All Stories

  1. Pseudoathetotic Pseudodystonia as a Manifestation of Isolated Medullary Demyelination in Neuromyelitis Optica Spectrum Disorder
  2. Motor stereotypies, Dhat syndrome, and gaming disorder: A masquerading presentation of Wilson's disease
  3. Propranolol for Tremors in Spinocerebellar Ataxia Type 12: A Randomized Clinical Trial
  4. Focal leptomeningeal metastases causing binocular vision loss
  5. Focused Ultrasound versus Radiofrequency Ablation for Pallidothalamic Tractotomy: Looking beyond the Bilateral Effects
  6. VPS16‐Related Dystonia: Expanding the Clinical Spectrum and Therapeutic Insights
  7. CSF Tap Test Parameters and Short-Term Outcomes in operated and non-operated patients with idiopathic Normal Pressure Hydrocephalus: A Cohort Study
  8. Pallidothalamic Tractotomy after Pallidotomy for Medication‐Refractory Dystonia: Preliminary Short‐Term Results from a Case Series of Five Patients
  9. L‐2‐Hydroxyglutaric Aciduria Complicated by Cerebral Neoplasm
  10. Long-term Probiotics Intervention Facilitates Recovery of Motor and Non-motor Functions by Regulating Inflammation and Modulating Gut-brain Axis in 6-OHDA Rat Model of Parkinson’s Disease
  11. CSF1R-Related Adult-Onset Leukoencephalopathy With Axonal Spheroids: A Case Series of Four Asian Indian Patients
  12. The Expanding Spectrum of Anti-IgLON5 Disease: A Case Series from an Indian Cohort
  13. Botulinum neurotoxin and immunomodulation for treatment of hemimasticatory spasms associated with hemifacial atrophy and morphea
  14. Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) as a cause of new-onset refractory status epilepticus (NORSE): Case report and review of literature
  15. Genetic Landscape of Dystonia in Asian Indians
  16. Clinical Reasoning: A 50-Year-Old Man With Ataxia, Dystonia, and Abnormal Ocular Movements
  17. The Genomic Landscape of Wilson Disease in a Pan India Disease Cohort and Population‐Scale Data
  18. Unprecedented Co-occurrence: Identification of a Pathogenic Genetic Variant in the KMT2B Gene in a Wilson Disease Patient with a Pathogenic ATP7B Mutation
  19. Phenomenological patterns and aetiological spectrum in patients visiting a tertiary care Movement disorders service in India: An observational study
  20. Loss of Ambulation Due to Calcific Myonecrosis: A Rare but Reversible Complication of Wilson’s Disease
  21. Fatigue in Parkinson’s disease—A narrative review
  22. From writer's cramp to blepharoclonus: An atypical journey with a novel KMT2B variant
  23. Twist of Fate: Rare Vascular Pattern Behind Stroke in a Septuagenarian
  24. Safety and Efficacy of Injection Tenecteplase in 4.5 to 24 Hours Imaging Eligible Window Patients with Acute Ischemic Stroke (EAST-AIS) - Study Protocol
  25. Palatal Tremor, Periocular and Perioral Myokymia, and Pseudoathetosis in a Patient with Whipple’s Disease
  26. Juvenile Parkinsonism and Cognitive Impairment in a Patient with Compound Heterozygous Variants in the BTD Gene‐ an Unusual Presentation of Biotinidase Deficiency
  27. Acute acquired comitant esotropia heralding neuromyelitis optica spectrum disorder
  28. Acute bilateral sensorineural hearing loss as presentation of leptomeningeal metastases
  29. Polyneuropathy Unveiling a Hidden Hepatic Plasmacytoma: An Extremely Rare Association
  30. Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration
  31. Atypical Parkinsonism with Positive Anti-amphiphysin Antibodies: Expanding the Phenotypic Spectrum
  32. Dystonic Leg Cramps and Cataracts with Low Ferritin and Normal Neuroimaging: An Overlapping Spectrum of FTL Gene Related Disorders
  33. Clinical approaches and managements of sleep-related movement disorders
  34. Primary Coenzyme Q10 Deficiency‐4 Causing Young Onset Ataxia‐Dystonia
  35. Essential Tremor and Essential Tremor Plus Are Essentially Similar Electrophysiologically
  36. Sarcoidosis presenting as progressive multifocal leukoencephalopathy in an apparently immunocompetent adult
  37. De Novo Movement Disorders Associated with COVID-19- A Systematic Review of Individual Patients
  38. Systemic Vasculitis Presenting with Central and Peripheral Involvement
  39. Neuropathic Tremor in Guillain‐Barré Syndrome
