Wolfram Syndrome 1: A Pediatrician's and Pediatric Endocrinologist's Perspective.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
12 Feb 2023
Historique:
received: 28 12 2022
revised: 21 01 2023
accepted: 10 02 2023
entrez: 25 2 2023
pubmed: 26 2 2023
medline: 3 3 2023
Statut: epublish

Résumé

Wolfram syndrome 1 (WS1) is a rare autosomal recessive neurodegenerative disease caused by mutations in

Identifiants

pubmed: 36835101
pii: ijms24043690
doi: 10.3390/ijms24043690
pmc: PMC9960967
pii:
doi:

Substances chimiques

Membrane Proteins 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Anastasios Serbis (A)

Department of Pediatrics, School of Medicine, University of Ioannina, 451 10 Ioannina, Greece.

Dimitrios Rallis (D)

Neonatal Intensive Care Unit, School of Medicine, University of Ioannina, 451 10 Ioannina, Greece.

Vasileios Giapros (V)

Neonatal Intensive Care Unit, School of Medicine, University of Ioannina, 451 10 Ioannina, Greece.

Assimina Galli-Tsinopoulou (A)

Second Department of Pediatrics, School of Medicine, Faculty of Health Sciences, AHEPA University General Hospital, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece.

Ekaterini Siomou (E)

Department of Pediatrics, School of Medicine, University of Ioannina, 451 10 Ioannina, Greece.

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Classifications MeSH