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G Brunier
C Turpin

Showing results (111-120 of 131) with videos related to

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Revue Neurologique|April 1, 2005
[Presentation of Niemann-Pick type C disease with psychiatric disturbance in an adult]L Tyvaert, T Stojkovic, J-M Cuisset, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Molecular characterization of Charcot-Marie-Tooth patients in 15 pedigrees from FranceG Lucotte, S Berriche, C Bathelier, et al.
American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
The Journal of Molecular Diagnostics : JMD|June 29, 2011
Comparison of allelic discrimination by dHPLC, HRM, and TaqMan in the detection of BRAF mutation V600EPablo Carbonell, María C Turpin, Daniel Torres-Moreno, et al.
Magnetic Resonance in Chemistry : MRC|March 31, 2007
Solid-state 13C NMR and quantum chemical investigation of metal diene complexesZhiru Ma, Julio C Facelli, Ronald J Pugmire, et al.
Annals of Neurology|May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Infection and Immunity|July 1, 1997
Rickettsia rickettsii infection of cultured human endothelial cells induces NF-kappaB activationL A Sporn, S K Sahni, N B Lerner, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Pageof 14

Showing results (111-120 of 131) with videos related to

Sort By:
Pageof 14
Revue Neurologique|April 1, 2005
[Presentation of Niemann-Pick type C disease with psychiatric disturbance in an adult]L Tyvaert, T Stojkovic, J-M Cuisset, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Molecular characterization of Charcot-Marie-Tooth patients in 15 pedigrees from FranceG Lucotte, S Berriche, C Bathelier, et al.
American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
The Journal of Molecular Diagnostics : JMD|June 29, 2011
Comparison of allelic discrimination by dHPLC, HRM, and TaqMan in the detection of BRAF mutation V600EPablo Carbonell, María C Turpin, Daniel Torres-Moreno, et al.
Magnetic Resonance in Chemistry : MRC|March 31, 2007
Solid-state 13C NMR and quantum chemical investigation of metal diene complexesZhiru Ma, Julio C Facelli, Ronald J Pugmire, et al.
Annals of Neurology|May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Infection and Immunity|July 1, 1997
Rickettsia rickettsii infection of cultured human endothelial cells induces NF-kappaB activationL A Sporn, S K Sahni, N B Lerner, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Pageof 14