Proesmans W - Search Results

1

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene.

van Lieburg AF, Verdijk MA, Knoers VV, van Essen AJ, Proesmans W, Mallmann R, Monnens LA, van Oost BA, van Os CH, Deen PM. van Lieburg AF, et al. Among authors: proesmans w. Am J Hum Genet. 1994 Oct;55(4):648-52. Am J Hum Genet. 1994. PMID: 7524315 Free PMC article.

2

Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin 2 gene.

van Lieburg AF, Knoers VV, Mallmann R, Proesmans W, van den Heuvel LP, Monnens LA. van Lieburg AF, et al. Among authors: proesmans w. Nephron. 1996;72(4):544-6. doi: 10.1159/000188936. Nephron. 1996. PMID: 8730418 Clinical Trial.

3

Verocytotoxin-producing Escherichia coli infection in hemolytic uremic syndrome in part of western Europe.

van de Kar NC, Roelofs HG, Muytjens HL, Tolboom JJ, Roth B, Proesmans W, Reitsma-Bierens WC, Wolff ED, Karmali MA, Chart H, Monnens LA. van de Kar NC, et al. Among authors: proesmans w. Eur J Pediatr. 1996 Jul;155(7):592-5. doi: 10.1007/BF01957911. Eur J Pediatr. 1996. PMID: 8831084

4

Renal transplantation in 20 children with hemolytic-uremic syndrome.

Eijgenraam FJ, Donckerwolcke RA, Monnens LA, Proesmans W, Wolff ED, van Damme B. Eijgenraam FJ, et al. Among authors: proesmans w. Clin Nephrol. 1990 Feb;33(2):87-93. Clin Nephrol. 1990. PMID: 2311309

5

Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations.

Schimmenti LA, Cunliffe HE, McNoe LA, Ward TA, French MC, Shim HH, Zhang YH, Proesmans W, Leys A, Byerly KA, Braddock SR, Masuno M, Imaizumi K, Devriendt K, Eccles MR. Schimmenti LA, et al. Among authors: proesmans w. Am J Hum Genet. 1997 Apr;60(4):869-78. Am J Hum Genet. 1997. PMID: 9106533 Free PMC article.

6

Diaphragmatic hernia in Denys-Drash syndrome.

Devriendt K, Deloof E, Moerman P, Legius E, Vanhole C, de Zegher F, Proesmans W, Devlieger H. Devriendt K, et al. Among authors: proesmans w. Am J Med Genet. 1995 May 22;57(1):97-101. doi: 10.1002/ajmg.1320570120. Am J Med Genet. 1995. PMID: 7645607

7

Indomethacin therapy in Bartter syndrome.

Proesmans W, Muaka BK, Monnens L. Proesmans W, et al. Acta Paediatr Belg. 1977 Jan-Mar;30(1):31-6. Acta Paediatr Belg. 1977. PMID: 860644 No abstract available.

8

Reversible deficient prostacyclin release in childhood hemolytic uremic syndrome.

Chamone DA, Proesmans WC, Monnens LA, Binda ki Muaka P, Vermylen JG. Chamone DA, et al. Among authors: proesmans wc. Int J Pediatr Nephrol. 1982 Mar;3(1):13-6. Int J Pediatr Nephrol. 1982. PMID: 7049977

9

The complement system in hemolytic-uremic syndrome in childhood.

Monnens L, Molenaar J, Lambert PH, Proesmans W, van Munster P. Monnens L, et al. Among authors: proesmans w. Clin Nephrol. 1980 Apr;13(4):168-71. Clin Nephrol. 1980. PMID: 7379368

10

Defective tubular reabsorption of pyruvic and L-lactic acid.

Jaeken J, De Cock P, Proesmans W, Corbeel E, Eggermont E, Eeckels R, Monnens L, Bakkeren J. Jaeken J, et al. Among authors: proesmans w. N Engl J Med. 1980 Sep 18;303(12):706. doi: 10.1056/NEJM198009183031227. N Engl J Med. 1980. PMID: 7402267 No abstract available.

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