| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A confused child: Answer
|
Fitzpatrick, Emer
|
|
|
22 |
3 |
p. 356-357
|
artikel
|
| 2 |
A confused child: Question
|
Fitzpatrick, Emer
|
|
|
22 |
3 |
p. 355
|
artikel
|
| 3 |
Acute post-streptococcal glomerulonephritis in a 14-month-old boy: why is this uncommon?
|
Bingler, Michael A.
|
|
|
22 |
3 |
p. 448-450
|
artikel
|
| 4 |
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome
|
Geelen, Joyce
|
|
|
22 |
3 |
p. 371-375
|
artikel
|
| 5 |
Ca2+-Mg2+-dependent ATP-ase activity and calcium homeostasis in children with chronic kidney disease
|
Polak-Jonkisz, Dorota
|
|
|
22 |
3 |
p. 414-419
|
artikel
|
| 6 |
Chronic kidney disease: common, harmful and treatable—World Kidney Day 2007
|
Levey, Andrew S.
|
|
|
22 |
3 |
p. 321-325
|
artikel
|
| 7 |
Doppler ultrasonographic indices in diagnosing nutcracker syndrome in children
|
Shin, Jae Il
|
|
|
22 |
3 |
p. 409-413
|
artikel
|
| 8 |
Erratum to: Cystatin C, kidney function and cardiovascular disease
|
Bökenkamp, Arend
|
|
|
22 |
3 |
p. 475
|
artikel
|
| 9 |
Fluid balance of pediatric hematopoietic stem cell transplant recipients and intensive care unit admission
|
Benoit, Geneviève
|
|
|
22 |
3 |
p. 441-447
|
artikel
|
| 10 |
Foreign body in the bladder mimicking nephritis
|
Benz, Marcus R.
|
|
|
22 |
3 |
p. 467-470
|
artikel
|
| 11 |
Gitelman’s syndrome: towards genotype-phenotype correlations?
|
Riveira-Munoz, Eva
|
|
|
22 |
3 |
p. 326-332
|
artikel
|
| 12 |
Gitelman syndrome and glomerulonephritis
|
Watanabe, Toru
|
|
|
22 |
3 |
p. 474
|
artikel
|
| 13 |
Growth impairment shows an age-dependent pattern in boys with chronic kidney disease
|
Živičnjak, Miroslav
|
|
|
22 |
3 |
p. 420-429
|
artikel
|
| 14 |
High-sensitivity C-reactive protein (hs-CRP) level in children with nephrotic syndrome
|
Wasilewska, Anna
|
|
|
22 |
3 |
p. 403-408
|
artikel
|
| 15 |
HLA-DRB1* alleles in Egyptian children with post-streptococcal acute glomerulonephritis
|
Bakr, Ashraf
|
|
|
22 |
3 |
p. 376-379
|
artikel
|
| 16 |
Hyponatremia resulting from Arginine Vasopressin Receptor 2 gene mutation
|
Bes, David Francisco
|
|
|
22 |
3 |
p. 463-466
|
artikel
|
| 17 |
Idiopathic collapsing focal segmental glomerulosclerosis in pediatric patients
|
El-Refaey, Ahmed M.
|
|
|
22 |
3 |
p. 396-402
|
artikel
|
| 18 |
Ifosfamide toxicity in cultured proximal renal tubule cells
|
Springate, James
|
|
|
22 |
3 |
p. 358-365
|
artikel
|
| 19 |
Intraperitoneal treatment with darbepoetin for children on peritoneal dialysis
|
Rijk, Yvonne
|
|
|
22 |
3 |
p. 436-440
|
artikel
|
| 20 |
Mutational analysis in 119 families with nephronophthisis
|
O’Toole, John F.
|
|
|
22 |
3 |
p. 366-370
|
artikel
|
| 21 |
Obesity and other clinical endpoints in steroid-sensitive nephrotic syndrome
|
Neuhaus, Thomas J.
|
|
|
22 |
3 |
p. 471
|
artikel
|
| 22 |
Pathophysiology of focal segmental glomerulosclerosis
|
Reidy, Kimberly
|
|
|
22 |
3 |
p. 350-354
|
artikel
|
| 23 |
Primary focal segmental glomerular sclerosis in children: clinical course and prognosis
|
Paik, Kyung Hoon
|
|
|
22 |
3 |
p. 389-395
|
artikel
|
| 24 |
Procalcitonin serum levels in children undergoing chronic haemodialysis
|
Lorton, Fleur
|
|
|
22 |
3 |
p. 430-435
|
artikel
|
| 25 |
Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth
|
Boyer, Olivia
|
|
|
22 |
3 |
p. 380-388
|
artikel
|
| 26 |
Risk of hypertension in primary vesicoureteral reflux
|
Simoes e Silva, Ana C.
|
|
|
22 |
3 |
p. 459-462
|
artikel
|
| 27 |
Role of fibroblast growth factor receptor signaling in kidney development
|
Bates, Carlton M.
|
|
|
22 |
3 |
p. 343-349
|
artikel
|
| 28 |
The challenge of renal function in heart transplant children
|
Filippo, Sylvie Di
|
|
|
22 |
3 |
p. 333-342
|
artikel
|
| 29 |
The importance of a ‘cohort effect’ in comparisons of groups with glucocorticoid-induced obesity
|
Foster, Bethany J.
|
|
|
22 |
3 |
p. 472-473
|
artikel
|
| 30 |
Unusual histological findings in a child with idiopathic nephrotic syndrome
|
Springate, James
|
|
|
22 |
3 |
p. 451-453
|
artikel
|
| 31 |
WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis
|
Kanemoto, Katsuyoshi
|
|
|
22 |
3 |
p. 454-458
|
artikel
|
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