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Showing results (141-150 of 157) with videos related to

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TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|March 31, 2007
The use of MapPop1.0 for choosing a QTL mapping sample from an advanced backcross populationC Birolleau-Touchard, E Hanocq, A Bouchez, et al.
Annals of Neurology|November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patientsM R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Molecular Genetics and Metabolism|August 5, 2008
Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduriaM A Cosson, G Touati, F Lacaille, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Journal of Inherited Metabolic Disease|June 23, 2000
Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosisJ M Saudubray, P de Lonlay, G Touati, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
D-2-hydroxyglutaric aciduria: further clinical delineationM S van der Knaap, C Jakobs, G F Hoffmann, et al.
European Journal of Pediatrics|March 1, 1996
Clinical outcome and long-term management of 17 patients with propionic acidaemiaS B van der Meer, F Poggi, M Spada, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patientsJ M Saudubray, D Martin, P de Lonlay, et al.
Journal of Inherited Metabolic Disease|March 12, 2009
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B(12)V Valayannopoulos, L Hubert, J F Benoist, et al.
Journal of Inherited Metabolic Disease|December 20, 2012
Treatment of acute decompensation of maple syrup urine disease in adult patients with a new parenteral amino-acid mixtureA Servais, J B Arnoux, C Lamy, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|March 31, 2007
The use of MapPop1.0 for choosing a QTL mapping sample from an advanced backcross populationC Birolleau-Touchard, E Hanocq, A Bouchez, et al.
Annals of Neurology|November 18, 1998
Clinical approach to inherited peroxisomal disorders: a series of 27 patientsM R Baumgartner, B T Poll-The, N M Verhoeven, et al.
Molecular Genetics and Metabolism|August 5, 2008
Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduriaM A Cosson, G Touati, F Lacaille, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Journal of Inherited Metabolic Disease|June 23, 2000
Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosisJ M Saudubray, P de Lonlay, G Touati, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
D-2-hydroxyglutaric aciduria: further clinical delineationM S van der Knaap, C Jakobs, G F Hoffmann, et al.
European Journal of Pediatrics|March 1, 1996
Clinical outcome and long-term management of 17 patients with propionic acidaemiaS B van der Meer, F Poggi, M Spada, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patientsJ M Saudubray, D Martin, P de Lonlay, et al.
Journal of Inherited Metabolic Disease|March 12, 2009
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B(12)V Valayannopoulos, L Hubert, J F Benoist, et al.
Journal of Inherited Metabolic Disease|December 20, 2012
Treatment of acute decompensation of maple syrup urine disease in adult patients with a new parenteral amino-acid mixtureA Servais, J B Arnoux, C Lamy, et al.
Pageof 16