J L Laplanche|P Beaudry|L Ripoll|J M Launay - JoVE Visualize

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Pathologie-Biologie|February 1, 1995

[Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies]J L Laplanche, P Beaudry, L Ripoll, et al.

Neurology|October 1, 1993

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob diseaseL Ripoll, J L Laplanche, M Salzmann, et al.

Dementia and Geriatric Cognitive Disorders|March 6, 1999

14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseP Beaudry, P Cohen, J P Brandel, et al.

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.

Bulletin Et Memoires De L'Academie Royale De Medecine De Belgique|October 26, 2000

[Recent data on prion diseases]C Dreux, J M Launay, J L Laplanche

Annales Pharmaceutiques Francaises|January 1, 1995

[Molecular genetics of familial and sporadic forms of human prion diseases]J L Laplanche, J M Launay, C Dreux

Annales De Biologie Clinique|January 1, 1990

[Proteins, genes and early diagnosis of Alzheimer's disease]J L Laplanche, J Chatelain, J M Launay, et al.

Lancet (London, England)|November 12, 1994

The apolipoprotein E alleles as major susceptibility factors for Creutzfeldt-Jakob disease. The French Research Group on Epidemiology of Human Spongiform EncephalopathiesP Amouyel, O Vidal, J M Launay, et al.

The Journal of General Virology|August 1, 1995

Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapieC Clouscard, P Beaudry, J M Elsen, et al.

Revue Neurologique|May 5, 1999

[Creutzfeldt-Jakob disease: diagnostic value of protein 14-3-3 and neuronal specific enolase assay in cerebrospinal fluid]J P Brandel, P Beaudry, N Delasnerie-Lauprêtre, et al.

Pageof 31

Showing results (1-10 of 302) with videos related to

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Pageof 31

Pathologie-Biologie|February 1, 1995

[Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies]J L Laplanche, P Beaudry, L Ripoll, et al.

Neurology|October 1, 1993

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob diseaseL Ripoll, J L Laplanche, M Salzmann, et al.

Dementia and Geriatric Cognitive Disorders|March 6, 1999

14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseP Beaudry, P Cohen, J P Brandel, et al.

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.

Bulletin Et Memoires De L'Academie Royale De Medecine De Belgique|October 26, 2000

[Recent data on prion diseases]C Dreux, J M Launay, J L Laplanche

Annales Pharmaceutiques Francaises|January 1, 1995

[Molecular genetics of familial and sporadic forms of human prion diseases]J L Laplanche, J M Launay, C Dreux

Annales De Biologie Clinique|January 1, 1990

[Proteins, genes and early diagnosis of Alzheimer's disease]J L Laplanche, J Chatelain, J M Launay, et al.

Lancet (London, England)|November 12, 1994

The apolipoprotein E alleles as major susceptibility factors for Creutzfeldt-Jakob disease. The French Research Group on Epidemiology of Human Spongiform EncephalopathiesP Amouyel, O Vidal, J M Launay, et al.

The Journal of General Virology|August 1, 1995

Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapieC Clouscard, P Beaudry, J M Elsen, et al.

Revue Neurologique|May 5, 1999

[Creutzfeldt-Jakob disease: diagnostic value of protein 14-3-3 and neuronal specific enolase assay in cerebrospinal fluid]J P Brandel, P Beaudry, N Delasnerie-Lauprêtre, et al.

Pageof 31