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Items: 12

1.

Unmet needs and challenges for follow-up and treatment of autosomal dominant polycystic kidney disease: the paediatric perspective.

De Rechter S, Bammens B, Schaefer F, Liebau MC, Mekahli D.

Clin Kidney J. 2018 Dec;11(Suppl 1):i14-i26. doi: 10.1093/ckj/sfy088. Epub 2018 Dec 17. Review.

2.

Simultaneous determination of allantoin and adenosine in human urine using liquid chromatography - UV detection.

Andries A, De Rechter S, Janssens P, Mekahli D, Van Schepdael A.

J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Oct 1;1096:201-207. doi: 10.1016/j.jchromb.2018.08.026. Epub 2018 Aug 27.

PMID:
30176509
3.

Renal progression factors in young patients with tuberous sclerosis complex: a retrospective cohort study.

Janssens P, Van Hoeve K, De Waele L, De Rechter S, Claes KJ, Van de Perre E, Wissing KM, Bammens B, Jansen A, Mekahli D.

Pediatr Nephrol. 2018 Nov;33(11):2085-2093. doi: 10.1007/s00467-018-4003-6. Epub 2018 Jul 9.

PMID:
29987458
4.

Prevalence of Hypertension in Children with Early-Stage ADPKD.

Massella L, Mekahli D, Paripović D, Prikhodina L, Godefroid N, Niemirska A, Ağbaş A, Kalicka K, Jankauskiene A, Mizerska-Wasiak M, Afonso AC, Salomon R, Deschênes G, Ariceta G, Özçakar ZB, Teixeira A, Duzova A, Harambat J, Seeman T, Hrčková G, Lungu AC, Papizh S, Peco-Antic A, De Rechter S, Giordano U, Kirchner M, Lutz T, Schaefer F, Devuyst O, Wühl E, Emma F.

Clin J Am Soc Nephrol. 2018 Jun 7;13(6):874-883. doi: 10.2215/CJN.11401017. Epub 2018 Apr 19.

PMID:
29674338
5.

Is Autosomal Dominant Polycystic Kidney Disease Becoming a Pediatric Disorder?

De Rechter S, Breysem L, Mekahli D.

Front Pediatr. 2017 Dec 20;5:272. doi: 10.3389/fped.2017.00272. eCollection 2017. Review.

6.

3DUS as an alternative to MRI for measuring renal volume in children with autosomal dominant polycystic kidney disease.

Breysem L, De Rechter S, De Keyzer F, Smet MH, Bammens B, Van Dyck M, Hofmans M, Oyen R, Levtchenko E, Mekahli D.

Pediatr Nephrol. 2018 May;33(5):827-835. doi: 10.1007/s00467-017-3862-6. Epub 2018 Jan 6.

PMID:
29306987
7.

Evidence for Bone and Mineral Metabolism Alterations in Children With Autosomal Dominant Polycystic Kidney Disease.

De Rechter S, Bacchetta J, Godefroid N, Dubourg L, Cochat P, Maquet J, Raes A, De Schepper J, Vermeersch P, Van Dyck M, Levtchenko E, D'Haese P, Evenepoel P, Mekahli D.

J Clin Endocrinol Metab. 2017 Nov 1;102(11):4210-4217. doi: 10.1210/jc.2017-01157.

PMID:
29092060
8.

Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease.

De Rechter S, Kringen J, Janssens P, Liebau MC, Devriendt K, Levtchenko E, Bergmann C, Jouret F, Bammens B, Borry P, Schaefer F, Mekahli D.

PLoS One. 2017 Sep 29;12(9):e0185779. doi: 10.1371/journal.pone.0185779. eCollection 2017.

9.

Expanding the role of vasopressin antagonism in polycystic kidney diseases: From adults to children?

Janssens P, Weydert C, De Rechter S, Wissing KM, Liebau MC, Mekahli D.

Pediatr Nephrol. 2018 Mar;33(3):395-408. doi: 10.1007/s00467-017-3672-x. Epub 2017 Apr 28. Review.

PMID:
28455745
10.

The Case | Hypercalcemia in a child with chronic kidney disease.

De Rechter S, Levtchenko E, Evenepoel P, Mekahli D.

Kidney Int. 2016 Jul;90(1):233-4. doi: 10.1016/j.kint.2015.12.060. No abstract available.

PMID:
27312459
11.

Autophagy in renal diseases.

De Rechter S, Decuypere JP, Ivanova E, van den Heuvel LP, De Smedt H, Levtchenko E, Mekahli D.

Pediatr Nephrol. 2016 May;31(5):737-52. doi: 10.1007/s00467-015-3134-2. Epub 2015 Jul 4. Review.

PMID:
26141928
12.

Charcot-Marie-Tooth: are you testing for proteinuria?

De Rechter S, De Waele L, Levtchenko E, Mekahli D.

Eur J Paediatr Neurol. 2015 Jan;19(1):1-5. doi: 10.1016/j.ejpn.2014.08.004. Epub 2014 Aug 28. Review.

PMID:
25439738

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