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C Caillaud

Showing results (61-70 of 80) with videos related to

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La Revue De Medecine Interne|April 4, 2018
[Type 3 Gaucher disease, also an adult disease?]A Leurs, A Chepy, C Detonellaere, et al.
Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.
Genomics|November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuriaV Abadie, S Lyonnet, N Maurin, et al.
Neuroreport|May 9, 1994
In vivo transfer of a marker gene to study motoneuronal developmentF Lisovoski, J Cadusseau, S Akli, et al.
The Journal of Biological Chemistry|May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuriaC Caillaud, S Lyonnet, F Rey, et al.
International Journal of Clinical Practice|August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome SurveyO Lidove, U Ramaswami, R Jaussaud, et al.
Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.
American Journal of Human Genetics|December 1, 1988
Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in FranceF Rey, M Berthelon, C Caillaud, et al.
Human Genetics|April 1, 1992
Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in PortugalC Caillaud, L Vilarinho, A Vilarinho, et al.
Gene Therapy|September 10, 2003
Widespread distribution of beta-hexosaminidase activity in the brain of a Sandhoff mouse model after coinjection of adenoviral vector and mannitolC Bourgoin, C Emiliani, E J Kremer, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
La Revue De Medecine Interne|April 4, 2018
[Type 3 Gaucher disease, also an adult disease?]A Leurs, A Chepy, C Detonellaere, et al.
Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.
Genomics|November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuriaV Abadie, S Lyonnet, N Maurin, et al.
Neuroreport|May 9, 1994
In vivo transfer of a marker gene to study motoneuronal developmentF Lisovoski, J Cadusseau, S Akli, et al.
The Journal of Biological Chemistry|May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuriaC Caillaud, S Lyonnet, F Rey, et al.
International Journal of Clinical Practice|August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome SurveyO Lidove, U Ramaswami, R Jaussaud, et al.
Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.
American Journal of Human Genetics|December 1, 1988
Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in FranceF Rey, M Berthelon, C Caillaud, et al.
Human Genetics|April 1, 1992
Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in PortugalC Caillaud, L Vilarinho, A Vilarinho, et al.
Gene Therapy|September 10, 2003
Widespread distribution of beta-hexosaminidase activity in the brain of a Sandhoff mouse model after coinjection of adenoviral vector and mannitolC Bourgoin, C Emiliani, E J Kremer, et al.
Pageof 8