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                             27 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of nephrogenic diabetes insipidus with a novel missense mutation in the AVPR2 gene Ashida, Akira

22 5 p. 670-673
artikel
2 ACE inhibition in nutcracker syndrome with orthostatic proteinuria: how about a hemodynamic effect? Shin, Jae Il

22 5 p. 758
artikel
3 ACE inhibition in orthostatic proteinuria associated with nutcracker syndrome would be individualized Ha, Tae-Sun

22 5 p. 759-760
artikel
4 Adolescent dialysis patient transition to adult care: a cross-sectional survey Bell, Lorraine

22 5 p. 720-726
artikel
5 A multicenter study of the pharmacokinetics of lisinopril in pediatric patients with hypertension Hogg, Ronald J.

22 5 p. 695-701
artikel
6 Association of isolated preauricular tags and nephrourological anomalies: case-control study Lizama, Macarena

22 5 p. 658-660
artikel
7 Ceftriaxone associated nephrolithiasis: a prospective study in 284 children Mohkam, Masoumeh

22 5 p. 690-694
artikel
8 Darbepoetin, effective treatment of anaemia in paediatric patients with chronic renal failure André, Jean-Luc

22 5 p. 708-714
artikel
9 Diagnosis of Alport syndrome without biopsy? Gubler, Marie Claire

22 5 p. 621-625
artikel
10 Diagnosis of de novo localized thrombotic microangiopathy by surveillance biopsy Hastings, M. Colleen

22 5 p. 742-746
artikel
11 Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)? Zhang, Ke Wei

22 5 p. 645-651
artikel
12 Effect of carnitine supplementation on lipid profile and anemia in children on chronic dialysis Verrina, Enrico

22 5 p. 727-733
artikel
13 Effects of deflazacort vs. methylprednisone: a randomized study in kidney transplant patients Ferraris, Jorge R.

22 5 p. 734-741
artikel
14 Erratum to: Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations Landau, Daniel

22 5 p. 761
artikel
15 Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations Landau, Daniel

22 5 p. 661-669
artikel
16 Genetics of focal segmental glomerulosclerosis Woroniecki, Robert P.

22 5 p. 638-644
artikel
17 How to define anemia in children with chronic kidney disease? Filler, Guido

22 5 p. 702-707
artikel
18 In memory of Dr. Johannes Brodehl, born 20 October 1931 and died 2 September 2006 Brandis, Matthias

22 5 p. 762-763
artikel
19 Is mesangial hypercellularity with glomerular immaturity a variant of glomerulosclerosis? Ostalska-Nowicka, Danuta

22 5 p. 674-683
artikel
20 Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease Assadi, Farahnak

22 5 p. 750-752
artikel
21 Malaria-induced renal damage: facts and myths Ehrich, Jochen H. H.

22 5 p. 626-637
artikel
22 Meningococcal disease associated with an acute post-streptococcal complement deficiency Daskas, Nikolaos

22 5 p. 747-749
artikel
23 Metabolic disturbances following the use of inadequate solutions for hemofiltration in acute renal failure Soysal, Demet Demirkol

22 5 p. 715-719
artikel
24 Nine novel COL4A3 and COL4A4 mutations and polymorphisms identified in inherited membrane diseases Rana, Kesha

22 5 p. 652-657
artikel
25 Renal scarring sequelae in childhood Kawasaki disease Wang, Jieh-Neng

22 5 p. 684-689
artikel
26 Severe anemia caused by the angiotensin receptor blocker irbesartan after renal transplantation Simonetti, Giacomo D.

22 5 p. 756-757
artikel
27 Superior sagittal sinus thrombosis and bilateral sixth-nerve palsy in a child with nephrotic syndrome Zaragoza-Casares, Pablo

22 5 p. 753-755
artikel
                             27 gevonden resultaten
 
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