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NCBA, R-CALF, COOL, USDA (No Politics!)
Two cases of variant Creutzfeldt-Jakob disease SPAIN 07-08
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<blockquote data-quote="flounder" data-source="post: 524887" data-attributes="member: 3519"><p>Rapid communications </p><p> </p><p>Two cases of variant Creutzfeldt-Jakob disease reported in Spain in 2007 and 2008 </p><p></p><p></p><p>volume 13 </p><p>issue 15 </p><p>publication date April 2008 </p><p> </p><p> </p><p>How to cite this article, click here. </p><p> </p><p>Indexed in MedLine as: Euro Surveill 2008;13(15) Published online April 2008 </p><p>Two cases of variant Creutzfeldt-Jakob disease reported in Spain in 2007 and 2008 </p><p> </p><p></p><p> </p><p></p><p>J de Pedro Cuesta (<a href="mailto:jpedro@isciii.es">jpedro@isciii.es</a>" onclick="window.open(this.href);return false<img src="data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7" class="smilie smilie--sprite smilie--sprite2" alt=";)" title="Wink ;)" loading="lazy" data-shortname=";)" />, Instituto de Salud Carlos III, Department of Applied Epidemiology, National Centre of Epidemiology, Madrid, Spain</p><p></p><p> </p><p></p><p>--------------------------------------------------------------------------------</p><p> </p><p>In 2005, the first case of variant Creutzfeldt-Jakob disease (vCJD) was reported in Spain, in a woman born in 1978 with clinical onset of symptoms in 2004 [1]. She subsequently died in 2005.</p><p></p><p>Recently, two more laboratory-confirmed vCJD cases were reported to the Spanish CJD state registry. In February 2006, a woman born in 1957 developed progressive cognitive deterioration, and died in December 2007 with suspected sporadic CJD (typical EEG in October 2007) MM at codon 129 and no mutations in PRPN gene. A man born in 1967 had onset in May 2007 with psychiatric symptoms, and after several months developed progressive cognitive decline with dementia, typical MRI, MM at codon 129, no mutations in PRPN gene. He died in February 2008. Post-mortem, neuropathology with histochemistry confirmed vCJD in both cases. No clear specific dietary habits, blood donations or reception were recorded. Neither case appears to have visited the United Kingdom before 2004. </p><p></p><p>The latest two cases were resident in the same region of the country, Castilla y Leon, but no link between them was established.</p><p> </p><p></p><p>--------------------------------------------------------------------------------</p><p> </p><p>References </p><p></p><p>Centro Nacional de Epidemiología, Instituto de Salud Carlos III. First case of vCJD reported in Spain. Euro Surveill. 2005;10(8):E050804.1. Available from: <a href="http://www.eurosurveillance.org/ew/2005/050804.asp#1" target="_blank">http://www.eurosurveillance.org/ew/2005/050804.asp#1</a></p><p></p><p> </p><p></p><p></p><p> </p><p></p><p>Citation style for this article: . Two cases of variant Creutzfeldt-Jakob disease reported in Spain in 2007 and 2008. Euro Surveill 2008;13(15). Available online: <a href="http://www.eurosurveillance.org/edition/v13n15/080410_3.asp" target="_blank">http://www.eurosurveillance.org/edition ... 0410_3.asp</a> </p><p></p><p></p><p>*Acquired in UK</p><p>** Acquired in Saudi Arabia</p><p>*** Includes 17 inconclusive and 9 pending (1 from 2006, 8 from 2007.</p><p>**** Includes 17 non-vCJD type unknown (2 from 1996, 2 from 1997, 1</p><p>from 2001, 1 from 2003, 4 from 2004, 3 from 2005, 4 from 2006) and 36</p><p>type pending (2 from 2005, 8 from 2006, 26 from 2007).</p><p></p><p>Notes:</p><p></p><p>-- Cases are listed based on the year of death when available. If the</p><p>year of death is not available, the year of sample receipt is used.</p><p></p><p>-- Referrals: Cases with possible or probable prion disease from</p><p>which brain tissue or blood in the case of familial disease were</p><p>submitted.</p><p></p><p>-- Inconclusive: Cases in which the samples were not sufficient to</p><p>make a diagnosis.</p><p></p><p>-- Non-vCJD type unknown are cases in which the tissue submitted was</p><p>adequate to establish the presence but not the type; in all cases,</p><p>vCJD could be excluded.</p><p></p><p>--</p><p></p><p>Terry S. Singeltary Sr. <flounder9@verizon.net></p><p></p><p>[In submitting these data, Terry S. Singeltary Sr. draws attention to</p><p>the steady increase in the "type unknown" category, which, according</p><p>to their definition, comprises cases in which vCJD could be excluded.</p><p>The total of 26 cases for the current year (2007) is disturbing,</p><p>possibly symptomatic of the circulation of novel agents.</p><p>Characterization of these agents should be given a high priority. -</p><p>Mod.CP]</p><p></p><p><a href="http://www.promedmail.org/pls/askus/f?p=2400:1001:6833194127530602005::NO::F2400_P1001_BACK_PAGE,F2400_P1001_PUB_MAIL_ID:1010,39963" target="_blank">http://www.promedmail.org/pls/askus/f?p ... 1010,39963</a></p><p></p><p>There is a growing number of human CJD cases, and they were presented</p><p>last week in San Francisco by Luigi Gambatti(?) from his CJD</p><p>surveillance collection.</p><p></p><p>He estimates that it may be up to 14 or 15 persons which display</p><p>selectively SPRPSC and practically no detected RPRPSC proteins.</p><p></p><p><a href="http://www.fda.gov/ohrms/dockets/ac/06/transcripts/1006-4240t1.htm" target="_blank">http://www.fda.gov/ohrms/dockets/ac/06/ ... 4240t1.htm</a></p><p></p><p><a href="http://www.fda.gov/ohrms/dockets/ac/06/transcripts/2006-4240t1.pdf" target="_blank">http://www.fda.gov/ohrms/dockets/ac/06/ ... 4240t1.pdf</a></p><p></p><p>JOURNAL OF NEUROLOGY</p><p></p><p>MARCH 26, 2003</p><p></p><p>RE-Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob</p><p></p><p>disease in the United States</p><p></p><p>Email Terry S. Singeltary:</p><p></p><p><a href="mailto:flounder@wt.net">flounder@wt.net</a>" onclick="window.open(this.href);return false;</p><p></p><p>I lost my mother to hvCJD (Heidenhain Variant CJD). I would like to</p><p></p><p>comment on the CDC's attempts to monitor the occurrence of emerging</p><p></p><p>forms of CJD. Asante, Collinge et al [1] have reported that BSE</p><p></p><p>transmission to the 129-methionine genotype can lead to an alternate</p><p></p><p>phenotype that is indistinguishable from type 2 PrPSc, the commonest</p><p></p><p>sporadic CJD. However, CJD and all human TSEs are not reportable</p><p></p><p>nationally. CJD and all human TSEs must be made reportable in every</p><p></p><p>state and internationally. I hope that the CDC does not continue to</p><p></p><p>expect us to still believe that the 85%+ of all CJD cases which are</p><p></p><p>sporadic are all spontaneous, without route/source. We have many TSEs in</p><p></p><p>the USA in both animal and man. CWD in deer/elk is spreading rapidly and</p><p></p><p>CWD does transmit to mink, ferret, cattle, and squirrel monkey by</p><p></p><p>intracerebral inoculation. With the known incubation periods in other</p><p></p><p>TSEs, oral transmission studies of CWD may take much longer. Every</p><p></p><p>victim/family of CJD/TSEs should be asked about route and source of this</p><p></p><p>agent. To prolong this will only spread the agent and needlessly expose</p><p></p><p>others. In light of the findings of Asante and Collinge et al, there</p><p></p><p>should be drastic measures to safeguard the medical and surgical arena</p><p></p><p>from sporadic CJDs and all human TSEs. I only ponder how many sporadic</p><p></p><p>CJDs in the USA are type 2 PrPSc?</p><p></p><p><a href="http://www.neurology.org/cgi/eletters/60/2/176#535" target="_blank">http://www.neurology.org/cgi/eletters/60/2/176#535</a></p><p></p><p>THE PATHOLOGICAL PROTEIN</p><p></p><p>Hardcover, 304 pages plus photos and illustrations. ISBN 0-387-95508-9</p><p></p><p>June 2003</p><p></p><p>BY Philip Yam</p><p></p><p>CHAPTER 14 LAYING ODDS</p><p></p><p>Answering critics like Terry Singeltary, who feels that the U.S.</p><p>under-counts CJD, Schonberger conceded that the current surveillance</p><p>system has errors but stated that most of the errors will be confined</p><p>to the older population.</p><p></p><p><a href="http://www.thepathologicalprotein.com/" target="_blank">http://www.thepathologicalprotein.com/</a></p><p></p><p>doi:10.1016/S1473-3099(03)00715-1</p><p>Copyright © 2003 Published by Elsevier Ltd.</p><p>Newsdesk</p><p></p><p>Tracking spongiform encephalopathies in North America</p><p></p><p>Xavier Bosch</p><p></p><p>Available online 29 July 2003.</p><p>Volume 3, Issue 8, August 2003, Page 463</p><p></p><p>My name is Terry S Singeltary Sr, and I live in Bacliff, Texas. I lost</p><p>my mom to hvCJD (Heidenhain variant CJD) and have been searching for</p><p>answers ever since. What I have found is that we have not been told</p><p>the truth. CWD in deer and elk is a small portion of a much bigger</p><p>problem." ...</p><p></p><p><a href="http://www.thelancet.com/journals/laninf/article/PIIS1473309903007151/fulltext" target="_blank">http://www.thelancet.com/journals/lanin ... 1/fulltext</a></p><p></p><p><a href="http://download.thelancet.com/pdfs/journals/1473-3099/PIIS1473309903007151.pdf" target="_blank">http://download.thelancet.com/pdfs/jour ... 007151.pdf</a></p><p></p><p>Diagnosis and Reporting of Creutzfeldt-Jakob Disease</p><p></p><p>Singeltary, Sr et al. JAMA.2001; 285: 733-734.</p><p></p><p><a href="http://jama.ama-assn.org/http://www.neurology.org/cgi/eletters/60/2/176#535" target="_blank">http://jama.ama-assn.org/http://www.neu ... /2/176#535</a></p><p></p><p>APHIS-2006-0041-0006 TSE advisory committee for the meeting December</p><p>15, 2006</p><p></p><p><a href="http://www.regulations.gov/fdmspublic/ContentViewer?objectId=09000064801f3413&disposition=attachment&contentType=msw8" target="_blank">http://www.regulations.gov/fdmspublic/C ... tType=msw8</a></p><p></p><p>Subject: [Docket No. FSIS-2006-0011] FSIS Harvard Risk Assessment of</p><p>Bovine Spongiform Encephalopathy (BSE)</p><p></p><p><a href="http://www.fsis.usda.gov/OPPDE/Comments/2006-0011/2006-0011-1.pdf" target="_blank">http://www.fsis.usda.gov/OPPDE/Comments ... 0011-1.pdf</a></p><p></p><p>[Docket No. 03-025IFA] FSIS Prohibition of the Use of Specified Risk</p><p>Materials for Human Food and Requirement for the Disposition of</p><p>Non-Ambulatory Disabled Cattle</p><p></p><p>9/13/2005</p><p></p><p><a href="http://www.fsis.usda.gov/OPPDE/Comments/03-025IFA/03-025IFA-2.pdf" target="_blank">http://www.fsis.usda.gov/OPPDE/Comments ... 5IFA-2.pdf</a></p><p></p><p>2 January 2000</p><p></p><p>British Medical Journal</p><p></p><p>U.S. Scientist should be concerned with a CJD epidemic in the U.S., as</p><p>well</p><p></p><p><a href="http://www.bmj.com/cgi/eletters/320/7226/8/b#6117" target="_blank">http://www.bmj.com/cgi/eletters/320/7226/8/b#6117</a></p><p></p><p>15 November 1999</p><p></p><p>British Medical Journal</p><p></p><p>vCJD in the USA * BSE in U.S.</p><p></p><p><a href="http://www.bmj.com/cgi/eletters/319/7220/1312/b#5406" target="_blank">http://www.bmj.com/cgi/eletters/319/7220/1312/b#5406</a></p><p></p><p>Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob</p><p>disease in the United States</p><p></p><p><a href="http://cjdusa.blogspot.com/" target="_blank">http://cjdusa.blogspot.com/</a></p><p></p><p>Creutzfeldt Jakob Disease</p><p></p><p><a href="http://creutzfeldt-jakob-disease.blogspot.com/" target="_blank">http://creutzfeldt-jakob-disease.blogspot.com/</a></p><p></p><p>Creutzfeldt-Jakob Disease, Prion Protein Gene Codon 129VV, and a Novel</p><p>PrPSc ype in a Young British Woman</p><p></p><p><a href="http://creutzfeldt-jakob-disease.blogspot.com/2008/01/creutzfeldt-jakob-disease-prion-protein.html" target="_blank">http://creutzfeldt-jakob-disease.blogsp ... otein.html</a></p><p></p><p>CJD QUESTIONNAIRE</p><p></p><p><a href="http://cjdquestionnaire.blogspot.com/" target="_blank">http://cjdquestionnaire.blogspot.com/</a></p><p></p><p>ANIMAL HEALTH REPORT 2006 (BSE h-BASE EVENT IN ALABAMA, Scrapie, and CWD)</p><p></p><p><a href="http://animalhealthreport2006.blogspot.com/" target="_blank">http://animalhealthreport2006.blogspot.com/</a></p><p></p><p>CREUTZFELDT JAKOB DISEASE MAD COW BASE UPDATE USA</p><p></p><p><a href="http://cjdmadcowbaseoct2007.blogspot.com/" target="_blank">http://cjdmadcowbaseoct2007.blogspot.com/</a></p><p></p><p>Friday, January 11, 2008</p><p></p><p>CJD HUMAN TSE REPORT UK, USA, CANADA, and Mexico JANUARY 2008</p><p></p><p><a href="http://cjdmadcowbaseoct2007.blogspot.com/2008/01/cjd-human-tse-report-uk-usa-canada-and.html" target="_blank">http://cjdmadcowbaseoct2007.blogspot.co ... a-and.html</a></p><p></p><p>Friday, February 8, 2008</p><p></p><p>Creutzfeldt Jakob Disease Delaware UPDATE</p><p></p><p><a href="http://cjdmadcowbaseoct2007.blogspot.com/2008/02/creutzfeldt-jakob-disease-delaware.html" target="_blank">http://cjdmadcowbaseoct2007.blogspot.co ... aware.html</a></p><p></p><p>CREUTZFELDT JAKOB DISEASE TEXAS</p><p></p><p><a href="http://cjdtexas.blogspot.com/" target="_blank">http://cjdtexas.blogspot.com/</a></p><p></p><p>Friday, January 25, 2008</p><p></p><p>January 2008 Update on Feed Enforcement Activities to Limit the Spread</p><p>of BSE</p><p></p><p><a href="http://madcowspontaneousnot.blogspot.com/2008/01/january-2008-update-on-feed-enforcement.html" target="_blank">http://madcowspontaneousnot.blogspot.co ... ement.html</a></p><p></p><p><a href="http://madcowspontaneousnot.blogspot.com/" target="_blank">http://madcowspontaneousnot.blogspot.com/</a></p><p></p><p>BSE BASE MAD COW TESTING TEXAS, USA, AND CANADA</p><p></p><p><a href="http://madcowtesting.blogspot.com/" target="_blank">http://madcowtesting.blogspot.com/</a></p><p></p><p>NOR-98 ATYPICAL SCRAPIE USA UPDATE AS AT OCT 2007</p><p></p><p><a href="http://nor-98.blogspot.com/" target="_blank">http://nor-98.blogspot.com/</a></p><p></p><p><a href="http://scrapie-usa.blogspot.com/" target="_blank">http://scrapie-usa.blogspot.com/</a></p><p></p><p>Sunday, March 16, 2008</p><p></p><p>MAD COW DISEASE terminology UK c-BSE (typical), atypical BSE H or L,</p><p>and or Italian L-BASE</p><p></p><p><a href="http://bse-atypical.blogspot.com/2008/03/mad-cow-disease-terminology-uk-c-bse.html" target="_blank">http://bse-atypical.blogspot.com/2008/0 ... c-bse.html</a></p><p></p><p>SCHOOL LUNCH PROGRAM FROM DOWNER CATTLE UPDATE</p><p></p><p><a href="http://downercattle.blogspot.com/" target="_blank">http://downercattle.blogspot.com/</a></p><p></p><p>SRM MAD COW RECALL 406 THOUSAND POUNDS CATTLE HEADS WITH TONSILS KANSAS</p><p></p><p><a href="http://cjdmadcowbaseoct2007.blogspot.com/2008/04/srm-mad-cow-recall-406-thousand-pounds.html" target="_blank">http://cjdmadcowbaseoct2007.blogspot.co ... ounds.html</a></p><p></p><p>SPECIFIED RISK MATERIALS</p><p></p><p><a href="http://madcowspontaneousnot.blogspot.com/2008/02/specified-risk-materials-srm.html" target="_blank">http://madcowspontaneousnot.blogspot.co ... s-srm.html</a></p><p></p><p></p><p>TSS</p></blockquote><p></p>
[QUOTE="flounder, post: 524887, member: 3519"] Rapid communications Two cases of variant Creutzfeldt-Jakob disease reported in Spain in 2007 and 2008 volume 13 issue 15 publication date April 2008 How to cite this article, click here. Indexed in MedLine as: Euro Surveill 2008;13(15) Published online April 2008 Two cases of variant Creutzfeldt-Jakob disease reported in Spain in 2007 and 2008 J de Pedro Cuesta ([email=jpedro@isciii.es]jpedro@isciii.es[/email]" onclick="window.open(this.href);return false;), Instituto de Salud Carlos III, Department of Applied Epidemiology, National Centre of Epidemiology, Madrid, Spain -------------------------------------------------------------------------------- In 2005, the first case of variant Creutzfeldt-Jakob disease (vCJD) was reported in Spain, in a woman born in 1978 with clinical onset of symptoms in 2004 [1]. She subsequently died in 2005. Recently, two more laboratory-confirmed vCJD cases were reported to the Spanish CJD state registry. In February 2006, a woman born in 1957 developed progressive cognitive deterioration, and died in December 2007 with suspected sporadic CJD (typical EEG in October 2007) MM at codon 129 and no mutations in PRPN gene. A man born in 1967 had onset in May 2007 with psychiatric symptoms, and after several months developed progressive cognitive decline with dementia, typical MRI, MM at codon 129, no mutations in PRPN gene. He died in February 2008. Post-mortem, neuropathology with histochemistry confirmed vCJD in both cases. No clear specific dietary habits, blood donations or reception were recorded. Neither case appears to have visited the United Kingdom before 2004. The latest two cases were resident in the same region of the country, Castilla y Leon, but no link between them was established. -------------------------------------------------------------------------------- References Centro Nacional de Epidemiología, Instituto de Salud Carlos III. First case of vCJD reported in Spain. Euro Surveill. 2005;10(8):E050804.1. Available from: [url=http://www.eurosurveillance.org/ew/2005/050804.asp#1]http://www.eurosurveillance.org/ew/2005/050804.asp#1[/url] Citation style for this article: . Two cases of variant Creutzfeldt-Jakob disease reported in Spain in 2007 and 2008. Euro Surveill 2008;13(15). Available online: [url=http://www.eurosurveillance.org/edition/v13n15/080410_3.asp]http://www.eurosurveillance.org/edition ... 0410_3.asp[/url] *Acquired in UK ** Acquired in Saudi Arabia *** Includes 17 inconclusive and 9 pending (1 from 2006, 8 from 2007. **** Includes 17 non-vCJD type unknown (2 from 1996, 2 from 1997, 1 from 2001, 1 from 2003, 4 from 2004, 3 from 2005, 4 from 2006) and 36 type pending (2 from 2005, 8 from 2006, 26 from 2007). Notes: -- Cases are listed based on the year of death when available. If the year of death is not available, the year of sample receipt is used. -- Referrals: Cases with possible or probable prion disease from which brain tissue or blood in the case of familial disease were submitted. -- Inconclusive: Cases in which the samples were not sufficient to make a diagnosis. -- Non-vCJD type unknown are cases in which the tissue submitted was adequate to establish the presence but not the type; in all cases, vCJD could be excluded. -- Terry S. Singeltary Sr. <flounder9@verizon.net> [In submitting these data, Terry S. Singeltary Sr. draws attention to the steady increase in the "type unknown" category, which, according to their definition, comprises cases in which vCJD could be excluded. The total of 26 cases for the current year (2007) is disturbing, possibly symptomatic of the circulation of novel agents. Characterization of these agents should be given a high priority. - Mod.CP] [url=http://www.promedmail.org/pls/askus/f?p=2400:1001:6833194127530602005::NO::F2400_P1001_BACK_PAGE,F2400_P1001_PUB_MAIL_ID:1010,39963]http://www.promedmail.org/pls/askus/f?p ... 1010,39963[/url] There is a growing number of human CJD cases, and they were presented last week in San Francisco by Luigi Gambatti(?) from his CJD surveillance collection. He estimates that it may be up to 14 or 15 persons which display selectively SPRPSC and practically no detected RPRPSC proteins. [url=http://www.fda.gov/ohrms/dockets/ac/06/transcripts/1006-4240t1.htm]http://www.fda.gov/ohrms/dockets/ac/06/ ... 4240t1.htm[/url] [url=http://www.fda.gov/ohrms/dockets/ac/06/transcripts/2006-4240t1.pdf]http://www.fda.gov/ohrms/dockets/ac/06/ ... 4240t1.pdf[/url] JOURNAL OF NEUROLOGY MARCH 26, 2003 RE-Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob disease in the United States Email Terry S. Singeltary: [email=flounder@wt.net]flounder@wt.net[/email]" onclick="window.open(this.href);return false; I lost my mother to hvCJD (Heidenhain Variant CJD). I would like to comment on the CDC's attempts to monitor the occurrence of emerging forms of CJD. Asante, Collinge et al [1] have reported that BSE transmission to the 129-methionine genotype can lead to an alternate phenotype that is indistinguishable from type 2 PrPSc, the commonest sporadic CJD. However, CJD and all human TSEs are not reportable nationally. CJD and all human TSEs must be made reportable in every state and internationally. I hope that