Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference31 articles.
1. Fanconi G, Bickel H. [Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease]. Helv Paediatr Acta 1949; 4: 359-396
2. Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome
3. Fanconi–Bickel Syndrome
4. Mutation Analysis of the GLUT2 Gene in Patients with Fanconi-Bickel Syndrome
5. Fanconi Bickel Syndrome: Novel Mutations inGLUT 2Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families
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1. Clinical, genetic profile and therapy evaluation of 11 Chinese paediatric patients with Fanconi-Bickel syndrome;2023-11-07
2. GLUT2, glucose and oxygen sensing in CD8+ T cells;Nature Metabolism;2023-10-26
3. The glucose transporter 2 regulates CD8+ T cell function via environment sensing;Nature Metabolism;2023-10-26
4. Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome;Biomedicines;2022-08-29
5. Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient;Frontiers in Endocrinology;2022-05-18
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