Glycogen storage disease type I: clinical and laboratory profile

Glycogen storage disease type I: clinical and laboratory profile

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Objectives: To characterize the clinical, laboratory, and anthropometric profile of a sample of Brazilian patients with glycogen storage disease type I managed at an outpatient referral clinic for inborn errors of metabolism. Methods: This was a cross‐sectional outpatient study based on a convenienc...

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Bibliographic Details
Main Authors: Berenice L. Santos, Carolina F.M. de Souza, Lavinia Schuler‐Faccini, Lilia Refosco, Matias Epifanio, Tatiele Nalin, Sandra M.G. Vieira, Ida V.D. Schwartz
Format: Article
Language:Portuguese
Published: Brazilian Society of Pediatrics 2014-11-01
Series:Jornal de Pediatria (Versão em Português)
Subjects:
Inborn errors of metabolism
Glycogen storage disease type I
Clinical aspects
Diagnoses
Nutritional status
Online Access:http://www.sciencedirect.com/science/article/pii/S2255553614001220

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http://www.sciencedirect.com/science/article/pii/S2255553614001220

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