the CDC does not continue to expect us to still believe that the 85%+ of all CJD cases which are sporadic are all spontaneous, without route/source. We have many TSEs in the USA in both animal and man. CWD in deer/elk is spreading rapidly and CWD does transmit to mink, ferret, cattle, and squirrel monkey by intracerebral inoculation. With the known incubation periods in other TSEs, oral transmission studies of CWD may take much longer. Every victim/family of CJD/TSEs should be asked about route and source of this agent. To prolong this will only spread the agent and needlessly expose others. In light of the findings of Asante and Collinge et al, there should be drastic measures to safeguard the medical and surgical arena from sporadic CJDs and all human TSEs. I only ponder how many sporadic CJDs in the USA are type 2 PrPSc? [url=http://www.neurology.org/cgi/eletters/60/2/176#535]http://www.neurology.org/cgi/eletters/60/2/176#535[/url] THE PATHOLOGICAL PROTEIN Hardcover, 304 pages plus photos and illustrations. ISBN 0-387-95508-9 June 2003 BY Philip Yam CHAPTER 14 LAYING ODDS Answering critics like Terry Singeltary, who feels that the U.S. under-counts CJD, Schonberger conceded that the current surveillance system has errors but stated that most of the errors will be confined to the older population. [url=http://www.thepathologicalprotein.com/]http://www.thepathologicalprotein.com/[/url] doi:10.1016/S1473-3099(03)00715-1 Copyright © 2003 Published by Elsevier Ltd. Newsdesk Tracking spongiform encephalopathies in North America Xavier Bosch Available online 29 July 2003. Volume 3, Issue 8, August 2003, Page 463 My name is Terry S Singeltary Sr, and I live in Bacliff, Texas. I lost my mom to hvCJD (Heidenhain variant CJD) and have been searching for answers ever since. What I have found is that we have not been told the truth. CWD in deer and elk is a small portion of a much bigger problem." ... [url=http://www.thelancet.com/journals/laninf/article/PIIS1473309903007151/fulltext]http://www.thelancet.com/journals/lanin ... 1/fulltext[/url] [url=http://download.thelancet.com/pdfs/journals/1473-3099/PIIS1473309903007151.pdf]http://download.thelancet.com/pdfs/jour ... 007151.pdf[/url] Diagnosis and Reporting of Creutzfeldt-Jakob Disease Singeltary, Sr et al. JAMA.2001; 285: 733-734. [url=http://jama.ama-assn.org/http://www.neurology.org/cgi/eletters/60/2/176#535]http://jama.ama-assn.org/http://www.neu ... /2/176#535[/url] APHIS-2006-0041-0006 TSE advisory committee for the meeting December 15, 2006 [url=http://www.regulations.gov/fdmspublic/ContentViewer?objectId=09000064801f3413&disposition=attachment&contentType=msw8]http://www.regulations.gov/fdmspublic/C ... tType=msw8[/url] Subject: [Docket No. FSIS-2006-0011] FSIS Harvard Risk Assessment of Bovine Spongiform Encephalopathy (BSE) [url=http://www.fsis.usda.gov/OPPDE/Comments/2006-0011/2006-0011-1.pdf]http://www.fsis.usda.gov/OPPDE/Comments ... 0011-1.pdf[/url] [Docket No. 03-025IFA] FSIS Prohibition of the Use of Specified Risk Materials for Human Food and Requirement for the Disposition of Non-Ambulatory Disabled Cattle 9/13/2005 [url=http://www.fsis.usda.gov/OPPDE/Comments/03-025IFA/03-025IFA-2.pdf]http://www.fsis.usda.gov/OPPDE/Comments ... 5IFA-2.pdf[/url] 2 January 2000 British Medical Journal U.S. Scientist should be concerned with a CJD epidemic in the U.S., as well [url=http://www.bmj.com/cgi/eletters/320/7226/8/b#6117]http://www.bmj.com/cgi/eletters/320/7226/8/b#6117[/url] 15 November 1999 British Medical Journal vCJD in the USA * BSE in U.S. [url=http://www.bmj.com/cgi/eletters/319/7220/1312/b#5406]http://www.bmj.com/cgi/eletters/319/7220/1312/b#5406[/url] Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob disease in the United States [url=http://cjdusa.blogspot.com/]http://cjdusa.blogspot.com/[/url] Creutzfeldt Jakob Disease [url=http://creutzfeldt-jakob-disease.blogspot.com/]http://creutzfeldt-jakob-disease.blogspot.com/[/url] Creutzfeldt-Jakob Disease, Prion Protein Gene Codon 129VV, and a Novel PrPSc ype in a Young British Woman [url=http://creutzfeldt-jakob-disease.blogspot.com/2008/01/creutzfeldt-jakob-disease-prion-protein.html]http://creutzfeldt-jakob-disease.blogsp ... otein.html[/url] CJD QUESTIONNAIRE [url=http://cjdquestionnaire.blogspot.com/]http://cjdquestionnaire.blogspot.com/[/url] ANIMAL HEALTH REPORT 2006 (BSE h-BASE EVENT IN ALABAMA, Scrapie, and CWD) [url=http://animalhealthreport2006.blogspot.com/]http://animalhealthreport2006.blogspot.com/[/url] CREUTZFELDT JAKOB DISEASE MAD COW BASE UPDATE USA [url=http://cjdmadcowbaseoct2007.blogspot.com/]http://cjdmadcowbaseoct2007.blogspot.com/[/url] Friday, January 11, 2008 CJD HUMAN TSE REPORT UK, USA, CANADA, and Mexico JANUARY 2008 [url=http://cjdmadcowbaseoct2007.blogspot.com/2008/01/cjd-human-tse-report-uk-usa-canada-and.html]http://cjdmadcowbaseoct2007.blogspot.co ... a-and.html[/url] Friday, February 8, 2008 Creutzfeldt Jakob Disease Delaware UPDATE [url=http://cjdmadcowbaseoct2007.blogspot.com/2008/02/creutzfeldt-jakob-disease-delaware.html]http://cjdmadcowbaseoct2007.blogspot.co ... aware.html[/url] CREUTZFELDT JAKOB DISEASE TEXAS [url=http://cjdtexas.blogspot.com/]http://cjdtexas.blogspot.com/[/url] Friday, January 25, 2008 January 2008 Update on Feed Enforcement Activities to Limit the Spread of BSE [url=http://madcowspontaneousnot.blogspot.com/2008/01/january-2008-update-on-feed-enforcement.html]http://madcowspontaneousnot.blogspot.co ... ement.html[/url] [url=http://madcowspontaneousnot.blogspot.com/]http://madcowspontaneousnot.blogspot.com/[/url] BSE BASE MAD COW TESTING TEXAS, USA, AND CANADA [url=http://madcowtesting.blogspot.com/]http://madcowtesting.blogspot.com/[/url] NOR-98 ATYPICAL SCRAPIE USA UPDATE AS AT OCT 2007 [url=http://nor-98.blogspot.com/]http://nor-98.blogspot.com/[/url] [url=http://scrapie-usa.blogspot.com/]http://scrapie-usa.blogspot.com/[/url] Sunday, March 16, 2008 MAD COW DISEASE terminology UK c-BSE (typical), atypical BSE H or L, and or Italian L-BASE [url=http://bse-atypical.blogspot.com/2008/03/mad-cow-disease-terminology-uk-c-bse.html]http://bse-atypical.blogspot.com/2008/0 ... c-bse.html[/url] SCHOOL LUNCH PROGRAM FROM DOWNER CATTLE UPDATE [url=http://downercattle.blogspot.com/]http://downercattle.blogspot.com/[/url] SRM MAD COW RECALL 406 THOUSAND POUNDS CATTLE HEADS WITH TONSILS KANSAS [url=http://cjdmadcowbaseoct2007.blogspot.com/2008/04/srm-mad-cow-recall-406-thousand-pounds.html]http://cjdmadcowbaseoct2007.blogspot.co ... ounds.html[/url] SPECIFIED RISK MATERIALS [url=http://madcowspontaneousnot.blogspot.com/2008/02/specified-risk-materials-srm.html]http://madcowspontaneousnot.blogspot.co ... s-srm.html[/url] TSS [/QUOTE]
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