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Serological detection of verocytotoxin-producing Escherichia coli in patients with haemolytic uraemic syndrome in Western Europe
by CHART, H
European journal of clinical microbiology & infectious diseases, 1993, Vol.12 (9), p.707-709
2.
Serological detection of verocytotoxin-producingEscherichia coli in patients with haemolytic uraemic syndrome in Western Europe
by Chart, H.
European journal of clinical microbiology & infectious diseases, 1993, Vol.12 (9), p.707-709
3.
Switch in FGFR3 and -4 Expression Profile During Human Renal Development May Account for Transient Hypercalcemia in Patients With Sotos Syndrome due to 5q35 Microdeletions
by Mutsaers, Henricus A. M
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (7), p.E1361-E1367
4.
Interactions of Shiga-like toxin with human peripheral blood monocytes
by Geelen, J.M
Pediatric nephrology (Berlin, West), 2007, Vol.22 (8), p.1181-1187
5.
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation
by Lieburg, A.F. van
Human genetics, 1995, Vol.96 (1), p.70-78
6.
Strict cysteamine dose regimen is required to prevent nocturnal cystine accumulation in cystinosis
by Levtchenko, E.N
Pediatric nephrology (Berlin, West), 2006, Vol.21 (1), p.110-113
7.
PATIENTS WITH AUTOSOMAL NEPHROGENIC DIABETES-INSIPIDUS HOMOZYGOUS FOR MUTATIONS IN THE AQUAPORIN-2 WATER-CHANNEL GENE
by VANLIEBURG, AF
American journal of human genetics, 1994, Vol.55 (4), p.648-652
8.
Decreased intracellular ATP content and intact mitochondrial energy generating capacity in human cystinotic fibroblasts
by Levtchenko, E.N
Pediatric research, 2006, Vol.59 (2), p.287-292
9.
Hereditary Isolated Renal Magnesium Loss Maps to Chromosome 11q23
by Meij, Iwan C
American journal of human genetics, 1999, Vol.64 (1), p.180-188
10.
Advances in haemolytic uraemic syndrome
by Taylor, C M
Archives of disease in childhood, 1998, Vol.78 (2), p.190-193
11.
Monocyte chemoattractant protein-1 and interleukin-8 levels in urine and serum of patents with hemolytic uremic syndrome
by VAN SETTEN, P. A
Pediatric research, 1998, Vol.43 (6), p.759-767
12.
Detection of apoptosis in kidney biopsies of patients with D+ hemolytic uremic syndrome
by Loo, D.M.W.M. te
Pediatric research, 2001, Vol.49 (3), p.413--6
13.
Switch in FGFR3 and -4 expression profile during human renal development may account for transient hypercalcemia in patients with Sotos syndrome due to 5q35 microdeletions
by Mutsaers, Henricus A M
The journal of clinical endocrinology and metabolism, 2014, Vol.99 (7), p.E1361
14.
Treatment of hyperhomocysteinemia in children on dialysis by folic acid
by SCHRÖDER, C. H
Pediatric nephrology (Berlin, West), 1999, Vol.13 (7), p.583-585
15.
Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families
by Lemmink, H.H
Pediatric nephrology (Berlin, West), 1996, Vol.10 (4), p.403-407
16.
Intraperitoneal hypercoagulation and hypofibrinolysis is present in childhood peritonitis
by DE BOER, A. W
Pediatric nephrology (Berlin, West), 1999, Vol.13 (4), p.284-287
17.
Hereditary disorders of the glomerular basement membrane
by Smeets, H.J.M
Pediatric nephrology (Berlin, West), 1996, Vol.10 (6), p.779-788
18.
The fibrinolytic system in the hemolytic uremic syndrome : in vivo and in vitro studies
by VAN DE KAR, N. C. A. J
Pediatric research, 1994, Vol.36 (2), p.257-264
19.
Effects of oral and intramuscular vitamin K prophylaxis on vitamin K1, PIVKA-II, and clotting factors in breast fed infants
by Cornelissen, E A
Archives of disease in childhood, 1992, Vol.67 (10), p.1250-1254
20.
Verocytotoxin-producing Escherichia coli infection in hemolytic uremic syndrome in part of western Europe
by vandeKar, NCAJ
European journal of pediatrics, 1996, Vol.155 (7), p.592-595
