Archana Desurkar

Sheffield, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Zorevunersen in Children and Adolescents with Dravet Syndrome.

Zorevunersen in Children and Adolescents with Dravet Syndrome.

Journal: The New England journal of medicine

Published: March 04, 2026

The use of cannabidiol in patients with Lennox-Gastaut syndrome and Dravet syndrome in the UK Early Access Program: A retrospective chart review study.

The use of cannabidiol in patients with Lennox-Gastaut syndrome and Dravet syndrome in the UK Early Access Program: A retrospective chart review study.

Journal: Epilepsy & behavior reports

Published: June 14, 2024

Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study.

Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 14, 2024

Classic ketogenic diet versus further antiseizure medicine in infants with drug-resistant epilepsy (KIWE): a UK, multicentre, open-label, randomised clinical trial.

Classic ketogenic diet versus further antiseizure medicine in infants with drug-resistant epilepsy (KIWE): a UK, multicentre, open-label, randomised clinical trial.

Journal: The Lancet. Neurology

Published: June 26, 2023

Retrospective chart review study of use of cannabidiol (CBD) independent of concomitant clobazam use in patients with Lennox-Gastaut syndrome or Dravet syndrome.

Retrospective chart review study of use of cannabidiol (CBD) independent of concomitant clobazam use in patients with Lennox-Gastaut syndrome or Dravet syndrome.

Journal: Seizure

Published: January 24, 2023

Assessing the role of ketogenic dietary therapy in ring chromosome 20 syndrome: A patient-led approach.

Assessing the role of ketogenic dietary therapy in ring chromosome 20 syndrome: A patient-led approach.

Journal: Epilepsia open

Published: October 07, 2019

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures.

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures.

Journal: Epilepsia

Published: August 07, 2019

SLC35A2-related congenital disorder of glycosylation: Defining the phenotype.

SLC35A2-related congenital disorder of glycosylation: Defining the phenotype.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: May 30, 2018

Crossing the lines between epilepsy syndromes: a myoclonic epilepsy variant with prominent eyelid myoclonia and atonic components.

Crossing the lines between epilepsy syndromes: a myoclonic epilepsy variant with prominent eyelid myoclonia and atonic components.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: November 25, 2017

Functional mRNA analysis reveals aberrant splicing caused by novel intronic mutation in WDR45 in NBIA patient.

Functional mRNA analysis reveals aberrant splicing caused by novel intronic mutation in WDR45 in NBIA patient.

Journal: American journal of medical genetics. Part A

Published: October 26, 2017

Effectiveness and tolerability of Perampanel in children, adolescents and young adults with refractory epilepsy: A UK national multicentre study.

Effectiveness and tolerability of Perampanel in children, adolescents and young adults with refractory epilepsy: A UK national multicentre study.

Journal: Seizure

Published: May 11, 2017

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.

Journal: Neurology

Published: November 07, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026