All Stories

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