Familial LCAT deficiency and cardiovascular disease: the game is not over. A case of dramatic multivessel atherosclerosis.

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第一作者： Federico,Bigazzi

第一单位： Lipoapheresis Unit, Reference Center for the Diagnosis and Treatment of Inherited Dyslipidemias, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy.

作者： Federico,Bigazzi ^[1] ; Beatrice,Dal Pino ^[1] ; Chiara,Pavanello ^[2] ; Francesco,Sbrana ^[3] ; Giovanni D,Aquaro ^[4] ; Vinicio,Napoli ^[5] ; Cataldo,Palmieri ^[6] ; Andrea,Barison ^[4] ; Laura,Calabresi ^[2] ; Tiziana,Sampietro ^[1]

作者单位： Lipoapheresis Unit, Reference Center for the Diagnosis and Treatment of Inherited Dyslipidemias, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy. ^[1] E. Grossi Paoletti Center, Department of Pharmacology and Biomolecular Sciences, University of Milan, Milan, Italy. ^[2] Lipoapheresis Unit, Reference Center for the Diagnosis and Treatment of Inherited Dyslipidemias, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy - francesco.sbrana@ftgm.com. ^[3] MRI Lab, Department of Cardiology, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy. ^[4] Department of Translational Research and New Technologies in Medicine and Surgery, Pisa University, Pisa, Italy. ^[5] Division of Interventional Cardiology, Fondazione Toscana "Gabriele Monasterio", Pisa, Italy. ^[6]

主题词人类(Humans);心血管疾病(Cardiovascular Diseases);动脉粥样硬化(Atherosclerosis);突变(Mutation)

DOI 10.23736/S0026-4806.20.06633-1

PMID 32486613

发布时间 2023-08-11

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