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Neurology
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December 1, 1994
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies
J L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
BMJ (Clinical Research Ed.)
|
March 20, 1993
Inherited prion disease
J 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 sclerosis
N 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 phenotype
K 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 1992-7
J 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 gene
J 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 controls
H J T Ward, D Everington, E A Croes, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 60) with videos related to
Sort By:
Page
of 6
Neurology
|
December 1, 1994
Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies
J L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
BMJ (Clinical Research Ed.)
|
March 20, 1993
Inherited prion disease
J 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 sclerosis
N 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 phenotype
K 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 1992-7
J 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 gene
J 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 controls
H J T Ward, D Everington, E A Croes, et al.
Page
of 6