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From: TSS ()
Subject: Re: Scrapie program on hold in Vermont
Date: September 25, 2006 at 10:20 am PST

In Reply to: Scrapie program on hold in Vermont posted by TSS on September 25, 2006 at 9:57 am:

1997 TO 2006. SPORADIC CJD CASES TRIPLED, with phenotype
of 'UNKNOWN' strain growing. ...

Classification of sporadic Creutzfeldt–Jakob disease revisited

Ignazio Cali1, Rudolph Castellani3, Jue Yuan1, Amer Al-Shekhlee2, Mark L. Cohen1, Xiangzhu Xiao1, Francisco J. Moleres1, Piero Parchi4, Wen-Quan Zou1 and Pierluigi Gambetti1
1 Department of Pathology, Case Western Reserve University Cleveland, OH, USA 2 Department of Neurology, Case Western Reserve University Cleveland, OH, USA 3 Division of Neuropathology, Department of Pathology University of Maryland, Baltimore, MD, USA 4 Dipartimento di Scienze Neurologiche, Università di Bologna Bologna, Italy;article=3092;title=CJD%20WATCH

Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD

Anna Krasnianski1, Walter J. Schulz-Schaeffer2, Kai Kallenberg3, Bettina Meissner1, Donald A. Collie5, Sigrun Roeber4, Mario Bartl1, Uta Heinemann1, Daniela Varges1, Hans A. Kretzschmar4 and Inga Zerr1
1 Department of Neurology, Georg-August University Göttingen Germany 2 Department of Neuropathology, Georg-August University Göttingen Germany 3 Department of Neuroradiology, Georg-August University Göttingen Germany 4 Department of Neuropathology, Ludwig-Maximillian University Munich Germany 5 Department of Neuroradiology, Western General Hospital Edinburgh UK;article=3093;title=CJD%20WATCH

Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt–Jakob disease

S. J. Collins1,*, P. Sanchez-Juan2,*, C. L. Masters1, G. M. Klug1, C. van Duijn2, A. Poleggi3, M. Pocchiari3, S. Almonti3, N. Cuadrado-Corrales4, J. de Pedro-Cuesta4, H. Budka5, E. Gelpi5, M. Glatzel6,13, M. Tolnay6, E. Hewer6, I. Zerr7, U. Heinemann7, H. A. Kretszchmar8, G. H. Jansen9, E. Olsen9, E. Mitrova10, A. Alpérovitch11, J.-P. Brandel11, J. Mackenzie12, K. Murray12 and R. G. Will12;article=3090;title=CJD%20WATCH

Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity

Simon Mead, Mark Poulter, Jon Beck, Thomas E. F. Webb, Tracy A. Campbell, Jacqueline M. Linehan, Melanie Desbruslais, Susan Joiner, Jonathan D. F. Wadsworth, Andrew King, Peter Lantos and John Collinge
MRC Prion Unit, Department of Neurodegenerative Diseases, Institute of Neurology and Department of Neuropathology, King's College Hospital London, UK;article=3087;title=CJD%20WATCH


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