Natalie Trump
Developmental Neurosciences, UCL Great Ormond Street Institute Of Child Health
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 11 publications
Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study.
Journal: Annals of neurology
Published: February 09, 2024
KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation.
Journal: Brain : a journal of neurology
Published: May 15, 2020
Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Journal: Neurology
Published: November 07, 2016
Autosomal dominant SCN8A mutation with an unusually mild phenotype.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: January 04, 2016
Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?
Journal: Molecular genetics and metabolism
Published: October 03, 2015
GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy.
Journal: Developmental medicine and child neurology
Published: September 29, 2015
Delineation of the movement disorders associated with FOXG1 mutations.
Journal: Neurology
Published: September 28, 2015
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
Journal: Journal of medical genetics
Published: May 11, 2015
Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Journal: Prenatal diagnosis
Published: April 24, 2015
Familial recurrences of FOXG1-related disorder: Evidence for mosaicism.
Journal: American journal of medical genetics. Part A
Published: March 04, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026