012
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- Publication type:
- Report
Commentary to ‘Comorbidity in Finnish migraine families’.
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- Journal of Headache & Pain, 2006, v. 7, n. 5, p. 320, doi. 10.1007/s10194-006-0328-9
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- Article
MRI features of neurodegenerative Langerhans cell histiocytosis.
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- 2006
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- Publication type:
- journal article
Pediatric post-operative cerebellar mutism syndrome, cerebellar cognitive affective syndrome, and posterior fossa syndrome: historical review and proposed resolution to guide future study.
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- Child's Nervous System, 2020, v. 36, n. 6, p. 1205, doi. 10.1007/s00381-019-04253-6
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- Publication type:
- Article
Trihexyphenidyl for treatment of dystonia in ataxia telangiectasia: a case report.
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- Child's Nervous System, 2020, v. 36, n. 4, p. 873, doi. 10.1007/s00381-019-04399-3
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- Publication type:
- Article
Brain pathology of spinocerebellar ataxias.
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- Acta Neuropathologica, 2012, v. 124, n. 1, p. 1, doi. 10.1007/s00401-012-1000-x
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- Publication type:
- Article
A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.
- Published in:
- 2011
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- Publication type:
- Report
New neuropathological findings in Unverricht-Lundborg disease: neuronal intranuclear and cytoplasmic inclusions.
- Published in:
- 2011
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- Publication type:
- Report
Chiari anomaly type II without cerebellar herniation.
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- Acta Neuropathologica, 2003, v. 105, n. 2, p. 193, doi. 10.1007/s00401-002-0628-3
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- Publication type:
- Article
Abnormalities of cerebellar foliation in rats prenatally exposed to ethanol.
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- Acta Neuropathologica, 2001, v. 102, n. 1, p. 36, doi. 10.1007/s004010000345
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- Publication type:
- Article
Huge Arachnoid Cyst of the Posterior Fossa with Cerebellar Tentorium Dysplasia Associated with Juvenile Polyposis.
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- Pediatric Neurosurgery, 2003, v. 38, n. 5, p. 253, doi. 10.1159/000069819
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- Publication type:
- Article
Identification of genes that modify ataxin-1-induced neurodegeneration.
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- Nature, 2000, v. 408, n. 6808, p. 101, doi. 10.1038/35040584
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- Publication type:
- Article
The caudal limit of Otx2 expression positions the isthmic organizer.
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- Nature, 1999, v. 401, n. 6749, p. 164, doi. 10.1038/43670
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- Publication type:
- Article
Quantitative Changes in Gait Parameters after Cycling among Multiple Sclerosis Patients with Ataxia: A Pilot Study.
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- Journal of Modern Rehabilitation, 2022, v. 16, n. 4, p. 355, doi. 10.18502/jmr.v16i4.10763
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- Publication type:
- Article
Diligent family history to detect a mitochondrial disorder in disguise: Lessons from a case of myoclonic epilepsy.
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- Annals of Movement Disorders, 2024, v. 7, n. 3, p. 211, doi. 10.4103/aomd.aomd_22_24
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- Article
Mitochondrial ataxia - Unravelling the puzzle.
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- Annals of Movement Disorders, 2024, v. 7, n. 2, p. 78, doi. 10.4103/aomd.aomd_63_24
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- Article
Onconeural antibody-associated cerebellar ataxia: An analysis.
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- Annals of Movement Disorders, 2024, v. 7, n. 2, p. 102, doi. 10.4103/aomd.aomd_24_24
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- Publication type:
- Article
Anti-glutamic acid decarboxylase antibodies-associated cerebellar ataxia: A treatable ataxia.
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- Annals of Movement Disorders, 2024, v. 7, n. 1, p. 13, doi. 10.4103/aomd.aomd_23_23
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- Publication type:
- Article
Paraneoplastic cerebellar degeneration heralding recurrent metastatic carcinoma breast.
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- Annals of Movement Disorders, 2023, v. 6, n. 1, p. 33, doi. 10.4103/aomd.aomd_5_22
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- Publication type:
- Article
A juvenile-onset case of autosomal recessive spastic ataxia of Charlevoix–Saguenay with a novel mutation in the SACS gene.
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- Annals of Movement Disorders, 2023, v. 6, n. 1, p. 36, doi. 10.4103/aomd.aomd_15_22
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- Article
Boucher Neuhauser syndrome in twins: Rare and unusual cause of cerebellar ataxia.
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- 2022
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- Abstract
Cerebellar ataxia with intracranial calcification: Cockayne syndrome.
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- 2022
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- Publication type:
- Abstract
AREA MEASUREMENTS WITHIN THE FORAMEN MAGNUM: COMPARISON OF 171 PATIENTS WITH SYMPTOMATIC AND ASYMPTOMATIC CHIARI MALFORMATION TYPE 1.
