Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Kirkinen Pertti"'
Autor:
Tomas Eija, Sly William S, Waheed Abdul, Pastorek Jaromir, Pastorekova Silvia, Hämäläinen Jonna M, Hynninen Piritta, Kirkinen Pertti, Parkkila Seppo
Publikováno v:
Reproductive Biology and Endocrinology, Vol 2, Iss 1, p 73 (2004)
Abstract Background Carbonic anhydrase (CA) classically catalyses the reversible hydration of dissolved CO2 to form bicarbonate ions and protons. The twelve active CA isozymes are thought to regulate a variety of cellular functions including several
Externí odkaz:
https://doaj.org/article/099e3d18c7394b4baae41bf6427643be
Publikováno v:
BMC Women's Health, Vol 3, Iss 1, p 1 (2003)
Abstract Background To investigate obstetric prognosis in sisters of preeclamptic women. Methods We identified consecutive 635 sib pairs from the Birth Registry data of Kuopio University Hospital who had their first delivery between January 1989 and
Externí odkaz:
https://doaj.org/article/b25104f7070444979f39cb145d034f6d
Autor:
Paakki, Pauliina, Stockmann, Helene, Kantola, Marjatta, Wagner, Peruka, Lauper, Urs, Huch, Renate, Elovaara, Eivor, Kirkinen, Pertti, Pasanen, Markku
Publikováno v:
Environmental Health Perspectives, 2000 Feb 01. 108(2), 141-145.
Externí odkaz:
https://www.jstor.org/stable/3454512
Publikováno v:
Scandinavian Journal of Public Health, 2010 Nov 01. 38(7), 756-760.
Externí odkaz:
https://www.jstor.org/stable/45150330
Publikováno v:
In European Journal of Obstetrics and Gynecology 2004 112(1):84-88
Publikováno v:
In Urology 2004 63(1):67-71
Publikováno v:
In Human Pathology July 2000 31(7):841-846
Autor:
Rinne, Kirsi M. *, Kirkinen, Pertti P.
Publikováno v:
In European Journal of Obstetrics and Gynecology May 1999 84(1):23-25
Autor:
Heinonen, Seppo *, Kirkinen, Pertti
Publikováno v:
In Obstetrics & Gynecology 1999 94(2):189-193
Autor:
Markku Ryynänen, Elisa Kajanoja, Minna Makkonen, Kirkinen Pertti, Arto Mannermaa, Seppo Heinonen
Publikováno v:
European Journal of Human Genetics. 7:212-216
Fragile X syndrome is the second leading cause of mental retardation after Down syndrome. Most women carriers of the fragile X mutation are unaware of their condition. We critically evaluated whether screening pregnant women at low risk for FMR1 muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b061193fafc18b4830a3541bc07e9a6
https://doi.org/10.1038/sj.ejhg.5200285
https://doi.org/10.1038/sj.ejhg.5200285