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10篇 您的检索式：作者名="Epailly"

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		题名	作者	年代	出处	被引量
	1	Transient reduction without normalization of brain natriuretic peptide early after heart transplantation显示文摘	Geny B Follenius M Epailly E	1998	J Thorac Cardiovasc Surg1998，115，2：	1
	2	Is a prosthetic ring required for mitral repair of mitral insufficiency due to posterior leaflet prolapse? Long-term results in 96 patients submitted to repair with no ring 1显示文摘	Bernard Eisenmann Arnaud Charpentier Sorin Popescu Eric Epailly Philippe Billaud Amine Jirari	1998	European Journal of Cardio-Thoracic Surgery1998，，6：	1
	3	Endothelial cell activation contributes to the release of procoagulant microparticles during acute cardiac allograft rejection显示文摘	Morel O Ohlmann P Epailly E		0，，：	1
	4	Endothelial cell activation contributes to the release of procoagulant microparticles during acute cardiac allograft rejection显示文摘	Morel O Ohlmann P Epailly E	2008	J Heart Lung Transplant2008，27，1：	1
	5	Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease显示文摘	Echaniz-Laguna A Mohr M Epailly E	2006	Muscle Nerve2006，33，3：	1
	6	Transient reduction without normalization of brain natriuretic peptide early after heart transplantation显示文摘	Geny B Follenius M Epailly E		0，，02：	1
	7	Endothelial Cell Activation Contributes to the Release of Procoagulant Microparticles During Acute Cardiac Allograft Rejection显示文摘	Morel O Ohlmann P Epailly E	2008	J Heart Lung Transplant2008，27，1：	1
	8	Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease 显示文摘	Echaniz-Laguna A Mohr M Epailly E	2006	Muscle Nerve2006，33，3：	1
	9	Endothelial cell activation contributes to the release of procoagulant microparticles during acute cardiac allograft rejection显示文摘	Morel O Ohlmann P Epailly E	2008	Heart Lung Transplant2008，27，1：	1
	10	在一个Danon病大家族中的新LAMP-2基因突变与成功的心脏移植治疗显示文摘Lysosome-associated membrane protein-2 deficiency (LAMP2 deficiency), or Danon disease, is a rare X-linked lysosomal disease characterized by cardiomyopathy, vacuolar myopathy, and mental retardation. Less than 20 families with mutations of the Lamp-2 gene have been reported. We describe a family from Sardinia with eight affected patients (4 females and 4 males) and a novel mutation in exon 2 of the Lamp-2 gene (c.102103delAG). Females developed isolated cardiomyopathy in adulthood, whereas males presented with cardiomyopathy, myopathy, and mental retardation before the age of 20 years. Cardiomyopathy was lethal in three females in their 40s and in three males before the age 20 years. One patient was su ccessfully treated by heart transplantation with more than 5-year follow-up. T his study demonstrates that Danon disease is a frequently fatal condition that i s potentially treatable with heart transplantation.	Echaniz-Laguna A. Mohr M. Epailly E. 牛亚利	2006	世界核心医学期刊文摘(神经病学分册)2006，2，6：	0

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