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
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy.
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
Association of Child Neurology (AOCN) – Indian Epilepsy Society (IES) Consensus Guidelines for the Diagnosis and Management of West Syndrome
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
Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy.
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
Association of Child Neurology (AOCN) – Indian Epilepsy Society (IES) Consensus Guidelines for the Diagnosis and Management of West Syndrome
Revisiting magnetic resonance imaging pattern of Krabbe disease – Lessons from an Indian cohort
Teaching NeuroImages: Acute necrotizing encephalopathy of childhood Neuroimaging findings
The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study
Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent
Study of Refractory Status Epilepticus from a Tertiary Care Center.
Novel imag Novel imaging finding and novel mutation in an infant with molybdenum cofactor deficiency, a mimicker of hypoxic-ischaemic encephalopathy
Predictors of Outcome in Children with Status Epilepticus during Resuscitation in Pediatric Emergency Department: A Retrospective Observational Study
Recurrent Painful Ophthalmoplegic Neuropathy: A Cause of Headache
Imaging findings in TRPM6-Related hypomagnesemia with secondary hypocalcemia
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder
"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.
NTRK2-related developmental and epileptic encephalopathy: Report of 5 new cases
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.
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
Ghosal hematodiaphyseal dysplasia and response to corticosteroid therapy.
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder.
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
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.
Unusual Presentation of Adrenal Hypoplasia Congenita.
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
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.
Association of Child Neurology (AOCN) Consensus Statement on the Diagnosis and Management of Febrile Seizures.
Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent.
Clinico-Etiological Spectrum and Functional Outcomes of Children with Pre-Status Dystonicus and Status Dystonicus (SD): A Descriptive Study.
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.
Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic Disorder.
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder.