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- Journal of Turkish Spinal Surgery, 2023, v. 34, n. 4, p. 156, doi. 10.4274/jtss.galenos.2023.92400
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- Publication type:
- Article
A malignancy phantom: a rare clinical case report of metastatic renal cell carcinoma with no evidence of a primary lesion presenting as cerebellar ataxia.
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- European Journal of Medical Case Reports, 2024, v. 8, n. 3, p. 44, doi. 10.24911/ejmcr.173-1685921237
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- Publication type:
- Article
Histological study in the brain of the reelin/ Dab1-compound mutant mouse.
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- Anatomical Science International, 2009, v. 84, n. 3, p. 200, doi. 10.1007/s12565-008-0009-7
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- Article
A cerebellar ataxia patient harboring 229 pure GAA repeat units in FGF14 presenting with grip myotonia.
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- 2024
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- Publication type:
- Case Study
A patient presenting downbeat positioning nystagmus with 19/11 CAG repeats in the CACNA1A gene: A case report.
- Published in:
- Neurology & Clinical Neuroscience, 2024, v. 12, n. 6, p. 359, doi. 10.1111/ncn3.12824
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- Publication type:
- Article
Autoimmunity to voltage‐gated calcium channels.
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- Neurology & Clinical Neuroscience, 2024, v. 12, n. 3, p. 150, doi. 10.1111/ncn3.12707
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- Publication type:
- Article
Paraneoplastic cerebellar degeneration after improvement of Lambert–Eaton myasthenic syndrome.
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- Neurology & Clinical Neuroscience, 2024, v. 12, n. 2, p. 118, doi. 10.1111/ncn3.12783
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- Article
Possible association of crossed cerebellar diaschisis with cerebellar ataxia in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
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- Neurology & Clinical Neuroscience, 2023, v. 11, n. 3, p. 164, doi. 10.1111/ncn3.12702
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- Article
Cerebellar ataxia following antitubercular therapy.
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- Neurology & Clinical Neuroscience, 2022, v. 10, n. 3, p. 160, doi. 10.1111/ncn3.12585
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- Article
A case of cutis verticis gyrata‐mental retardation syndrome accompanied by various neurological abnormalities.
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- Neurology & Clinical Neuroscience, 2021, v. 9, n. 6, p. 487, doi. 10.1111/ncn3.12549
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- Publication type:
- Article
Successful treatment of anti‐GAD antibody‐associated autoimmune cerebellar ataxia with combined immunotherapies.
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- Neurology & Clinical Neuroscience, 2021, v. 9, n. 6, p. 474, doi. 10.1111/ncn3.12541
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- Article
Superficial siderosis by a dural foramen.
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- Neurology & Clinical Neuroscience, 2021, v. 9, n. 5, p. 414, doi. 10.1111/ncn3.12532
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- Publication type:
- Article
Gait apraxia as a presenting sign of Gerstmann‐Sträussler‐Scheinker disease.
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- Neurology & Clinical Neuroscience, 2021, v. 9, n. 4, p. 339, doi. 10.1111/ncn3.12511
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- Publication type:
- Article
MRI abnormality of the bilateral middle cerebellar peduncles and long‐term follow‐up in hypoglycemic encephalopathy: A case report.
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- Neurology & Clinical Neuroscience, 2021, v. 9, n. 1, p. 130, doi. 10.1111/ncn3.12467
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- Publication type:
- Article
Recurrent severe and long‐lasting cerebellar ataxia attacks in adult‐onset neuronal intranuclear inclusion disease.
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- Neurology & Clinical Neuroscience, 2021, v. 9, n. 1, p. 107, doi. 10.1111/ncn3.12454
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- Publication type:
- Article
Juvenile/adult‐onset galactosialidosis with remarkable clinical variabilities in two Japanese siblings.
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- Neurology & Clinical Neuroscience, 2019, v. 7, n. 4, p. 218, doi. 10.1111/ncn3.12294
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- Publication type:
- Article
Case of congenital fibrosis of the extraocular muscles type 1 with progressive cerebellar ataxia.
- Published in:
- 2018
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- Publication type:
- Case Study
Wearable gait sensors to measure ataxia due to spinocerebellar degeneration.
- Published in:
- Neurology & Clinical Neuroscience, 2018, v. 6, n. 1, p. 9, doi. 10.1111/ncn3.12174
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- Publication type:
- Article
Case of myasthenia gravis and Lambert-Eaton myasthenic syndrome overlap syndrome accompanied by autoimmune encephalitis and cerebellar ataxia with multiple neuronal antibodies.
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- Neurology & Clinical Neuroscience, 2017, v. 5, n. 5, p. 152, doi. 10.1111/ncn3.12134
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- Publication type:
- Article