92 a Glycogen Storage Disease Type I and Iii(gsdi, Iii) and Pyruvate Carboxylase Deficiency (Pcd): Nocturnal Gastric Drip Feeding Versus Administration of Uncooked Corn Starch!

Pediatric Research - United States
doi 10.1203/00006450-198610000-00146
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Liver Transplantation for Glycogen Storage Disease Types I, III, and IV

European Journal of Pediatrics
Child HealthPediatricsPerinatology
1999English

Markedly Elevated Serum Transaminases in Glycogen Storage Disease Type III

Journal of Pediatric Gastroenterology and Nutrition
Child HealthPediatricsPerinatologyGastroenterology
2011English

Pyruvate Carboxylase Deficiency

2020English

Glycogen Storage Disease Due to Muscle and Heart Glycogen Synthase Deficiency

2020English

Pulmonary Arterial Hypertension in Glycogen Storage Disease Type I

Journal of Inborn Errors of Metabolism and Screening
Child HealthGeneticsEndocrinologyPerinatologyPediatricsMetabolismDiabetes
2017English

753 an Intraoral Prosthesis Facilitates Continuous Noc-Turnal Feedings (Cnf) in Glycogen Storage Diseases, Types I and Iii (Gsd I/Iii)

Pediatric Research
Child HealthPediatricsPerinatology
1981English

181: A Patient With Pyruvate Carboxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1976English

Beneficial Effects of Ketogenic Diet on Phosphofructokinase Deficiency (Glycogen Storage Disease Type VII)

Frontiers in Neurology
Neurology
2020English

Glycogen Storage Disease Due to Phosphorylase Kinase Deficiency

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy