nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A comparative proteomic study of nephrogenesis in intrauterine growth restriction
|
Shen, Qian |
|
2010 |
25 |
6 |
p. 1063-1072 |
artikel |
2 |
Bone metabolism in oxalosis: a single-center study using new imaging techniques and biomarkers
|
Bacchetta, Justine |
|
2010 |
25 |
6 |
p. 1081-1089 |
artikel |
3 |
Chronic treatment with lisinopril decreases proliferative and apoptotic pathways in autosomal recessive polycystic kidney disease
|
Jia, Guangfu |
|
2010 |
25 |
6 |
p. 1139-1146 |
artikel |
4 |
Cisplatin pharmacokinetics in a child receiving peritoneal dialysis
|
Sebestyen, Judit |
|
2010 |
25 |
6 |
p. 1185-1189 |
artikel |
5 |
Cryptogenic organizing pneumonia after rituximab therapy for presumed post-kidney transplant lymphoproliferative disease
|
Bitzan, Martin |
|
2010 |
25 |
6 |
p. 1163-1167 |
artikel |
6 |
Enzymatic disease of the podocyte
|
Kistler, Andreas D. |
|
2010 |
25 |
6 |
p. 1017-1023 |
artikel |
7 |
Evaluation of peritoneal capacity for peritoneal dialysis after abdominal surgery
|
Cho, Min Hyun |
|
2010 |
25 |
6 |
p. 1195-1196 |
artikel |
8 |
First-year response to rhGH therapy in children with CKD: a National Cooperative Growth Study Report
|
Mahan, John D. |
|
2010 |
25 |
6 |
p. 1125-1130 |
artikel |
9 |
Glomerular basement membrane lipidosis in Alagille syndrome
|
Davis, Jessica |
|
2010 |
25 |
6 |
p. 1181-1184 |
artikel |
10 |
HNF1B alterations associated with congenital anomalies of the kidney and urinary tract
|
Nakayama, Makiko |
|
2010 |
25 |
6 |
p. 1073-1079 |
artikel |
11 |
IgG subclasses and complement pathway in segmental and global membranous nephropathy
|
Segawa, Yoshie |
|
2010 |
25 |
6 |
p. 1091-1099 |
artikel |
12 |
Imaging in the evaluation of renovascular disease
|
Tullus, Kjell |
|
2009 |
25 |
6 |
p. 1049-1056 |
artikel |
13 |
Large vessel vasculitis
|
Gulati, Ashima |
|
2009 |
25 |
6 |
p. 1037-1048 |
artikel |
14 |
Levels of urinary transforming growth factor β-1 in children with D+ hemolytic uremic syndrome
|
Caletti, María Gracia |
|
2010 |
25 |
6 |
p. 1177-1180 |
artikel |
15 |
Long-term outcome of children with steroid-resistant nephrotic syndrome treated with tacrolimus
|
Roberti, Isabel |
|
2010 |
25 |
6 |
p. 1117-1124 |
artikel |
16 |
Molecular anatomy of the kidney: what have we learned from gene expression and functional genomics?
|
Rumballe, Bree |
|
2009 |
25 |
6 |
p. 1005-1016 |
artikel |
17 |
Mutant-type α5(IV) collagen in a mild form of Alport syndrome has residual ability to form a heterotrimer
|
Kobayashi, Takehiro |
|
2010 |
25 |
6 |
p. 1169-1172 |
artikel |
18 |
Neurogenic bladder in twins: answer
|
Özçakar, Z. Birsin |
|
2009 |
25 |
6 |
p. 1059-1061 |
artikel |
19 |
Neurogenic bladder in twins: question
|
Özçakar, Z. Birsin |
|
2009 |
25 |
6 |
p. 1057 |
artikel |
20 |
New therapies, new concerns: rituximab-associated lung injury
|
Lands, Larry C. |
|
2010 |
25 |
6 |
p. 1001-1003 |
artikel |
21 |
Orthostatic proteinuria and the spectrum of diurnal variability of urinary protein excretion in healthy children
|
Brandt, John Robert |
|
2010 |
25 |
6 |
p. 1131-1137 |
artikel |
22 |
Outcome of accidental peritoneal dialysis catheter holes or tip exposure
|
Silverstein, Douglas M. |
|
2010 |
25 |
6 |
p. 1147-1151 |
artikel |
23 |
Predictors and consequences of higher estimated glomerular filtration rate at dialysis initiation
|
Atkinson, Meredith A. |
|
2010 |
25 |
6 |
p. 1153-1161 |
artikel |
24 |
Predictors of outcome in Henoch–Schönlein nephritis
|
Edström Halling, Stella |
|
2010 |
25 |
6 |
p. 1101-1108 |
artikel |
25 |
Quality of life or health status in children with chronic kidney disease
|
Maxwell, Hilary |
|
2009 |
25 |
6 |
p. 1191-1192 |
artikel |
26 |
Rituximab efficiency in children with steroid-dependent nephrotic syndrome
|
Sellier-Leclerc, Anne-Laure |
|
2010 |
25 |
6 |
p. 1109-1115 |
artikel |
27 |
Severe respiratory adverse events associated with rituximab infusion
|
Kamei, Koichi |
|
2009 |
25 |
6 |
p. 1193 |
artikel |
28 |
Small vessel vasculitis
|
Brogan, Paul |
|
2009 |
25 |
6 |
p. 1025-1035 |
artikel |
29 |
Two families with compound heterozygosity for adenine phosphoribosyltransferase deficiency
|
Iwaki, Takuma |
|
2010 |
25 |
6 |
p. 1173-1176 |
artikel |