Bert Bammens
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Explore the profile of Bert Bammens including associated specialties, affiliations and a list of published articles.
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104
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Recent Articles
21.
Dai L, Meijers B, Bammens B, de Loor H, Schurgers L, Qureshi A, et al.
Toxins (Basel)
. 2020 May;
12(6).
PMID: 32471179
Gut microbial metabolism is not only an important source of uremic toxins but may also help to maintain the vitamin K stores of the host. We hypothesized that sevelamer therapy,...
22.
Keddar M, Muylle T, Carrie E, Trefois P, Nachit M, Crott R, et al.
Front Physiol
. 2020 Mar;
11:130.
PMID: 32161551
Fat accumulation in skeletal muscle was recently established as a major risk factor for cardiovascular disease (CVD) in the general population, but its relevance for patients with kidney failure is...
23.
Janssens P, Jouret F, Bammens B, Liebau M, Schaefer F, Dandurand A, et al.
Sci Rep
. 2020 Mar;
10(1):4294.
PMID: 32152377
It is unknown whether early diagnosis of autosomal dominant polycystic kidney disease (ADPKD) can enable earlier management and improve outcomes. We conducted a post hoc analysis of data from the...
24.
Andrei G, Van Loon E, Lerut E, Victoor J, Meijers B, Bammens B, et al.
Antiviral Res
. 2019 Jun;
168:203-209.
PMID: 31212020
Cytomegalovirus (CMV) is one of the most common opportunistic infections after transplantation. To prevent CMV infections, universal prophylaxis and pre-emptive therapy with ganciclovir or its prodrug valganciclovir is applied. However,...
25.
Burgmaier K, Kilian S, Bammens B, Benzing T, Billing H, Buscher A, et al.
Sci Rep
. 2019 May;
9(1):7919.
PMID: 31138820
Autosomal recessive polycystic kidney disease (ARPKD) is a severe pediatric hepatorenal disorder with pronounced phenotypic variability. A substantial number of patients with early diagnosis reaches adulthood and some patients are...
26.
Evenepoel P, Claes K, Meijers B, Laurent M, Bammens B, Naesens M, et al.
Kidney Int
. 2019 Mar;
95(6):1461-1470.
PMID: 30922664
Kidney transplant recipients are at increased risk of fractures. This prospective observational study investigated whether areal bone mineral density (aBMD) as assessed by dual-energy x-ray absorptiometry can predict incident fragility...
27.
Evenepoel P, Claes K, Cavalier E, Meijers B, Stenvinkel P, Behets G, et al.
Kidney Int
. 2019 Jan;
95(2):412-419.
PMID: 30665572
Autosomal dominant polycystic kidney disease (ADPKD) is among the most common hereditary nephropathies. Low bone turnover osteopenia has been reported in mice with conditional deletion of the PKD1 and PKD2...
28.
De Rechter S, Bammens B, Schaefer F, Liebau M, Mekahli D
Clin Kidney J
. 2018 Dec;
11(Suppl 1):i14-i26.
PMID: 30581562
Awareness is growing that the clinical course of autosomal dominant polycystic kidney disease (ADPKD) already begins in childhood, with a broad range of both symptomatic and asymptomatic features. Knowing that...
29.
Evenepoel P, Claes K, Meijers B, Laurent M, Bammens B, Naesens M, et al.
J Bone Miner Res
. 2018 Nov;
34(2):262-269.
PMID: 30427544
Chronic kidney disease and osteoporosis are major public health problems associated with an aging population. Vitamin K insufficiency is prevalent among patients with end-stage renal disease (ESRD). Preliminary data indicate...
30.
Evenepoel P, Claes K, Meijers B, Laurent M, Bammens B, Naesens M, et al.
Nephrol Dial Transplant
. 2018 Oct;
35(4):697-705.
PMID: 30339234
The skeletal effects of renal transplantation are not completely understood, especially in patients managed with a steroid minimization immunosuppressive protocol and long term. We enrolled 69 adult transplant recipients (39...