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Items: 1 to 50 of 282

1.

Switch in FGFR3 and -4 expression profile during human renal development may account for transient hypercalcemia in patients with Sotos syndrome due to 5q35 microdeletions.

Mutsaers HA, Levtchenko EN, Martinerie L, Pertijs JC, Allegaert K, Devriendt K, Masereeuw R, Monnens LA, Lombès M.

J Clin Endocrinol Metab. 2014 Jul;99(7):E1361-7. doi: 10.1210/jc.2014-1123. Epub 2014 Mar 26.

2.

Pre-treatment of dairy and breast milk with sevelamer hydrochloride and sevelamer carbonate to reduce phosphate.

Raaijmakers R, Houkes LM, Schröder CH, Willems JL, Monnens LA.

Perit Dial Int. 2013 Sep-Oct;33(5):565-72. doi: 10.3747/pdi.2012.00063. Epub 2013 May 1.

3.

In memoriam: Professor Cornelis Schroder--8 April 1951-19 September 2012.

Monnens LA, Van de Walle J, Knoll J, Levtchenko EN; European Society of Pediatric Nephrology.

Pediatr Nephrol. 2013 May;28(5):833-4. doi: 10.1007/s00467-013-2422-y. Epub 2013 Feb 23. No abstract available.

PMID:
23436175
4.

The paradox of hyperdopaminuria in aromatic L-amino Acid deficiency explained.

Wassenberg T, Monnens LA, Geurtz BP, Wevers RA, Verbeek MM, Willemsen MA.

JIMD Rep. 2012;4:39-45. doi: 10.1007/8904_2011_84. Epub 2011 Nov 2.

5.

Drug-induced alterations in Mg2+ homoeostasis.

Lameris AL, Monnens LA, Bindels RJ, Hoenderop JG.

Clin Sci (Lond). 2012 Jul;123(1):1-14. doi: 10.1042/CS20120045. Review.

PMID:
22409531
6.

Apparent mineralocorticoid excess: time of manifestation and complications despite treatment.

Knops NB, Monnens LA, Lenders JW, Levtchenko EN.

Pediatrics. 2011 Jun;127(6):e1610-4. doi: 10.1542/peds.2010-1928. Epub 2011 May 2.

PMID:
21536617
7.

Renal transplantation for fibromuscular dysplasia.

Knops NB, Cornelissen EA, Monnens LA.

Am J Transplant. 2011 Apr;11(4):852-6. doi: 10.1111/j.1600-6143.2011.03455.x.

8.

Cysteamine restores glutathione redox status in cultured cystinotic proximal tubular epithelial cells.

Wilmer MJ, Kluijtmans LA, van der Velden TJ, Willems PH, Scheffer PG, Masereeuw R, Monnens LA, van den Heuvel LP, Levtchenko EN.

Biochim Biophys Acta. 2011 Jun;1812(6):643-51. doi: 10.1016/j.bbadis.2011.02.010. Epub 2011 Feb 28.

9.

Nephrogenic syndrome of inappropriate antidiuresis.

Levtchenko EN, Monnens LA.

Nephrol Dial Transplant. 2010 Sep;25(9):2839-43. doi: 10.1093/ndt/gfq324. Epub 2010 Jun 13.

PMID:
20543212
10.

Involvement of claudin 3 and claudin 4 in idiopathic infantile hypercalcaemia: a novel hypothesis?

Lameris AL, Huybers S, Burke JR, Monnens LA, Bindels RJ, Hoenderop JG.

Nephrol Dial Transplant. 2010 Nov;25(11):3504-9. doi: 10.1093/ndt/gfq221. Epub 2010 Apr 20.

PMID:
20466674
11.

Novel conditionally immortalized human proximal tubule cell line expressing functional influx and efflux transporters.

Wilmer MJ, Saleem MA, Masereeuw R, Ni L, van der Velden TJ, Russel FG, Mathieson PW, Monnens LA, van den Heuvel LP, Levtchenko EN.

Cell Tissue Res. 2010 Feb;339(2):449-57. doi: 10.1007/s00441-009-0882-y. Epub 2009 Nov 10.

12.

Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review.

