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Incidence of malignant disease in biopsy-proven inflammatory myopathy. A population-based cohort study

Annals of internal medicine, 2001-06, Vol.134 (12), p.1087

2001

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Diagnostic criteria for respiratory chain disorders in adults and children

Neurology, 2002-11, Vol.59 (9), p.1406-1411

2002

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Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder

Neurology, 1999-04, Vol.52 (6), p.1255-1255

1999

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Quadriceps muscle wasting persists 5 months after total hip arthroplasty for osteoarthritis of the hip: a pilot study

Internal medicine journal, 2001-01, Vol.31 (1), p.7-14

2001

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Clinical course correlates poorly with muscle pathology in nemaline myopathy

Neurology, 2003-02, Vol.60 (4), p.665-673

2003

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Benign acute childhood myositis: laboratory and clinical features

Neurology, 1999-12, Vol.53 (9), p.2127-2127

1999

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Mitochondrial theory of senescence: Respiratory chain protein studies in human skeletal muscle

Mechanisms of ageing and development, 1991-11, Vol.60 (3), p.295-302

1991

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Contrasting histochemical features of various mitochondrial syndromes

Acta neurologica Scandinavica, 1995-04, Vol.91 (4), p.287-293

1995

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Elevated aminotransferase as a presenting finding in a patient with occult muscle disease

Journal of paediatrics and child health, 2000-04, Vol.36 (2), p.189-190

2000

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A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I

American journal of human genetics, 1992-09, Vol.51 (3), p.457-468

1992

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Haycocknema perplexum n. g., n. sp. (Nematoda: Robertdollfusidae): an intramyofibre parasite in man

Systematic parasitology, 1999-06, Vol.43 (2), p.123-131

1999

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Idiopathic granulomatous myositis: does the clinical spectrum include polymyalgia rheumatica?

Journal of clinical neuroscience, 1999-05, Vol.6 (3), p.255-259

1999

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Biochemical and morphological studies of skeletal muscle in experimental chronic alcoholic myopathy

Acta neurologica Scandinavica, 1990-12, Vol.82 (6), p.386-391

1990

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Biopsy Proven Polymyositis in Victoria 1982–1987: Analysis of Prognostic Factors

Journal of the Royal Society of Medicine, 1994-06, Vol.87 (6), p.323-326

1994

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Emetine myopathy in a patient with an eating disorder

Medical journal of Australia, 1993-12, Vol.159 (11-12), p.757-760

1993

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Oxidative energy failure in post-mitotic cells : a major factor in senescence

Revue neurologique, 1991, Vol.147 (6-7), p.532-535

1991

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Incidence of inflammatory myopathies in Victoria, Australia, and evidence of spatial clustering

Journal of rheumatology, 1999-05, Vol.26 (5), p.1094

1999

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Idiopathic inflammatory myopathies: clinical aspects

Bailliere's clinical neurology, 1993-11, Vol.2 (3), p.499

1993

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Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions : an immunocytochemical study

Acta neuropathologica, 1991-01, Vol.82 (3), p.185-192

1991

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Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation product

Neurology, 1987-09, Vol.37 (9), p.1530-1530

1987

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Current perspectives in the study of human mitochondriopathies

Medical journal of Australia, 1988-07, Vol.149 (1), p.30-33

1988

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Functional respiratory chain studies in mitochondrial cytopathies: support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndrome

Acta neuropathologica, 1991-01, Vol.81 (3), p.318-323

1991

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Endomyocardial biopsy in infants and children with cardiomyopathy

Clinical cardiology (Mahwah, N.J.), 1991-11, Vol.14 (11), p.903-907

1991

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Critical care myopathy: An electrophysiological and histological study

Muscle & nerve, 1996-04, Vol.19 (4), p.516-518

1996

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G.O.2 A clinical and pathological study of congenital fibre type disproportion

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.646-646

2006

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Incidence of malignant disease in biopsy-proven inflammatory myopathy. A population-based cohort study

Diagnostic criteria for respiratory chain disorders in adults and children

Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder

Quadriceps muscle wasting persists 5 months after total hip arthroplasty for osteoarthritis of the hip: a pilot study

Clinical course correlates poorly with muscle pathology in nemaline myopathy

Benign acute childhood myositis: laboratory and clinical features

Mitochondrial theory of senescence: Respiratory chain protein studies in human skeletal muscle

Contrasting histochemical features of various mitochondrial syndromes

Elevated aminotransferase as a presenting finding in a patient with occult muscle disease

A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I

Haycocknema perplexum n. g., n. sp. (Nematoda: Robertdollfusidae): an intramyofibre parasite in man

Idiopathic granulomatous myositis: does the clinical spectrum include polymyalgia rheumatica?

Biochemical and morphological studies of skeletal muscle in experimental chronic alcoholic myopathy

Biopsy Proven Polymyositis in Victoria 1982–1987: Analysis of Prognostic Factors

Emetine myopathy in a patient with an eating disorder

Oxidative energy failure in post-mitotic cells : a major factor in senescence

Incidence of inflammatory myopathies in Victoria, Australia, and evidence of spatial clustering

Idiopathic inflammatory myopathies: clinical aspects

Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions : an immunocytochemical study

Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation product

Current perspectives in the study of human mitochondriopathies

Functional respiratory chain studies in mitochondrial cytopathies: support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndrome

Endomyocardial biopsy in infants and children with cardiomyopathy

Critical care myopathy: An electrophysiological and histological study

G.O.2 A clinical and pathological study of congenital fibre type disproportion

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