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Cecile Acquaviva-Bourdain

Showing results (1-10 of 4) with videos related to

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Molecular Genetics and Metabolism|June 2, 2006
A novel MOCS2 mutation reveals coordinated expression of the small and large subunit of molybdopterin synthaseRita Hahnewald, Silke Leimkühler, Antonia Vilaseca, et al.
Urolithiasis|May 31, 2020
Plasma oxalate: comparison of methodologiesFelicity Stokes, Cecile Acquaviva-Bourdain, Bernd Hoppe, et al.
Muscle & Nerve|February 16, 2011
Subacute myopathy in a mature patient due to multiple acyl-coenzyme A dehydrogenase deficiencyPierre Kaminsky, Cecile Acquaviva-Bourdain, Jacques Jonas, et al.
Pediatric Neurology|August 24, 2024
Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental DisorderMaria Carla Borroto, Heena Patel, Siddharth Srivastava, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Molecular Genetics and Metabolism|June 2, 2006
A novel MOCS2 mutation reveals coordinated expression of the small and large subunit of molybdopterin synthaseRita Hahnewald, Silke Leimkühler, Antonia Vilaseca, et al.
Urolithiasis|May 31, 2020
Plasma oxalate: comparison of methodologiesFelicity Stokes, Cecile Acquaviva-Bourdain, Bernd Hoppe, et al.
Muscle & Nerve|February 16, 2011
Subacute myopathy in a mature patient due to multiple acyl-coenzyme A dehydrogenase deficiencyPierre Kaminsky, Cecile Acquaviva-Bourdain, Jacques Jonas, et al.
Pediatric Neurology|August 24, 2024
Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental DisorderMaria Carla Borroto, Heena Patel, Siddharth Srivastava, et al.
Pageof 1