Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

Por Bishop, Matthew T., Will, Robert G., Manson, Jean C.
Publicado em 2010

The regulatory challenge /

Por Bishop, Matthew, Kay, John Anderson, Mayer, Colin P.
Publicado em 1996

Neurosurgical strategies for Gilles de la Tourette’s syndrome

Por Mukhida, Karim, Bishop, Matthew, Hong, Murray, Mendez, Ivar
Publicado em 2008

Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease

Por Bishop, Matthew T, Sanchez-Juan, Pascual, Knight, Richard SG
Publicado em 2013

Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease

Por Bishop, Matthew T, Kovacs, Gabor G, Sanchez-Juan, Pascual, Knight, Richard SG
Publicado em 2008

PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism

Por Bishop, Matthew T, Pennington, Catherine, Heath, Craig A, Will, Robert G, Knight, Richard SG
Publicado em 2009

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease

Por Bishop, Matthew T., Diack, Abigail B., Ritchie, Diane L., Ironside, James W., Will, Robert G., Manson, Jean C.
Publicado em 2013

Functional properties of dopamine neurons and co-expression of vasoactive intestinal polypeptide in the dorsal raphe nucleus and ventro-lateral periaqueductal grey

Por Dougalis, Antonios G., Matthews, Gillian A. C., Bishop, Matthew W., Brischoux, Frédéric, Kobayashi, Kazuto, Ungless, Mark A.
Publicado no Eur J Neurosci (2012)

Hyperexcitable Substantia Nigra Dopamine Neurons in PINK1- and HtrA2/Omi-Deficient Mice

Por Bishop, Matthew W., Chakraborty, Subhojit, Matthews, Gillian A. C., Dougalis, Antonios, Wood, Nicholas W., Festenstein, Richard, Ungless, Mark A.
Publicado em 2010

Gerstmann-Straüssler-Scheinker disease: Novel PRNP mutation and VGKC-complex antibodies

Por Jones, Matthew, Odunsi, Sola, du Plessis, Daniel, Vincent, Angela, Bishop, Matthew, Head, Mark W., Ironside, James W., Gow, David
Publicado em 2014

No Major Change in vCJD Agent Strain after Secondary Transmission via Blood Transfusion

Por Bishop, Matthew T., Ritchie, Diane L., Will, Robert G., Ironside, James W., Head, Mark W., Thomson, Val, Bruce, Moira, Manson, Jean C.
Publicado em 2008

A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease

Por Sanchez-Juan, Pascual, Bishop , Matthew T, Croes , Esther A, Knight , Richard SG, Will , Robert G, van Duijn , Cornelia M, Manson , Jean C
Publicado em 2011

No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

Por Sánchez-Juan, Pascual, Bishop, Matthew T, Green, Alison, Giannattasio, Claudia, Arias-Vasquez, Alejandro, Poleggi, Anna, Knight, Richard SG, van Duijn, Cornelia M
Publicado em 2007

Considerations for Exchanging and Sharing Medical Images for Improved Collaboration and Patient Care: HIMSS-SIIM Collaborative White Paper

Por Vreeland, Amy, Persons, Kenneth R., Primo, Henri (Rik), Bishop, Matthew, Garriott, Kimberley M., Doyle, Matthew K., Silver, Elliott, Brown, Danielle M., Bashall, Chris
Publicado no J Digit Imaging (2016)

Emergency Physician-performed Transesophageal Echocardiography in Simulated Cardiac Arrest

Por Byars, Don V., Tozer, Jordan, Joyce, John M., Vitto, Michael J., Taylor, Lindsay, Kayagil, Turan, Jones, Matt, Bishop, Matthew, Knapp, Barry, Evans, David
Publicado no West J Emerg Med (2017)

Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study

Por Ironside, James W, Bishop, Matthew T, Connolly, Kelly, Hegazy, Doha, Lowrie, Suzanne, Le Grice, Margaret, Ritchie, Diane L, McCardle, Linda M, Hilton, David A
Publicado em 2006

Peripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob Disease : An Immunohistochemical, Quantitative, and Biochemical Study

Por Head, Mark W., Ritchie, Diane, Smith, Nadine, McLoughlin, Victoria, Nailon, William, Samad, Sazia, Masson, Stephen, Bishop, Matthew, McCardle, Linda, Ironside, James W.
Publicado em 2004

Constant Transmission Properties of Variant Creutzfeldt-Jakob Disease in 5 Countries

Por Diack, Abigail B., Ritchie, Diane, Bishop, Matthew, Pinion, Victoria, Brandel, Jean-Philippe, Haik, Stephane, Tagliavini, Fabrizio, Van Duijn, Cornelia, Belay, Ermias D., Gambetti, Pierluigi, Schonberger, Lawrence B., Piccardo, Pedro, Will, Robert G., Manson, Jean C.
Publicado em 2012

Human Prion Diseases in The Netherlands (1998–2009): Clinical, Genetic and Molecular Aspects

Por Jansen, Casper, Parchi, Piero, Capellari, Sabina, Ibrahim-Verbaas, Carla A., Schuur, Maaike, Strammiello, Rosaria, Corrado, Patrizia, Bishop, Matthew T., van Gool, Willem A., Verbeek, Marcel M., Baas, Frank, van Saane, Wesley, Spliet, Wim G. M., Jansen, Gerard H., van Duijn, Cornelia M., Rozemuller, Annemieke J. M.
Publicado em 2012

A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk

Por Sanchez-Juan, Pascual, Bishop, Matthew T., Kovacs, Gabor G., Calero, Miguel, Aulchenko, Yurii S., Ladogana, Anna, Boyd, Alison, Lewis, Victoria, Ponto, Claudia, Calero, Olga, Poleggi, Anna, Carracedo, Ángel, van der Lee, Sven J., Ströbel, Thomas, Rivadeneira, Fernando, Hofman, Albert, Haïk, Stéphane, Combarros, Onofre, Berciano, José, Uitterlinden, Andre G., Collins, Steven J., Budka, Herbert, Brandel, Jean-Philippe, Laplanche, Jean Louis, Pocchiari, Maurizio, Zerr, Inga, Knight, Richard S. G., Will, Robert G., van Duijn, Cornelia M.
Publicado no PLoS One (2015)