Bijvoet SM - Search Results

1

Cardiotocography plus ST analysis of fetal electrocardiogram compared with cardiotocography only for intrapartum monitoring: a randomized controlled trial.

Westerhuis MEMH, Visser GHA, Moons KGM, van Beek E, Benders MJ, Bijvoet SM, van Dessel HJHM, Drogtrop AP, van Geijn HP, Graziosi GC, Groenendaal F, van Lith JMM, Nijhuis JG, Oei SG, Oosterbaan HP, Porath MM, Rijnders RJP, Schuitemaker NWE, Sopacua LM, van der Tweel I, Wijnberger LDE, Willekes C, Zuithoff NPA, Mol BWJ, Kwee A. Westerhuis MEMH, et al. Among authors: bijvoet sm. Obstet Gynecol. 2010 Jun;115(6):1173-1180. doi: 10.1097/AOG.0b013e3181dfffd6. Obstet Gynecol. 2010. PMID: 20502287 Clinical Trial.

2

A randomised clinical trial on cardiotocography plus fetal blood sampling versus cardiotocography plus ST-analysis of the fetal electrocardiogram (STAN) for intrapartum monitoring.

Westerhuis ME, Moons KG, van Beek E, Bijvoet SM, Drogtrop AP, van Geijn HP, van Lith JM, Mol BW, Nijhuis JG, Oei SG, Porath MM, Rijnders RJ, Schuitemaker NW, van der Tweel I, Visser GH, Willekes C, Kwee A. Westerhuis ME, et al. Among authors: bijvoet sm. BMC Pregnancy Childbirth. 2007 Jul 26;7:13. doi: 10.1186/1471-2393-7-13. BMC Pregnancy Childbirth. 2007. PMID: 17655764 Free PMC article. Clinical Trial.

3

Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo event.

Henderson HE, Bijvoet SM, Mannens MA, Bruin T, Erkelens DW, Hayden MR, Kastelein JJ. Henderson HE, et al. Among authors: bijvoet sm. Am J Med Genet. 1998 Jul 24;78(4):313-6. doi: 10.1002/(sici)1096-8628(19980724)78:4<313::aid-ajmg1>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9714430

4

Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiency.

Bijvoet SM, Wiebusch H, Ma Y, Reymer PW, Bruin T, Bakker HD, Funke H, Assmann G, Hayden MR, Kastelein JJ. Bijvoet SM, et al. Neth J Med. 1996 Nov;49(5):189-95. doi: 10.1016/0300-2977(96)00043-5. Neth J Med. 1996. PMID: 8973094

5

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia.

Reymer PW, Groenemeyer BE, Gagné E, Miao L, Appelman EE, Seidel JC, Kromhout D, Bijvoet SM, van de Oever K, Bruin T, et al. Reymer PW, et al. Among authors: bijvoet sm. Hum Mol Genet. 1995 Sep;4(9):1543-9. doi: 10.1093/hmg/4.9.1543. Hum Mol Genet. 1995. PMID: 8541837

6

Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana.

Tuzgöl S, Bijvoet SM, Bruin T, Kastelein JJ, Hayden MR. Tuzgöl S, et al. Among authors: bijvoet sm. J Med Genet. 1994 Aug;31(8):622-6. doi: 10.1136/jmg.31.8.622. J Med Genet. 1994. PMID: 7815420 Free PMC article.

7

Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descent.

Bijvoet SM, Bruin T, Tuzgöl S, Bakker HD, Hayden MR, Kastelein JJ. Bijvoet SM, et al. Hum Genet. 1994 Mar;93(3):339-43. doi: 10.1007/BF00212035. Hum Genet. 1994. PMID: 8125488

8

The familial hyperchylomicronaemia syndrome.

Bijvoet SM, Bruin T, Kastelein JJ. Bijvoet SM, et al. Neth J Med. 1993 Feb;42(1-2):36-44. Neth J Med. 1993. PMID: 8446222 Review.

9

Mismatch PCR: a rapid method to screen for the Pro207-->Leu mutation in the lipoprotein lipase (LPL) gene.

Bijvoet SM, Hayden MR. Bijvoet SM, et al. Hum Mol Genet. 1992 Oct;1(7):541. doi: 10.1093/hmg/1.7.541. Hum Mol Genet. 1992. PMID: 1307255 No abstract available.

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