Molecular characterization of WFS1 in patients with Wolfram syndrome

Autor: Van den Ouweland, JMW, Cryns, K, Pennings, RJE, Walraven, [No Value], Janssen, GMC, Maassen, JA, Veldhuijzen, BFE, Arntzenius, AB, Lindhout, D, Cremers, CWRJ, Van Camp, G, Dikkeschei, LD

Publikováno v: Journal of molecular diagnostics, 5(2), 88-95. ELSEVIER SCIENCE INC

Wolfram (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness) syndrome is a rare autosomal-recessive neurodegenerative disorder that is characterized by juvenile-onset diabetes mellitus, optic atrophy, diabetes insipidus, and sensorine

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https://research.rug.nl/en/publications/a060ba3a-7215-433e-ae55-713a39dd3fc7

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18F-fluorodeoxyglucose positron emission tomography in elderly patients with an elevated erythrocyte sedimentation rate of unknown origin.

Autor: Lensen KJ; Department of Internal Medicine and the Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, Amsterdam, The Netherlands., Voskuyl AE, van der Laken CJ, Comans EF, van Schaardenburg D, Arntzenius AB, Zwijnenburg T, Stam F, Gompelman M, Zant FM, van Paassen AQ, Voerman BJ, Smit F, Anten S, Siegert CE, Binnerts A, Smulders YM

Publikováno v: PloS one [PLoS One] 2013; Vol. 8 (3), pp. e58917. Date of Electronic Publication: 2013 Mar 19.

Hypomagnesaemia due to use of proton pump inhibitors--a review.

Autor: Kuipers MT; Department of Internal Medicine, Spaarne Hospital, Hoofddorp, the Netherlands., Thang HD, Arntzenius AB

Publikováno v: The Netherlands journal of medicine [Neth J Med] 2009 May; Vol. 67 (5), pp. 169-72.

[Tumors outside of the central nervous system in Von Hippel-Lindau disease].

Autor: Veltman GA; Afd. Interne Geneeskunde, Academisch Ziekenhuis, Leiden., Arntzenius AB, Oosterwijk JC, Lycklamaá Nijeholt AA, Roelfsema F

Publikováno v: Nederlands tijdschrift voor geneeskunde [Ned Tijdschr Geneeskd] 1996 Apr 13; Vol. 140 (15), pp. 823-6.