van Oost BA - 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: van oost ba. Nat Genet. 1992 Oct;2(2):99-102. doi: 10.1038/ng1092-99. Nat Genet. 1992. PMID: 1303271

2

Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe.

van Oost BA, Smits AP, Dreesen JC, van den Ouweland AM, Oostra BA. van Oost BA, et al. Among authors: van den ouweland am. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):320-7. doi: 10.1002/ajmg.1320430149. Am J Med Genet. 1992. PMID: 1605205

3

Linkage analyses in families with nephrogenic diabetes insipidus.

Knoers NV, van der Heyden H, van Oost BA, Monnens L, Willems J, Ropers HH. Knoers NV, et al. Among authors: van oost ba, van der heyden h. Prog Clin Biol Res. 1989;305:149-55. Prog Clin Biol Res. 1989. PMID: 2569742 No abstract available.

4

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. Among authors: van oost ba, van der heyden h. Genomics. 1989 Apr;4(3):434-7. doi: 10.1016/0888-7543(89)90352-2. Genomics. 1989. PMID: 2714800

5

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. Among authors: van oost ba, van der heyden h. Hum Genet. 1988 Sep;80(1):31-8. doi: 10.1007/BF00451451. Hum Genet. 1988. PMID: 2843456

6

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: van essen aj, van os ch, van oost ba. Am J Hum Genet. 1994 Oct;55(4):648-52. Am J Hum Genet. 1994. PMID: 7524315 Free PMC article.

7

Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.

van Lieburg AF, Verdijk MA, Schoute F, Ligtenberg MJ, van Oost BA, Waldhauser F, Dobner M, Monnens LA, Knoers NV. van Lieburg AF, et al. Among authors: van oost ba. Hum Genet. 1995 Jul;96(1):70-8. doi: 10.1007/BF00214189. Hum Genet. 1995. PMID: 7607658 Free article. Review.

8

Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus.

Knoers NV, van den Ouweland AM, Verdijk M, Monnens LA, van Oost BA. Knoers NV, et al. Among authors: van oost ba, van den ouweland am. Kidney Int. 1994 Jul;46(1):170-6. doi: 10.1038/ki.1994.256. Kidney Int. 1994. PMID: 7933835 Free article.

9

Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine.

Deen PM, Verdijk MA, Knoers NV, Wieringa B, Monnens LA, van Os CH, van Oost BA. Deen PM, et al. Among authors: van os ch, van oost ba. Science. 1994 Apr 1;264(5155):92-5. doi: 10.1126/science.8140421. Science. 1994. PMID: 8140421

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. Among authors: van oost ba, van den ouweland a. Pediatr Nephrol. 1993 Oct;7(5):685-8. doi: 10.1007/BF00852579. Pediatr Nephrol. 1993. PMID: 8251344 Review.

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