Karine Lascelles

Guy's And St Thomas' NHS Trust
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 29 publications

Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency.

Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency.

Journal: Brain communications

Published: January 28, 2025

Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype.

Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype.

Journal: Clinical dysmorphology

Published: May 17, 2023

Location, symptoms, and management of plexiform neurofibromas in 127 children with neurofibromatosis 1, attending the National Complex Neurofibromatosis 1 service, 2018-2019.

Location, symptoms, and management of plexiform neurofibromas in 127 children with neurofibromatosis 1, attending the National Complex Neurofibromatosis 1 service, 2018-2019.

Journal: American journal of medical genetics. Part A

Published: June 18, 2021

A recent surge of fulminant and early onset subacute sclerosing panencephalitis (SSPE) in the United Kingdom: An emergence in a time of measles.

A recent surge of fulminant and early onset subacute sclerosing panencephalitis (SSPE) in the United Kingdom: An emergence in a time of measles.

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

Published: December 16, 2020

Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2.

Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: November 25, 2020

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

Ischemic Stroke Following Ergotamine Overdose.

Ischemic Stroke Following Ergotamine Overdose.

Journal: Pediatric neurology

Published: June 14, 2019

Early predictors of epilepsy and subsequent relapse in children with acute disseminated encephalomyelitis.

Early predictors of epilepsy and subsequent relapse in children with acute disseminated encephalomyelitis.

Journal: Multiple sclerosis (Houndmills, Basingstoke, England)

Published: February 08, 2019

PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics.

PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 27, 2018

Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severity.

Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severity.

Journal: Clinical genetics

Published: November 23, 2018

The spectrum of intermediate SCN8A-related epilepsy.

The spectrum of intermediate SCN8A-related epilepsy.

Journal: Epilepsia

Published: October 29, 2018

Cerebral vasculopathy in childhood neurofibromatosis type 2: cause for concern?

Cerebral vasculopathy in childhood neurofibromatosis type 2: cause for concern?

Journal: Developmental medicine and child neurology

Published: April 06, 2018

Showing 1-12 of 29

Last Updated: 09/26/2026