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About 253 results for "variant creutzfeldt jakob"

Variant CJD May Be Misdiagnosed in Older Patients

Reuters Health Information By Reuters Staff February03,2015 NEW YORK (Reuters Health) - Variant Creutzfeldt-Jakob Disease (vCJD) may be misdiagnosed in patients older than 55, given their somewhat different clinical phenotype from younger ... Diabetes Care, 1 month ago

1 images for "variant creutzfeldt jakob"

Scientific American, 6 days ago

Guidance: Current measures to reduce the risk of vCJD transmission by blood

SaBTO summary of measures currently in place in the UK to reduce the risk of transmitting variant Creutzfeldt-Jakob disease (vCJD) via blood. Document PDF, 171KB, 3 pages Detail Summary published by the Advisory Committee on the Safety of ...
 UK Department of Health1 month ago

Blood Safety (Variant Creutzfeldt-Jakob Disease)

Frank Dobson (Holborn and St Pancras, Labour) I start by declaring two peculiar interests. When I was Secretary of State for Health, I introduced the leucodepletion of the blood supply, which led to the establishment of the prion unit that now ...
 They Work For You1 month ago

Enforcement Report for March 18, 2015

Devices Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers while on a mattress. All Pressure IQ Evolve mattresses ...
 U.S. Food and Drug Administration1 week ago

Anavex Appoints Scientific Advisory Board Member With Expertise in Protein Misfolding Neurodegenerative Diseases

(MENAFN Press) NEW YORK March 5 2015 — Anavex Life Sciences Corp. ("Anavex" or the "Company") (AVXL) a clinical-stage biopharmaceutical company developing drug candidates to treat Alzheimer's disease other central nervous system (CNS) diseases ...
 MENAFN2 weeks ago Anavex Appoints Corinne Lasmézas to Scientific Advisory Board  Citybizlist3 weeks ago Anavex Life Sciences Corp. (AVXL: OTCQX U.S.) | Anavex Appoints Scientific Advisory Board Member With Expertise in Protein Misfolding Neurodegenerative Diseases  Pink Sheets3 weeks ago Anavex (AVXL) Appoints Scientific Advisory Board Member With Expertise In Protein Misfolding Neurodegenerative Diseases  FierceBiotech3 weeks ago
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Baxter BioScience Announces Positive Phase III Results for BAX 817, Investigational Recombinant Treatment for Hemophila A and B Patients with Inhibitors

Baxter International Inc. ( NYSE:BAX ) today announced positive results from its Phase III clinical trial evaluating the safety and efficacy of BAX 817, an investigational recombinant factor VIIa (rFVIIa) treatment for people ...
 Fat Pitch Financials2 weeks ago Baxter BioScience Corporation Announces Positive Phase III Results For BAX 817, Investigational Recombinant Treatment For Hemophila A And B Patients With Inhibitors  BioSpace2 weeks ago BAXTER : BioScience Announces Positive Phase III Results for BAX 817, Investigational Recombinant Treatment for Hemophila A and B Patients with Inhibitors  4 Traders2 weeks ago
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A chronology of brain-wasting diseases

CALGARY - An early chronology of brain-wasting diseases: 1732: Scrapie, a fatal neurological disease that produces subacute spongiform encephalopathy in adult sheep, is first recorded. Similar disease occurs naturally in goats and captive mule ...
 Alaska Highway News2 weeks ago
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EVARREST® Fibrin Sealant Patch a Potential Solution for Aortic Reconstruction Surgery

"These findings demonstrate the potential clinical usefulness of the EVARREST Fibrin Sealant Patch when surgically repairing an aortic aneurysm or aortic dissection," said Sina L. Moainie The current standard of care for controlling anastomotic ...
 Pettinga Financial Advisors2 weeks ago
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Changes in Retinal Function and Morphology Are Early Clinical Signs of Disease in Cattle with Bovine Spongiform Encephalopathy

Affiliation: Virus and Prion Research Unit, National Animal Disease Center, Ames, IA 50010, United States of America Current address: Department of Veterinary Pathology, Iowa State University, Ames, IA 50010, United States of America ⨯ ...
 Plosone.org2 weeks ago

Octapharma USA: FDA Approves Octaplas(TM) License Supplement, Increasing Post Thaw Permitted Storage Time

Labeling Also Increases Shelf Life for Solvent/Detergent Treated, Pooled Human Plasma HOBOKEN, N.J.--(BUSINESS WIRE)-- Octapharma USA today announced the U.S. Food and Drug Administration (FDA) has approved revised product labeling for ...
 CNBC2 weeks ago Octapharma USA, Inc.: FDA Approves Octaplas License Supplement, Increasing Post Thaw Permitted Storage Time 3/9/2015  ClinicSpace2 weeks ago OCTAPHARMA USA : FDA Approves Octaplas License Supplement, Increasing Post Thaw Permitted Storage Time  4 Traders2 weeks ago
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