Late Diagnosis of Fanconi-Bickel Syndrome-Reference-Cited by-同舟云学术

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Late Diagnosis of Fanconi-Bickel Syndrome

Published:2016-07-29 Issue: Volume:4 Page:232640981667943
ISSN:2326-4098
Container-title:Journal of Inborn Errors of Metabolism and Screening
language:en
Short-container-title:Journal of Inborn Errors of Metabolism and Screening

Author:

Gupta Nirupama¹,Nambam Bimota²,Weinstein David A.³,Shoemaker Lawrence R.¹

Affiliation:

1. Division of Nephrology, Department of Pediatrics, University of Florida, Gainesville, FL, USA

2. Division of Endocrinology, Department of Pediatrics, University of Florida, Gainesville, FL, USA

3. Glycogen Storage Disease Program, Department of Pediatrics, University of Florida, Gainesville, FL, USA

Publisher

FapUNIFESP (SciELO)

Subject

Genetics(clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/2326409816679430

Reference28 articles.

1. Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome

2. GLUT2, glucose sensing and glucose homeostasis

3. Organization of the Human GLUT2 (Pancreatic β-Cell and Hepatocyte) Glucose Transporter Gene

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1. Current Clinical Guidelines for the Management of Patients with Glycogen Storage Disease;Pediatric pharmacology;2024-07-04

2. Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care;Reviews in Endocrine and Metabolic Disorders;2024-04-01

3. Idiopathic Pathological Ketotic Hypoglycemia: Finding the Needle in a Haystack;Hormone Research in Paediatrics;2024-03-21

4. Fanconi-Bickel Syndrome: A Rare Etiology of Hypophosphatemic Rickets;Paediatric Nephrology Journal of Bangladesh;2024-01

5. Nutritional support in glycogen storage diseases: evolution of treatment and unresolved contradictions;Annals of the Russian academy of medical sciences;2023-11-01

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