J. Marsh

Cardiac involvement in hereditary myopathy with early respiratory failure

J. Bourke, P. Chinnery, V. Straub, 2016, Neurology.

CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies

A. Schapira, G. Ravenscroft, N. Laing, 2016, Neuromuscular Disorders.

In vitro screening for putative psoriasis‐specific antigens among wheat proteins and peptides

P. Shewry, J. Skavland, J. Marsh, 2012, The British journal of dermatology.

Titin mutation segregates with hereditary myopathy with early respiratory failure.

M. Santibanez-Koref, P. Chinnery, R. Horvath, 2012, Brain : a journal of neurology.

Late onset bone marrow failure associated with proximal fusion of radius and ulna: a new syndrome

P. Ganly, I. Dokal, J. Hows, 1989, British journal of haematology.

Recessive desmin-null muscular dystrophy with central nuclei and mitochondrial abnormalities

Robert W. Taylor, K. Bushby, I. Horrocks, 2013, Acta Neuropathologica.

Clinical management and survival outcomes of gliosarcomas in the era of multimodality therapy

K. McDonald, O. Damodaran, M. Bynevelt, 2014, Journal of Clinical Neuroscience.