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An estimate of amyotrophic lateral sclerosis heritability using twin data

Journal of neurology, neurosurgery and psychiatry, 2010-12, Vol.81 (12), p.1324-1326

2010

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Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-04, Vol.156B (3), p.285-290

2011

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Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS inclusions

Neuropathology and applied neurobiology, 2013-08, Vol.39 (5), p.553-561

2013

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Prolonged survival in motor neuron disease: a descriptive study of the King’s database 1990–2002

Journal of neurology, neurosurgery and psychiatry, 2003-07, Vol.74 (7), p.995-997

2003

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Racial and Ethnic Disparities in Survival in Lung Transplant Candidates with Idiopathic Pulmonary Fibrosis

American journal of transplantation, 2006-02, Vol.6 (2), p.398-403

2006

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Is language impairment more common than executive dysfunction in amyotrophic lateral sclerosis?

Journal of neurology, neurosurgery and psychiatry, 2013-05, Vol.84 (5), p.494-498

2013

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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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Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 1998-12, Vol.65 (6), p.950-951

1998

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Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

Clinical genetics, 2009-05, Vol.75 (5), p.485-489

2009

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Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS

Journal of neurology, neurosurgery and psychiatry, 2005-09, Vol.76 (9), p.1279-1285

2005

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Low index-to-ring finger length ratio in sporadic ALS supports prenatally defined motor neuronal vulnerability

Journal of neurology, neurosurgery and psychiatry, 2011-06, Vol.82 (6), p.635-637

2011

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Endothelial vasodilator production by uterine and systemic arteries. II. Pregnancy effects on NO synthase expression

American journal of physiology. Heart and circulatory physiology, 1997-04, Vol.272 (4), p.H1730-H1740

1997

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Clinical Versus Actuarial Predictions of Violence in Patients With Mental Illnesses

Journal of consulting and clinical psychology, 1996-06, Vol.64 (3), p.602-609

1996

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Phosphorylation of neurofilament heavy chain side-arms by stress activated protein kinase-1b/Jun N-terminal kinase-3

Journal of cell science, 2000-02, Vol.113 ( Pt 3) (3), p.401-407

2000

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Regression Analyses of Counts and Rates: Poisson, Overdispersed Poisson, and Negative Binomial Models

Psychological bulletin, 1995-11, Vol.118 (3), p.392-404

1995

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Phenotypic differences between African and white patients with motor neuron disease: a case-control study

Journal of neurology, neurosurgery and psychiatry, 2000-08, Vol.69 (2), p.251-253

2000

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PATH46 Familial mutations in the RNA binding gene FUS result in cellular mislocalisation of the protein

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.e20-e20

2010

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Establishing the UK DNA Bank for motor neuron disease (MND)

BMC genetics, 2015-07, Vol.16 (1), p.84, Article 84

2015

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PATH45 Cytoskeletal and inflammatory protein biomarkers for amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.e20-e20

2010

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Vibrio cholerae O395 tcpA pilin gene sequence and comparison of predicted protein structural features to those of type 4 pilins

Infection and Immunity, 1990-09, Vol.58 (9), p.3042-3049

1990

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Endothelium-Derived Nitric Oxide Synthase Protein Expression in Ovine Placental Arteries

Biology of reproduction, 2001-05, Vol.64 (5), p.1494-1499

2001

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Glutamate Slows Axonal Transport of Neurofilaments in Transfected Neurons

The Journal of cell biology, 2000-07, Vol.150 (1), p.165-175

2000

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CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2008-07, Vol.79 (7), p.849-850

2008

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Endothelial vasodilator production by uterine and systemic arteries. VII. Estrogen and progesterone effects on eNOS

American journal of physiology. Heart and circulatory physiology, 2001-04, Vol.280 (4), p.H1699-H1705

2001

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Endothelial vasodilator production by uterine and systemic arteries. III. Ovarian and estrogen effects on NO synthase

American journal of physiology. Heart and circulatory physiology, 1998-11, Vol.275 (5), p.H1845-H1856

1998

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An estimate of amyotrophic lateral sclerosis heritability using twin data

Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis

Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS inclusions

Prolonged survival in motor neuron disease: a descriptive study of the King’s database 1990–2002

Racial and Ethnic Disparities in Survival in Lung Transplant Candidates with Idiopathic Pulmonary Fibrosis

Is language impairment more common than executive dysfunction in amyotrophic lateral sclerosis?

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

Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis

Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

Abnormal cortical excitability in sporadic but not homozygous D90A SOD1 ALS

Low index-to-ring finger length ratio in sporadic ALS supports prenatally defined motor neuronal vulnerability

Endothelial vasodilator production by uterine and systemic arteries. II. Pregnancy effects on NO synthase expression

Clinical Versus Actuarial Predictions of Violence in Patients With Mental Illnesses

Phosphorylation of neurofilament heavy chain side-arms by stress activated protein kinase-1b/Jun N-terminal kinase-3

Regression Analyses of Counts and Rates: Poisson, Overdispersed Poisson, and Negative Binomial Models

Phenotypic differences between African and white patients with motor neuron disease: a case-control study

PATH46 Familial mutations in the RNA binding gene FUS result in cellular mislocalisation of the protein

Establishing the UK DNA Bank for motor neuron disease (MND)

PATH45 Cytoskeletal and inflammatory protein biomarkers for amyotrophic lateral sclerosis

Vibrio cholerae O395 tcpA pilin gene sequence and comparison of predicted protein structural features to those of type 4 pilins

Endothelium-Derived Nitric Oxide Synthase Protein Expression in Ovine Placental Arteries

Glutamate Slows Axonal Transport of Neurofilaments in Transfected Neurons

CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis

Endothelial vasodilator production by uterine and systemic arteries. VII. Estrogen and progesterone effects on eNOS

Endothelial vasodilator production by uterine and systemic arteries. III. Ovarian and estrogen effects on NO synthase

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