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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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Natural history and clinical features of the flail arm and flail leg ALS variants

Neurology, 2009-03, Vol.72 (12), p.1087

2009

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Proteome-based plasma biomarkers for Alzheimer's disease

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3042-3050

2006

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Preprocessing surface EMG data removes voluntary muscle activity and enhances SPiQE fasciculation analysis

Clinical neurophysiology, 2020-01, Vol.131 (1), p.265-273

2020

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Fasciculation electromechanical latency is prolonged in amyotrophic lateral sclerosis

Clinical neurophysiology, 2023-01, Vol.145, p.71-80

2023

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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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Proteomic analyses reveal that loss of TDP-43 affects RNA processing and intracellular transport

Neuroscience, 2015-05, Vol.293, p.157-170

2015

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SOD1 and cognitive dysfunction in familial amyotrophic lateral sclerosis

Journal of neurology, 2009-02, Vol.256 (2), p.234-241

2009

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Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [ 11C](R)-PK11195 positron emission tomography study

Neurobiology of disease, 2004-04, Vol.15 (3), p.601-609

2004

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A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS

Neurology, 2009-07, Vol.73 (1), p.16

2009

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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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Amyotrophic lateral sclerosis mutant vesicle-associated membrane protein-associated protein-B transgenic mice develop TAR-DNA-binding protein-43 pathology

Neuroscience, 2010-05, Vol.167 (3), p.774-785

2010

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A proposed staging system for amyotrophic lateral sclerosis

Brain (London, England : 1878), 2012-03, Vol.135 (3), p.847-852

2012

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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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New VAPB deletion variant and exclusion of VAPB mutations in familial ALS

Neurology, 2008-04, Vol.70 (14), p.1179

2008

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[11C]-WAY100635 PET demonstrates marked 5-HT1A receptor changes in sporadic ALS

Brain (London, England : 1878), 2005-04, Vol.128 (4), p.896-905

2005

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Distinct cerebral lesions in sporadic and ‘D90A’ SOD1 ALS: studies with [11C]flumazenil PET

Brain (London, England : 1878), 2005-06, Vol.128 (6), p.1323-1329

2005

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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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Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry)

Neuroepidemiology, 2007-11, Vol.29 (1-2), p.44-48

2007

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Demystifying the spontaneous phenomena of motor hyperexcitability

Clinical neurophysiology, 2021-08, Vol.132 (8), p.1830-1844

2021

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Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria

Human molecular genetics, 2012-05, Vol.21 (9), p.1979-1988

2012

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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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Deletions of the Heavy Neurofilament Subunit Tail in Amyotrophic Lateral Sclerosis

Human molecular genetics, 1999-02, Vol.8 (2), p.157-164

1999

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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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An estimate of amyotrophic lateral sclerosis heritability using twin data

Natural history and clinical features of the flail arm and flail leg ALS variants

Proteome-based plasma biomarkers for Alzheimer's disease

Preprocessing surface EMG data removes voluntary muscle activity and enhances SPiQE fasciculation analysis

Fasciculation electromechanical latency is prolonged in amyotrophic lateral sclerosis

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

Proteomic analyses reveal that loss of TDP-43 affects RNA processing and intracellular transport

SOD1 and cognitive dysfunction in familial amyotrophic lateral sclerosis

Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [ 11C](R)-PK11195 positron emission tomography study

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS

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

Amyotrophic lateral sclerosis mutant vesicle-associated membrane protein-associated protein-B transgenic mice develop TAR-DNA-binding protein-43 pathology

A proposed staging system for amyotrophic lateral sclerosis

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

New VAPB deletion variant and exclusion of VAPB mutations in familial ALS

[11C]-WAY100635 PET demonstrates marked 5-HT1A receptor changes in sporadic ALS

Distinct cerebral lesions in sporadic and ‘D90A’ SOD1 ALS: studies with [11C]flumazenil PET

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

Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry)

Demystifying the spontaneous phenomena of motor hyperexcitability

Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria

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

Deletions of the Heavy Neurofilament Subunit Tail in Amyotrophic Lateral Sclerosis

Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis

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