| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ACE I/D gene polymorphism predicts renal damage in congenital uropathies
|
Hohenfellner, K.
|
|
1999
|
13 |
6 |
p. 514-518
|
artikel
|
| 2 |
ACE inhibition scintigraphy in the management of hypertension in children
|
Chandar, Jayanthi J.
|
|
1999
|
13 |
6 |
p. 493-500
|
artikel
|
| 3 |
A patient with pseudohypoaldosteronism type 1 and respiratory distress syndrome
|
Malagon-Rogers, Maricarmen
|
|
1999
|
13 |
6 |
p. 484-486
|
artikel
|
| 4 |
Autosomal dominant inheritance of multicystic dysplastic kidney
|
Srivastava, T.
|
|
1999
|
13 |
6 |
p. 481-483
|
artikel
|
| 5 |
Collecting duct morphogenesis
|
Davies, J. A.
|
|
1999
|
13 |
6 |
p. 535-541
|
artikel
|
| 6 |
Cystatin C as a marker for glomerular filtration rate in pediatric patients
|
Ylinen, Elisa A.
|
|
1999
|
13 |
6 |
p. 506-509
|
artikel
|
| 7 |
Diabetes mellitus in patients with infantile cystinosis after renal transplantation
|
Robert, J.-J.
|
|
1999
|
13 |
6 |
p. 524-529
|
artikel
|
| 8 |
Diagnostic sensitivity of serum cystatin for impaired glomerular filtration rate
|
Filler, G.
|
|
1999
|
13 |
6 |
p. 501-505
|
artikel
|
| 9 |
Henoch-Schönlein purpura and pulmonary hemorrhage: a report and literature review
|
Vats, Kalyani R.
|
|
1999
|
13 |
6 |
p. 530-534
|
artikel
|
| 10 |
Hereditary glomerulopathy associated with a mitochondrial tRNALeu gene mutation
|
Cheong, H. I.
|
|
1999
|
13 |
6 |
p. 477-480
|
artikel
|
| 11 |
Hypercalcemia of the newborn: etiology, evaluation, and management
|
Rodd, Celia
|
|
1999
|
13 |
6 |
p. 542-547
|
artikel
|
| 12 |
Influence of hyperfiltration on the measurement of urinary N-acetyl-β-D-glucosaminidase
|
Müller, D.
|
|
1999
|
13 |
6 |
p. 519-523
|
artikel
|
| 13 |
IPNA Newsletter
|
,
|
|
1999
|
13 |
6 |
p. 554-556
|
artikel
|
| 14 |
Markers of endothelial cell activation and injury in childhood haemolytic uraemic syndrome
|
Nevard, Corinne H. F.
|
|
1999
|
13 |
6 |
p. 487-492
|
artikel
|
| 15 |
Sodium-lithium countertransport in children with nephrotic syndrome
|
Tulassay, T.
|
|
1999
|
13 |
6 |
p. 510-513
|
artikel
|
| 16 |
The burden of genetic disease and attitudes towards gene testing in Alport syndrome
|
Pajari, Heli
|
|
1999
|
13 |
6 |
p. 471-476
|
artikel
|
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