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Leucine-rich Glioma Inactivated 1 (LGI-1) Limbic Encephalitis Presenting with Psychotic Symptoms without Seizures: A Case Report with Five-year Follow-up and Review of Literature.
- Published in:
- 2024
- By:
- Publication type:
- Letter
Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.
- Published in:
- 2024
- By:
- Publication type:
- Letter
OPA1 Mutation Presenting as Ethambutol-Induced Optic Neuropathy.
- Published in:
- 2024
- By:
- Publication type:
- Letter to the Editor
Pontine Tegmental Cap Dysplasia: A Rare Brainstem Malformation Mimicking Hereditary Sensory Autonomic Neuropathy.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Role of Optical Coherence Tomography in Predicting Visual Outcome after Surgery for Sellar and Supra-Sellar Tumors.
- Published in:
- Neurology India, 2024, v. 72, n. 1, p. 50, doi. 10.4103/neurol-india.Neurol-India-D-23-00654
- By:
- Publication type:
- Article
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
Yoga in Parkinson’s Disease: Movement from Disorder to Order.
- Published in:
- Neurology India, 2023, v. 71, n. 3, p. 570, doi. 10.4103/0028-3886.378699
- 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
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
Cervical dystonia with cerebellar ataxia in KCNA1 mutation: A phenotypic expansion.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Ayurveda for management of migraine: A narrative review of clinical evidence.
- Published in:
- Journal of Family Medicine & Primary Care, 2022, v. 11, n. 8, p. 4228, doi. 10.4103/jfmpc.jfmpc_2109_21
- By:
- Publication type:
- Article
Management of acute stroke.
- Published in:
- APIK Journal of Internal Medicine, 2022, v. 10, n. 3, p. 153, doi. 10.4103/ajim.ajim_66_20
- By:
- Publication type:
- Article
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
Smartphone-Based Telestroke Vs"Stroke Physician" led Acute Stroke Management (SMART INDIA): A Protocol for a Cluster-Randomized Trial.
- Published in:
- Annals of Indian Academy of Neurology, 2022, v. 25, n. 3, p. 422, doi. 10.4103/aian.aian_1052_21
- By:
- Publication type:
- Article
Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence.
- 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
Retinal Changes in Parkinson's Disease: A Longitudinal Follow-up Study.
- Published in:
- 2022
- By:
- Publication type:
- Journal 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
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
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
The Rationale of Yoga in Parkinson's Disease: A Critical Review.
- Published in:
- 2021
- By:
- Publication type:
- journal 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
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
Medication Overuse Headache.
- Published in:
- 2021
- By:
- Publication type:
- journal 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
A Rare Case of Ataxia-Telangiectasia-Like Disorder With MRE11 Mutation.
- Published in:
- Journal of Pediatric Neurosciences, 2020, v. 15, n. 3, p. 283, doi. 10.4103/jpn.JPN_152_19
- By:
- Publication type:
- Article
Electroencephalography as a Diagnostic Aid in a Girl with Neuroregression and Stereotypies.
- Published in:
- Journal of Neurosciences in Rural Practice, 2020, v. 11, n. 2, p. 359, doi. 10.1055/s-0040-1709264
- By:
- Publication type:
- Article
Tumors masquerading as neurological diseases: A caution for clinicians in planning diagnosis and treatment.
- Published in:
- 2020
- By:
- Publication type:
- journal article
'All that waddles is not dystrophy'.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Blink Reflex is Significantly Altered in Patients with Multisystem Atrophy Compared to Patients with Progressive Supranuclear Palsy, Alzheimer's Disease, and Frontotemporal Dementia ‑ A Pilot Study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
N-methyl- d -aspartate encephalitis our experience with diagnostic dilemmas, clinical features, and outcome.
- Published in:
- Journal of Pediatric Neurosciences, 2018, v. 13, n. 4, p. 423, doi. 10.4103/JPN.JPN_96_18
- By:
- Publication type:
- Article
Review of tremor in Parkinson's disease and atypical parkinsonian disorders.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Sensory tricks in dystonia: Phenomenology and mechanisms.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Sporadic Hyperekplexia Plus Syndrome.
- Published in:
- Journal of Pediatric Neurosciences, 2017, v. 12, n. 1, p. 36, doi. 10.4103/jpn.JPN_170_16
- By:
- Publication type:
- Article
An uncommon cause of bifacial weakness and non-length-dependent demyelinating neuropathy.
- Published in:
- Annals of Indian Academy of Neurology, 2015, v. 18, n. 4, p. 445, doi. 10.4103/0972-2327.169641
- By:
- Publication type:
- Article
Episodic neurological dysfunction in hereditary peripheral neuropathy.
- Published in:
- Annals of Indian Academy of Neurology, 2015, v. 18, n. 1, p. 111, doi. 10.4103/0972-2327.144314
- By:
- Publication type:
- Article