Work

Co-Occurrence of Two Rare Diseases: A Child with Phenylketonuria and WNT1 Osteoporosis

Year: 2024

Type: article

Study design: Case Report

Source: Hormone Research in Paediatrics

DOI: 10.1159/000541378

Authors: Artemis Doulgeraki, Fan Wang, Anastasia Skouma, Eleana Petropoulou, Symeon Tournis, Alice Costantini, Outi Mäkitie

Institutions: Institute of Child Health, Karolinska Institutet, KAT General Hospital of Attica, University of Helsinki, Helsinki University Hospital, Folkhälsans Forskningscentrum

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4404813976

FWCI:

Cites: 38

Cited by:

Related to: 10