Digitale Bibliotheek
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                             45 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of psoriasis with ANCA-negative pauci-immune crescentic glomerulonephritis in children Prasad, Narayan

26 7 p. 1173-1174
artikel
2 Acute antibody-mediated rejection in paediatric renal transplant recipients Kranz, Birgitta

26 7 p. 1149-1156
artikel
3 Acute antibody-mediated rejection in paediatric renal transplant recipients Kranz, Birgitta

26 7 p. 1149-1156
artikel
4 An unusual case of hyperkalaemia in infancy: answer Formosa, Mireille

26 7 p. 1067-1069
artikel
5 An unusual case of hyperkalaemia in infancy: answer Formosa, Mireille

26 7 p. 1067-1069
artikel
6 An unusual case of hyperkalaemia in infancy: question Formosa, Mireille

26 7 p. 1065
artikel
7 An unusual case of hyperkalaemia in infancy: question Formosa, Mireille

26 7 p. 1065
artikel
8 Assessment of long-term renal complications in extremely low birth weight children Kwinta, Przemko

26 7 p. 1095-1103
artikel
9 Assessment of long-term renal complications in extremely low birth weight children Kwinta, Przemko

26 7 p. 1095-1103
artikel
10 Ciliopathies: an expanding disease spectrum Waters, Aoife M.

26 7 p. 1039-1056
artikel
11 Ciliopathies: an expanding disease spectrum Waters, Aoife M.

26 7 p. 1039-1056
artikel
12 Clinical course and outcome of children with steroid-sensitive nephrotic syndrome Esfahani, Seyed Taher

26 7 p. 1089-1093
artikel
13 Clinical course and outcome of children with steroid-sensitive nephrotic syndrome Esfahani, Seyed Taher

26 7 p. 1089-1093
artikel
14 Clinical outcomes in children with Henoch–Schönlein purpura nephritis grade IIIa or IIIb Xia, Yonghui

26 7 p. 1083-1088
artikel
15 Clinical outcomes in children with Henoch–Schönlein purpura nephritis grade IIIa or IIIb Xia, Yonghui

26 7 p. 1083-1088
artikel
16 Development of uveitis during systemic corticosteroid therapy in TINU syndrome Lava, Sebastiano A. G.

26 7 p. 1177-1178
artikel
17 Development of uveitis during systemic corticosteroid therapy in TINU syndrome Lava, Sebastiano A. G.

26 7 p. 1177-1178
artikel
18 Elevated systolic blood pressure in preterm very-low-birth-weight infants ≤3 years of life Duncan, Andrea F.

26 7 p. 1115-1121
artikel
19 Elevated systolic blood pressure in preterm very-low-birth-weight infants ≤3 years of life Duncan, Andrea F.

26 7 p. 1115-1121
artikel
20 Eye examination is important in patients with tubulointerstitial nephritis Jahnukainen, Timo

26 7 p. 1179
artikel
21 Eye examination is important in patients with tubulointerstitial nephritis Jahnukainen, Timo

26 7 p. 1179
artikel
22 Genetic susceptibility to renal scar formation after urinary tract infection: a systematic review and meta-analysis of candidate gene polymorphisms Zaffanello, Marco

26 7 p. 1017-1029
artikel
23 Genetic susceptibility to renal scar formation after urinary tract infection: a systematic review and meta-analysis of candidate gene polymorphisms Zaffanello, Marco

26 7 p. 1017-1029
artikel
24 Heat shock proteins in chronic kidney disease Musiał, Kinga

26 7 p. 1031-1037
artikel
25 Heat shock proteins in chronic kidney disease Musiał, Kinga

26 7 p. 1031-1037
artikel
26 Hydatid disease and tubulointerstitial nephritis Nickavar, Azar

26 7 p. 1171-1172
artikel
27 Karyomegalic-like nephropathy, Ewing’s sarcoma and ifosfamide therapy McCulloch, Tom

26 7 p. 1163-1166
artikel
28 Karyomegalic-like nephropathy, Ewing’s sarcoma and ifosfamide therapy McCulloch, Tom

26 7 p. 1163-1166
artikel
29 Morphine and hyperkalaemia in a boy with sickle cell crisis Boussemart, Thierry

26 7 p. 1175-1176
artikel
30 No difference in meeting hemoglobin and albumin targets for dialyzed children with urologic disorders Lestz, Rachel M.

26 7 p. 1129-1136
artikel
31 No difference in meeting hemoglobin and albumin targets for dialyzed children with urologic disorders Lestz, Rachel M.

26 7 p. 1129-1136
artikel
32 Novel DNA mutation in the GATA3 gene in an Emirati boy with HDR syndrome and hypomagnesemia Al-Shibli, Amar

26 7 p. 1167-1170
artikel
33 Novel DNA mutation in the GATA3 gene in an Emirati boy with HDR syndrome and hypomagnesemia Al-Shibli, Amar

26 7 p. 1167-1170
artikel
34 Pathogenesis and therapy of focal segmental glomerulosclerosis: an update Gbadegesin, Rasheed

26 7 p. 1001-1015
artikel
35 Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes Babayeva, Sima

26 7 p. 1071-1081
artikel
36 Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation Baskin, Esra

26 7 p. 1157-1161
artikel
37 Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation Baskin, Esra

26 7 p. 1157-1161
artikel
38 Serum osteoprotegerin, RANKL and fibroblast growth factor-23 in children with chronic kidney disease Siomou, Ekaterini

26 7 p. 1105-1114
artikel
39 Serum osteoprotegerin, RANKL and fibroblast growth factor-23 in children with chronic kidney disease Siomou, Ekaterini

26 7 p. 1105-1114
artikel
40 Serum uric acid is associated with high blood pressure in pediatric hemodialysis patients Silverstein, Douglas M.

26 7 p. 1123-1128
artikel
41 Serum uric acid is associated with high blood pressure in pediatric hemodialysis patients Silverstein, Douglas M.

26 7 p. 1123-1128
artikel
42 Solutions for peritoneal dialysis in children: recommendations by the European Pediatric Dialysis Working Group Schmitt, Claus Peter

26 7 p. 1137-1147
artikel
43 Solutions for peritoneal dialysis in children: recommendations by the European Pediatric Dialysis Working Group Schmitt, Claus Peter

26 7 p. 1137-1147
artikel
44 TRPC channel modulation in podocytes—inching toward novel treatments for glomerular disease Hindi, Shafic El

26 7 p. 1057-1064
artikel
45 TRPC channel modulation in podocytes—inching toward novel treatments for glomerular disease El Hindi, Shafic

26 7 p. 1057-1064
artikel
                             45 gevonden resultaten
 
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