Multicenter randomized controlled trial to evaluate the efficacy and tolerability of frozen gloves for the prevention of chemotherapy-induced peripheral neuropathy

Autor: Beijers, A.J.M., Bonhof, C.S., Mols, F., Ophorst, J., de Vos-Geelen, J., Jacobs, E.M.G., van de Poll-Franse, L.V., Vreugdenhil, G.

Publikováno v: In Annals of Oncology January 2020 31(1):131-136

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Morbidity and mortality in first-degree relatives of C282Y homozygous probands with clinically detected haemochromatosis compared with the general population: the HEmochromatosis FAmily Study (HEFAS)

Autor: Jacobs, E.M.G., Hendriks, J.C.M., Marx, J.J.M., Deursen, C.T. van, Kreeftenberg, H.G., Vries, R.A. de, Stalenhoef, A.F.H., Verbeek, A.L.M., Swinkels, D.W.

Publikováno v: Netherlands Journal of Medicine, 65(11), 425-433. van Zuiden Communications BV.
Netherlands Journal of Medicine, 65, 11, pp. 425-33
Netherlands Journal of Medicine, 65, 425-33

Background: Family screening has been suggested as a sophisticated model for the early detection of HFE-related hereditary haemochromatosis (HH). However, until now, controlled studies on the morbidity and mortality in families with HH are lacking. M

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9b98356c6d6de89d8f0a03b225d265b6
https://hdl.handle.net/2066/51639

Atrial natriuretic peptide increases albuminuria in type I diabetic patients: evidence for blockade of tubular protein reabsorption

Autor: Jacobs, E.M.G., Vervoort, G.M.M., Branten, A.J.W., Klasen, I.S., Smits, P., Wetzels, J.F.M.

Publikováno v: European Journal of Clinical Investigation, 29, 109-115
European Journal of Clinical Investigation, 29, pp. 109-115

Item does not contain fulltext

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a044ef8dc1d7fe9990564752e4a541a3
https://doi.org/10.1046/j.1365-2362.1999.00422.x

On the early management of hereditary hemochromatosis

Autor: Jacobs, E.M.G.

Contains fulltext : 53320.pdf (Publisher’s version ) (Open Access) Homozygosity for the C282Y mutation is one of the most common genetic disorders, which predisposes to iron overload related disease known as hereditary hemochromatosis (HH). Severen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e0838f24df32c6e0af46e588ab11eed0
http://hdl.handle.net/2066/53320