Zobrazeno 1 - 10
of 524
pro vyhledávání: '"L. Viinikka"'
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 53:649-652
Publikováno v:
Arteriosclerosis: An Official Journal of the American Heart Association, Inc.. 10:653-657
Prostacyclin (PGI2) is an antithrombotic factor, which may prevent the initiation and the complications of arteriosclerosis. The most important site of PGI2 production is the vascular endothelium, but little is known about how this process is regulat
Autor:
Per Winkel, E. E. A. Leskinen, B. Lindblad, A. P. W. Nyberg, R Gräsbeck, V. Nántö, P. D. Wimberley, L. Viinikka, P. J. Moe, T Alström, H. Hertz, H. E. Solberg, A. Bo Hansen, C. Holmberg
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 50:99-104
Reference values should be produced under standardized conditions. To enable comparison it is desirable to use the same procedure also in other clinical situations. A procedure for the collection of venous blood from children with special reference t
Publikováno v:
Gynecological Endocrinology. 10:20-22
Autor:
L, Viinikka
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 116(23)
Publikováno v:
Archives of disease in childhood. Fetal and neonatal edition. 84(1)
OBJECTIVES—To evaluate in a randomised blind study the effect on puncture site lesions of two different incision devices used to obtain blood samples from preterm infants by repeated heel sticks. SETTING—The neonatal intensive care unit at the Ho
Publikováno v:
Journal of cellular physiology. 176(1)
Optimal vascular homeostasis requires efficient control of both proliferation and elimination of vascular endothelial cells. Programmed cell death, or apoptosis, is the main mechanism controlling cell elimination, and it is an essential component of
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(2)
Women with prior preeclampsia are characterized by hyperinsulinemia and a 2- to 3-fold excess risk of hypertension and ischemic heart disease in later life. We therefore studied whether these women present changes in pituitary, ovarian, and endotheli
Publikováno v:
Prenatal diagnosis. 17(10)
Hereditary tyrosinaemia type 1 is a rare but serious metabolic disorder with an autosomal recessive mode of inheritance. We describe the prenatal diagnosis of an affected fetus performed by DNA-mutation analysis and a subsequent pregnancy with a heal
Autor:
A, Ristimäki, L, Viinikka
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 112(5)