Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome

Autor: A V, Vanlander, P G, Jorens, J, Smet, B, De Paepe, W, Verbrugghe, G G, Van den Eynden, F, Meire, P, Pauwels, N, Van der Aa, S, Seneca, W, Lissens, J G, Okun, R, Van Coster

Publikováno v: Acta anaesthesiologica Scandinavica. 56(4)

Propofol is an anesthetic agent widely used for induction and maintenance of anesthesia, and sedation in children. Although generally considered as reliable and safe, administration of propofol can occasionally induce a potentially fatal complication

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1a0d026a5fd7044ce87ec7f499fc1f97
https://pubmed.ncbi.nlm.nih.gov/22260353

Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism

Autor: J. G. Okun, Thomas Meissner, P. Bärtsch, Timo Otonkoski, B. Friedmann, T. Bauer, M. A. Schwab, Ertan Mayatepek

Publikováno v: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 37(11)

Exercise-induced hyperinsulinism (EIHI) is a recently described entity characterised by recurrent episodes of hypoglycaemia induced by physical exercise. The index patient for this disorder and a matched control were subjected to aerobic and anaerobi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fd2cc1dd756af57f9f0d5eae6512583
https://pubmed.ncbi.nlm.nih.gov/16308838

Targeted Metabolomic Profiling of Total Fatty Acids in Human Plasma by Liquid Chromatography-Tandem Mass Spectrometry.

Autor: Aidaros AA; Department of Genetics & Genomics, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain 17666, UAE., Sharma C; Department of Internal Medicine, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain 17666, UAE., Langhans CD; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, 69120 Heidelberg, Germany., G Okun J; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, 69120 Heidelberg, Germany., Hoffmann GF; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, 69120 Heidelberg, Germany., Dasouki M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 3354, Saudi Arabia., Chakraborty P; Metabolics and Newborn Screening, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.; Department of Pediatrics, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Aljasmi F; Department of Genetics & Genomics, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain 17666, UAE.; Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain 17666, UAE., Y Al-Dirbashi O; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 3354, Saudi Arabia.; Metabolics and Newborn Screening, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada.; Department of Pediatrics, University of Ottawa, Ottawa, ON K1N 6N5, Canada.; Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain 17666, UAE.

Publikováno v: Metabolites [Metabolites] 2020 Oct 09; Vol. 10 (10). Date of Electronic Publication: 2020 Oct 09.