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	Less protease-resistant PrP in a patient with sporadic CJD treated with intraventricular pentosan polysulphate. [My Copy] Acta neurologica Scandinavica (5 October 2009) by T. Terada, Y. Tsuboi, T. Obi, et al.K. Doh-Ura, S. Murayama, T. Kitamoto, T. Yamada, K. Mizoguchi posted to treatment scjd pentosan cjd by applebyb on 2009-10-09 12:41:59 as
	Updated clinical diagnostic criteria for sporadic Creutzfeldt Jakob disease. [My Copy] Brain : a journal of neurology (22 September 2009) by I. Zerr, K. Kallenberg, D. M. Summers, et al.C. Romero, A. Taratuto, U. Heinemann, M. Breithaupt, D. Varges, B. Meissner, A. Ladogana, M. Schuur, S. Haik, S. J. Collins, Gerard H. Jansen, G. B. Stokin, J. Pimentel, E. Hewer, D. Collie, P. Smith, H. Roberts, J. P. Brandel, C. van Duijn, M. Pocchiari, C. Begue, P. Cras, R. G. Will, P. Sanchez-Juan posted to scjd neuroimaging mri diagnosis cjd by applebyb on 2009-09-24 20:11:57 as
	MRI lesion profiles in sporadic Creutzfeldt-Jakob disease. [My Copy] Neurology, Vol. 72, No. 23. (9 June 2009), pp. 1994-2001. by B. Meissner, K. Kallenberg, P. Sanchez-Juan, et al.D. Collie, D. M. Summers, S. Almonti, S. J. Collins, P. Smith, P. Cras, G. H. Jansen, J. P. Brandel, M. B. Coulthart, H. Roberts, B. Van Everbroeck, D. Galanaud, V. Mellina, R. G. Will, I. Zerr posted to cjd diagnosis mri scjd by applebyb on 2009-08-07 19:49:31 as
	Increased frequency of positive family history of dementia in sporadic CJD [My Copy] Neurobiology of Aging, Vol. 30, No. 4. (April 2009), pp. 615-621. by Anna Krasnianski, Nicolas von Ahsen, Uta Heinemann, et al.Bettina Meissner, Walter J. Schulz-Schaeffer, Hans A. Kretzschmar, Victor W. Armstrong, Inga Zerr posted to cjd genetics risk scjd by applebyb on 2009-06-26 11:59:31 as
	Innocent white blood cells in sporadic Creutzfeldt-Jakob disease? [My Copy] Laboratory investigation; a journal of technical methods and pathology, Vol. 89, No. 6. (June 2009), pp. 612-613. by S. T. Lee, J. K. Roh posted to cjd pathogenesis prion scjd by applebyb on 2009-06-19 12:34:09 as
	The role of cerebrospinal fluid proteins as early diagnostic markers for sporadic Creutzfeldt-Jakob disease. [My Copy] Neuroscience letters, Vol. 455, No. 1. (8 May 2009), pp. 56-59. by Catherine Pennington, Gurjit Chohan, Jan Mackenzie, et al.Mary Andrews, Robert Will, Richard Knight, Alison Green posted to cjd csf diagnosis scjd by applebyb on 2009-05-15 18:17:39 as along with 1 person nns1987
	'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2 [My Copy] J Neurol Neurosurg Psychiatry, Vol. 80, No. 2. (1 February 2009), pp. 244-246. by C. La Morgia, P. Parchi, S. Capellari, et al.R. Lodi, C. Tonon, R. Rinaldi, S. Mondini, F. Cirignotta posted to genetics phenotype prion scjd by applebyb on 2009-01-17 01:10:48 as
	De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis [My Copy] Proceedings of the National Academy of Sciences, Vol. 106, No. 1. (6 January 2009), pp. 304-309. by Christina J. Sigurdson, Nilsson, Simone Hornemann, et al.Mathias Heikenwalder, Giuseppe Manco, Petra Schwarz, David Ott, Thomas Rülicke, Pawel P. Liberski, Christian Julius, Jeppe Falsig, Lothar Stitz, Kurt Wüthrich, Adriano Aguzzi posted to prion scjd by applebyb on 2009-01-13 01:41:37 as
	Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profiles [My Copy] Journal of Neurology, Vol. 255, No. 10. (1 October 2008), pp. 1464-1472. by Katharina Stoeck, Klaus Hess, Lorenz Amsler, et al.Tobias Eckert, Dieter Zimmermann, Adriano Aguzzi, Markus Glatzel posted to cjd phenotype prion_disease scjd by applebyb on 2008-11-21 14:37:22 as
	An unusually presenting case of sCJD-The VV1 subtype. [My Copy] Clinical neurology and neurosurgery (6 November 2008) by Kaloyan S S. Tanev, Mimi Yilma posted to cjd molecular_subtype phenotype prion_disease scjd vv1 by applebyb on 2008-11-21 14:33:03 as
	Review. The origin of the prion agent of kuru: molecular and biological strain typing. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3747-3753. by Jonathan D. Wadsworth, Susan Joiner, Jacqueline M. Linehan, Emmanuel A. Asante, Sebastian Brandner, John Collinge posted to cjd icjd kuru phenotype prion prpsc scjd strain by applebyb on 2008-10-19 23:57:27 as along with 1 person bmezmer
	Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients. [My Copy] Acta neuropathologica (28 August 2008) by Atsushi Kobayashi, Kunimasa Arima, Masafumi Ogawa, Miho Murata, Takahiro Fukuda, Tetsuyuki Kitamoto posted to mm1 plaques scjd survival by applebyb on 2008-09-01 23:06:15 as
	First Report of Creutzfeldt-Jakob Disease Occurring in 2 Siblings Unexplained by PRNP Mutation. [My Copy] Journal of neuropathology and experimental neurology (19 August 2008) by Thomas E. Webb, Suvankar Pal, Durrenajaf Siddique, et al.Dominic C. Heaney, Jacqueline M. Linehan, Jonathan D. Wadsworth, Susan Joiner, Jon Beck, Stephen J. Wroe, Valerie Stevenson, Sebastian Brandner, Simon Mead, John Collinge posted to fcjd prnp scjd by applebyb on 2008-08-26 02:14:43 as
	An atypical form of sporadic panencephalopathic Creutzfeldt-Jakob disease in Japan. [My Copy] Neuropathol Appl Neurobiol, Vol. 29, No. 1. (February 2003), pp. 77-80. by S. Yamamoto, H. Furukawa, T. Kitamoto, et al.Y. Takamaru, N. Morita, M. Yasuda, Y. Okada, H. Sawa, K. Nagashima posted to prion_diseases scjd cjd by applebyb on 2008-03-30 23:02:20 as
	Classification of sporadic CreutzfeldtJakob disease revisited [My Copy] Brain, Vol. 129, No. 9. (September 2006), pp. 2266-2277. by Cali, Ignazio, Castellani, et al. Rudolph, Yuan, Jue, Al-Shekhlee, Amer, Cohen, L. Mark, Xiao, Xiangzhu, Moleres, J. Francisco, Parchi, Piero, Zou, Wen-Quan, Gambetti, Pierluigi posted to classification prion_diseases scjd cjd by applebyb on 2008-03-30 23:00:34 as
	Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice [My Copy] Proceedings of the National Academy of Sciences, Vol. 105, No. 10. (11 March 2008), pp. 3885-3890. by Jonathan D. Wadsworth, Susan Joiner, Jacqueline M. Linehan, et al.Melanie Desbruslais, Katie Fox, Sharon Cooper, Sabrina Cronier, Emmanuel A. Asante, Simon Mead, Sebastian Brandner, Andrew F. Hill, John Collinge posted to cre kuru scjd by applebyb on 2008-03-12 00:47:51 as
	14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes. [My Copy] Neurobiology of aging, Vol. 30, No. 11. (5 November 2009), pp. 1842-1850. by K. Gmitterová, U. Heinemann, M. Bodemer, et al.A. Krasnianski, B. Meissner, H. A. Kretzschmar, I. Zerr posted to 14-3-3 codon129 scjd by applebyb on 2008-03-12 00:40:41 as

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Tag scjd [17 articles] Export Sort

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