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Language, Ideology, and the Human: New Interventions

2012

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Fractal Zeta Functions and Fractal Drums: Higher-Dimensional Theory of Complex Dimensions

1, 2017

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The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

Journal of neurology, 2019-04, Vol.266 (4), p.876-887

2019

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A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy

Brain (London, England : 1878), 2011-01, Vol.134 (Pt 1), p.171-182

2011

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Rituximab in the treatment of pembrolizumab-induced myasthenia gravis

European journal of cancer (1990), 2018-10, Vol.102, p.49-51

2018

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Factors influencing kidney transplantation rates: a study from the ERA Registry

Nephrology, dialysis, transplantation, 2023-05, Vol.38 (6), p.1540-1551

2023

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Myth and Violence in the Contemporary Female Text: New Cassandras

1, 2011

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Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Neuromuscular disorders : NMD, 2013-07, Vol.23 (7), p.540-548

2013

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Brown-Vialetto-Van Laere syndrome: a 28-year follow-up

Journal of neurology, neurosurgery and psychiatry, 2016-06, Vol.87 (6), p.681-682

2016

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FRI0352 Small Fibre Neuropathy and Ganglionopathy in Primary Sjogren's Syndrome (PSS)

Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.562-562

2016

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[OP.8D.02] FIRST IN MAN TREATMENT OF SEVERE BP VARIABILITY WITH BAROREFLEX ACTIVATION THERAPY

Journal of hypertension, 2016-09, Vol.34 Suppl 2 - ESH 2016 Abstract Book (Supplement 2), p.e105-e105

2016

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Increased mitochondrial superoxide dismutase activity in Parkinson's disease but not amyotrophic lateral sclerosis motor cortex

Neuroscience letters, 1997-12, Vol.239 (2), p.105-108

1997

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Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

Journal of neurology, neurosurgery and psychiatry, 1996-12, Vol.61 (6), p.565-572

1996

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Mobility shift of beta-dystroglycan combined with reduced laminin alpha2 expression is a marker of genetic defects in the GMPPB gene

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S166-S166

2016

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P67 Characterisation of the expression of Polycomb Group Genes in human neuromuscular diseases

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S24-S25

2014

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A novel bleeding disorder associated with RYR1 mutations

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S89-S90

2016

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Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease

Cochrane database of systematic reviews, 2017-10, Vol.10 (6), p.CD004427-CD004427

2017

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Copper and zinc levels in familial amyotrophic lateral sclerosis patients with cuznsod gene mutations

Annals of neurology, 1997-07, Vol.42 (1), p.130-131

1997

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P32 Polycomb group genes and the regenerative process in the aged and pathological human muscle

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S15-S15

2012

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AB1078 USE OF MYOSITIS SPECIFIC AUTOANTIBODIES TEST ACROSS A LARGE NHS HOSPITAL TRUST

Annals of the rheumatic diseases, 2020-06, Vol.79 (Suppl 1), p.1827-1828

2020

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Leprosy: a 'common' and curable cause of peripheral neuropathy with skin lesions

The Journal of the Royal College of Physicians of Edinburgh, 2015-01, Vol.45 (1), p.38-42

2015

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Mutations in all five exons of SOD-1 may cause ALS

Annals of neurology, 1998-03, Vol.43 (3), p.390-394

1998

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P.15.7 A founder mutation in the titin gene is a common cause of myofibrillar myopathy with early respiratory failure

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.820-820

2013

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Cuznsod-associated amyotrophic lateral sclerosis

Annals of neurology, 1997-08, Vol.42 (2), p.273-274

1997

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Cells from individuals with SOD-1 associated familial amyotrophic lateral sclerosis do not have an increased susceptibility to radiation-induced free radical production or DNA damage

Journal of the neurological sciences, 1999-03, Vol.164 (1), p.89-92

1999

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Language, Ideology, and the Human: New Interventions

Fractal Zeta Functions and Fractal Drums: Higher-Dimensional Theory of Complex Dimensions

The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy

Rituximab in the treatment of pembrolizumab-induced myasthenia gravis

Factors influencing kidney transplantation rates: a study from the ERA Registry

Myth and Violence in the Contemporary Female Text: New Cassandras

Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

Brown-Vialetto-Van Laere syndrome: a 28-year follow-up

FRI0352 Small Fibre Neuropathy and Ganglionopathy in Primary Sjogren's Syndrome (PSS)

[OP.8D.02] FIRST IN MAN TREATMENT OF SEVERE BP VARIABILITY WITH BAROREFLEX ACTIVATION THERAPY

Increased mitochondrial superoxide dismutase activity in Parkinson's disease but not amyotrophic lateral sclerosis motor cortex

Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

Mobility shift of beta-dystroglycan combined with reduced laminin alpha2 expression is a marker of genetic defects in the GMPPB gene

P67 Characterisation of the expression of Polycomb Group Genes in human neuromuscular diseases

A novel bleeding disorder associated with RYR1 mutations

Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease

Copper and zinc levels in familial amyotrophic lateral sclerosis patients with cuznsod gene mutations

P32 Polycomb group genes and the regenerative process in the aged and pathological human muscle

AB1078 USE OF MYOSITIS SPECIFIC AUTOANTIBODIES TEST ACROSS A LARGE NHS HOSPITAL TRUST

Leprosy: a 'common' and curable cause of peripheral neuropathy with skin lesions

Mutations in all five exons of SOD-1 may cause ALS

P.15.7 A founder mutation in the titin gene is a common cause of myofibrillar myopathy with early respiratory failure

Cuznsod-associated amyotrophic lateral sclerosis

Cells from individuals with SOD-1 associated familial amyotrophic lateral sclerosis do not have an increased susceptibility to radiation-induced free radical production or DNA damage

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