Hulsbeek M - Search Results

1

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Among authors: hulsbeek m. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

2

Cardiac conduction defects associate with mutations in SCN5A.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Among authors: hulsbeek m. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.

3

Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysis.

Boon M, Nolte IM, Bruinenberg M, Spijker GT, Terpstra P, Raelson J, De Keyser J, Zwanikken CP, Hulsbeek M, Hofstra RM, Buys CH, te Meerman GJ. Boon M, et al. Among authors: hulsbeek m. Neurogenetics. 2001 Oct;3(4):221-30. doi: 10.1007/s100480100121. Neurogenetics. 2001. PMID: 11714103

4

Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis.

van den Berg A, Hulsbeek MF, de Jong D, Kok K, Veldhuis PM, Roche J, Buys CH. van den Berg A, et al. Among authors: hulsbeek mf. Genes Chromosomes Cancer. 1996 Jan;15(1):64-72. doi: 10.1002/(SICI)1098-2264(199601)15:1<64::AID-GCC9>3.0.CO;2-2. Genes Chromosomes Cancer. 1996. PMID: 8824727

5

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: hulsbeek m. J Clin Endocrinol Metab. 1996 Aug;81(8):2881-4. doi: 10.1210/jcem.81.8.8768845. J Clin Endocrinol Metab. 1996. PMID: 8768845

6

3D printing of patient-specific neck splints for the treatment of post-burn neck contractures.

Visscher DO, Te Slaa S, Jaspers ME, van de Hulsbeek M, Borst J, Wolff J, Forouzanfar T, van Zuijlen PP. Visscher DO, et al. Among authors: van de hulsbeek m. Burns Trauma. 2018 Jun 8;6:15. doi: 10.1186/s41038-018-0116-1. eCollection 2018. Burns Trauma. 2018. PMID: 29930950 Free PMC article. No abstract available.

7

Further delineation of the chromosome 14q terminal deletion syndrome.

van Karnebeek CD, Quik S, Sluijter S, Hulsbeek MM, Hoovers JM, Hennekam RC. van Karnebeek CD, et al. Among authors: hulsbeek mm. Am J Med Genet. 2002 Jun 1;110(1):65-72. doi: 10.1002/ajmg.10207. Am J Med Genet. 2002. PMID: 12116274 Review.

8

A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3.

Timmer T, Terpstra P, van den Berg A, Veldhuis PM, Ter Elst A, Voutsinas G, Hulsbeek MM, Draaijers TG, Looman MW, Kok K, Naylor SL, Buys CH. Timmer T, et al. Among authors: hulsbeek mm. Eur J Hum Genet. 1999 May-Jun;7(4):478-86. doi: 10.1038/sj.ejhg.5200334. Eur J Hum Genet. 1999. PMID: 10352938

9

Analysis of multiple renal cell adenomas and carcinomas suggests allelic loss at 3p21 to be a prerequisite for malignant development.

van den Berg A, Dijkhuizen T, Draaijers TG, Hulsbeek MM, Maher ER, van den Berg E, Störkel S, Buys CH. van den Berg A, et al. Among authors: hulsbeek mm. Genes Chromosomes Cancer. 1997 Aug;19(4):228-32. doi: 10.1002/(sici)1098-2264(199708)19:4<228::aid-gcc4>3.0.co;2-z. Genes Chromosomes Cancer. 1997. PMID: 9258657

10

Ordering of polymorphic markers in the chromosome region 3p21.

van den Berg A, Kooy RF, Hulsbeek MM, de Jong D, Kok K, van der Veen AY, Buys CH. van den Berg A, et al. Among authors: hulsbeek mm. Cytogenet Cell Genet. 1996;72(2-3):225-8. doi: 10.1159/000134196. Cytogenet Cell Genet. 1996. PMID: 8978783

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