Publications by authors named "Gary McCullagh"

Claim this Profile
F
Fifteen-minute consultation: Approach to a child with congenital insensitivity to pain.
Muhamad Azamin Anuar, Emily Rose Whitehouse, Uma Varma, Gary McCullagh, Imelda Hughes

Arch Dis Child Educ Pract Ed· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
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.
Vasantha Gowda, Mark Atherton, Archana Murugan, Laurent Servais, Jennie Sheehan, Gary McCullagh

Lancet Reg Health Eur· February 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Francesca Peluso, Stefano G Caraffi, Gianluca Contrò, Lara Valeri, Manuela Napoli, Gary McCullagh

J Med Genet· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial.
Richard S Finkel, Craig M McDonald, H Lee Sweeney, Erika Finanger, Erin Neil Knierbein, Gary McCullagh

J Neuromuscul Dis· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fifteen-minute consultation: A structured approach to the management of stroke in a child.
Ailva O'Reilly, Gary McCullagh

Arch Dis Child Educ Pract Ed· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
T2-highlighted U-fibres and rapid parenchymal volume loss in AESD: An under-recognised subtype of paediatric acute encephalopathy syndromes.
Saipriya Ramji, Gary McCullagh, Dipak Ram, Grace Vassallo, Julija Pavaine

J Neuroradiol· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Kathleen M Gorman, Esther Meyer, Detelina Grozeva, Egidio Spinelli, Amy McTague, Gary McCullagh

Am J Hum Genet· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A patient with a novel CNTNAP2 homozygous variant: further delineation of the CASPR2 deficiency syndrome and review of the literature.
Florence Riccardi, Jill Urquhart, Gary McCullagh, Peter Lawrence, Sofia Douzgou

Clin Dysmorphol· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period.
Maria Sframeli, Anna Sarkozy, Marta Bertoli, Guja Astrea, Judith Hudson, Gary McCullagh

Neuromuscul Disord· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.
Gillian I Rice, Naoki Kitabayashi, Magalie Barth, Tracy A Briggs, Annabel C E Burton, Gary McCullagh

Neuropediatrics· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
A Reghan Foley, Manoj P Menezes, Amelie Pandraud, Michael A Gonzalez, Ahmad Al-Odaib, B Gary McCullagh

Brain· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A valuable non-invasive diagnostic investigation for paediatric idiopathic brachial neuritis.
Grace Vassallo, Tim Martland, Wellesley Forbes, Gary McCullagh

Dev Med Child Neurol· October 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis