Les instruments chirurgicaux inactivés = The sterilised surgery instrumentsBARLET, P.CETIM informations. 1998, Num 157, issn 0399-0001, p. 45Article

MR imaging of Creutzfeldt-Jakob diseaseFINKENSTAEDT, M; SZUDRA, A; ZERR, I et al.Radiology. 1996, Vol 199, Num 3, pp 793-798, issn 0033-8419Article

Modélisation de l'épidémie de variant de la maladie de Creutzfeldt Jakob en FranceCHADEAU, Marc.2005, non paginé [212 p.]Thesis

Maladie de Creutzfeldt-Jakob et maladies apparentées : données épidémio-cliniquesDELASNERIE LAUPRETRE, N; SALOMON, D.Journal de pédiatrie et de puériculture. 2002, Vol 15, Num 6, pp 326-332, issn 0987-7983Article

A test for transmissible spongiform encephalopathyKLASS, Michael R; HODGES, Steven; SAYERS, Riona et al.American biotechnology laboratory. 2002, Vol 20, Num 12, pp 34-36, issn 0749-3223, 2 p.Article

TRANSFORMATION OF CELL CULTURES DERIVED FROM HUMAN BRAINS = TRANSFORMATION DE CULTURES DE CELLULES DERIVEES DE CERVEAUX HUMAINSKATZ M; KOPROWSKY H; MOORHEAD PS et al.1973; SCIENCE; U.S.A.; DA. 1973; VOL. 179; NO 4077; PP. 1019-1020; BIBL. 8REF.Serial Issue

ANIMAL MODEL OF HUMAN DISEASE KURU, CREUTZFELD-JAKOB DISEASE. (SLOW VIRUS INFECTIONS)MARSH RF.1972; AMER. J. PATHOL.,; U.S.A.; DA. 1972; VOL. 69; NO 1; PP. 209-212; BIBL. 7REF.Serial Issue

SPONTANEOUS TRANSFORMATION OF HUMAN BRAIN CELLS GROWN IN VITRO AND DESCRIPTION OF ASSOCIATED VIRUS PARTICLES = TRANSFORMATION SPONTANEE DE CELLULES DE CERVEAU HUMAIN SE DEVELOPPANT IN VITRO ET DESCRIPTION DES PARTICULES DE VIRUS ASSOCIEESHOOKS J; GIBBS CJ JR; CHOPRA H et al.1972; SCIENCE; U.S.A.; DA. 1972; VOL. 176; NO 4042; PP. 1420-1422; BIBL. 5REF.Serial Issue

Onset of Creutzfeldt-Jakob disease mimicking an acute cerebrovascular eventDEPOLD HOHLER, Anna; FLYNN, Frederick G.Neurology. 2006, Vol 67, Num 3, pp 538-539, issn 0028-3878, 2 p.Article

Variante de la maladie de creutzfeldt-jakob, 10 ans après = Variant Creutzfeldt-Jakob disease, 10 years laterBRANDEL, Jean-Philippe.La Presse médicale (1983). 2006, Vol 35, Num 1, pp 15-16, issn 0755-4982, 2 p., CAH1Article

Actualités sur le risque iatrogène d'infection par agent à transmission non conventionnelle lors de la transfusion sanguine et d'un acte invasifHARTEMANN, P.Hygiènes (Lyon). 2006, Vol 14, Num 6, pp 417-422, issn 1249-0075, 6 p.Article

Sporadic Creutzfeldt-Jakob disease : Clinical and diagnostic characteristics of the rare VV1 typeBOSQUE, Patrick; MEISSNER, B; SCHULZ-SCHAEFFER, W. J et al.Neurology. 2005, Vol 65, Num 10, pp 1520-1521, issn 0028-3878, 9 p.Article

Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob diseaseTABATON, Massimo; MONACO, Salvatore; CORDONE, Maria Paola et al.Annals of neurology. 2004, Vol 55, Num 2, pp 294-296, issn 0364-5134, 3 p.Article

Plasminogen activities and concentrations in patients with sporadic Creutzfeldt-Jakob diseaseZERR, Inga; BODEMER, Monika; KABOTH, Ulrich et al.Neuroscience letters. 2004, Vol 371, Num 2-3, pp 163-166, issn 0304-3940, 4 p.Article

Traitement des dispositifs médicaux thermosensibles. Revue des dispositifs thermostables en consultation d'Oto Rhino Laryngologie2003, 42 p.Book

Les agents transmissibles non conventionnels, ou prions : risques de santé publiqueDORMONT, Dominique.Actualité et dossier en santé publique. 2002, Num 38, pp 66-68, issn 1243-275XArticle

Les encéphalopathies subaiguës spongiformes transmissibles ou maladies à prions = Spongiform subacute encephlopathy or prion diseasesDORMONT, Dominique.MHA (Sousse). 2002, pp 6-8, issn 0330-8030, 3 p., HSConference Paper

Les mécanismes de la mort neuronale = The mecanism of the neuronal deathDORMONT, Dominique.Biofutur (Puteaux). 2001, pp 22-25, issn 0294-3506, HSArticle

Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotypeVAN EVERBROECK, Bart; CROES, Esther A; PALS, Philippe et al.Neuroscience letters. 2001, Vol 313, Num 1-2, pp 69-72, issn 0304-3940Article

Risques liés au prion pour les enfantsBEAUVAIS, P.Journal de pédiatrie et de puériculture. 2001, Vol 14, Num 8, pp 480-485, issn 0987-7983Article

The spatial pattern of the vacuolation in patients with sporadic Creutzfeldt-Jakob diseaseARMSTRONG, R. A; CAIRNS, N. J; LANTOS, P. L et al.Neuroscience letters. 2000, Vol 281, Num 2-3, pp 187-190, issn 0304-3940Article

A rapid and efficient method for the detection of point mutations of the human prion protein gene (PRNP) by direct sequencingPETRAROLI, R; VACCARI, G; POCCHIARI, M et al.Journal of neuroscience methods. 2000, Vol 99, Num 1-2, pp 59-63, issn 0165-0270Article

Clinical aspects of human spongiform encephalopathies, with the exception of iatrogenic forms : Human prion diseaseBRANDEL, J. P.Biomedicine & pharmacotherapy. 1999, Vol 53, Num 1, pp 14-18, issn 0753-3322Article

Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob diseaseSALVATORE, M; SEEBER, A. C; NACMIAS, B et al.Neuroscience letters. 1997, Vol 227, Num 2, pp 140-142, issn 0304-3940Article

The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbanceNOZAKI, I; HAMAGUCHI, T; NOGUCHI-SHINOHARA, M et al.Neurology. 2006, Vol 67, Num 3, pp 531-533, issn 0028-3878, 3 p.Article