Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening-Reference-Cited by-同舟云学术

Long‐term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening

Published:2022-10-04 Issue:1 Volume:46 Page:15-27
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J of Inher Metab Disea

Author:

Mütze Ulrike¹^ORCID,Garbade Sven F.¹,Gleich Florian¹,Lindner Martin²,Freisinger Peter³,Hennermann Julia B.⁴,Thimm Eva⁵,Gramer Gwendolyn¹⁶,Posset Roland¹,Krämer Johannes⁷,Grünert Sarah C.⁸,Hoffmann Georg F.¹,Kölker Stefan¹

Affiliation:

1. Division of Child Neurology and Metabolic Medicine, Center for Child and Adolescent Medicine and Dietmar Hopp Metabolic Center University Hospital Heidelberg Heidelberg Germany

2. Division of Pediatric Neurology University Children's Hospital Frankfurt Frankfurt Germany

3. Children's Hospital Reutlingen Klinikum am Steinenberg, Reutlingen Germany

4. Villa Metabolica, Center for Pediatric and Adolescent Medicine Mainz University Medical Center Mainz Germany

5. Department of General Pediatrics, Neonatology, and Pediatric Cardiology University Children's Hospital, Heinrich Heine University Düsseldorf Düsseldorf Germany

6. University Medical Center Hamburg‐Eppendorf University Children's Hospital Hamburg Germany

7. Ulm Department of Pediatric and Adolescent Medicine Ulm University Medical School Ulm Germany

8. Department of General Pediatrics, Adolescent Medicine and Neonatology Medical Center ‐ University of Freiburg, Faculty of Medicine Freiburg Germany

Funder

Medizinischen Fakultät Heidelberg, Universität Heidelberg

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12563

Reference29 articles.

1. Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany *

2. Long-term Outcomes of Individuals With Metabolic Diseases Identified Through Newborn Screening

3. Newborn screening and disease variants predict neurological outcome in isovaleric aciduria

4. Growth and Final Height Among Children With Phenylketonuria

5. The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation

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