Gabriel S. Chow
Hucknall Road
Nottingham, ENG, United Kingdom
Nottingham, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 16 publications
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain.
Journal: Journal of neuromuscular diseases
Published: January 08, 2024
Quality of life and neurological disability in children and young people with ataxia telangiectasia.
Quality of life and neurological disability in children and young people with ataxia telangiectasia.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: March 10, 2022
Accumulation of Brain Hypointense Foci on Susceptibility-Weighted Imaging in Childhood Ataxia Telangiectasia.
Journal: AJNR. American journal of neuroradiology
Published: November 16, 2020
LBSL: Case Series and DARS2 Variant Analysis in Early Severe Forms With Unexpected Presentations.
Journal: Neurology. Genetics
Published: September 15, 2020
Multiparametric cerebellar imaging and clinical phenotype in childhood ataxia telangiectasia.
Journal: NeuroImage. Clinical
Published: August 20, 2019
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Journal: Brain : a journal of neurology
Published: December 17, 2018
Evaluation of an internet-based animated preparatory video for children undergoing non-sedated MRI.
Journal: The British journal of radiology
Published: April 25, 2018
Early discharge and rehabilitation in paediatric acquired brain and neurological injury: a transferable model.
Journal: Archives of disease in childhood. Education and practice edition
Published: March 07, 2018
Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya.
Journal: Neurology
Published: June 12, 2017
Longitudinal analysis of the neurological features of ataxia-telangiectasia.
Journal: Developmental medicine and child neurology
Published: December 15, 2015
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain.
Journal: American journal of human genetics
Published: September 02, 2015
Trismus in the paediatric population.
Journal: Developmental medicine and child neurology
Published: October 13, 2014
Last Updated: 09/26/2026