Congenital disorders of glycosylation in children – Histopathological and ultrastructural changes in the liver
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference17 articles.
1. The challenge of CDG diagnosis;Francisco;Mol Genet Metab,2019
2. Congenital disorders of glycosylation (CDG): Quo vadis?;Péanne;Eur J Med Genet,2018
3. Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature;Marques-da-Silva;J Inherit Metab Dis,2017
4. CCDC115-CDG: a new rare and misleading inherited cause of liver disease;Girard;Mol Genet Metab,2018
5. Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation;Vajro;Orphanet J Rare Dis,2018
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1. Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review;International Journal of Molecular Sciences;2023-05-11
2. A rare case of SRD5A3‐CDG in a patient with ataxia and telangiectasia: A case report;Clinical Case Reports;2022-11
3. Stroke-like Episodes in Inherited Neurometabolic Disorders;Metabolites;2022-09-30
4. Liver Involvement in Congenital Disorders of Glycosylation and Deglycosylation;Frontiers in Pediatrics;2021-07-05
5. Liver Involvement in Congenital Disorders of Glycosylation: A Systematic Review;Journal of Pediatric Gastroenterology & Nutrition;2021-06-24
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