Hayley J. Durling

Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1)

Christopher S. Meredith, Ralf Herrmann, Cheryl Parry et al. · The American Journal of Human Genetics · 2004 · 227 citations · Full text

Mitochondrial Myopathy, Muscle Function, Skeletal Muscle +8

Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene

Biljana Ilkovski, Sandra T. Cooper, Kristen L. Nowak et al. · The American Journal of Human Genetics · 2001 · 157 citations · Full text

Muscle Physiology, Muscle Function, Health Sciences +10

Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)

J. M. Schr�der, Hayley J. Durling, Nigel G. Laing · Acta Neuropathologica · 2004 · 60 citations

Mechanobiology, Medicine, Molecular Biology +8

De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

Hayley J. Durling, Peter Reilich, Josef Müller‐Höcker et al. · Neuromuscular Disorders · 2002 · 37 citations

Genetic Disorder, Medicine, Genetics +5

Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive

Phillipa J. Lamont, David R. Thorburn, Vicki Fabian et al. · Neuropediatrics · 2004 · 26 citations

Neurological Disorder, Isolated Deficiency, Mitochondrial Myopathy +20