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First characterization of a large deletion of the PDHA 1 gene.
Brivet M, Moutard ML, Zater M, Venet L, Chenel C, Mine M, Legrand A. Brivet M, et al. Among authors: zater m. Mol Genet Metab. 2005 Dec;86(4):456-61. doi: 10.1016/j.ymgme.2005.08.009. Epub 2005 Oct 25. Mol Genet Metab. 2005. PMID: 16256390
Molecular characterization of 82 patients with pyruvate dehydrogenase complex deficiency. Structural implications of novel amino acid substitutions in E1 protein.
Imbard A, Boutron A, Vequaud C, Zater M, de Lonlay P, de Baulny HO, Barnerias C, Miné M, Marsac C, Saudubray JM, Brivet M. Imbard A, et al. Among authors: zater m. Mol Genet Metab. 2011 Dec;104(4):507-16. doi: 10.1016/j.ymgme.2011.08.008. Epub 2011 Aug 18. Mol Genet Metab. 2011. PMID: 21914562
A Novel Mutation in CPT1A Resulting in Hepatic CPT Deficiency.
Fontaine M, Dessein AF, Douillard C, Dobbelaere D, Brivet M, Boutron A, Zater M, Mention-Mulliez K, Martin-Ponthieu A, Vianey-Saban C, Briand G, Porchet N, Vamecq J. Fontaine M, et al. Among authors: zater m. JIMD Rep. 2012;6:7-14. doi: 10.1007/8904_2011_94. Epub 2012 Jan 31. JIMD Rep. 2012. PMID: 23430932 Free PMC article.
Prenatal molecular diagnosis of inherited cholestatic diseases.
Jung C, Driancourt C, Baussan C, Zater M, Hadchouel M, Meunier-Rotival M, Guiochon-Mantel A, Jacquemin E. Jung C, et al. Among authors: zater m. J Pediatr Gastroenterol Nutr. 2007 Apr;44(4):453-8. doi: 10.1097/MPG.0b013e318036a569. J Pediatr Gastroenterol Nutr. 2007. PMID: 17414143
Urinary cystatin C as a specific marker of tubular dysfunction.
Conti M, Moutereau S, Zater M, Lallali K, Durrbach A, Manivet P, Eschwège P, Loric S. Conti M, et al. Among authors: zater m. Clin Chem Lab Med. 2006;44(3):288-91. doi: 10.1515/CCLM.2006.050. Clin Chem Lab Med. 2006. PMID: 16519600
11 results