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13篇 您的检索式：作者名="Brivet M"

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		题名	作者	年代	出处	被引量
	1	A deletion in the human QP-C gene causes a complex Ill deficiency resulting in hypoglycaemia and lactic acidosis 显示文摘	Haut S Brivet M Touati G	2003	Hum Genet2003，113，2：	1
	2	Antibody neutralization of HIV-1 and the potential for vaccine design显示文摘	MOULARD M BRIVET B	1999	Immunol Lett1999，66，13：	1
	3	Necrotizing fasciitis, bacteremia, and multiorgan failure caused by Ochrobactrum anthropi 显示文摘	Brivet F Guibert M Kiredjian M	1993	Clin Infect Dis1993，17，3：	1
	4	Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block: translocase assay in permeabilized fibroblasts J显示文摘	Pande S V Brivet M Stama A	1993	Clin Invest1993，91，：	1
	5	Impaired mitochondrial pyruvate importation in a patient and a fetus at risk 显示文摘	Brivet M Garcia-Cazorla A Lyonnet S	2003	Mol Genet Metab2003，78，3：	1
	6	A large genomic deletion in the PDHX gene caused by the retrotranspositional insertion of a fulllength LINE-1 element显示文摘	Mine M Chen JM Brivet M	2007	Hum Mutat2007，28，2：	1
	7	Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 pa- tients 显示文摘	Vianey-Saban C Divry P Brivet M	1998	Clin Chim Acta1998，269，1：	1
	8	Defects in activation and transport of fatty acids显示文摘	Brivet M Boutron A Slama A	1999	J Inherit Metab Dis1999，22，：	1
	9	A novel gross deletion caused by non-homologous recombination of the PDHX gene in a patient with pyruvate dehydrogenase deficiency显示文摘	Mine M Brivet M Schiff M	2006	Mol Genet Metab2006，89，12：	1
	10	Leigh's disease due to a new mutation in the PDHX gene显示文摘	Schiff M Mine M Brivet M	2006	Ann Neurol2006，59，4：	1
	11	Mitochandrial very-long- chain acyl-coenzyme A dehydmgenase deficiency: clinical characteristics and diagnostic considerations in 30 patients 显示文摘	Vianey-Saban C Divry P Brivet M	1998	Clin Chim Acta1998，269，1：	1
	12	A large genomic deletion in the PDHX gene caused by the retrotranspositional insertion of a full-length LINE-1 element显示文摘	Miné M Chen JM Brivet M		0，，02：	1
	13	A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis显示文摘	Haut S Brivet M Touati G Rustin P Lebon S Garcia-Cazorla A	2003	Hum Genet2003，113，：	1

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