Found: 105
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Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.
- Published in:
- 2024
- By:
- Publication type:
- Letter
Novel Insights into the Genetic Basis of Progressive Supranuclear Palsy in Asian–Indian Population.
- Published in:
- Movement Disorders, 2024, v. 39, n. 4, p. 753, doi. 10.1002/mds.29740
- By:
- Publication type:
- Article
Revisiting Friedreich's Ataxia: Phenotypic and Imaging Characteristics.
- Published in:
- Annals of Indian Academy of Neurology, 2024, v. 27, n. 2, p. 152, doi. 10.4103/aian.aian_1001_23
- By:
- Publication type:
- Article
Pontine Tegmental Cap Dysplasia: A Rare Brainstem Malformation Mimicking Hereditary Sensory Autonomic Neuropathy.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Morphometric alterations of the mesocorticolimbic network in Parkinson's disease with impulse control disorders.
- Published in:
- Journal of Neural Transmission, 2024, v. 131, n. 3, p. 229, doi. 10.1007/s00702-023-02735-1
- By:
- Publication type:
- Article
Sexual dysfunction in men with young onset Parkinson's disease.
- Published in:
- Journal of Neural Transmission, 2024, v. 131, n. 2, p. 149, doi. 10.1007/s00702-023-02729-z
- By:
- Publication type:
- Article
Painless legs and moving toes in chronic inflammatory demyelinating polyradiculoneuropathy.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Rare Encephalitis-Like Presentation of a Pediatric Patient with Dual Positive Aquaporin-4 and Myelin Oligodendrocyte Antibodies: A Case Report with Review of Literature.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Spastic ataxia with sensory neuropathy sans cerebral leukodystrophy in probable adult polyglucosan body disease.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Collagen XII-Related Myopathy: An Emerging Spectrum of Extracellular Matrix-Related Myopathy.
- Published in:
- Neurology India, 2023, v. 71, n. 6, p. 1257, doi. 10.4103/0028-3886.391402
- By:
- Publication type:
- Article
Adult-Onset Ischemic Moyamoya Disease: Reasoning and Decision-Making.
- Published in:
- Neurology India, 2023, v. 71, n. 5, p. 1065, doi. 10.4103/0028-3886.388102
- By:
- Publication type:
- Article
Olfactory Bulb Volume, Olfactory Sulcus Depth in Parkinson's Disease, Atypical Parkinsonism.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 5, p. 794, doi. 10.1002/mdc3.13733
- By:
- Publication type:
- Article
Anti-GAD antibodies associated autoimmunity presenting as isolated dementia: an expansion of GAD antibody-spectrum disorders.
- Published in:
- 2023
- By:
- Publication type:
- Letter
Pediatric neurobrucellosis: a systematic review with case report.
- Published in:
- Journal of Tropical Pediatrics, 2023, v. 69, n. 1, p. 1, doi. 10.1093/tropej/fmad004
- By:
- Publication type:
- Article
Geste antagoniste in dystonia: Demystifying the tricks.
- Published in:
- Annals of Movement Disorders, 2023, v. 6, n. 1, p. 7, doi. 10.4103/aomd.aomd_51_22
- By:
- Publication type:
- Article
Clinical Spectrum, Radiological Correlation and Outcome of Movement Disorders in Wilson's Disease.
- Published in:
- Tremor & Other Hyperkinetic Movements, 2023, v. 13, p. 1, doi. 10.5334/tohm.794
- By:
- Publication type:
- Article
Neuro-Bechet's disease: a case series from India.
- Published in:
- Egyptian Journal of Neurology, Psychiatry & Neurosurgery, 2022, v. 58, p. 1, doi. 10.1186/s41983-022-00586-3
- By:
- Publication type:
- Article
Autoimmune Encephalitis Following Severe Traumatic Brain Injury.
- Published in:
- Primary Care Companion for CNS Disorders (2155-7772), 2022, v. 24, n. 6, p. e1, doi. 10.4088/PCC.21cr03198
- By:
- Publication type:
- Article
Sleep architecture in progressive supranuclear palsy: A video-polysomnography study.
- Published in:
- Annals of Indian Academy of Neurology, 2022, v. 25, n. 5, p. 858, doi. 10.4103/aian.aian_1096_21
- By:
- Publication type:
- Article
Spectrum of movement disorder emergencies in a tertiary care center in India: A prospective observational study.
- Published in:
- Annals of Indian Academy of Neurology, 2022, v. 25, n. 5, p. 890, doi. 10.4103/aian.aian_295_22
- By:
- Publication type:
- Article
Cervical dystonia with cerebellar ataxia in KCNA1 mutation: A phenotypic expansion.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Role of middle latency auditory evoked potentials in parkinsonism: An electrophysiological clue.
