van Amstel HK - Search Results

1

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: van amstel hk. Nature. 1994 Jan 27;367(6461):375-6. doi: 10.1038/367375a0. Nature. 1994. PMID: 7906866

2

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: van amstel hk. Am J Med. 1996 Dec;101(6):635-41. doi: 10.1016/s0002-9343(96)00330-0. Am J Med. 1996. PMID: 9003111

3

Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young children.

van Heurn LW, Schaap C, Sie G, Haagen AA, Gerver WJ, Freling G, van Amstel HK, Heineman E. van Heurn LW, et al. Among authors: van amstel hk. J Pediatr Surg. 1999 Apr;34(4):568-71. doi: 10.1016/s0022-3468(99)90075-1. J Pediatr Surg. 1999. PMID: 10235324

4

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

Eng C, Clayton D, Schuffenecker I, Lenoir G, Cote G, Gagel RF, van Amstel HK, Lips CJ, Nishisho I, Takai SI, Marsh DJ, Robinson BG, Frank-Raue K, Raue F, Xue F, Noll WW, Romei C, Pacini F, Fink M, Niederle B, Zedenius J, Nordenskjöld M, Komminoth P, Hendy GN, Mulligan LM, et al. Eng C, et al. Among authors: van amstel hk. JAMA. 1996 Nov 20;276(19):1575-9. JAMA. 1996. PMID: 8918855

5

A novel germline mutation of PTEN associated with brain tumours of multiple lineages.

Staal FJ, van der Luijt RB, Baert MR, van Drunen J, van Bakel H, Peters E, de Valk I, van Amstel HK, Taphoorn MJ, Jansen GH, van Veelen CW, Burgering B, Staal GE. Staal FJ, et al. Among authors: van drunen j, van veelen cw, van amstel hk, van bakel h, van der luijt rb. Br J Cancer. 2002 May 20;86(10):1586-91. doi: 10.1038/sj.bjc.6600206. Br J Cancer. 2002. PMID: 12085208 Free PMC article.

6

X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.

van den Berg IE, van Beurden EA, Malingré HE, van Amstel HK, Poll-The BT, Smeitink JA, Lamers WH, Berger R. van den Berg IE, et al. Among authors: van beurden ea, van amstel hk. Am J Hum Genet. 1995 Feb;56(2):381-7. Am J Hum Genet. 1995. PMID: 7847371 Free PMC article.

7

Tetranucleotide repeat polymorphism in the vWF gene.

van Amstel HK, Reitsma PH. van Amstel HK, et al. Nucleic Acids Res. 1990 Aug 25;18(16):4957. doi: 10.1093/nar/18.16.4957-a. Nucleic Acids Res. 1990. PMID: 2395671 Free PMC article.

8

Mutational analysis of endothelial cells derived from von Hippel-Lindau-related renal cancer.

Los M, Kerckhaert OA, Zewald R, van Amstel HK, Voest EE. Los M, et al. Among authors: van amstel hk. J Natl Cancer Inst. 2000 Oct 18;92(20):1688-9. doi: 10.1093/jnci/92.20.1688. J Natl Cancer Inst. 2000. PMID: 11036115 No abstract available.

9

Molecular basis of hereditary protein C and protein S deficiency.

Reitsma PH, van Amstel HK, Poort BR, van der Velden PA, Bertina RM. Reitsma PH, et al. Among authors: van der velden pa, van amstel hk. Curr Stud Hematol Blood Transfus. 1991;(58):94-9. doi: 10.1159/000419345. Curr Stud Hematol Blood Transfus. 1991. PMID: 1835438 Review. No abstract available.

10

No pathogenic mutations in the uroplakin III gene of 25 patients with primary vesicoureteral reflux.

Giltay JC, van de Meerakker J, van Amstel HK, de Jong TP. Giltay JC, et al. Among authors: van de meerakker j, van amstel hk. J Urol. 2004 Feb;171(2 Pt 1):931-2. doi: 10.1097/01.ju.0000094802.50650.3d. J Urol. 2004. PMID: 14713856

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