Browsing by Author "Bay, Luisa."
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Liver disease and dyslipidemia as a manifestation of lysosomal acid lipase deficiency (LAL-D). Clinical and diagnostic aspects, and a new treatment. An update.
Bay, Luisa.; Cañero Velasco, Cristina.; Ciocca, Mirta.; Cotti, Andrea.; Cuarterolo, Miriam.; Fainboim, Alejandro.; Piñero, Federico.; et al. (Sociedad Argentina de Pediatría., 2017-06-01)Lysosomal acid lipase deficiency (LAL-D) is still a little recognized genetic disease with significant morbidity and mortality in children and adults. This document provides guidance on when to suspect LAL-D and how to ... -
New recommendations for the care of patients with mucopolysaccharidosis type I
Amartino, Hernán.; Bay, Luisa.; Antacle, Alejandra.; Et al. (Sociedad argentina de pediatría, 2021-04)Abstract in English, Spanish Considering the advances made on mucopolysaccharidosis type I after the consensus study published by a group of experts in Argentina in 2008, recommendations about genetic testing, cardiological ...