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G Debray

Showing results (11-20 of 21) with videos related to

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Revue Medicale De Liege|June 5, 2020
[Current and new therapeutic options in inborn errors of metabolism]F G Debray, L Weekers, C Dadoumont, et al.
Revue Medicale De Liege|March 26, 2009
[Osteogenesis imperfecta]J F Kaux, C Le Goff, F G Debray, et al.
Revue Medicale De Liege|December 31, 2010
[How to explore ... congenital isolated hypogonadotrophic hypogonadism]H Valdes-Socin, F G Debray, A S Parent, et al.
Neuropediatrics|May 28, 2008
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxiaF-G Debray, M Lambert, R Gagne, et al.
European Journal of Pediatrics|March 23, 2006
Intermittent peripheral weakness as the presenting feature of pyruvate dehydrogenase deficiencyFrancois-G Debray, Marie Lambert, Michel Vanasse, et al.
Scientific Reports|December 17, 2017
A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseasesF Boemer, C Fasquelle, S d'Otreppe, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
Clinical Genetics|April 2, 2015
Diagnostic pitfall in antenatal manifestations of CPT II deficiencyF Boemer, M Deberg, R Schoos, et al.
Cell Transplantation|August 15, 2012
Hepatocyte transplantation using the domino concept in a child with tetrabiopterin nonresponsive phenylketonuriaX Stéphenne, F G Debray, F Smets, et al.
Neurology|July 2, 2008
Reduced brain choline in homocystinuria due to remethylation defectsF-G Debray, Y Boulanger, A Khiat, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Revue Medicale De Liege|June 5, 2020
[Current and new therapeutic options in inborn errors of metabolism]F G Debray, L Weekers, C Dadoumont, et al.
Revue Medicale De Liege|March 26, 2009
[Osteogenesis imperfecta]J F Kaux, C Le Goff, F G Debray, et al.
Revue Medicale De Liege|December 31, 2010
[How to explore ... congenital isolated hypogonadotrophic hypogonadism]H Valdes-Socin, F G Debray, A S Parent, et al.
Neuropediatrics|May 28, 2008
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxiaF-G Debray, M Lambert, R Gagne, et al.
European Journal of Pediatrics|March 23, 2006
Intermittent peripheral weakness as the presenting feature of pyruvate dehydrogenase deficiencyFrancois-G Debray, Marie Lambert, Michel Vanasse, et al.
Scientific Reports|December 17, 2017
A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseasesF Boemer, C Fasquelle, S d'Otreppe, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
Clinical Genetics|April 2, 2015
Diagnostic pitfall in antenatal manifestations of CPT II deficiencyF Boemer, M Deberg, R Schoos, et al.
Cell Transplantation|August 15, 2012
Hepatocyte transplantation using the domino concept in a child with tetrabiopterin nonresponsive phenylketonuriaX Stéphenne, F G Debray, F Smets, et al.
Neurology|July 2, 2008
Reduced brain choline in homocystinuria due to remethylation defectsF-G Debray, Y Boulanger, A Khiat, et al.
Pageof 3