Löwik MM, Groenen PJ, Levtchenko EN, Monnens LA, van den Heuvel LP.

Eur J Pediatr. 2009 Nov;168(11):1291-304. doi: 10.1007/s00431-009-1017-x. Epub 2009 Jun 27. Review.

13.

Mitochondrial complex V expression and activity in cystinotic fibroblasts.

Wilmer MJ, van den Heuvel LP, Rodenburg RJ, Vogel RO, Nijtmans LG, Monnens LA, Levtchenko EN.

Pediatr Res. 2008 Nov;64(5):495-7. doi: 10.1203/PDR.0b013e318183fd67.

PMID:
18596576
14.

Urinary protein excretion pattern and renal expression of megalin and cubilin in nephropathic cystinosis.

Wilmer MJ, Christensen EI, van den Heuvel LP, Monnens LA, Levtchenko EN.

Am J Kidney Dis. 2008 Jun;51(6):893-903. doi: 10.1053/j.ajkd.2008.03.010. Epub 2008 May 2.

PMID:
18455850
15.

Proteomic profiling and identification in peritoneal fluid of children treated by peritoneal dialysis.

Raaijmakers R, Pluk W, Schröder CH, Gloerich J, Cornelissen EA, Wessels HJ, Willems JL, Monnens LA, van den Heuvel LP.

Nephrol Dial Transplant. 2008 Jul;23(7):2402-5. doi: 10.1093/ndt/gfn212. Epub 2008 Apr 19.

PMID:
18424818
16.

[From gene to disease; Dent's disease caused by abnormalities in the CLCN5 and OCRL1 genes].

Levtchenko EN, Monnens LA, Bökenkamp A, Knoers NV.

Ned Tijdschr Geneeskd. 2007 Oct 27;151(43):2377-80. Review. Dutch.

PMID:
18019214
17.

Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemia.

Cairo ER, Friedrich T, Swarts HG, Knoers NV, Bindels RJ, Monnens LA, Willems PH, De Pont JJ, Koenderink JB.

Biochim Biophys Acta. 2008 Feb;1778(2):398-404. Epub 2007 Oct 17.

18.

Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation.

Löwik MM, Groenen PJ, Pronk I, Lilien MR, Goldschmeding R, Dijkman HB, Levtchenko EN, Monnens LA, van den Heuvel LP.

Kidney Int. 2007 Nov;72(10):1198-203. Epub 2007 Aug 22.

19.

Cystine dimethylester model of cystinosis: still reliable?

Wilmer MJ, Willems PH, Verkaart S, Visch HJ, de Graaf-Hess A, Blom HJ, Monnens LA, van den Heuvel LP, Levtchenko EN.

Pediatr Res. 2007 Aug;62(2):151-5.

PMID:
17597653
20.

Interactions of Shiga-like toxin with human peripheral blood monocytes.

Geelen JM, van der Velden TJ, van den Heuvel LP, Monnens LA.

Pediatr Nephrol. 2007 Aug;22(8):1181-7. Epub 2007 May 22.

21.

Adult and paediatric patients with minimal change nephrotic syndrome show no major alterations in glomerular expression of sulphated heparan sulphate domains.

Wijnhoven TJ, Geelen JM, Bakker M, Lensen JF, Rops AL, Kramer AB, Navis G, van den Hoven MJ, van der Vlag J, Berden JH, Wetzels JF, van den Heuvel LP, Monnens LA, van Kuppevelt TH.

Nephrol Dial Transplant. 2007 Oct;22(10):2886-93. Epub 2007 May 25.

PMID:
17526541
22.

[From gene to disease; 'apparent mineralocorticoid excess' syndrome, a syndrome with an apparent excess of mineral corticoids].

Levtchenko EN, Deinum J, Knoers NV, Hermus AR, Monnens LA, Lenders JW.

Ned Tijdschr Geneeskd. 2007 Mar 24;151(12):692-4. Review. Dutch.

PMID:
17447595
23.

[From gene to disease; the haemolytic uraemic syndrome can be caused by mutations in regulating factors of the alternative route of the complement system].

Geelen JM, Klasen IS, van den Heuvel LP, Monnens LA.

