Gustavo H. Cabrera

San Isidro, B, Argentina

Last Updated: 09/26/2026

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Found 14 publications

Diagnosis, treatment, and follow-up of Fabry disease in pediatrics.

Diagnosis, treatment, and follow-up of Fabry disease in pediatrics.

Journal: Molecular genetics and metabolism

Published: October 09, 2025

New Drugs Available for Fabry Disease.

New Drugs Available for Fabry Disease.

Journal: Kidney & blood pressure research

Published: December 30, 2024

Argentine program of home infusions with enzyme replacement therapy for lysosomal diseases: Results in safety, quality of life and adherence.

Argentine program of home infusions with enzyme replacement therapy for lysosomal diseases: Results in safety, quality of life and adherence.

Journal: Molecular genetics and metabolism

Published: December 09, 2024

Clinical outcomes among young patients with Fabry disease who initiated agalsidase beta treatment before 30 years of age: An analysis from the Fabry Registry.

Clinical outcomes among young patients with Fabry disease who initiated agalsidase beta treatment before 30 years of age: An analysis from the Fabry Registry.

Journal: Molecular genetics and metabolism

Published: July 30, 2022

Fabry disease and COVID-19: international expert recommendations for management based on real-world experience.

Fabry disease and COVID-19: international expert recommendations for management based on real-world experience.

Journal: Clinical kidney journal

Published: October 17, 2020

The clinical profiles of female patients with Fabry disease in Latin America: A Fabry Registry analysis of natural history data from 169 patients based on enzyme replacement therapy status.

The clinical profiles of female patients with Fabry disease in Latin America: A Fabry Registry analysis of natural history data from 169 patients based on enzyme replacement therapy status.

Journal: JIMD reports

Published: January 15, 2019

Fabry disease. A potential pitfall A family with a novel intronic mutation.

Fabry disease. A potential pitfall A family with a novel intronic mutation.

Journal: Molecular genetics and metabolism reports

Published: May 02, 2018

Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?

Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 13, 2018

Effectiveness of enzyme replacement therapy in Fabry disease: Long term experience in Argentina.

Effectiveness of enzyme replacement therapy in Fabry disease: Long term experience in Argentina.

Journal: Molecular genetics and metabolism reports

Published: November 23, 2016

Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry.

Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry.

Journal: Molecular genetics and metabolism

Published: April 26, 2016

Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry.

Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry.

Journal: Journal of medical genetics

Published: August 26, 2015

Guidelines for diagnosis, monitoring and treatment of Fabry disease

Guidelines for diagnosis, monitoring and treatment of Fabry disease

Journal: Medicina

Published: October 25, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026