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D Rabier

Showing results (81-90 of 157) with videos related to

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Journal of Inherited Metabolic Disease|January 26, 2006
Severe hypoglycaemia in isolated 3-methylcrotonyl-CoA carboxylase deficiency; a rare, severe clinical presentationH G M Oude Luttikhuis, G Touati, D Rabier, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Methylmalonic and propionic acidaemias: management and outcomeH Ogier de Baulny, J F Benoist, O Rigal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 1989
Ornithine carbamoyltransferase deficiency. A new variant with subnormal enzyme activityD Rabier, A Benoit, F Petit, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Arginase deficiency in two brothersM Candito, B Bebin, C Vianey-Saban, et al.
Clinical Nutrition (Edinburgh, Scotland)|June 1, 1997
Tolerance to starvation in children on long-term total parenteral nutritionB François, V Colomb, J P Bonnefont, et al.
Annales De Biologie Clinique|January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]A Pelet, E Toumas, D Rabier, et al.
Prenatal Diagnosis|July 6, 2006
Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experienceB Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Circulation|December 1, 1999
Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in childrenD Bonnet, D Martin, Pascale De Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1994
[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]J C Netter, G Cossarizza, C Narcy, et al.
Biochemical and Biophysical Research Communications|November 16, 1992
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, F Poggi, et al.
Pageof 16

Showing results (81-90 of 157) with videos related to

Sort By:
Pageof 16
Journal of Inherited Metabolic Disease|January 26, 2006
Severe hypoglycaemia in isolated 3-methylcrotonyl-CoA carboxylase deficiency; a rare, severe clinical presentationH G M Oude Luttikhuis, G Touati, D Rabier, et al.
Journal of Inherited Metabolic Disease|May 4, 2005
Methylmalonic and propionic acidaemias: management and outcomeH Ogier de Baulny, J F Benoist, O Rigal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 1989
Ornithine carbamoyltransferase deficiency. A new variant with subnormal enzyme activityD Rabier, A Benoit, F Petit, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Arginase deficiency in two brothersM Candito, B Bebin, C Vianey-Saban, et al.
Clinical Nutrition (Edinburgh, Scotland)|June 1, 1997
Tolerance to starvation in children on long-term total parenteral nutritionB François, V Colomb, J P Bonnefont, et al.
Annales De Biologie Clinique|January 1, 1988
[Genetic counseling in ornithine carbamoyltransferase deficiency]A Pelet, E Toumas, D Rabier, et al.
Prenatal Diagnosis|July 6, 2006
Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experienceB Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Circulation|December 1, 1999
Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in childrenD Bonnet, D Martin, Pascale De Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1994
[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]J C Netter, G Cossarizza, C Narcy, et al.
Biochemical and Biophysical Research Communications|November 16, 1992
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, F Poggi, et al.
Pageof 16