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Vassili Valayannopoulos

Researcher at Necker-Enfants Malades Hospital

Publications -  175
Citations -  7079

Vassili Valayannopoulos is an academic researcher from Necker-Enfants Malades Hospital. The author has contributed to research in topics: Lysosomal acid lipase deficiency & Sebelipase alfa. The author has an hindex of 41, co-authored 168 publications receiving 5959 citations. Previous affiliations of Vassili Valayannopoulos include Paris Descartes University & Genzyme.

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Suggested guidelines for the diagnosis and management of urea cycle disorders

TL;DR: These guidelines aim at providing a trans-European consensus to guide practitioners, set standards of care and help awareness campaigns, and help to harmonise practice, set common standards and spread good practices with a positive impact on the outcomes of UCD patients.
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Congenital hyperinsulinism: current trends in diagnosis and therapy

TL;DR: Congenital hyperinsulinism is an inappropriate insulin secretion by the pancreatic β-cells secondary to various genetic disorders and Genetics and 18F-fluoro-L-DOPA positron emission tomography (PET) help to diagnose diffuse or focal forms of HI.
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A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase Deficiency.

TL;DR: Sbelipase alfa therapy resulted in a reduction in multiple disease-related hepatic and lipid abnormalities in children and adults with lysosomal acid lipase deficiency and observed improvements in lipid levels and reduction in hepatic fat content.