A5013830001- Epilepsy research and treatment
- Pharmacological Effects and Toxicity Studies
- Genetics and Neurodevelopmental Disorders
- Autoimmune Neurological Disorders and Treatments
- Metabolism and Genetic Disorders
- Parasitic infections in humans and animals
- Infectious Diseases and Tuberculosis
- Neonatal and fetal brain pathology
- Glycogen Storage Diseases and Myoclonus
- Hereditary Neurological Disorders
- Cerebrospinal fluid and hydrocephalus
- Infectious Encephalopathies and Encephalitis
- Peripheral Neuropathies and Disorders
- Neurogenetic and Muscular Disorders Research
- Bacterial Infections and Vaccines
- Neurological and metabolic disorders
- Cerebral Palsy and Movement Disorders
- Congenital Anomalies and Fetal Surgery
- Botulinum Toxin and Related Neurological Disorders
- Genomics and Rare Diseases
- Mitochondrial Function and Pathology
- Traumatic Brain Injury and Neurovascular Disturbances
- Neurological diseases and metabolism
- Vitamin D Research Studies
- Hematological disorders and diagnostics
All India Institute of Medical Sciences Rishikesh
2019-2025
Post Graduate Institute of Medical Education and Research
2017-2025
All India Institute of Medical Sciences Raipur
2022-2025
All India Institute of Medical Sciences Bhopal
2022-2025
Safdarjang Hospital
2016-2018
Vardhman Mahavir Medical College & Safdarjung Hospital
2016-2018
Febrile seizure (FS) is the single most common type of seen in children between 6 months to 5 years age. The purpose our study was identify risk factors associated with first episode febrile seizures, which would help better management and preventive measures at for FS episodes.To evaluate seizures Indian children.This a hospital based, case control study. this children. Seventy (70) age their were compared 70 fever but without based on various factors.The mean 24.90±16.11 cases 26.34±16.93...
Abstract Objective Literature on the genotypic spectrum of Infantile Epileptic Spasms Syndrome (IESS) in children is scarce developing countries. This multicentre collaboration evaluated and phenotypic landscape genetic IESS Indian children. Methods Between January 2021 June 2022, this cross‐sectional study was conducted at six centers India. Children with genetically confirmed IESS, without definite structural‐genetic structural‐metabolic etiology, were recruited underwent detailed...
Background: The ongoing COVID-19 pandemic and the lockdown measures have forced clinicians across world to look on telemedicine. Although migraine as such seems an ideal option for telemedicine, a systematic study reviewing feasibility, efficacy, advantages of current advanced telecommunication technologies in children with is lacking. Methods: Clinical details telephonic consultations performed between March 25 June 4, 2020, including characteristics, analgesic/prophylactic drug regimens,...
Objectives: To compare the diagnostic accuracy of ultrasonography-guided optic nerve sheath diameter with transcranial Doppler-guided middle cerebral artery flow indices against gold standard invasive intraparenchymal intracranial pressure values in children. Design: A single-center prospective cohort study. Setting: PICU a tertiary care teaching hospital North India. Patients: Eligible children (2–12 yr) are admitted to ICU and undergoing monitoring using an catheter. Observations parallel...
Exact information about the efficacy of various medications proposed by regulatory bodies in children with COVID-19 is limited due to lack controlled trials existing literature.Different electronic databases (MEDLINE, EMBASE, Web Science, COCHRANE CENTRAL, LitCovid, medRxiv, and bioRxiv) were searched for articles describing management cases 18 shortlisted medications. Prospective/retrospective studies/case series (with at least 20 cases) reporting patients aged ≤14 years collect regarding...
Opsoclonus myoclonus ataxia syndrome (OMAS) is a rare neuroinflammatory disorder that typically associated with paraneoplastic and postinfectious processes. has not been previously reported in association tuberculous meningitis (TBM). This report presents unique case which TBM manifested as OMAS, highlighting the complex interplay between tuberculosis autoimmune neurological conditions. A 1.5-year-old healthy girl, presented acute-onset jerky movements, opsoclonus, irritability, reduced...