Leren TP - Search Results

1

Genetics of hypertrophic cardiomyopathy in Norway.

Berge KE, Leren TP. Berge KE, et al. Among authors: leren tp. Clin Genet. 2014 Oct;86(4):355-60. doi: 10.1111/cge.12286. Epub 2013 Oct 23. Clin Genet. 2014. PMID: 24111713

2

StyI polymorphism in an enhancer region of the second intron of the apolipoprotein B gene in hyper- and hypocholesterolemic subjects.

Røsby O, Poledne R, Hjermann I, Tonstad S, Berg K, Leren TP. Røsby O, et al. Among authors: leren tp. Clin Genet. 1992 Nov;42(5):217-23. doi: 10.1111/j.1399-0004.1992.tb03244.x. Clin Genet. 1992. PMID: 1362528

3

A 9.6 kilobase deletion in the low density lipoprotein receptor gene in Norwegian familial hypercholesterolemia subjects.

Rødningen OK, Røsby O, Tonstad S, Ose L, Berg K, Leren TP. Rødningen OK, et al. Among authors: leren tp. Clin Genet. 1992 Dec;42(6):288-95. doi: 10.1111/j.1399-0004.1992.tb03258.x. Clin Genet. 1992. PMID: 1362925

4

A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjects.

Leren TP, Solberg K, Røsby O, Rødningen OK, Tonstad S, Ose L, Berg K. Leren TP, et al. Clin Genet. 1992 Nov;42(5):224-8. doi: 10.1111/j.1399-0004.1992.tb03245.x. Clin Genet. 1992. PMID: 1486698

5

Haplotype analysis at the low density lipoprotein receptor locus in normal and familial hypercholesterolemia Norwegian subjects.

Rødningen OK, Leren TP, Røsby O, Tonstad S, Ose L, Berg K. Rødningen OK, et al. Among authors: leren tp. Clin Genet. 1993 Oct;44(4):214-20. doi: 10.1111/j.1399-0004.1993.tb03883.x. Clin Genet. 1993. PMID: 7903228

6

Short report on DNA marker at candidate locus.

Solberg K, Rødningen OK, Tonstad S, Ose L, Berg K, Leren TP. Solberg K, et al. Among authors: leren tp. Clin Genet. 1993 Aug;44(2):111. Clin Genet. 1993. PMID: 8275559 No abstract available.

7

Two novel missense mutations in the LDL receptor gene causing familial hypercholesterolemia.

Gundersen KE, Solberg K, Rødningen OK, Tonstad S, Ose L, Berg K, Leren TP. Gundersen KE, et al. Among authors: leren tp. Clin Genet. 1996 Feb;49(2):85-7. doi: 10.1111/j.1399-0004.1996.tb04333.x. Clin Genet. 1996. PMID: 8740918

8

Molecular genetics of familial hypercholesterolaemia in Norway.

Leren TP, Tonstad S, Gundersen KE, Bakken KS, Rødningen OK, Sundvold H, Ose L, Berg K. Leren TP, et al. J Intern Med. 1997 Mar;241(3):185-94. doi: 10.1046/j.1365-2796.1997.78119000.x. J Intern Med. 1997. PMID: 9104431 Free article.

9

Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia.

Leren TP. Leren TP. Clin Genet. 2004 May;65(5):419-22. doi: 10.1111/j.0009-9163.2004.0238.x. Clin Genet. 2004. PMID: 15099351

10

Application of molecular genetics for diagnosing familial hypercholesterolemia in Norway: results from a family-based screening program.

Leren TP, Manshaus T, Skovholt U, Skodje T, Nossen IE, Teie C, Sørensen S, Bakken KS. Leren TP, et al. Semin Vasc Med. 2004 Feb;4(1):75-85. doi: 10.1055/s-2004-822989. Semin Vasc Med. 2004. PMID: 15199436 Review.

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