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Results: 26-33/33
Authors:
Schroder, CH
de Boer, AW
Giesen, AM
Monnens, LAH
Blom, H
Citation: Ch. Schroder et al., Treatment of hyperhomocysteinemia in children on dialysis by folic acid, PED NEPHROL, 13(7), 1999, pp. 583-585
Authors:
de Boer, AW
Levi, M
Reddingius, RE
Willems, JL
van den Bosch, S
Schroder, CH
Monnens, LAH
Citation: Aw. De Boer et al., Intraperitoneal hypercoagulation and hypofibrinolysis is present in childhood peritonitis, PED NEPHROL, 13(4), 1999, pp. 284-287
Authors:
de Boer, AW
van Schaijk, TCJG
Willems, HL
de Haan, AFJ
Monnens, LAH
Schroder, CH
Citation: Aw. De Boer et al., Follow-up study of peritoneal fluid kinetics in infants and children on peritoneal dialysis, PERIT DIA I, 19(6), 1999, pp. 572-577
Authors:
Heuvelink, AE
Van de Kar, NCAJ
Van der Velden, TJAM
Chart, H
Monnens, LAH
Citation: Ae. Heuvelink et al., Verocytotoxin-producing Escherichia coli infection in household members ofchildren with hemolytic-uremic syndrome in the Netherlands, PEDIAT INF, 18(8), 1999, pp. 709-714
Authors:
Van der Loop, FTL
Monnens, LAH
Schroder, CH
Lemmink, HH
Breuning, MH
Timmer, EDJ
Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4 A5 defects in Alport's syndrome by immunohistochemistry of skin (vol 55, pg 1217, 1999), KIDNEY INT, 56(6), 1999, pp. 2337-2337
Authors:
van der Loop, FTL
Monnens, LAH
Schroder, CH
Lemmink, HH
Breuning, MH
Timmer, EDJ
Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin, KIDNEY INT, 55(4), 1999, pp. 1217-1224
Authors:
Meij, IC
Saar, K
van den Heuvel, LPWJ
Nuernberg, G
Vollmer, M
Hildebrandt, F
Reis, A
Monnens, LAH
Knoers, NVAM
Citation: Ic. Meij et al., Hereditary isolated renal magnesium loss maps to chromosome 11q23, AM J HU GEN, 64(1), 1999, pp. 180-188
Authors:
van de Kar, NCAJ
Monnens, LAH
Citation: Ncaj. Van De Kar et Lah. Monnens, The haemolytic-uraemic syndrome in childhood, BAIL CLIN H, 11(2), 1998, pp. 497-507