Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Markku Ryynänen"'
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Maternal gestational diabetes (GDM), small (SGA) and large (LGA) for gestational age neonates are associated with increased morbidity in both mother and child. We studied how different levels of first trimester pregnancy associate
Externí odkaz:
https://doaj.org/article/50f93823e80b469cb6c66ea7d45efba4
Publikováno v:
Journal of Human Reproductive Sciences, Vol 4, Iss 1, Pp 34-38 (2011)
Objectives : Endometriosis and uterine fibroids are common gynecological disorders in fertile women. It has been suggested that these two disorders may be associated with each other. In this study, we tested whether this connection exists. In additio
Externí odkaz:
https://doaj.org/article/20ea2fedc1c74cbf967357fe5282bbcb
Publikováno v:
Prenatal diagnosis. 36(2)
The objective of this article is to estimate whether the maternal serum levels of A disintegrin and metalloprotease domain 12 (ADAM12-s), pregnancy-associated plasma protein-A (PAPP-A), and free beta human chorionic gonadotrophin (fβ-hCG) are altere
Publikováno v:
Fetal Diagnosis and Therapy. 22:45-50
Objective: To evaluate whether first trimester screening markers are altered in pregnancies affected both by other chromosomal defects than trisomy 21 and structural anomalies and whether it is possible to detect these pregnancies by combined ultraso
Publikováno v:
Brain Topography. 15:165-171
We compared the N1 responses of the auditory event-related brain potentials (ERPs) in school-aged children with fragile X syndrome to age-matched controls in order to assess auditory processing. Event-related potentials to non-attended standard and d
Publikováno v:
BJOG: An International Journal of Obstetrics and Gynaecology. 107:969-972
Objective To evaluate pregnancy outcome in women who are carriers of fragile X. Design Cross-sectional case-control study. Setting Department of Obstetrics and Gynaecology, Kuopio University Hospital, Finland. Sample Sixty-three singleton pregnancies
Publikováno v:
Clinical Genetics. 58:111-115
The aim of the present study was to evaluate prospectively the dynamics of the FMR1 gene. The risk of full mutation among pregnant women and the carriers, and the risk of expansion of a premutation allele to a full mutation were estimated. We identif
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 79:15-18
Background. This investigation was undertaken to study the conditions resulting in midtrimester fetal hydrops and to evaluate its overall prognosis as regards counseling purposes. Material and methods. The etiology of midtrimester non-immune fetal hy
Autor:
Anne M. Koivisto, Markku Ryynänen, Hilkka Soininen, Maarit Lehtovirta, Mikko Hiltunen, Arto Mannermaa, Piia Valonen, Seppo Helisalmi
Publikováno v:
Journal of Neurology. 246:821-824
Apolipoprotein E (APOE) epsilon4 allele is a major risk factor for the development of Alzheimer's disease (AD). It has been suggested that the quantitative expression of APOE alleles results from mutations in the promoter region of this gene. We stud
Autor:
Mikko Hiltunen, Anne M. Koivisto, Hilkka Soininen, Paavo J. Riekkinen, Maarit Lehtovirta, Seppo Helisalmi, Arto Mannermaa, Markku Ryynänen
Publikováno v:
European Journal of Human Genetics. 7:652-658
Alzheimer's disease (AD) is a complex neurodegenerative disorder, for which several disease-associated loci have been located on different chromosomes. We have used a population-based linkage disequilibrium mapping approach in order to find potential