A GPHN point mutation leading to molybdenum cofactor deficiency
Reiss, J, Lenz, U, Aquaviva-Bourdain, C, Joriot-Chekaf, S, Mention-Mulliez, K, Holder-Espinasse, M
Published in Clinical genetics (01.12.2011)
Published in Clinical genetics (01.12.2011)
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Creatine biosynthesis and transport in health and disease
Joncquel-Chevalier Curt, Marie, Voicu, Pia-Manuela, Fontaine, Monique, Dessein, Anne-Frédérique, Porchet, Nicole, Mention-Mulliez, Karine, Dobbelaere, Dries, Soto-Ares, Gustavo, Cheillan, David, Vamecq, Joseph
Published in Biochimie (01.12.2015)
Published in Biochimie (01.12.2015)
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Fluxomic evidence for impaired contribution of short-chain acyl-CoA dehydrogenase to mitochondrial palmitate β-oxidation in symptomatic patients with ACADS gene susceptibility variants
Dessein, Anne-Frédérique, Fontaine, Monique, Joncquel-Chevalier Curt, Marie, Briand, Gilbert, Sechter, Claire, Mention-Mulliez, Karine, Dobbelaere, Dries, Douillard, Claire, Lacour, Arnaud, Redonnet-Vernhet, Isabelle, Lamireau, Delphine, Barth, Magalie, Minot-Myhié, Marie-Christine, Kuster, Alice, de Lonlay, Pascale, Gregersen, Niels, Acquaviva, Cécile, Vianey-Saban, Christine, Vamecq, Joseph
Published in Clinica chimica acta (01.08.2017)
Published in Clinica chimica acta (01.08.2017)
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Diagnosis and course to follow for hepatic insufficiency
Mulliez, K Mention
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2015)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2015)
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Journal Article
Opioid Facilitation of β-Adrenergic Blockade: A New Pharmacological Condition?
Vamecq, Joseph, Mention-Mulliez, Karine, Leclerc, Francis, Dobbelaere, Dries
Published in Pharmaceuticals (Basel, Switzerland) (25.09.2015)
Published in Pharmaceuticals (Basel, Switzerland) (25.09.2015)
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