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Peter H N Oomen

Explore the profile of Peter H N Oomen including associated specialties, affiliations and a list of published articles. Areas
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Articles 5
Citations 39
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Recent Articles
1.
Pellikaan K, van Weijen P, Rosenberg A, Hoekstra F, Vermaak M, Oomen P, et al.
Front Endocrinol (Lausanne) . 2023 Apr; 14:1145066. PMID: 37033248
Context: Prader-Willi syndrome (PWS) is a complex rare genetic syndrome. Mortality in patients with PWS is 3% per year. In nearly half of the patients, the cause of death is...
2.
Arendz I, Oomen P, Wolthuis A, van der Velde N, Kroese J, van der Veen I, et al.
Ned Tijdschr Geneeskd . 2013 May; 157(18):A5409. PMID: 23635500
Objective: To determine the prevalence of gestational diabetes mellitus in high-risk pregnancies during the second or third trimester diagnosed by screening with the 75-gram oral glucose tolerance test (75 g-OGTT)...
3.
de Heide L, Glaudemans A, Oomen P, Apers J, Totte E, van Beek A
J Clin Endocrinol Metab . 2012 Apr; 97(6):E963-7. PMID: 22466332
Context: Hyperinsulinemic hypoglycemia after Roux-en-Y gastric bypass (RYGB) has been increasingly reported. It is induced by β-cell hyperplasia often referred to as nesidioblastosis. Positron emission tomography (PET) with [11C]-5-hydroxytryptophan ((11)C-HTP)...
4.
Dullaart R, Oomen P, Sluiter W
Eur J Intern Med . 2007 Apr; 18(3):193-5. PMID: 17449390
Background: Circulating levels of vascular endothelial growth factor (VEGF) may predict microvascular complications in type 1 diabetes mellitus and are elevated when metabolic control is poor. We tested whether serum...
5.
Bayley J, van Minderhout I, Weiss M, Jansen J, Oomen P, Menko F, et al.
BMC Med Genet . 2006 Jan; 7:1. PMID: 16405730
Background: Germline mutations of the SDHD, SDHB and SDHC genes, encoding three of the four subunits of succinate dehydrogenase, are a major cause of hereditary paraganglioma and pheochromocytoma, and demonstrate...