Matthew J. Parton
Queen Square
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
A Novel Variant in TPM3 Causing Muscle Weakness and Concomitant Hypercontractile Phenotype.
Journal: International journal of molecular sciences
Published: October 12, 2023
Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice.
Journal: Journal of the American Heart Association
Published: November 29, 2022
Differential Diagnoses of Inclusion Body Myositis.
Journal: Neurologic clinics
Published: July 25, 2020
Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair.
Journal: Human genetics
Published: August 06, 2019
Calpainopathy with macrophage-rich, regional inflammatory infiltrates.
Journal: Neuromuscular disorders : NMD
Published: November 19, 2016
Seizure: acute investigation and management.
Journal: British journal of hospital medicine (London, England : 2005)
Published: September 20, 2016
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
Journal: Neurobiology of aging
Published: March 17, 2016
Ongoing developments in sporadic inclusion body myositis.
Journal: Current rheumatology reports
Published: November 18, 2014
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Journal: Brain : a journal of neurology
Published: November 03, 2014
Cerebellar ataxia and epilepsy with anti-GAD antibodies: treatment with IVIG and plasmapheresis.
Journal: BMJ case reports
Published: January 15, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026