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J Chatelain

Showing results (31-40 of 41) with videos related to

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Neurology|April 1, 1996
Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein geneJ C Antoine, J L Laplanche, J F Mosnier, et al.
Human Molecular Genetics|June 1, 1995
Two novel insertions in the prion protein gene in patients with late-onset dementiaJ L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
Genomics|January 1, 1993
PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresisJ L Laplanche, J Chatelain, D Westaway, et al.
Medical Care|March 19, 2026
A Qualitative Study of the Implementation of Referral Coordination for Specialty Care Referrals in the Veterans Health AdministrationAnna Zogas, Varsha G Vimalananda, Megan B McCullough, et al.
BMJ (Clinical Research Ed.)|March 20, 1993
Inherited prion diseaseJ L Laplanche, J Chatelain, M Dussaucy, et al.
Revue Neurologique|January 1, 1982
[Creutzfeldt-Jakob disease in France: an epidemiological update (author's transl)]F Cathala, P Brown, S Raharison, 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.
Experimental Hematology|November 1, 1987
Recombinant human interleukin-2 restores in vitro T-cell colony formation by peripheral blood mononuclear cells after autologous bone marrow transplantationA E Bosly, P J Staquet, C M Doyen, 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.
Acta Neuropathologica|January 1, 1994
Creutzfeldt-Jakob disease and cerebral amyloid angiopathyF Gray, F Chrétien, P Cesaro, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Neurology|April 1, 1996
Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein geneJ C Antoine, J L Laplanche, J F Mosnier, et al.
Human Molecular Genetics|June 1, 1995
Two novel insertions in the prion protein gene in patients with late-onset dementiaJ L Laplanche, N Delasnerie-Lauprêtre, J P Brandel, et al.
Genomics|January 1, 1993
PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresisJ L Laplanche, J Chatelain, D Westaway, et al.
Medical Care|March 19, 2026
A Qualitative Study of the Implementation of Referral Coordination for Specialty Care Referrals in the Veterans Health AdministrationAnna Zogas, Varsha G Vimalananda, Megan B McCullough, et al.
BMJ (Clinical Research Ed.)|March 20, 1993
Inherited prion diseaseJ L Laplanche, J Chatelain, M Dussaucy, et al.
Revue Neurologique|January 1, 1982
[Creutzfeldt-Jakob disease in France: an epidemiological update (author's transl)]F Cathala, P Brown, S Raharison, 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.
Experimental Hematology|November 1, 1987
Recombinant human interleukin-2 restores in vitro T-cell colony formation by peripheral blood mononuclear cells after autologous bone marrow transplantationA E Bosly, P J Staquet, C M Doyen, 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.
Acta Neuropathologica|January 1, 1994
Creutzfeldt-Jakob disease and cerebral amyloid angiopathyF Gray, F Chrétien, P Cesaro, et al.
Pageof 5