Search Results - "Mackenzie, Jan"

Iatrogenic Creutzfeldt-Jakob disease, final assessment by Brown, Paul, Brandel, Jean-Philippe, Sato, Takeshi, Nakamura, Yosikazu, MacKenzie, Jan, Will, Robert G, Ladogana, Anna, Pocchiari, Maurizio, Leschek, Ellen W, Schonberger, Lawrence B

“…The era of iatrogenic Creutzfeldt-Jakob disease (CJD) has nearly closed; only occasional cases with exceptionally long incubation periods are still appearing…”
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Sporadic Creutzfeldt-Jakob Disease in 2 Plasma Product Recipients, United Kingdom by Urwin, Patrick, Thanigaikumar, Kumar, Ironside, James W, Molesworth, Anna, Knight, Richard S, Hewitt, Patricia E, Llewelyn, Charlotte, Mackenzie, Jan, Will, Robert G

“…Sporadic Creutzfeldt-Jakob disease (sCJD) has not been previously reported in patients with clotting disorders treated with fractionated plasma products. We…”
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Validation of diagnostic criteria for variant Creutzfeldt-Jakob disease by Heath, Craig A., Cooper, Sarah A., Murray, Katy, Lowman, Andrea, Henry, Colm, MacLeod, Margaret A., Stewart, Gillian E., Zeidler, Martin, MacKenzie, Jan M., Ironside, James W., Summers, David M., Knight, Richard S. G., Will, Robert G.

“…Objective Variant Creutzfeldt–Jakob disease (vCJD), a novel form of human prion disease, was recognized in 1996. The disease affected a younger cohort than…”
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The role of cerebrospinal fluid proteins as early diagnostic markers for sporadic Creutzfeldt–Jakob disease by Pennington, Catherine, Chohan, Gurjit, Mackenzie, Jan, Andrews, Mary, Will, Robert, Knight, Richard, Green, Alison

“…The utility of cerebrospinal fluid (CSF) proteins such as 14-3-3, tau protein and S-100b as diagnostic markers in the early stages of sporadic…”
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Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain by Brandel, Jean-Philippe, Heath, Craig A., Head, Mark W., Levavasseur, Etienne, Knight, Richard, Laplanche, Jean-Louis, Langeveld, Jan PM, Ironside, James W., Hauw, Jean-Jacques, Mackenzie, Jan, Alpérovitch, Annick, Will, Robert G., Haïk, Stéphane

“…Objective Variant Creutzfeldt–Jakob disease (vCJD) was first reported in the United Kingdom in 1996. Since then, the majority of cases have been observed in…”
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Sporadic Creutzfeldt-Jakob Disease in Adults over 80 Years: A 10-year Review of United Kingdom Surveillance (S18.005) by McDermott, Eugene Ace, Watson, Neil, Tam, Johnny, Centola, John, Kurucu, Hatice, Mackenzie, Jan, Summers, David, Green, Alison, Barria, Marcelo, Smith, Colin, Pal, Suvankar

“…Abstract only…”
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Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance by McDermott, Eugene Ace, Watson, Neil, Tam, Johnny, Centola, John, Kurucu King, Hatice, Mackenzie, Jan, Summers, David, Green, Alison, Barria, Marcelo A, Smith, Colin, Pal, Suvankar

“…Abstract Introduction Sporadic Creutzfeldt-Jakob disease (sCJD) is a rapidly progressive neurodegenerative disease with public health implications. Mean age of…”
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Non-white cases of sporadic Creutzfeldt-Jakob disease: A 28 year review of United Kingdom National Surveillance Data by Langlands, Gavin, Mackenzie, Jan, Graham, Cat, Watson, Neil, Molesworth, Anna, Summers, David, Green, Alison, Smith, Colin, Pal, Suvankar

“…Descriptions of sporadic Creutzfeldt-Jakob disease (sCJD) in non-White populations are limited. Improved understanding may aid diagnoses and case ascertainment…”
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Variant Creutzfeldt‐Jakob disease in a transfusion recipient: coincidence or cause? by Chohan, Gurjit, Llewelyn, Charlotte, Mackenzie, Jan, Cousens, Simon, Kennedy, Angus, Will, Robert, Hewitt, Patricia

