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Results:
1-16
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Results: 16
Authors:
Jones, AO
Tzenova, J
Frappier, D
Crumley, MJ
Roslin, NM
Kos, CH
Tieder, M
Langman, CB
Proesmans, W
Carpenter, TO
Rice, A
Anderson, D
Morgan, K
Fujiwara, TM
Tenehouse, HS
Citation: Ao. Jones et al., Hereditary hypophosphatemic pickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene, J AM S NEPH, 12(3), 2001, pp. 507-514
Authors:
Van Dyck, M
Proesmans, W
Citation: M. Van Dyck et W. Proesmans, Growth hormone therapy in chronic renal failure induces catch-up of head circumference, PED NEPHROL, 16(8), 2001, pp. 631-636
Authors:
Proesmans, W
Citation: W. Proesmans, Untitled, PED NEPHROL, 16(6), 2001, pp. 532-532
Authors:
Proesmans, W
De Rooster, A
Van Dyck, M
Citation: W. Proesmans et al., Intravenous cyclosporine A for patients with nephrotic syndrome, PED NEPHROL, 16(2), 2001, pp. 196-197
Authors:
Van Dyck, M
Gyssels, A
Proesmans, W
Nijs, J
Eeckels, R
Citation: M. Van Dyck et al., Growth hormone treatment enhances bone mineralisation in children with chronic renal failure, EUR J PED, 160(6), 2001, pp. 359-363
Authors:
Schiepers, C
Mesotten, L
Proesmans, W
Vereecken, R
Verbruggen, A
De Roo, M
Citation: C. Schiepers et al., Surgical correction of vesicoureteral reflux: 5-year follow-up with Tc-99(m)-DMSA scintigraphy, NUCL MED C, 22(2), 2001, pp. 217-224
Authors:
Proesmans, W
Citation: W. Proesmans, The role of coagulation and fibrinolysis in the pathogenesis of diarrhea-associated hemolytic uremic syndrome, SEM THROMB, 27(3), 2001, pp. 201-205
Authors:
Proesmans, W
Van Molhem, S
Lateur, L
Citation: W. Proesmans et al., A 16-year-old boy with medullary sponge kidneys, osteoporosis, and premature loss of all teeth, PED NEPHROL, 14(3), 2000, pp. 259-262
Authors:
Zaman, Z
Proesmans, W
Citation: Z. Zaman et W. Proesmans, Dysmorphic erythrocytes and G1 cells as markers of glomerular hematuria, PED NEPHROL, 14(10-11), 2000, pp. 980-984
Authors:
Proesmans, W
Knockaert, H
Trouet, D
Citation: W. Proesmans et al., Enalapril in paediatric patients with Alport syndrome: 2 years' experience, EUR J PED, 159(6), 2000, pp. 430-433
Authors:
Vereecken, RL
Proesmans, W
Citation: Rl. Vereecken et W. Proesmans, Extensive surgery on the trigone for complete ureteral duplication does not cause incontinence or voiding problems, UROLOGY, 55(2), 2000, pp. 267-270
Authors:
Vereecken, RL
Proesmans, W
Citation: Rl. Vereecken et W. Proesmans, Urethral instability as an important element of dysfunctional voiding, J UROL, 163(2), 2000, pp. 585-588
Authors:
Feather, SA
Malcolm, S
Woolf, AS
Wright, V
Blaydon, D
Reid, CJD
Flinter, FA
Proesmans, W
Devriendt, K
Carter, J
Warwicker, P
Goodship, THJ
Goodship, JA
Citation: Sa. Feather et al., Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1, AM J HU GEN, 66(4), 2000, pp. 1420-1425
Authors:
Van Dyck, M
Bilem, N
Proesmans, W
Citation: M. Van Dyck et al., Conservative treatment for chronic renal failure from birth: a 3-year follow-up study, PED NEPHROL, 13(9), 1999, pp. 865-869
Authors:
Vereecken, RL
Proesmans, W
Citation: Rl. Vereecken et W. Proesmans, A review of ninety-two obstructive megaureters in children, EUR UROL, 36(4), 1999, pp. 342-347
Authors:
Kohlhase, J
Taschner, PEM
Burfeind, P
Pasche, B
Newman, B
Blanck, C
Breuning, MH
ten Kate, LP
Maaswinkel-Mooy, P
Mitulla, B
Seidel, J
Kirkpatrick, SJ
Pauli, RM
Wargowski, DS
Devriendt, K
Proesmans, W
Gabrielli, O
Coppa, GV
Wesby-van Swaay, E
Trembath, RC
Schinzel, AA
Reardon, W
Seemanova, E
Engel, W
Citation: J. Kohlhase et al., Molecular analysis of SALL1 mutations in Townes-Brocks syndrome, AM J HU GEN, 64(2), 1999, pp. 435-445
Risultati:
1-16
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