Christian Medical College Vellore, Ida Scudder Road, Vellore – 632004, Tamil Nadu, India
Publications
Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India
Revisiting magnetic resonance imaging pattern of Krabbe disease – Lessons from an Indian cohor
Renal Tubular Function, Bone Health and Body Composition in Wilson's Disease: A Cross-Sectional Study from India
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy.
Decompressive craniectomy in cerebral venous thrombosis: a single centre experience.
Status dystonicus: Diagnosis and management of a rare and challenging entity
Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India
Revisiting magnetic resonance imaging pattern of Krabbe disease – Lessons from an Indian cohor
Renal Tubular Function, Bone Health and Body Composition in Wilson's Disease: A Cross-Sectional Study from India
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy.
Decompressive craniectomy in cerebral venous thrombosis: a single centre experience.
Status dystonicus: Diagnosis and management of a rare and challenging entity
Phosphoproteomic analysis reveals Akt isoform-specific regulation of cytoskeleton proteins in human temporal lobe epilepsy with hippocampal sclerosis
An Unusual Cause of Chronic Headache in an Adolescent Boy: A Case Report
Validation of a drooling questionnaire in Indian children with cerebral palsy
Renal Tubular Function, Bone Health and Body Composition in Wilson's Disease: A Cross-Sectional Study from India
Revisiting magnetic resonance imaging pattern of Krabbe disease – Lessons from an Indian cohort
Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort
The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study
Therapeutic Drug Monitoring of Levetiracetam and Lamotrigine: Is There a Need?
Novel imag Novel imaging finding and novel mutation in an infant with molybdenum cofactor deficiency, a mimicker of hypoxic-ischaemic encephalopathy
Recurrent Painful Ophthalmoplegic Neuropathy: A Cause of Headache
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder
Natural history of multiple sclerosis from the Indian perspective: Experience from a tertiary care hospital.
"Eye of tiger sign" mimic in an adolescent boy with mitochondrial membrane protein associated neurodegeneration (MPAN).
Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder
Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability
Never Miss Sleep Disorder in Children with Drop Attacks.
Neuroregression as an initial manifestation in a toddler with acquired pernicious anaemia.
Megalencephalic leukoencephalopathy with subcortical cysts in an adult.
NTRK2-related developmental and epileptic encephalopathy: Report of 5 new cases
First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1.
Clustering of Juvenile Canavan disease in an Indian community due to population bottleneck and isolation: genomic signatures of a founder event
Menkes disease and response to copper histidine: An Indian case series
An Inherited Cause of Stroke Mimic in a Toddler
Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort.
PHACES syndrome with moyamoya vasculopathy – a case report.
Unusual MRI findings in 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency
Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinent
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.
Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations.
Unusual Magnetic Resonance Imaging Findings in 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency.
Never Miss Sleep Disorder in Children with Drop Attacks
A Treatable Cause of Intellectual Disability and Autism in a Young Child
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy.
Hypomyelination, Hypodontia, Hypogonadotropic Hypogonadism (4H) Syndrome With Vertebral Anomalies: A Novel Association.
SGCE Myoclonus-Dystonia: An Inherited Movement Disorder
First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1
Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1.
SGCE Myoclonus-Dystonia: An Inherited Movement Disorder
Stroke in a Child with Dengue Encephalopathy.
Recurrent Painful Ophthalmoplegic Neuropathy: A Cause of Headache.
An Inherited Cause of Stroke Mimic in a Toddler.
Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based Review
Subsultus Tendinum in a Child with Typhoid Fever.
EEG lateralization and seizure outcome following peri-insular hemispherotomy for pediatric hemispheric epilepsy
Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder.
Pulmonary distress following attempted suicidal hanging.
Clinico-Etiological Spectrum and Functional Outcomes of Children with Pre-Status Dystonicus and Status Dystonicus (SD): A Descriptive Study.
Neurotrophic keratitis and congenital insensitivity to pain with anhidrosis–a case report with 10-year follow-up.
Management of Children and Adolescents with Wilson Disease and Neurological Worsening Following D-Penicillamine Therapy: A Single Centre Experience
Eye signs in a child with ROBO3 gene mutation.
Oculodigital Sign: A Clinical Clue for Diagnosis.
Fumaric Aciduria: A Rare Cause of Refractory Epilepsy.
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder.
A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage: Lupus Anticoagulant Hypoprothombinemia Syndrome
Ocular Features and Visual Outcome in Children with Moyamoya Disease and Moyamoya Syndrome: A Case Series.
