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Multiple mitochondrial DNA deletions in monozygotic twins with OPMD

Journal of neurology, neurosurgery and psychiatry, 2008-01, Vol.79 (1), p.68-71

2008

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Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease

Cochrane database of systematic reviews, 2007-01, Vol.2011 (1), p.CD002829

2007

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PONM14 A novel homozygous missense mutation in the GNE gene of two brothers with hereditary inclusion body myopathy type 2

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.e64-e64

2010

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Enterovirus related metabolic myopathy: a postviral fatigue syndrome

Journal of neurology, neurosurgery and psychiatry, 2003-10, Vol.74 (10), p.1382-1386

2003

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Phenotypic variability in siblings with type III spinal muscular atrophy

Journal of neurology, neurosurgery and psychiatry, 2004-12, Vol.75 (12), p.1762-1764

2004

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Barraquer-Simons lipodystrophy, Raynaud's phenomenon and cutaneous vasculitis

Clinical and experimental dermatology, 2000-06, Vol.25 (4), p.277-280

2000

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Muscle fibre characteristics and lactate responses to exercise in chronic fatigue syndrome

Journal of neurology, neurosurgery and psychiatry, 1998-03, Vol.64 (3), p.362-367

1998

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A diagnostic dilemma of intracranial pathology: coincidence or the result of cranial trauma?

BMJ case reports, 2010-11, Vol.2010 (nov22 1), p.bcr0720103167-bcr0720103167

2010

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Oculomotor function in amyotrophic lateral sclerosis: Evidence for frontal impairment

Annals of neurology, 1995-07, Vol.38 (1), p.38-44

1995

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Familial cramp due to potassium-aggravated myotonia

Journal of neurology, neurosurgery and psychiatry, 1998-10, Vol.65 (4), p.569-572

1998

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Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA

Journal of general virology, 1990-06, Vol.71 (6), p.1399-1402

1990

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Dermatomyositis in association with transitional cell carcinoma of the bladder

Clinical and experimental dermatology, 1999-03, Vol.24 (2), p.94-96

1999

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Cytochrome c Oxidase Deficiency Associated with the First Stop-Codon Point Mutation in Human mtDNA

American journal of human genetics, 1998-07, Vol.63 (1), p.29-36

1998

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Histological surprise: callosal tuberculoma presenting as malignant glioma

Journal of neurology, neurosurgery and psychiatry, 1997-07, Vol.63 (1), p.98-99

1997

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Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease

Cochrane database of systematic reviews, 2005-01 (1), p.CD002829

2005

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Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis

Neurology, 1997-03, Vol.48 (3), p.746-751

1997

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Recurrent Epistaxes in Hereditary Haemorrhagic Telangiectasia

Journal of the Royal Society of Medicine, 1997-05, Vol.90 (5), p.271-273

1997

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Clinical characteristics of SOD1 gene mutations in UK families with ALS

Journal of the neurological sciences, 1999-10, Vol.169 (1), p.56-60

1999

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Myopathy in HIV infection: the role of zidovudine and the significance of tubuloreticular inclusions

Neuropathology and applied neurobiology, 1993-10, Vol.19 (5), p.406-413

1993

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Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles

Journal of neurology, neurosurgery and psychiatry, 1995-09, Vol.59 (3), p.266-270

1995

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Transient myasthenia gravis in an elderly woman

Journal of neurology, neurosurgery and psychiatry, 2004-09, Vol.75 (9), p.1363-1363

2004

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A balanced autosomal translocation (3;9) associated with primary hypogonadism and dorsal spine stenosis

Clinical genetics, 1993-01, Vol.43 (1), p.44-45

1993

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Reports of the Midwest Category Seminar III

1969 edition, 2006

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Clinical features and management of two cases of encephalitis lethargica

Movement disorders, 1997-05, Vol.12 (3), p.354-359

1997

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Hyperammonaemia—An Important Cause of Encephalopathy: Three Case Reports

Annals of clinical biochemistry, 1993-03, Vol.30 (2), p.225-227

1993

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Multiple mitochondrial DNA deletions in monozygotic twins with OPMD

Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease

PONM14 A novel homozygous missense mutation in the GNE gene of two brothers with hereditary inclusion body myopathy type 2

Enterovirus related metabolic myopathy: a postviral fatigue syndrome

Phenotypic variability in siblings with type III spinal muscular atrophy

Barraquer-Simons lipodystrophy, Raynaud's phenomenon and cutaneous vasculitis

Muscle fibre characteristics and lactate responses to exercise in chronic fatigue syndrome

A diagnostic dilemma of intracranial pathology: coincidence or the result of cranial trauma?

Oculomotor function in amyotrophic lateral sclerosis: Evidence for frontal impairment

Familial cramp due to potassium-aggravated myotonia

Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA

Dermatomyositis in association with transitional cell carcinoma of the bladder

Cytochrome c Oxidase Deficiency Associated with the First Stop-Codon Point Mutation in Human mtDNA

Histological surprise: callosal tuberculoma presenting as malignant glioma

Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease

Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis

Recurrent Epistaxes in Hereditary Haemorrhagic Telangiectasia

Clinical characteristics of SOD1 gene mutations in UK families with ALS

Myopathy in HIV infection: the role of zidovudine and the significance of tubuloreticular inclusions

Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles

Transient myasthenia gravis in an elderly woman

A balanced autosomal translocation (3;9) associated with primary hypogonadism and dorsal spine stenosis

Reports of the Midwest Category Seminar III

Clinical features and management of two cases of encephalitis lethargica

Hyperammonaemia—An Important Cause of Encephalopathy: Three Case Reports

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