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 |