Výsledky vyhledávání - "E M G, Jacobs"

Atrial natriuretic peptide increases albuminuria in type 1 diabetic patients: evidence for blockade of tubular protein reabsorption

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

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

BACKGROUND It has been suggested that atrial natriuretic peptide (ANP) contributes to the glomerular hyperfiltration of diabetes mellitus. Infusion of ANP increases the urinary excretion of albumin in patients with type I diabetes mellitus (IDDM). Al

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7f05aba0fb1ea3d8c209240d9aaee84f
https://doi.org/10.1046/j.1365-2362.1999.00422.x

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Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosis

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

Publikováno v: The Netherlands journal of medicine. 65(11)

HFE-related hereditary haemochromatosis (HH) is an iron overload disease attributed to the highly prevalent homozygosity for the C282Y mutation in the HFE gene. The pathophysiology of this error in iron metabolism is not completely elucidated yet, al

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::642dd9a6df85323818809d5d0efdcd34
https://pubmed.ncbi.nlm.nih.gov/18079564

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

Publikováno v: The Netherlands journal of medicine. 65(11)

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.Data on iron p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b72c204dd10c1ff931e3481fb01c24e
https://pubmed.ncbi.nlm.nih.gov/18079565

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Impact of the introduction of a guideline on the targeted detection of hereditary haemochromatosis

Autor: E M G, Jacobs, C F M, Meulendijks, L, Elving, G J, van der Wilt, D W, Swinkels

Publikováno v: The Netherlands journal of medicine. 63(6)

In 1998 a clinical guideline for the targeted, accurate and early detection and treatment of HFE-related hereditary haemochromatosis (HH), which comprises a test for the causative HFE-gene mutations, was introduced in our outpatient department.The im

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::67563e920ab8884e2cdc66371f1218e0
https://pubmed.ncbi.nlm.nih.gov/16011012

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PTU-associated cutaneous vasculitis with ANCA anti-MPO and anti-PR3 antibodies

Autor: E M G, Jacobs, A, Hartkamp, H A H, Kaasjager

Publikováno v: The Netherlands journal of medicine. 61(9)

A 36-year-old woman presented at our clinic with symmetrical, tender, palpable purpuric lesions on her lower legs and buttocks after restarting PTU therapy for relapsing Graves' disease. PTU-induced vasculitis was diagnosed with remarkable ANCA anti-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ec1f5b8371cf82d87373b041da5b9d1f
https://pubmed.ncbi.nlm.nih.gov/14692444

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[From gene to disease; HFE-mutations in primary haemochromatosis]

Autor: D W, Swinkels, E M G, Jacobs

Publikováno v: Nederlands tijdschrift voor geneeskunde. 147(14)

Primary haemochromatosis is an autosomal recessive disorder with a high prevalence (1 in 200-400) among North-Europeans. Approximately 64-100% of patients with primary haemochromatosis are homozygous for a missense mutation that alters a major-histoc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a2c904ee258bcf91abb5a140e90cdd37
https://pubmed.ncbi.nlm.nih.gov/12712652

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[Diagnosis of 5 patients with possible primary hemochromatosis]

Autor: E M G, Jacobs, R A, de Vries, L D, Elving, A F H, Stalenhoef, D W, Swinkels

Publikováno v: Nederlands tijdschrift voor geneeskunde. 147(14)

In a 49-year-old man and a 28-year-old woman, both of whom complained of fatigue, HFE-gen related respectively non-HFE-gen related primary haemochromatosis was diagnosed, based on the elevated serum transferrin saturation, the elevated serum ferritin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::43cc37ac69298d584376fa94f11b8c59
https://pubmed.ncbi.nlm.nih.gov/12712648

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[Results from a general training hospital for the implementation of a diagnostic workup for pulmonary embolism according to the Dutch Institute for Health Care Improvement]

Autor: P W, Kamphuisen, E M G, Jacobs, J J, Mol, A J M, Rijnders, E F, Ullmann

Publikováno v: Nederlands tijdschrift voor geneeskunde. 146(44)

To evaluate the active implementation of the Dutch Institute for Healthcare Improvement's guideline for the diagnostic work-up for pulmonary embolism in a general training hospital, and to analyse reasons for not following the guideline strategy.Part

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fe2f58d4ca08d82c673e0bc2e827aea7
https://pubmed.ncbi.nlm.nih.gov/12448959

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