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Items: 23

1.

MTHFR C677T polymorphism is not associated with placental abruption or preeclampsia in Finnish women.

Jääskeläinen E, Keski-Nisula L, Toivonen S, Romppanen EL, Helisalmi S, Punnonen K, Heinonen S.

Hypertens Pregnancy. 2006;25(2):73-80.

PMID:
16867914
2.

Microdialysis detects postoperative perfusion failure in microvascular flaps.

Setälä L, Papp A, Romppanen EL, Mustonen P, Berg L, Härmä M.

J Reconstr Microsurg. 2006 Feb;22(2):87-96.

PMID:
16456768
3.

Endothelial nitric oxide synthase polymorphism is not associated with placental abruption in Finnish women.

Toivonen S, Keski-Nisula L, Romppanen EL, Helisalmi S, Punnonen K, Heinonen S.

Fetal Diagn Ther. 2005 Nov-Dec;20(6):508-11.

PMID:
16260885
4.

Low-activity haplotype of the microsomal epoxide hydrolase gene is protective against placental abruption.

Toivonen S, Romppanen EL, Hiltunen M, Helisalmi S, Keski-Nisula L, Punnonen K, Heinonen S.

J Soc Gynecol Investig. 2004 Dec;11(8):540-4.

PMID:
15582499
5.

M385T polymorphism in the factor V gene, but not Leiden mutation, is associated with placental abruption in Finnish women.

Jääskeläinen E, Toivonen S, Romppanen EL, Helisalmi S, Keski-Nisula L, Punnonen K, Heinonen S.

Placenta. 2004 Sep-Oct;25(8-9):730-4.

PMID:
15450391
6.

Susceptibility to pre-eclampsia in Finnish women is associated with R485K polymorphism in the factor V gene, not with Leiden mutation.

Faisel F, Romppanen EL, Hiltunen M, Helisalmi S, Laasanen J, Punnonen K, Salonen JT, Heinonen S.

Eur J Hum Genet. 2004 Mar;12(3):187-91.

7.

Plasminogen activator inhibitor-1 polymorphism in women with pre-eclampsia.

Häkli T, Romppanen EL, Hiltunen M, Helisalmi S, Punnonen K, Heinonen S.

Genet Test. 2003 Fall;7(3):265-8.

PMID:
14642005
8.

Polymorphism in the interleukin 1 receptor antagonist gene in women with preeclampsia.

Faisel F, Romppanen EL, Hiltunen M, Helisalmi S, Punnonen K, Salonen J, Heinonen S.

J Reprod Immunol. 2003 Oct;60(1):61-70.

PMID:
14568678
10.

Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are associated with polycystic ovary syndrome.

Korhonen S, Romppanen EL, Hiltunen M, Helisalmi S, Punnonen K, Hippeläinen M, Heinonen S.

Fertil Steril. 2003 Jun;79(6):1353-7.

PMID:
12798882
11.

Endothelial nitric oxide synthase polymorphism in preeclampsia.

Häkli T, Romppanen EL, Hiltunen M, Helisalmi S, Punnonen K, Heinonen S.

J Soc Gynecol Investig. 2003 Apr;10(3):154-7.

PMID:
12699878
12.

Microsatellite marker association at chromosome region 2p13 in Finnish patients with preeclampsia and obstetric cholestasis suggests a common risk locus.

Laasanen J, Hiltunen M, Romppanen EL, Punnonen K, Mannermaa A, Heinonen S.

Eur J Hum Genet. 2003 Mar;11(3):232-6.

13.

Lack of association between C-850T polymorphism of the gene encoding tumor necrosis factor-alpha and polycystic ovary syndrome.

Korhonen S, Romppanen EL, Hiltunen M, Mannermaa A, Punnonen K, Hippeläinen M, Heinonen S.

Gynecol Endocrinol. 2002 Aug;16(4):271-4.

PMID:
12396555
14.

Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.

Laasanen J, Romppanen EL, Hiltunen M, Helisalmi S, Mannermaa A, Punnonen K, Heinonen S.

Eur J Hum Genet. 2002 Sep;10(9):569-73.

15.

Polymorphism in the tumor necrosis factor-alpha gene in women with preeclampsia.

Heiskanen J, Romppanen EL, Hiltunen M, Iivonen S, Mannermaa A, Punnonen K, Heinonen S.

J Assist Reprod Genet. 2002 May;19(5):220-3.

16.

Oligonucleotide ligation assay: applications to molecular diagnosis of inherited disorders.

Romppanen EL.

Scand J Clin Lab Invest. 2001 Apr;61(2):123-9.

PMID:
11347979
18.

Optimal use of the fluorescent PicoGreen dye for quantitative analysis of amplified polymerase chain reaction products on microplate.

Romppanen EL, Savolainen K, Mononen I.

Anal Biochem. 2000 Mar 1;279(1):111-4. No abstract available.

PMID:
10683239
19.

PCR-oligonucleotide ligation assay from dried blood spots.

Romppanen EL, Mononen I.

Clin Chem. 1999 Nov;45(11):2022-5. No abstract available.

PMID:
10545079
20.

Molecular diagnosis of Finnish type infantile neuronal ceroid lipofuscinosis by restriction fragment length polymorphism and oligonucleotide ligation assay.

Romppanen EL, Valtonen P, Mononen T, Mononen I.

Clin Chem. 1998 Nov;44(11):2373-6. No abstract available.

PMID:
9799772
21.

Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by oligonucleotide ligation assay.

Romppanen EL, Mononen T, Mononen I.

Clin Chem. 1998 Jan;44(1):68-71.

PMID:
9550560
22.

Recombinant glycosylasparaginase and in vitro correction of aspartylglycosaminuria.

Mononen I, Heisterkamp N, Dunder U, Romppanen EL, Noronkoski T, Kuronen I, Groffen J.

FASEB J. 1995 Mar;9(5):428-33.

PMID:
7896015
23.

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