J. Morgan-Hughes

发表

Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

D. J. Hayes, J. Morgan-Hughes, J. Clark, 1985, Biochemical Society transactions.

Exacerbation of idiopathic Parkinson's disease by naproxen

S. Shaunak, P. Brown, J. Morgan-Hughes, 1995, BMJ.

INTERCOSTAL MUSCLE ACETYLCHOLINE RECEPTORS IN LONGSTANDING OCULAR MYASTHENIA

N. Murray, D. Landon, B. Lecky, 1980, The Lancet.

The effect of local pressure in diphtheritic neuropathy.

A. Hopkins, J. Morgan-Hughes, 1969, The Journal of physiology.

Cough seizures in patients with cerebral lesions.

J. Morgan-Hughes, 1966, British medical journal.

Tubular aggregates in skeletal muscle: their functional significance and mechanisms of pathogenesis.

J. Morgan-Hughes, 1998, Current opinion in neurology.

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

J. Clark, J. Clark, D. Landon, 1979, Journal of the Neurological Sciences.

The effect of local pressure in diphtheritic neuropathy.

A. Hopkins, J. Morgan-Hughes, 1969, Journal of neurology, neurosurgery, and psychiatry.

Mitochondrial myopathies: defects in mitochondrial metabolism in human skeletal muscle.

D. J. Hayes, J. Morgan-Hughes, J. Clark, 1983, Biochemical Society transactions.

Painful disorders of muscle.

J. Morgan-Hughes, 1979, British journal of hospital medicine.

Fifty year follow-up of a patient with central core disease shows slow but definite progression

V. Dubowitz, P. Lamont, M. Davis, 1998, Neuromuscular Disorders.

Isozyme patterns and protein profiles in neuromuscular disorders.

Y. Edwards, D. Hopkinson, J. Neerunjun, 1982, Journal of medical genetics.

Late‐onset cytoplasmic body myopathy resembling myotonic dystrophy

P. Brown, H. R. Morris, D. Landon, 1999, Muscle & nerve.

Central core disease or not? Observations on a family with a non-progressive myopathy.

E. Brett, F. Tomé, B. Lake, 1973, Brain : a journal of neurology.

Experimental diphtheritic neuropathy. A pathological and electrophysiological study.

J. Morgan-Hughes, 1968, Journal of the neurological sciences.

KINETIC ANALYSIS OF ACETYLCHOLINE RECEPTORS (ACHR) IN NORMAL AND MYASTHENIC HUMAN MUSCLE *

B. Lecky, J. Morgan-Hughes, 1981, Annals of the New York Academy of Sciences.

Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A)

N. Wood, A. Schapira, M. Hanna, 1998, Journal of neurology, neurosurgery, and psychiatry.

Hexosaminidase A deficiency presenting as juvenile progressive dystonia.

E. Young, R. Hardie, J. Morgan-Hughes, 1988, Journal of neurology, neurosurgery, and psychiatry.

A rapidly progressive adolescent‐onset oculopharyngeal somatic syndrome with rimmed vacuoles in two siblings

M. Rose, A. Papadimitriou, D. Landon, 1997, Annals of neurology.

AGRANULOCYTOSIS ASSOCIATED WITH IMIPRAMINE

J. Morgan-Hughes, I. Heald, 1960 .

Experimentally induced defects of mitochondrial metabolism in rat skeletal muscle. Biological effects of the NADH: coenzyme Q reductase inhibitor diphenyleneiodonium.

D. J. Hayes, E. Shoubridge, J. Clark, 1985, The Biochemical journal.

Dilutional hyponatraemia and myasthenic syndrome in a patient with bronchial carcinoma.

J. Hallpike, J. Morgan-Hughes, 1966, British medical journal.

A disorder of skeletal muscle associated with tubular aggregates.

W. Mair, P. Lascelles, J. Morgan-Hughes, 1970, Brain : a journal of neurology.

Pure neural tuberculoid leprosy.

J. Morgan-Hughes, W. Jopling, 1965, British medical journal.

Biochemical and molecular aspects of human mitochondrial respiratory chain disorders.

J. Cooper, A. Schapira, A. Harding, 1990, Biochemical Society transactions.

Mitochondrial myopathies: clinical defects.

J. Cooper, A. Schapira, A. Harding, 1990, Biochemical Society transactions.

DELETIONS OF MUSCLE MITOCHONDRIAL DNA

J. Cooper, A. Harding, I. Holt, 1988, The Lancet.

Changes in motor nerve conduction velocity in diphtheritic polyneuritis.

J. Morgan-Hughes, 1965, Rivista di patologia nervosa e mentale.

Mitochondrial myopathies: genetic defects.

J. Cooper, A. Schapira, A. Harding, 1990, Biochemical Society transactions.

The diagnosis of carnitine palmitoyltransferase II deficiency is now possible in small skeletal muscle biopsies

J. Land, S. Heales, S. Olpin, 2000, Journal of Inherited Metabolic Disease.