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M Odievre

Showing results (21-30 of 43) with videos related to

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Pediatric Research|February 1, 1983
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndromeM Brivet, N Moatti, A Corriat, et al.
European Journal of Nuclear Medicine|January 1, 1981
131I rose bengal: its use in the evaluation of infantile jaundiceJ Yvart, F Moati, F Alvarez, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 1990
Esophageal reflux in symptomatic and asymptomatic infants: postprandial and circadian variationsE Dreizzen, P Escourrou, M Odievre, et al.
Annales D'Anatomie Pathologique|January 1, 1980
[Oculo-cutaneous tyrosinosis (Richner-Hanhart syndrome). Histo-pathological study of a case]M Larregue, P de Giacomoni, M Odievre, et al.
Cancer Genetics and Cytogenetics|March 15, 1985
Radiation sensitivity of Bloom's syndrome lymphocytes during S and G2 phasesA Aurias, J L Antoine, R Assathiany, et al.
Human Genetics|July 1, 1988
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type IIE M Westphal, E Natt, T Grimm, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Point mutations in the tyrosine aminotransferase gene in tyrosinemia type IIE Natt, K Kida, M Odievre, et al.
Annals of Human Genetics|October 1, 1984
DNA analysis in patients with hereditary fructose intoleranceC Grégori, C Besmond, M Odievre, et al.
Neuropediatrics|April 1, 1997
Moyamoya disease in a child with glycogen storage disease type IaF Goutières, M Bourgeois, P Trioche, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Crigler-Najjar type II disease inheritance: a family studyP Labrune, A Myara, C Hennion, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Pediatric Research|February 1, 1983
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndromeM Brivet, N Moatti, A Corriat, et al.
European Journal of Nuclear Medicine|January 1, 1981
131I rose bengal: its use in the evaluation of infantile jaundiceJ Yvart, F Moati, F Alvarez, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 1990
Esophageal reflux in symptomatic and asymptomatic infants: postprandial and circadian variationsE Dreizzen, P Escourrou, M Odievre, et al.
Annales D'Anatomie Pathologique|January 1, 1980
[Oculo-cutaneous tyrosinosis (Richner-Hanhart syndrome). Histo-pathological study of a case]M Larregue, P de Giacomoni, M Odievre, et al.
Cancer Genetics and Cytogenetics|March 15, 1985
Radiation sensitivity of Bloom's syndrome lymphocytes during S and G2 phasesA Aurias, J L Antoine, R Assathiany, et al.
Human Genetics|July 1, 1988
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type IIE M Westphal, E Natt, T Grimm, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Point mutations in the tyrosine aminotransferase gene in tyrosinemia type IIE Natt, K Kida, M Odievre, et al.
Annals of Human Genetics|October 1, 1984
DNA analysis in patients with hereditary fructose intoleranceC Grégori, C Besmond, M Odievre, et al.
Neuropediatrics|April 1, 1997
Moyamoya disease in a child with glycogen storage disease type IaF Goutières, M Bourgeois, P Trioche, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Crigler-Najjar type II disease inheritance: a family studyP Labrune, A Myara, C Hennion, et al.
Pageof 5