A retrospective study of eating and psychosocial problems in patients with hepatic glycogen storage diseases and idiopathic ketotic hypoglycemia: Towards a standard set of patient‐reported outcome measures-Reference-Cited by-同舟云学术

A retrospective study of eating and psychosocial problems in patients with hepatic glycogen storage diseases and idiopathic ketotic hypoglycemia: Towards a standard set of patient‐reported outcome measures

Published:2021-10-10 Issue:1 Volume:63 Page:29-40
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Venema Annieke¹,Peeks Fabian¹,Bruijn‐van der Veen Marlies¹,Boer Foekje¹,Fokkert‐Wilts Marieke J.¹,Lubout Charlotte M. A.¹,Huskens Bibi²,Dumont Eric²³⁴,Mulkens Sandra²³⁴^ORCID,Derks Terry G. J.¹^ORCID

Affiliation:

1. Department of Metabolic Diseases, Beatrix Children's Hospital, University Medical Centre Groningen University of Groningen Groningen The Netherlands

2. SeysCentra, Center for Paediatric Eating Problems and Incontinence Malden The Netherlands

3. Department of Psychiatry and Neuropsychology, Faculty of Health, Medicine, and Life Sciences Maastricht University Maastricht The Netherlands

4. Department of Clinical Psychological Science, Faculty of Psychology and Neuroscience Maastricht University Maastricht The Netherlands

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12253

Reference35 articles.

1. Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics

2. Glycogen Storage Disease Type III diagnosis and management guidelines

3. Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

4. Guidelines for management of glycogen storage disease type I—European study on glycogen storage disease type I (ESGSD I)

5. Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome

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