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N Delasnerie

Showing results (41-50 of 60) with videos related to

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Neurology|December 1, 1994
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform EncephalopathiesJ L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
BMJ (Clinical Research Ed.)|March 20, 1993
Inherited prion diseaseJ L Laplanche, J Chatelain, M Dussaucy, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1983
[Familial Alzheimer's disease: a study of HLA markers]N Delasnerie-Lauprêtre, M Calot, E Ohayon, et al.
Journal of Clinical & Laboratory Immunology|July 1, 1981
Serum and cerebrospinal fluid C2 in multiple sclerosisN Delasnerie-Laupretre, D Prevot, C Martin-Mondiere, et al.
Human Mutation|May 2, 2000
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotypeK Peoc'h, P Manivet, P Beaudry, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2000
Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7J H d'Aignaux, J L Laplanche, N Delasnerie-Lauprêtre, et al.
Revue D'Epidemiologie Et De Sante Publique|March 13, 1998
[Incidence of Creutzfeldt-Jakob disease in France, 1992-1995]A Ruffié, N Delasnerie-Lauprêtre, J P Brandel, et al.
Brain : a Journal of Neurology|December 3, 1999
Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein geneJ L Laplanche, K H Hachimi, I Durieux, et al.
Revue Neurologique|October 17, 1998
[Diseases transmitted by non-conventional agents ("prions"): nosology and diagnosis]J J Hauw, F Lazarini, V Sazdovitch, et al.
Neurology|August 28, 2002
Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controlsH J T Ward, D Everington, E A Croes, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Neurology|December 1, 1994
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform EncephalopathiesJ L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
BMJ (Clinical Research Ed.)|March 20, 1993
Inherited prion diseaseJ L Laplanche, J Chatelain, M Dussaucy, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1983
[Familial Alzheimer's disease: a study of HLA markers]N Delasnerie-Lauprêtre, M Calot, E Ohayon, et al.
Journal of Clinical & Laboratory Immunology|July 1, 1981
Serum and cerebrospinal fluid C2 in multiple sclerosisN Delasnerie-Laupretre, D Prevot, C Martin-Mondiere, et al.
Human Mutation|May 2, 2000
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotypeK Peoc'h, P Manivet, P Beaudry, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2000
Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7J H d'Aignaux, J L Laplanche, N Delasnerie-Lauprêtre, et al.
Revue D'Epidemiologie Et De Sante Publique|March 13, 1998
[Incidence of Creutzfeldt-Jakob disease in France, 1992-1995]A Ruffié, N Delasnerie-Lauprêtre, J P Brandel, et al.
Brain : a Journal of Neurology|December 3, 1999
Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein geneJ L Laplanche, K H Hachimi, I Durieux, et al.
Revue Neurologique|October 17, 1998
[Diseases transmitted by non-conventional agents ("prions"): nosology and diagnosis]J J Hauw, F Lazarini, V Sazdovitch, et al.
Neurology|August 28, 2002
Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controlsH J T Ward, D Everington, E A Croes, et al.
Pageof 6