Ned Tijdschr Geneeskd. 2007 Jan 20;151(3):185-8. Review. Dutch.

PMID:
17288344
24.

In vivo degradation of heparan sulfates in the glomerular basement membrane does not result in proteinuria.

Wijnhoven TJ, Lensen JF, Wismans RG, Lamrani M, Monnens LA, Wevers RA, Rops AL, van der Vlag J, Berden JH, van den Heuvel LP, van Kuppevelt TH.

J Am Soc Nephrol. 2007 Mar;18(3):823-32. Epub 2007 Jan 24. Retraction in: J Am Soc Nephrol. 2008 Mar;19(3):647.

25.

Lack of specific binding of Shiga-like toxin (verocytotoxin) and non-specific interaction of Shiga-like toxin 2 antibody with human polymorphonuclear leucocytes.

Geelen JM, van der Velden TJ, Te Loo DM, Boerman OC, van den Heuvel LP, Monnens LA.

Nephrol Dial Transplant. 2007 Mar;22(3):749-55. Epub 2006 Nov 24.

PMID:
17127697
26.

Intestinal perforations in children on peritoneal dialysis.

Raaijmakers R, Monnens LA, Warris A, Schröder CH.

Perit Dial Int. 2006 Nov-Dec;26(6):712-4. No abstract available.

PMID:
17047240
27.

Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease.

Ludwig M, Utsch B, Monnens LA.

Nephrol Dial Transplant. 2006 Oct;21(10):2708-17. Epub 2006 Jul 20. Review. No abstract available.

PMID:
16861240
28.

No evidence of hearing loss in pseudohypoaldosteronism type 1 patients.

Peters TA, Levtchenko E, Cremers CW, Curfs JH, Monnens LA.

Acta Otolaryngol. 2006 Mar;126(3):237-9.

PMID:
16618647
29.

Decreased intracellular ATP content and intact mitochondrial energy generating capacity in human cystinotic fibroblasts.

Levtchenko EN, Wilmer MJ, Janssen AJ, Koenderink JB, Visch HJ, Willems PH, de Graaf-Hess A, Blom HJ, van den Heuvel LP, Monnens LA.

Pediatr Res. 2006 Feb;59(2):287-92.

PMID:
16439594
30.

Teaching molecular genetics: Chapter 1--Background principles and methods of molecular biology.

Knoers NV, Monnens LA.

Pediatr Nephrol. 2006 Feb;21(2):169-76. Epub 2005 Dec 31.

PMID:
16388390
31.

Strict cysteamine dose regimen is required to prevent nocturnal cystine accumulation in cystinosis.

Levtchenko EN, van Dael CM, de Graaf-Hess AC, Wilmer MJ, van den Heuvel LP, Monnens LA, Blom HJ.

Pediatr Nephrol. 2006 Jan;21(1):110-3. Epub 2005 Oct 27.

PMID:
16252107
32.

Elevated oxidized glutathione in cystinotic proximal tubular epithelial cells.

Wilmer MJ, de Graaf-Hess A, Blom HJ, Dijkman HB, Monnens LA, van den Heuvel LP, Levtchenko EN.

Biochem Biophys Res Commun. 2005 Nov 18;337(2):610-4. Epub 2005 Sep 23.

PMID:
16202976
33.

Sodium sieving in children.

Rusthoven E, Krediet RT, Willems HL, Monnens LA, Schröder CH.

Perit Dial Int. 2005 Feb;25 Suppl 3:S141-2.

PMID:
16048281
34.

Evaluation of intraperitoneal pressure and the effect of different osmotic agents on intraperitoneal pressure in children.

Rusthoven E, van der Vlugt ME, van Lingen-van Bueren LJ, van Schaijk TC, Willems HL, Monnens LA, Schröder CH.

Perit Dial Int. 2005 Jul-Aug;25(4):352-6.

PMID:
16022091
35.

[Lithium, a potentially dangerous drug].

Monnens LA, Levtchenko E.

Ned Tijdschr Geneeskd. 2005 Apr 30;149(18):1019; author reply 1019. Dutch. No abstract available.

PMID:
15903049
36.

