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Jenny Vaughan: Overturning injustice

BMJ (Online), 2019-03, p.l1024

2019

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Should NHS managers be regulated like doctors?

BMJ (Online), 2021-02, Vol.372, p.m4909

2021

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

Brain (London, England : 1878), 2005-12, Vol.128 (12), p.2786-2796

2005

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Post Bawa-Garba: how do we detoxify the climate of fear?

Bulletin of the Royal College of Surgeons of England, 2018-11, Vol.100 (8), p.325

Vaughan, Jenny

2018

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What implications does the Toombes vs Mitchell case have for other healthcare professionals?

BMJ (Online), 2022-01, Vol.376, p.o162

2022

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Criminalisation of unintentional error in healthcare in the UK: a perspective from New Zealand

BMJ (Online), 2019-03, Vol.364, p.l706

2019

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Sacrifice and risk in the time of COVID-19

Future healthcare journal, 2020-06, Vol.7 (2), p.158-160

2020

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Gross negligence manslaughter and the healthcare professional

Bulletin of the Royal College of Surgeons of England, 2016-02, Vol.98 (2), p.60-62

Vaughan, Jenny

2016

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The aftermath of the Sellu case for law and the medical profession

Bulletin of the Royal College of Surgeons of England, 2018-07, Vol.100 (5), p.207-209

2018

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27 Close, Newcastle upon Tyne: Archaeological Investigation, 1994

Archaeologia Aeliana, 2018-01, Vol.47, p.155

2018

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Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease

Neuroreport, 1999-02, Vol.10 (2), p.427-429

1999

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Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-07, Vol.136B (1), p.72-74

2005

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Medical manslaughter: where next?

Bulletin of the Royal College of Surgeons of England, 2018-09, Vol.100 (6), p.251-254

2018

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PARK11 is not linked with Parkinson's disease in European families

European journal of human genetics : EJHG, 2005-02, Vol.13 (2), p.193-197

2005

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Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

The New England journal of medicine, 2000-05, Vol.342 (21), p.1560-1567

2000

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Manslaughter and preventable harm

Trends in urology & men's health, 2015-07, Vol.6 (4), p.38-39

2015

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Excavations at Bamburgh: New Revelations in Light of Recent Investigations at the Core of the Castle Complex

Archaeological journal (London), 2017-01, Vol.174 (1), p.146-210

2017

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Undergraduate Research in Art: A Guide for Students

1, 2019

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Waggonways and brickworks : insights into the industrial heritage of Walker

Archaeologia Aeliana, 2013-01, Vol.42, p.269-304

2013

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Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

American journal of human genetics, 2001-03, Vol.68 (3), p.617-626

2001

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Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease

Neuroreport, 1999-02, Vol.10 (2), p.427-429

1999

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Sequencing of the α-Synuclein Gene in a Large Series of Cases of Familial Parkinson's Disease Fails to Reveal any Further Mutations

Human molecular genetics, 1998-04, Vol.7 (4), p.751-753

1998

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Atypical Parkinsonism‐Dystonia Syndrome Caused by a Novel DJ1 Mutation

Movement disorders clinical practice (Hoboken, N.J.), 2014-04, Vol.1 (1), p.45-49

2014

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The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

Annals of neurology, 1998-08, Vol.44 (2), p.270-273

1998

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The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

Neuroscience letters, 1999-07, Vol.270 (1), p.1-4

1999

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Jenny Vaughan: Overturning injustice

Should NHS managers be regulated like doctors?

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

Post Bawa-Garba: how do we detoxify the climate of fear?

What implications does the Toombes vs Mitchell case have for other healthcare professionals?

Criminalisation of unintentional error in healthcare in the UK: a perspective from New Zealand

Sacrifice and risk in the time of COVID-19

Gross negligence manslaughter and the healthcare professional

The aftermath of the Sellu case for law and the medical profession

27 Close, Newcastle upon Tyne: Archaeological Investigation, 1994

Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

Medical manslaughter: where next?

PARK11 is not linked with Parkinson's disease in European families

Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

Manslaughter and preventable harm

Excavations at Bamburgh: New Revelations in Light of Recent Investigations at the Core of the Castle Complex

Undergraduate Research in Art: A Guide for Students

Waggonways and brickworks : insights into the industrial heritage of Walker

Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease

Sequencing of the α-Synuclein Gene in a Large Series of Cases of Familial Parkinson's Disease Fails to Reveal any Further Mutations

Atypical Parkinsonism‐Dystonia Syndrome Caused by a Novel DJ1 Mutation

The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

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