Knoers NV - Search Results

1

Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus.

van den Ouweland AM, Dreesen JC, Verdijk M, Knoers NV, Monnens LA, Rocchi M, van Oost BA. van den Ouweland AM, et al. Among authors: knoers nv. Nat Genet. 1992 Oct;2(2):99-102. doi: 10.1038/ng1092-99. Nat Genet. 1992. PMID: 1303271

2

Evidence for intact V1-vasopressin receptors in congenital nephrogenic diabetes insipidus.

Knoers N, Janssens PM, Goertz J, Monnens LA. Knoers N, et al. Eur J Pediatr. 1992 May;151(5):381-3. doi: 10.1007/BF02113263. Eur J Pediatr. 1992. PMID: 1396896

3

Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatment.

Knoers N, Monnens LA. Knoers N, et al. Pediatr Nephrol. 1992 Sep;6(5):476-82. doi: 10.1007/BF00874020. Pediatr Nephrol. 1992. PMID: 1457333 Review.

4

A variant of nephrogenic diabetes insipidus: V2 receptor abnormality restricted to the kidney.

Knoers N, Monnens LA. Knoers N, et al. Eur J Pediatr. 1991 Mar;150(5):370-3. doi: 10.1007/BF01955943. Eur J Pediatr. 1991. PMID: 1828422

5

Fibrinolytic responses to 1-desamino-8-D-arginine-vasopressin in patients with congenital nephrogenic diabetes insipidus.

Knoers N, Brommer EJ, Willems H, van Oost BA, Monnens LA. Knoers N, et al. Nephron. 1990;54(4):322-6. doi: 10.1159/000185888. Nephron. 1990. PMID: 2109264

6

Amiloride-hydrochlorothiazide versus indomethacin-hydrochlorothiazide in the treatment of nephrogenic diabetes insipidus.

Knoers N, Monnens LA. Knoers N, et al. J Pediatr. 1990 Sep;117(3):499-502. doi: 10.1016/s0022-3476(05)81106-0. J Pediatr. 1990. PMID: 2391611 No abstract available.

7

Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus.

Knoers N, van der Heyden H, van Oost BA, Monnens L, Willems J, Ropers HH. Knoers N, et al. Genomics. 1989 Apr;4(3):434-7. doi: 10.1016/0888-7543(89)90352-2. Genomics. 1989. PMID: 2714800

8

Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome.

Knoers N, van der Heyden H, van Oost BA, Ropers HH, Monnens L, Willems J. Knoers N, et al. Hum Genet. 1988 Sep;80(1):31-8. doi: 10.1007/BF00451451. Hum Genet. 1988. PMID: 2843456

9

Linkage of X-linked nephrogenic diabetes insipidus with DXS52, a polymorphic DNA marker.

Knoers N, vd Heyden H, von Oost BA, Monnens L, Willems J, Ropers HH. Knoers N, et al. Nephron. 1988;50(3):187-90. doi: 10.1159/000185155. Nephron. 1988. PMID: 3226453

10

Nephrogenic diabetes insipidus: identification of the genetic defect.

Knoers N, van den Ouweland A, Dreesen J, Verdijk M, Monnens LA, van Oost BA. Knoers N, et al. Pediatr Nephrol. 1993 Oct;7(5):685-8. doi: 10.1007/BF00852579. Pediatr Nephrol. 1993. PMID: 8251344 Review.

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