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

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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
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  Data: Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis.
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  Data: <searchLink fieldCode="AU" term="%22Demaret+T%22">Demaret T</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Joyal+JS%22">Joyal JS</searchLink>; Service de Soins Intensifs Pédiatriques, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Karalis+A%22">Karalis A</searchLink>; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Parente+F%22">Parente F</searchLink>; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Delrue+MA%22">Delrue MA</searchLink>; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.<br /><searchLink fieldCode="AU" term="%22Mitchell+GA%22">Mitchell GA</searchLink>; Service de Génétique médicale, Department of Pediatrics, CHU Sainte-Justine and U Montréal, Montréal, Québec, Canada.
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  Data: <searchLink fieldCode="JN" term="%22101624422%22">Molecular genetics and metabolism reports</searchLink> [Mol Genet Metab Rep] 2024 Mar 21; Vol. 39, pp. 101073. <i>Date of Electronic Publication: </i>2024 Mar 21 (<i>Print Publication: </i>2024).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Inc%22">Elsevier Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101624422 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2214-4269 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2222144269%22">22144269 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab Rep <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1016/j.ymgmr.2024.101073
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      – TitleFull: Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis.
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              Text: 2024 Mar 21
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