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C Largilliere

Showing results (11-20 of 19) with videos related to

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European Journal of Pediatrics|December 1, 1983
Dihydrobiopterin biosynthesis deficiencyJ L Dhondt, B Leroux, J P Farriaux, et al.
LARC Medical|May 1, 1982
[Normal and pathologic metabolism of pteridines in man]J L Dhondt, Z Bellhasene, C Largilliere, et al.
Presse Medicale (Paris, France : 1983)|March 9, 1991
[Isolated thrombocytopenia under lipid emulsion in a 3-month old infant on parenteral feeding]K Francillette, F Gottrand, A Chiche, et al.
Clinical Chemistry|October 1, 1989
Biochemical contribution to diagnosis and study of a new case of D-glyceric acidemia/aciduriaM Fontaine, N Porchet, C Largilliere, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Persistent increase of serum activity of aminotransferases disclosing muscular diseases in children and adolescents]L Michaud, M Andrzejewski, C Largilliere, et al.
Presse Medicale (Paris, France : 1983)|June 18, 1988
[Third-degree atrioventricular block in typhoid fever]D Turck, H Ythier, C Francart, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
3-Methylglutaconic aciduria: neonatal onset with lactic acidosisC Largilliere, L Vallee, B Cartigny, et al.
Journal of Medical Genetics|July 1, 1992
Site specific screening for point mutations in ornithine transcarbamylase deficiencyD Feldmann, J M Rozet, A Pelet, et al.
Journal of Medical Genetics|August 1, 1995
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafnessS Manouvrier, A Rötig, G Hannebique, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
European Journal of Pediatrics|December 1, 1983
Dihydrobiopterin biosynthesis deficiencyJ L Dhondt, B Leroux, J P Farriaux, et al.
LARC Medical|May 1, 1982
[Normal and pathologic metabolism of pteridines in man]J L Dhondt, Z Bellhasene, C Largilliere, et al.
Presse Medicale (Paris, France : 1983)|March 9, 1991
[Isolated thrombocytopenia under lipid emulsion in a 3-month old infant on parenteral feeding]K Francillette, F Gottrand, A Chiche, et al.
Clinical Chemistry|October 1, 1989
Biochemical contribution to diagnosis and study of a new case of D-glyceric acidemia/aciduriaM Fontaine, N Porchet, C Largilliere, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Persistent increase of serum activity of aminotransferases disclosing muscular diseases in children and adolescents]L Michaud, M Andrzejewski, C Largilliere, et al.
Presse Medicale (Paris, France : 1983)|June 18, 1988
[Third-degree atrioventricular block in typhoid fever]D Turck, H Ythier, C Francart, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
3-Methylglutaconic aciduria: neonatal onset with lactic acidosisC Largilliere, L Vallee, B Cartigny, et al.
Journal of Medical Genetics|July 1, 1992
Site specific screening for point mutations in ornithine transcarbamylase deficiencyD Feldmann, J M Rozet, A Pelet, et al.
Journal of Medical Genetics|August 1, 1995
Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafnessS Manouvrier, A Rötig, G Hannebique, et al.
Pageof 2