  40. Social Cognition in Parkinson's Disease: A Case‐Control Study
  41. Tuberculosis of the spinal cord
  42. Electrophysiology and Magnetic Resonance Neurography Findings of Nontraumatic Ulnar Mononeuropathy From a Tertiary Care Center
  43. Zonisamide add-on in tremor-dominant Parkinson's disease- A randomized controlled clinical trial
  44. PSP‐Like Phenotype in Genetically ConfirmedSCA12
  45. A large cohort study of TB of the central nervous system: clinical outcomes
  46. Salt and Pepper Appearance of Brain‐Stem and Cerebellum in Anti‐Zic4 Associated Neurological Disorder
  47. Primary CNS vasculitis (PCNSV): a cohort study
  48. Fusiform Intracranial Aneurysms in a CADASIL Patient
  49. Subclavian Steal Syndrome due to Takayasu Arteritis
  50. Mucormycosis in COVID-19 Patients: A Case-Control Study
  51. Case of spontaneous intracranial hypotension: clinical, neuroimaging and treatment approach
  52. Allgrove Syndrome
  53. Unraveling movement disorders in spinocerebellar ataxia
  54. Mesenchymal Stem Cell Therapy in the Treatment of Neurodegenerative Cerebellar Ataxias: a Systematic Review and Meta-analysis
  55. Hemichorea in Rasmussen's Encephalitis—A Rare Case
  56. Comparison of Disease Profiles and Three-Month Outcomes of Patients with Neurological Disorders with and without COVID-19
  57. Linear Morphea
  58. DOK7 congenital myasthenic syndrome responsive to oral salbutamol
  59. Three territory sign in COVID-19
  60. GPi‐DBS for KMT2B‐Associated Dystonia: Systematic Review and Meta‐Analysis
  61. Infantile Ascending Hereditary Spastic Paralysis with Extrapyramidal and Extraocular Manifestations Associated with a Novel ALS2 Mutation
  62. How often does COVID-19 affect the nervous system ?
  63. Impact of SARS‐CoV‐2 Infection in Spinocerebellar Ataxia 12 Patients
  64. An atypical case of dermatomyositis associated with clear cell renal cell carcinoma
  65. Awareness of driving regulations amongst person with epilepsy and their caregivers
  66. Clinicoradiological profile of hypertrophic pachymeningitis and treatment outcomes: A retrospective cohort study
  67. Idiopathic Hypoparathyroidism Presenting As New Onset Refractory Status Epilepticus
  68. Syringomyelia after spinal anaesthesia: A case report
  69. Electrophysiological And Magnetic Resonance Neurography Correlate Of Non Traumatic Common Peroneal Neuropathy (4177)
  70. Levosulpiride-induced Movement Disorders
  71. Anti‐NMDA Receptor Encephalitis Associated with Coats‐Like Retinal Telangiectasia
  72. Patient Experience of a Neurology Tele-Follow-Up Program Initiated During the Coronavirus Disease 2019 Pandemic: A Questionnaire-Based Study
  73. Spinal Muscular Atrophy and Progressive Myoclonic Epilepsy: A Rare Association
  74. Managing Non-COVID Acute Neurology Amidst the Pandemic
  75. Dystonia and Myelopathy in a Case of Stress‐Induced Childhood‐Onset Neurodegeneration with Ataxia and Seizures (CONDSIAS)
  76. Hearing Loss in Migraine: An Uncommon Manifestation of a Common Disorder
  77. Acute onset vision loss as a presenting manifestation of carcinoma lung
  78. Toxic optic neuropathy: A rare but serious side effect of chloramphenicol and ciprofloxacin
  79. Conduct of virtual neurology DM final examination during COVID-19 pandemic
  80. Toxic optic neuropathy- An uncommon complication of commonly used antibiotics
  81. Lisch nodule—ophthalmologic marker of Neurofibroma 1
  82. Hemi Masticatory Spasm: Series of 7 Cases and Review of Literature
  83. Retinal astrocytic hamartoma-ophthalmologic marker of tuberous sclerosis
  84. Effect of providing sudden unexpected death in epilepsy (SUDEP) information to persons with epilepsy (PWE) and their caregivers-Experience from a tertiary care hospital
  85. Tenecteplase versus alteplase in acute ischemic stroke: systematic review and meta-analysis
  86. Nocardia: a rare cause of brain abscess
  87. Evaluation of various movement disorders in patients of genetically proven spinocerebellar ataxia: A study from a Tertiary Care Center in Northern India
  88. Parkinson's disease: A review
  89. Evaluation of various movement disorders in patients of genetically proven Spino Cerebellar Ataxia: A study from a tertiary care center in Northern India