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Executive dysfunction predicts social cognition impairment in amyotrophic lateral sclerosis

Journal of neurology, 2015-07, Vol.262 (7), p.1681-1690

2015

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Molecular classification of sporadic Creutzfeldt–Jakob disease

Brain (London, England : 1878), 2003-06, Vol.126 (6), p.1333-1346

2003

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The same prion strain causes vCJD and BSE

Nature (London), 1997-10, Vol.389 (6650), p.448-450

1997

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Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD

Nature (London), 1996-10, Vol.383 (6602), p.685-690

1996

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Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. [Addendum: Oct 2, 1997, v. 389 (6650), p. 526.]

Nature (London), 1995-12, Vol.378 (6559), p.779-783

1995

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Prion protein is necessary for normal synaptic function

Nature (London), 1994-07, Vol.370 (6487), p.295-297

1994

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Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-08, Vol.16 (5-6), p.316-323

2015

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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom : a systematic analysis of predisposing mutations and allelic variation in the PRNP gene

Human genetics, 1996-09, Vol.98 (3), p.259-264

1996

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Typing prion isoforms

Nature (London), 1997-03, Vol.386 (6622), p.233-234

1997

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Biochemical typing of scrapie strains

Nature (London), 1997-04, Vol.386 (6625), p.564-564

1997

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Addendum Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

Nature (London), 1997-10, Vol.389 (6650), p.526-526

1997

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Transmission of Creutzfeldt-Jakob Disease from Humans to Transgenic Mice Expressing Chimeric Human-Mouse Prion Protein

Proceedings of the National Academy of Sciences - PNAS, 1994-10, Vol.91 (21), p.9936-9940

1994

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Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

Nature (London), 1997-10, Vol.389 (6650), p.526-526

1997

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Inherited prion disease (PrP lysine 200) in Britain: two case reports

BMJ, 1993-01, Vol.306 (6873), p.301-302

International edition, 1993

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Review: Prion-like mechanisms of transactive response DNA binding protein of 43kDa (TDP-43) in amyotrophic lateral sclerosis (ALS)

Neuropathology and applied neurobiology, 2015-08, Vol.41 (5), p.578-597

2015

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Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

American journal of human genetics, 2013-03, Vol.92 (3), p.345-353

2013

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Administration of Riluzole Oral Suspension During the Different Stages of Amyotrophic Lateral Sclerosis

Frontiers in neurology, 2021-07, Vol.12, p.633854

2021

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Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion

Neurobiology of aging, 2015-01, Vol.36 (1), p.546.e1-546.e7

2015

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Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2014-05, Vol.85 (5), p.506-508

2014

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Molecular screening of sheep for bovine spongiform encephalopathy

Neuroscience letters, 1998-10, Vol.255 (3), p.159-162

1998

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Transmission of fatal familial insomnia to laboratory animals

The Lancet (British edition), 1995-08, Vol.346 (8974), p.569-570

1995

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CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementia

Brain (London, England : 1878), 2016-02, Vol.139 (Pt 2), p.e9-e9

2016

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An unusual presentation for SOD1-ALS: Isolated facial diplegia

Muscle & nerve, 2013-12, Vol.48 (6), p.994-995

2013

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

Nature genetics, 1995-02, Vol.9 (2), p.197-201

1995

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Deletions in the prion protein gene are not associated with CJD

Human molecular genetics, 1993-05, Vol.2 (5), p.541-544

1993

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Executive dysfunction predicts social cognition impairment in amyotrophic lateral sclerosis

Molecular classification of sporadic Creutzfeldt–Jakob disease

The same prion strain causes vCJD and BSE

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. [Addendum: Oct 2, 1997, v. 389 (6650), p. 526.]

Prion protein is necessary for normal synaptic function

Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom : a systematic analysis of predisposing mutations and allelic variation in the PRNP gene

Typing prion isoforms

Biochemical typing of scrapie strains

Addendum Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

Transmission of Creutzfeldt-Jakob Disease from Humans to Transgenic Mice Expressing Chimeric Human-Mouse Prion Protein

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein

Inherited prion disease (PrP lysine 200) in Britain: two case reports

Review: Prion-like mechanisms of transactive response DNA binding protein of 43kDa (TDP-43) in amyotrophic lateral sclerosis (ALS)

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

Administration of Riluzole Oral Suspension During the Different Stages of Amyotrophic Lateral Sclerosis

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion

Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis

Molecular screening of sheep for bovine spongiform encephalopathy

Transmission of fatal familial insomnia to laboratory animals

CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementia

An unusual presentation for SOD1-ALS: Isolated facial diplegia

Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

Deletions in the prion protein gene are not associated with CJD

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