Gary Mccullagh
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Fifteen-minute consultation: Approach to a child with congenital insensitivity to pain.
Journal: Archives of disease in childhood. Education and practice edition
Published: October 19, 2023
Efficacy and safety of onasemnogene abeparvovec in children with spinal muscular atrophy type 1: real-world evidence from 6 infusion centres in the United Kingdom.
Journal: The Lancet regional health. Europe
Published: September 26, 2023
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Journal: Journal of medical genetics
Published: January 03, 2023
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial.
Journal: Journal of neuromuscular diseases
Published: June 14, 2021
Fifteen-minute consultation: A structured approach to the management of stroke in a child.
Journal: Archives of disease in childhood. Education and practice edition
Published: March 05, 2020
T2-highlighted U-fibres and rapid parenchymal volume loss in AESD: An under-recognised subtype of paediatric acute encephalopathy syndromes.
Journal: Journal of neuroradiology = Journal de neuroradiologie
Published: July 05, 2019
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Journal: American journal of human genetics
Published: November 26, 2018
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.
Journal: Neuropediatrics
Published: June 01, 2017
Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period.
Journal: Neuromuscular disorders : NMD
Published: February 09, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026