RITODRINE HYDROCHLORIDE INDUCED CARDIOPULMONARY AND PLACENTAL HEMODYNAMIC CHANGES IN NORMAL AND HYPERTENSIVE LATE PREGNANCY.SUONIO S; RYYNANEN M; OLKKONEN H et al.1976; INTERNATION. J. GYNAECOL. OBSTETR.; U.S.A.; DA. 1976; VOL. 14; NO 3; PP. 268-272; BIBL. 9 REF.Article

First-trimester manifestation of intrahepatic cholestasis of pregnancy and high fetoplacental hormone production in a triploid fetus : a case reportKIRKINEN, P; RYYNÄNEN, M.Journal of reproductive medicine. 1995, Vol 40, Num 6, pp 471-473, issn 0024-7758Article

INCOMPLETE PRENATAL DIAGNOSIS OF G-TRISOMY MOSAICISM.SIMOLA K; AULA P; RYYNANEN M et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 6; PP. 500-503; BIBL. 11 REF.Article

Maternal serum alpha-fetoprotein and epithelial tumour marker concentrations are not increased by fetal sacrococcygeal teratomaKIRKINEN, P; HEINONEN, S; VANAMO, K et al.Prenatal diagnosis. 1997, Vol 17, Num 1, pp 47-50, issn 0197-3851Article

The effects on fetal development of high α-fetoprotein and maternal smokingHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.American journal of public health (1971). 1999, Vol 89, Num 4, pp 561-563, issn 0090-0036Article

Carrier diagnosis of the fragile X syndrome : a challenge in antenatal clinicsRYYNÄNEN, M; KIRKINEN, P; MANNERMAA, A et al.American journal of obstetrics and gynecology. 1995, Vol 172, Num 4, pp 1236-1239, issn 0002-9378, 1Conference Paper

Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patientsHILTUNEN, M; MANNERMAA, A; HELISALMI, S et al.Neuroscience letters. 1998, Vol 250, Num 1, pp 69-71, issn 0304-3940Article

Ultrasonic and magnetic resonance imaging of fetal sacrococcygeal teratomaKIRKINEN, P; PARTANEN, K; MERIKANTO, J et al.Acta obstetricia et gynecologica Scandinavica. 1997, Vol 76, Num 10, pp 917-922, issn 0001-6349Article

Effect of in vitro fertilization on human chorionic gonadotropin serum concentrations and Down's syndrome screeningHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.Fertility and sterility. 1996, Vol 66, Num 3, pp 398-403, issn 0015-0282Article

A severe loss of choline acetyltransferase in the frontal cortex of Alzheimer patients carrying apolipoprotein ε4 alleleSOININEN, H; KOSUNEN, O; HELISALMI, S et al.Neuroscience letters. 1995, Vol 187, Num 2, pp 79-82, issn 0304-3940Article

Apolipoprotein E polymorphism and Alzheimer's disease in Eastern FinlandLEHTOVIRTA, M; HELISALMI, S; MANNERMAA, A et al.Neuroscience letters. 1995, Vol 185, Num 1, pp 13-15, issn 0304-3940Article

Mapping of epidermolysis bullosa simplex mutation to chromosome 12RYYNANEN, M; KNOWLTON, R. G; UITTO, J et al.American journal of human genetics. 1991, Vol 49, Num 5, pp 978-984, issn 0002-9297Article

Translocation t(13; 14) in nine generations with a case of translocation homozygosityEKLUND, A; SIMOLA, K. O. J; RYYNANEN, M et al.Clinical genetics. 1988, Vol 33, Num 2, pp 83-86, issn 0009-9163Article

Etiology and outcome of second trimester non-immunologic fetal hydropsHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.Acta obstetricia et gynecologica Scandinavica. 2000, Vol 79, Num 1, pp 15-18, issn 0001-6349Article

Fragile-X syndrome in east Finland : molecular approach to genetic and prenatal diagnosisRYYNÄNEN, M; PULKKINEN, L; KIRKINEN, P et al.American journal of medical genetics. 1994, Vol 51, Num 4, pp 463-465, issn 0148-7299Article

Perinatal diagnostic evaluation of velamentous umbilical cord insertion : clinical, Doppler, and ultrasonic findingsHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.Obstetrics and gynecology (New York. 1953). 1996, Vol 87, Num 1, pp 112-117, issn 0029-7844Article

Uterine malformation : A cause of elevated maternal serum alpha-fetoprotein concentrationsHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.Prenatal diagnosis. 1996, Vol 16, Num 7, pp 635-640, issn 0197-3851, 5 p.Article

Recurrence risk of a serious, noninherited chromosomal abnormalityRYYNÄNEN, M; LESKINEN, S; HEINONEN, S et al.Fertility and sterility. 1997, Vol 68, Num 3, pp 439-442, issn 0015-0282Article

Results and views of women in population-wide pregnancy screening for trisomy 21 in East FinlandHEIKKILÄ, A; RYYNÄNEN, M; KIRKINEN, P et al.Fetal diagnosis and therapy. 1997, Vol 12, Num 2, pp 93-96, issn 1015-3837Conference Paper

MRI in Obstetrics : A Supplementary Method for UltrasonographyKIRKINEN, P; PARTANEN, K; VAINIO, P et al.Annals of medicine (Helsinki). 1996, Vol 28, Num 2, pp 131-136, issn 0785-3890Article

Velamentous umbilical cord insertion may be suspected from maternal serum α-fetoprotein and hCGHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.British journal of obstetrics and gynaecology (Print). 1996, Vol 103, Num 3, pp 209-213, issn 0306-5456Article

Dominant dystrophic epidermolysis bullosa : identification of a Gly→Ser substitution in the triple-helical domain of type VII collagenCHRISTIANO, A. M; RYYNÄNEN, M; UITTO, J et al.Proceedings of the National Academy of Sciences of the United States of America. 1994, Vol 91, Num 9, pp 3549-3553, issn 0027-8424Article

Antenatally diagnosted fetal hydronephrosis. Five year's follow upRYYNÄNEN, M; MARTIKAINEN, A; SAARIKOSKI, S et al.Journal of perinatal medicine. 1990, Vol 18, Num 4, pp 313-316, issn 0300-5577Article

Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutationKALLINEN, J; HEINONEN, S; MANNERMAA, A et al.Clinical genetics. 2000, Vol 58, Num 2, pp 111-115, issn 0009-9163Article

Endometrial and fetoplacental markers in pregnancies with fetal congenital nephrosisHEINONEN, S; RYYNÄNEN, M; KIRKINEN, P et al.Acta obstetricia et gynecologica Scandinavica. 1996, Vol 75, Num 6, pp 526-530, issn 0001-6349Article