IgG and complement receptor expression in children treated by peritoneal dialysis.

Bouts AH, Davin JC, Krediet RT, Schröder CH, Monnens LA, Nauta J, van de Winkel JG, Out TA.

Pediatr Nephrol. 2005 Aug;20(8):1161-7. Epub 2005 Apr 26.

PMID:
15856320
37.

Renal transplant nephrectomy in children: can an aggressive approach be recommended?

Zerouali F, Levtchenko EN, Feitz WF, Cornelissen EA, Monnens LA.

Pediatr Transplant. 2004 Dec;8(6):561-4.

PMID:
15598324
38.

Peritoneal transport characteristics with glucose polymer-based dialysis fluid in children.

Rusthoven E, Krediet RT, Willems HL, Monnens LA, Schröder CH.

J Am Soc Nephrol. 2004 Nov;15(11):2940-7.

39.

Intravenous iron supplementation in children on hemodialysis.

Leijn E, Monnens LA, Cornelissen EA.

J Nephrol. 2004 May-Jun;17(3):423-6.

PMID:
15365964
40.

Genetic disorders of transporters/channels in the inner ear and their relation to the kidney.

Peters TA, Monnens LA, Cremers CW, Curfs JH.

Pediatr Nephrol. 2004 Nov;19(11):1194-201. Epub 2004 Sep 9. Review.

PMID:
15365806
41.

Children with chronic renal failure have reduced numbers of memory B cells.

Bouts AH, Davin JC, Krediet RT, Monnens LA, Nauta J, Schröder CH, van Lier RA, Out TA.

Clin Exp Immunol. 2004 Sep;137(3):589-94.

42.

IGG and complement receptor expression on peripheral white blood cells in uraemic children.

Bouts AH, Krediet RT, Davin JC, Monnens LA, Nauta J, Schröder CH, van de Winkel JG, Out TA.

Nephrol Dial Transplant. 2004 Sep;19(9):2296-301. Epub 2004 Jul 20.

PMID:
15266033
43.

Fibrin glue used successfully in peritoneal dialysis catheter leakage in children.

Rusthoven E, van de Kar NA, Monnens LA, Schröder CH.

Perit Dial Int. 2004 May-Jun;24(3):287-9.

PMID:
15185778
44.

[From gene to disease: cystinosis].

Levtchenko EN, Wilmer M, de Graaf-Hess AC, van den Heuvel LP, Blom H, Monnens LA.

Ned Tijdschr Geneeskd. 2004 Mar 6;148(10):476-8. Review. Dutch.

PMID:
15042893
45.

[Tumor growth during the waiting period for radiotherapy in patients with oropharyngeal carcinoma].

Monnens LA.

Ned Tijdschr Geneeskd. 2003 Nov 29;147(48):2400-1; author reply 2401. Dutch. No abstract available.

PMID:
14677486
46.

Is biopsy required prior to cyclophosphamide in steroid-sensitive nephrotic syndrome?

Stadermann MB, Lilien MR, van de Kar NC, Monnens LA, Schröder CH.

Clin Nephrol. 2003 Nov;60(5):315-7.

PMID:
14640236
47.

Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections.

Artz MA, Steenbergen EJ, Hoitsma AJ, Monnens LA, Wetzels JF.

Transplantation. 2003 Sep 15;76(5):821-6.

PMID:
14501861
48.

Defective proximal tubular function in a patient with I-cell disease.

Bocca G, Monnens LA.

Pediatr Nephrol. 2003 Aug;18(8):830-2. Epub 2003 Jun 13.

PMID:
12811655
49.

Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K+-ATPase gamma-subunit.

Meij IC, Koenderink JB, De Jong JC, De Pont JJ, Monnens LA, Van Den Heuvel LP, Knoers NV.

Ann N Y Acad Sci. 2003 Apr;986:437-43. Review.

PMID:
12763862
50.

WT-1 and NPHS2 mutation analysis in patients with non-familial steroid-resistant focal-segmental glomerulosclerosis.

Löwik MM, Levtchenko EN, Monnens LA, van den Heuvel LP.

Clin Nephrol. 2003 Feb;59(2):143-6.

PMID:
12608558

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