“…BACKGROUND: To date there have been four instances of infection transmitted through blood transfusions derived from individuals who later developed variant…”
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Intensity of human prion disease surveillance predicts observed disease incidence by Klug, Genevieve M J A, Wand, Handan, Simpson, Marion, Boyd, Alison, Law, Matthew, Masters, Colin L, Matěj, Radoslav, Howley, Rachel, Farrell, Michael, Breithaupt, Maren, Zerr, Inga, van Duijn, Cornelia, Ibrahim-Verbaas, Carla, Mackenzie, Jan, Will, Robert G, Brandel, Jean-Philippe, Alperovitch, Annick, Budka, Herbert, Kovacs, Gabor G, Jansen, Gerard H, Coulthard, Michael, Collins, Steven J

“…Background Prospective national screening and surveillance programmes serve a range of public health functions. Objectively determining their adequacy and…”
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Investigation of Variant Creutzfeldt-Jakob Disease Implicated Organ or Tissue Transplantation in the United Kingdom by Molesworth, Anna, Yates, Philip, Hewitt, Patricia E, Mackenzie, Jan, Ironside, James W, Galea, George, Ward, Hester J.T

“…BACKGROUNDPerson-to-person transmission of variant Creutzfeldt-Jakob disease (vCJD) has occurred through blood transfusion and could also theoretically occur…”
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Diagnosing variant Creutzfeldt–Jakob disease: a retrospective analysis of the first 150 cases in the UK by Heath, C A, Cooper, S A, Murray, K, Lowman, A, Henry, C, MacLeod, M A, Stewart, G, Zeidler, M, McKenzie, J M, Knight, R S G, Will, R G

“…IntroductionEstablishing an early clinical diagnosis in variant Creutzfeldt–Jakob disease (vCJD) can be difficult, resulting in extended periods of uncertainty…”
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Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: U.K. cases 1991-2002 by Head, Mark W., Bunn, Tristan J. R., Bishop, Matthew T., McLoughlin, Victoria, Lowrie, Suzanne, McKimmie, Clive S., Williams, Michelle C., McCardle, Linda, MacKenzie, Jan, Knight, Richard, Will, Robert G., Ironside, James W.

“…Human prion diseases can occur as an idiopathic disorder (sporadic Creutzfeldt–Jakob disease) or can be acquired, as is the case for variant Creutzfeldt–Jakob…”
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Sporadic Creutzfeldt-Jakob disease and risk of blood transfusion in the United Kingdom by Molesworth, Anna M., Mackenzie, Jan, Everington, Dawn, Knight, Richard S.G., Will, Robert G.

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The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the United Kingdom: a 10 year review by Chohan, Gurjit, Pennington, Catherine, Mackenzie, Jan M, Andrews, Mary M, Everington, Dawn, Will, Robert G, Knight, Richard Sg, Green, Alison Je

“…It is 10 years since the detection of cerebrospinal fluid (CSF) 14-3-3 was included in the diagnostic criteria for sporadic Creutzfeldt-Jakob disease (sCJD) by…”
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Reply by Heath, Craig A., Cooper, Sarah A., Murray, Katy, Lowman, Andrea, Henry, Colm, MacLeod, Margaret A., Stewart, Gillian E., Zeidler, Martin, MacKenzie, Jan M., Ironside, James W., Summers, David M., Knight, Richard S. G., Will, Robert G.

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Reply by Heath, Craig A., Cooper, Sarah A., Murray, Katy, Lowman, Andrea, Henry, Colm, MacLeod, Margaret A., Stewart, Gillian E., Zeidler, Martin, MacKenzie, Jan M., Ironside, James W., Summers, David M., Knight, Richard S. G., Will, Robert G.

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Reply by Heath, Craig A., Cooper, Sarah A., Murray, Katy, Lowman, Andrea, Henry, Colm, MacLeod, Margaret A., Stewart, Gillian E., Zeidler, Martin, MacKenzie, Jan M., Ironside, James W., Summers, David M., Knight, Richard S. G., Will, Robert G.

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Reply by Heath, Craig A, Cooper, Sarah A, Murray, Katy, Lowman, Andrea, Henry, Colm, MacLeod, Margaret A, Stewart, Gillian E, Zeidler, Martin, MacKenzie, Jan M, Ironside, James W, Summers, David M, Knight, Richard S G, Will, Robert G

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Reply by Heath, Craig A, Cooper, Sarah A, Murray, Katy, Mb (Hons), Andrea Lowman, Colm Henrymrcpi, M R C G P, MacLeod, Margaret A, Stewart, Gillian E, Zeidler, Martin, MacKenzie, Jan M, Frcpath, James W Ironside, Summers, David M, Knight, Richard S G, Will, Robert G

“…No abstract is available for this article…”
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