Dinesh Talwar

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP

Krishna R. Veeramah, Janelle E. O’Brien, Miriam H. Meisler et al. · The American Journal of Human Genetics · 2012 · 439 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial

Lieven Lagae, Joseph Sullivan, Kelly G. Knupp et al. · The Lancet · 2019 · 366 citations

Medicine, Pharmacology, Pharmacotherapy +9

Exome sequencing reveals new causal mutations in children with epileptic encephalopathies

Krishna R. Veeramah, Laurel Johnstone, Tatiana M. Karafet et al. · Epilepsia · 2013 · 293 citations · Full text

Medicine, Genetics, Neurology +17

Principles and practice of sleep medicine in the child

Dinesh Talwar · Pediatric Neurology · 1996 · 280 citations

Nursing, Child Health, Pediatrics +10

The treatment of epilepsy: Principles and practice

Dinesh Talwar · Pediatric Neurology · 1993 · 235 citations

Medicine, Neurology, Pharmacotherapy +10