Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome

Author:

VANLANDER A. V.1,JORENS P. G.2,SMET J.1,DE PAEPE B.1,VERBRUGGHE W.2,VAN DEN EYNDEN G. G.3,MEIRE F.4,PAUWELS P.3,VAN DER AA N.5,SENECA S.6,LISSENS W.6,OKUN J. G.7,VAN COSTER R.1

Affiliation:

1. Department of Pediatrics; Division of Pediatric Neurology and Metabolism; Ghent University Hospital; Ghent; Belgium

2. Department of Critical Care Medicine; Antwerp University Hospital, Antwerp University; Edegem; Belgium

3. Department of Pathology; Antwerp University; Wilrijk; Belgium

4. Department of Pediatric Ophthalmology; Hôpital Universitaire des Enfants Reine Fabiola; Brussels; Belgium

5. Department of Medical Genetics; Antwerp University Hospital, Antwerp University; Edegem; Belgium

6. Center for Medical Genetics; UZ Brussel and Reproduction and Genetics (REGE); Vrije Universiteit Brussel; Brussels; Belgium

7. Department of General Pediatrics; Division of Inborn Metabolic Diseases; University Children's Hospital; Heidelberg; Germany

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,General Medicine

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