Landsvater RM - Search Results

1

Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.

Landsvater RM, Jansen RP, Hofstra RM, Buys CH, Lips CJ, Ploos van Amstel HK. Landsvater RM, et al. Hum Genet. 1996 Jan;97(1):11-4. doi: 10.1007/BF00218825. Hum Genet. 1996. PMID: 8557249

2

From medical history and biochemical tests to presymptomatic treatment in a large MEN 2A family.

Lips CJ, Landsvater RM, Höppener JW, Geerdink RA, Blijham GH, Jansen-Schillhorn van Veen JM, Feldberg MA, van Gils AP, Hoogenboom H, Berends MJ, et al. Lips CJ, et al. Among authors: landsvater rm. J Intern Med. 1995 Oct;238(4):347-56. doi: 10.1111/j.1365-2796.1995.tb01209.x. J Intern Med. 1995. PMID: 7595171

3

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma.

Hofstra RM, Landsvater RM, Ceccherini I, Stulp RP, Stelwagen T, Luo Y, Pasini B, Höppener JW, van Amstel HK, Romeo G, et al. Hofstra RM, et al. Among authors: landsvater rm. Nature. 1994 Jan 27;367(6461):375-6. doi: 10.1038/367375a0. Nature. 1994. PMID: 7906866

4

Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A.

Lips CJ, Landsvater RM, Höppener JW, Geerdink RA, Blijham G, van Veen JM, van Gils AP, de Wit MJ, Zewald RA, Berends MJ, et al. Lips CJ, et al. Among authors: landsvater rm. N Engl J Med. 1994 Sep 29;331(13):828-35. doi: 10.1056/NEJM199409293311302. N Engl J Med. 1994. PMID: 7915822 Free article.

5

The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred.

Landsvater RM, Rombouts AG, te Meerman GJ, Schillhorn-van Veen JM, Berends MJ, Geerdink RA, Struyvenberg A, Buys CH, Lips CJ. Landsvater RM, et al. Am J Hum Genet. 1993 Feb;52(2):335-42. Am J Hum Genet. 1993. PMID: 8094268 Free PMC article.

6

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases.

Hofstra RM, Stelwagen T, Stulp RP, de Jong D, Hulsbeek M, Kamsteeg EJ, van den Berg A, Landsvater RM, Vermey A, Molenaar WM, Lips CJ, Buys CH. Hofstra RM, et al. Among authors: landsvater rm. J Clin Endocrinol Metab. 1996 Aug;81(8):2881-4. doi: 10.1210/jcem.81.8.8768845. J Clin Endocrinol Metab. 1996. PMID: 8768845

7

Somatic mutations of the RET proto-oncogene are not required for tumor development in multiple endocrine neoplasia type 2 (MEN 2) gene carriers.

Landsvater RM, de Wit MJ, Zewald RA, Hofstra RM, Buys CH, Ploos van Amstel HK, Höppener JW, Lips CJ. Landsvater RM, et al. Cancer Res. 1996 Nov 1;56(21):4853-5. Cancer Res. 1996. PMID: 8895732

8

Exclusion of the phosphatidylinositol-specific phospholipase C beta 3 (PLC beta 3) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene.

de Wit MJ, Landsvater RM, Sinke RJ, Geurts van Kessel A, Lips CJ, Höppener JW. de Wit MJ, et al. Among authors: landsvater rm. Hum Genet. 1997 Jan;99(1):133-7. doi: 10.1007/s004390050327. Hum Genet. 1997. PMID: 9003511

9

Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10.

Landsvater RM, Mathew CG, Smith BA, Marcus EM, te Meerman GJ, Lips CJ, Geerdink RA, Nakamura Y, Ponder BA, Buys CH. Landsvater RM, et al. Genomics. 1989 Apr;4(3):246-50. doi: 10.1016/0888-7543(89)90327-3. Genomics. 1989. PMID: 2565874

10

Familial medullary thyroid carcinoma: not a distinct entity? Genotype-phenotype correlation in a large family.

Moers AM, Landsvater RM, Schaap C, Jansen-Schillhorn van Veen JM, de Valk IA, Blijham GH, Höppener JW, Vroom TM, van Amstel HK, Lips CJ. Moers AM, et al. Among authors: landsvater rm. Am J Med. 1996 Dec;101(6):635-41. doi: 10.1016/s0002-9343(96)00330-0. Am J Med. 1996. PMID: 9003111

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