Publications by authors named "Y de Keyzer"

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Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts.
Caroline Michot, Asmaa Mamoune, Joseph Vamecq, Mai Thao Viou, Lu-Sheng Hsieh, Yves de Keyzer

Biochim Biophys Acta· December 2013

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TMEM126A is a mitochondrial located mRNA (MLR) protein of the mitochondrial inner membrane.
Sylvain Hanein, Mathilde Garcia, Lucas Fares-Taie, Valérie Serre, Yves De Keyzer

Biochim Biophys Acta· June 2013

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Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome.
Anaïs Brassier, Chris Ottolenghi, Audrey Boutron, Anne-Marie Bertrand, Séverine Valmary-Degano, Yves de Keyzer

Mol Genet Metab· May 2013

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Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome.
Vassili Valayannopoulos, Naziha Bakouh, Michel Mazzuca, Luc Nonnenmacher, Laurence Hubert, Yves de Keyzer

J Inherit Metab Dis· January 2013

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Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia.
Caroline Michot, Laurence Hubert, Norma B Romero, Amr Gouda, Asmaa Mamoune, Yves de Keyzer

J Inherit Metab Dis· November 2012

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