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Jenny Vaughan

Showing results (1-10 of 6) with videos related to

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BMJ (Clinical Research Ed.)|February 24, 2021
Should NHS managers be regulated like doctors?Jenny Vaughan, Marcel Levi
Future Healthcare Journal|June 19, 2020
Sacrifice and risk in the time of COVID-19Julia Simons, Jenny Vaughan
BMJ (Clinical Research Ed.)|January 21, 2022
What implications does the Toombes vs Mitchell case have for other healthcare professionals?Ellen Welch, Jenny Vaughan, Kristina Rebecca Cranfield, et al.
BMJ (Clinical Research Ed.)|March 9, 2019
Criminalisation of unintentional error in healthcare in the UK: a perspective from New ZealandRohan Ameratunga, Hilary Klonin, Jenny Vaughan, et al.
Movement Disorders Clinical Practice|October 27, 2018
Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 MutationJose M Bras, Rita J Guerreiro, James T H Teo, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
BMJ (Clinical Research Ed.)|February 24, 2021
Should NHS managers be regulated like doctors?Jenny Vaughan, Marcel Levi
Future Healthcare Journal|June 19, 2020
Sacrifice and risk in the time of COVID-19Julia Simons, Jenny Vaughan
BMJ (Clinical Research Ed.)|January 21, 2022
What implications does the Toombes vs Mitchell case have for other healthcare professionals?Ellen Welch, Jenny Vaughan, Kristina Rebecca Cranfield, et al.
BMJ (Clinical Research Ed.)|March 9, 2019
Criminalisation of unintentional error in healthcare in the UK: a perspective from New ZealandRohan Ameratunga, Hilary Klonin, Jenny Vaughan, et al.
Movement Disorders Clinical Practice|October 27, 2018
Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 MutationJose M Bras, Rita J Guerreiro, James T H Teo, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Pageof 1