Liver transplantation in glycogen storage disease type Ib: The role of SGLT2 inhibitors
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference8 articles.
1. Longterm outcomes of living donor liver transplantation for glycogen storage disease type 1b;Shimizu;Liver Transpl.,2020
2. When considering liver transplant for children with glycogen storage disease 1b;Squires;Liver Transpl.,2020
3. Immunological features and complications in patients with glycogen storage disease 1b after living donor liver transplantation;Shimizu;Pediatr. Transplant.,2021
4. Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency;Veiga-da-Cunha;Proc. Natl. Acad. Sci. U. S. A.,2019
5. Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor;Wortmann;Blood,2020
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1. Outcomes of Pediatric Liver Transplantation in Glycogen Storage Disease Type 1b—A Single‐Center Experience;Pediatric Transplantation;2024-08-30
2. Dapagliflozin and Empagliflozin in Paediatric Indications: A Systematic Review;Pediatric Drugs;2024-04-18
3. Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop;Molecular Genetics and Metabolism;2024-03
4. DBS are suitable for 1,5-anhydroglucitol monitoring in GSD1b and G6PC3-deficient patients taking SGLT2 inhibitors to treat neutropenia;Molecular Genetics and Metabolism;2023-11
5. Glycogen storage diseases;Nature Reviews Disease Primers;2023-09-07
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