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Dr. Sarbani Raha - Pediatric Neurology in Vadodara

Dr. Sarbani Raha

MBBS, MD - Pediatrics, CCT - Clinical Neurophysiology

Pediatric NeurologyPediatric Neurology
  • Vadodara, Gujarat
  • 6 Awards

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Clinic Locations

Child Neurology & Epilepsy Clinic

401-402, Infinity Arcade, Baroda Dairy-ONGC Road, Vadodara, Gujarat, India,

Services

  • Gastroenteritis Treatment
  • Epilepsy In Children
  • Cerebral Plasy
  • Developmental Delay
  • Autism
  • Dyslexia Treatment
  • ADHD
  • Neurodegenerative Disorders
  • Inborn errors of metabolism
  • Migraine Treatment
  • Cluster Headache
  • Muscular dystrophy
  • Myopathy
  • Neuropathy
  • Myesthenia
  • Dystonia
  • Chorea
  • Tics
  • Pediatric Stroke
  • Craniovertebral Anomalies
  • Malformations of Cortical Development
  • Chromosomal Abnormalities
  • Neonatal Encephalopathy
  • Status Epilepticus
  • Traumatic brain injury rehabilitation
  • Meningitis
  • Encephalitis
  • GBS
  • Routine EEG
  • Bedside / Portable EEG
  • Video EEG
  • NCU
  • RNS
  • EMG
  • VEP
  • SSEP

Education

  • MP Shah Medical College,Jamnagar - 2000 Graduated
    MBBS
  • MP Shah Medical College,Jamnagar - 2004 Graduated
    MD - Pediatrics
  • Hinduja Hospital, Mumbai - 2009 Graduated
    Fellowship in Paediatric Neurology
  • Cleveland Clinic Foundation, Ohio, USA - 2011 Graduated
    CCT - Clinical Neurophysiology

Work & Experience

  • Amrita Institute of Medical Sciences Cochin
    Asst. Prof of Pediatrics
    2005-2006
  • Hinduja Hospital
    Fellowship in Pediatric Neurology
    2008-2009
  • Hinduja Hospital
    Associate/Junior Consultant
    2009-2013
  • Child Neurology and Epilepsy Clinic
    Consultant
    2013-2015

Awards

  • Paper published on Acute Infantile Encephalopathy Predominantly Affecting the Frontal Lobes (AIEF)

  • Paper published on Neurocognitive And Neurobehavioral Disabilities in Epilepsy with Electrical Status Epilepticus in Slow Sleep (ESES) and Related Syndromes

  • Paper published on Nonparaneoplastic Anti - N - Methyl D - Aspartate Receptor Encephalitis : A Case Series of Four Children

  • Paper published on Biotinidase Deficiency Presenting as Recurrent Myelopathy in a 7 - Year - Old Boy and a Review of the Literature

  • Paper published on Spectrum of MECP2 Gene Mutatios in a Cohort of Indian Patients with Rett Syndrome : Report of two Novel Mutations

  • Paper published on Novel Mutations in Cyclin - Dependent Kinase - Like 5 (CDKL5) Gene in Indian Cases of Rett Syndrome

Membership

  • Indian Medical Association (IMA)

  • Indian Academy of Paediatrics (IAP)

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