Jenny Vaughan: Overturning injustice

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Should NHS managers be regulated like doctors? by Vaughan, Jenny, Levi, Marcel

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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 by Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., Healy, Daniel G., Gilks, William P., Sweeney, Mary G., Ganguly, Milan, Gibbons, Vaneesha, Gandhi, Sonia, Vaughan, Jenny, Eunson, Louise H., Katzenschlager, Regina, Gayton, Juliet, Lennox, Graham, Revesz, Tamas, Nicholl, David, Bhatia, Kailash P., Quinn, Niall, Brooks, David, Lees, Andrew J., Davis, Mary B., Piccini, Paola, Singleton, Andrew B., Wood, Nicholas W.

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What implications does the Toombes vs Mitchell case have for other healthcare professionals? by Welch, Ellen, Vaughan, Jenny, Cranfield, Kristina Rebecca, Mehdian, Roshana

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Criminalisation of unintentional error in healthcare in the UK: a perspective from New Zealand by Ameratunga, Rohan, Klonin, Hilary, Vaughan, Jenny, Merry, Alan, Cusack, Jonathan

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Sacrifice and risk in the time of COVID-19 by Simons, Julia, Vaughan, Jenny

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Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease by Martinez, Maria, Brice, Alexis, Vaughan, Jenny R., Zimprich, Alexander, Breteler, Monique M.B., Meco, Giuseppe, Filla, Alessandro, Farrer, Matthew J., Bétard, Christine, Singleton, Andrew, Hardy, John, De Michele, Giuseppe, Bonifati, Vincenzo, Oostra, Ben A., Gasser, Thomas, Wood, Nick W., Dürr, Alexandra

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Manslaughter and preventable harm by Kirby, Roger, Franklin, Ian, Vaughan, Jenny

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Excavations at Bamburgh: New Revelations in Light of Recent Investigations at the Core of the Castle Complex by Kirton, Joanne, Young, Graeme

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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 by Periquet, Magali, Lücking, Christoph B., Vaughan, Jenny R., Bonifati, Vincenzo, Dürr, Alexandra, De Michele, Giuseppe, Horstink, Martin W., Farrer, Matt, Illarioshkin, Sergei N., Pollak, Pierre, Borg, Michel, Brefel-Courbon, Christine, Denefle, Patrice, Meco, Giuseppe, Gasser, Thomas, Breteler, Monique M.B., Wood, Nick W., Agid, Yves, Brice, Alexis

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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 by Vaughan, Jenny R., Farrer, Matthew J., Wszolek, Zbigniew K., Gasser, Thomas, Durr, Alexandra, Agid, Yves, Bonifati, Vincenzo, DeMichele, Giuseppe, Volpe, Gianpiero, Lincoln, Sarah, Breteler, Monique, Meco, Giuseppe, Brice, Alexis, David Marsden, C., Hardy, John, Wood, Nicholas W.

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Atypical Parkinsonism‐Dystonia Syndrome Caused by a Novel DJ1 Mutation by Bras, Jose M., Guerreiro, Rita J., Teo, James T.H., Darwent, Lee, Vaughan, Jenny, Molloy, Sophie, Hardy, John, Schneider, Susanne A.

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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 by Harhangi, B.Sanjay, Farrer, Matthew J., Lincoln, Sarah, Bonifati, Vincenzo, Meco, Giuseppe, De Michele, Giuseppe, Brice, Alexis, Dürr, Alexandra, Martinez, Maria, Gasser, Thomas, Bereznai, Benjamin, Vaughan, Jenny R., Wood, Nicholas W., Hardy, John, Oostra, Ben A., Breteler, Monique M.B.

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Detailed genotyping demonstrates association between the slow acetylator genotype for N-Acetyltransferase 2 (NAT2) and familial parkinson's disease by Bandmann, Oliver, Vaughan, Jenny R., Holmans, Peter, Marsden, C. David, Wood, Nicholas W.

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No pathogenic mutations in the synphilin-1 gene in Parkinson's disease by Bandopadhyay, Rina, de Silva, Rohan, Khan, Naheed, Graham, Elizabeth, Vaughan, Jenny, Engelender, Simone, Ross, Christopher, Morris, Huw, Morris, Christopher, Wood, Nicholas W, Daniel, Susan, Lees, Andrew

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Mutations in the gene encoding human persyn are not associated with amyotrophic lateral sclerosis or familial Parkinson's disease by Flowers, Joanna M, Leigh, P.Nigel, Davies, Alun M, Ninkina, Natalia N, Buchman, Vladimir L, Vaughan, Jenny, Wood, Nick W, Powell, John F

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CUTTING EDGE by Vaughan, Jenny

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Why Didn't I Know This Africa? by Vaughan, Jenny

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OMG! That's SO Five Decades Ago by Vaughan, Jenny

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Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 Mutation by Bras, Jose M, Guerreiro, Rita J, Teo, James T H, Darwent, Lee, Vaughan, Jenny, Molloy, Sophie, Hardy, John, Schneider, Susanne A

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