- Published in:
- Annals of Movement Disorders, 2022, v. 5, n. 3, p. 183, doi. 10.4103/AOMD.AOMD_18_22
- By:
- Publication type:
- Article
Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Delayed Cervical Dystonia with Tremors in a Patient with Wernicke Encephalopathy: An Expansion of Complication.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Study of assessment of olfactory bulb volume and olfactory sulcus depth using brain magnetic resonance imaging in Parkinson's disease and comparison with atypical Parkinsonism and vascular Parkinsonism.
- Published in:
- 2022
- By:
- Publication type:
- Abstract
Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Predictors of Late Seizures in Patients with Cerebral Venous Sinus Thrombosis: A Retrospective Analysis.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Vascular Parkinsonism with Dystonia in Moyamoya Disease: An Expansion of Movement Disorder Phenomenology.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Gender differences in progressive supranuclear palsy.
- Published in:
- Acta Neurologica Belgica, 2022, v. 122, n. 2, p. 357, doi. 10.1007/s13760-021-01599-0
- By:
- Publication type:
- Article
The Spectrum of Neuro-COVID: A Study of a Comprehensively Investigated Large Cohort from India.
- Published in:
- Annals of Indian Academy of Neurology, 2022, v. 25, n. 2, p. 194, doi. 10.4103/aian.aian_310_21
- By:
- Publication type:
- Article
Pseudo-neonatal Adrenoleukodystrophy: A Rare Peroxisomal Disorder.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Granulomatous Panuveitis in Multiple Sclerosis: A Rare Occurrence.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Disorders of Tetrahydrobiopterin Metabolism: Experience from South India.
- Published in:
- Metabolic Brain Disease, 2022, v. 37, n. 3, p. 743, doi. 10.1007/s11011-021-00889-z
- By:
- Publication type:
- Article
Spectrum of Movement Disorders in Niemann-Pick Disease Type C.
- Published in:
- Tremor & Other Hyperkinetic Movements, 2022, v. 12, p. 1, doi. 10.5334/tohm.701
- By:
- Publication type:
- Article
Clinical, Biochemical, Radiological, and Genetic Profile of Patients with Homocysteine Remethylation Pathway Defect and Spastic Paraplegia.
- Published in:
- Annals of Indian Academy of Neurology, 2021, v. 24, n. 6, p. 908, doi. 10.4103/aian.AIAN_223_21
- By:
- Publication type:
- Article
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Impact of Disrupted Botulinum Toxin Therapy in Movement Disorders Due to COVID-19 Pandemic.
- Published in:
- Annals of Indian Academy of Neurology, 2021, v. 24, n. 6, p. 1001, doi. 10.4103/aian.AIAN_573_20
- By:
- Publication type:
- Article
Reversible leukoencephalopathy and cerebral atrophy in homocystinuria due to MTHFR deficiency: A treatable metabolic disorder.
- Published in:
- Journal of Inherited Metabolic Disease, 2021, v. 44, n. 6, p. 1505, doi. 10.1002/jimd.12439
- By:
- Publication type:
- Article
Kennedy's disease: A second genetically confirmed report from India.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
ADCY5-related dyskinesia: A genetic cause of early-onset chorea-report of two cases and a novel mutation.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Does gender differences have a role in determining sleep quality in Parkinson's disease?
- Published in:
- Acta Neurologica Belgica, 2021, v. 121, n. 4, p. 1001, doi. 10.1007/s13760-020-01498-w
- By:
- Publication type:
- Article
Stroke-like episodes with cerebellar ataxia as presenting manifestation of adult-onset anti-N-methyl d-aspartate receptor encephalitis: an unusual presentation.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Electrophysiological Evaluation of Audiovestibular Pathway Dysfunction in Parkinson's Disease and Its Correlates: A Case Control Study.
- Published in:
- Annals of Indian Academy of Neurology, 2021, v. 24, n. 4, p. 531, doi. 10.4103/aian.AIAN_1011_20
- By:
- Publication type:
- Article
Upbeat Nystagmus in Late Onset Cerebellar Ataxia: Think of Anti-Glutamate Decarboxylase 65 Antibody-Associated Cerebellar Ataxia.
- Published in:
- 2021
- By:
- Publication type:
- Literary Criticism
Rapidly progressive spastic paraplegia due to hyperhomocysteinemia in child with MTHFR gene mutation and mitochondrial Complex I deficiency: A rare association.
- Published in:
- Journal of Pediatric Neurosciences, 2021, v. 16, n. 2, p. 153, doi. 10.4103/jpn.JPN_96_20
- By:
- Publication type:
- Article
Postpartum Optic Neuropathy: Think of Myelin Oligodendrocyte Glycoprotein Immunoglobulin G-Associated Optic Neuritis - Report of Two Cases.
- Published in:
- 2021
- By:
- Publication type:
- Letter to the Editor
Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation.
- Published in:
- 2021
- By:
- Publication type:
- Letter to the Editor
Subtypes of PSP and Prognosis: A Retrospective Analysis.
- Published in:
- Annals of Indian Academy of Neurology, 2021, v. 24, n. 1, p. 56, doi. 10.4103/aian.AIAN_611_20
- By:
- Publication type:
- Article