Luisa B. Bay
Buenos Aires, C, Argentina
Last Updated: 09/26/2026
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Found 10 publications
Natural history of cardiac findings in mucopolysaccharidosis type I: report from an international registry.
Journal: Cardiology in the young
Published: October 18, 2023
Growth in individuals with attenuated mucopolysaccharidosis type I during untreated and treated periods: Data from the MPS I registry.
Journal: American journal of medical genetics. Part A
Published: April 07, 2022
A few challenges in mucopolysaccharidosis type I.
Journal: Archivos argentinos de pediatria
Published: July 21, 2020
New recommendations for the care of patients with mucopolysaccharidosis type I.
Journal: Archivos argentinos de pediatria
Published: July 21, 2020
Growth patterns for untreated individuals with MPS I: Report from the international MPS I registry.
Journal: American journal of medical genetics. Part A
Published: June 21, 2019
Infantile-onset Pompe disease: Diagnosis and management.
Journal: Archivos argentinos de pediatria
Published: July 10, 2018
Liver disease and dyslipidemia as a manifestation of lysosomal acid lipase deficiency (LAL-D). Clinical and diagnostic aspects, and a new treatment. An update.
Journal: Archivos argentinos de pediatria
Published: August 22, 2016
Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships.
Journal: Orphanet journal of rare diseases
Published: May 26, 2015
Identification of 17 novel mutations in 40 Argentinean unrelated families with mucopolysaccharidosis type II (Hunter syndrome).
Journal: Molecular genetics and metabolism reports
Published: July 30, 2014
The importance of a law on time: presentation of a girl with biotinidase deficiency who was not picked up through the neonatal screening
Journal: Archivos argentinos de pediatria
Published: November 17, 2008
Showing 1-10 of 10
Last Updated: 09/26/2026