View in EDS

Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis.

Saved in:

Bibliographic Details
Title:	Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis.
Authors:	Demaret T; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.; Centre de Génétique Humaine, Institut de Pathologie et Génétique, Gosselies, Belgium., Joyal JS; Service de Soins Intensifs Pédiatriques, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada., Karalis A; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada., Parente F; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada., Delrue MA; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada., Mitchell GA; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.
Source:	Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2024 Mar 21; Vol. 39, pp. 101073. Date of Electronic Publication: 2024 Mar 21 (Print Publication: 2024).
Publication Type:	Case Reports; Journal Article
Journal Info:	Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101624422 Publication Model: eCollection Cited Medium: Print ISSN: 2214-4269 (Print) Linking ISSN: 22144269 NLM ISO Abbreviation: Mol Genet Metab Rep Subsets: PubMed not MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	2214-4269
DOI:	10.1016/j.ymgmr.2024.101073