phenylalanine and Abortion, Habitual

phenylalanine has been researched along with Abortion, Habitual in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Guo, J; Guo, Y; Jiang, H; Sa, Y; Song, J; Sun, Z; Wang, T; Wang, X; Xu, K; Yang, Y; Yuan, L1
Annichino-Bizzacchi, JM; Barbosa, HC; Barini, R; Carvalho, EC; Costa, DS; Siqueira, LH1
Huntley, CC; Stevenson, RE1
al-Awadi, SA; al-Ghanim, MM; al-Najdi, K; el-Badramany, MH; Farag, TI; Girish, Y; Uma, R; Usha, R1

Other Studies

4 other study(ies) available for phenylalanine and Abortion, Habitual

ArticleYear
Novel high-coverage targeted metabolomics method (SWATHtoMRM) for exploring follicular fluid metabolome alterations in women with recurrent spontaneous abortion undergoing in vitro fertilization.
    Scientific reports, 2019, 07-26, Volume: 9, Issue:1

    Topics: Abortion, Habitual; Adult; Chromatography, High Pressure Liquid; Dehydroepiandrosterone; Down-Regulation; Female; Fertilization in Vitro; Follicular Fluid; Humans; Mass Spectrometry; Metabolome; Metabolomics; Phenylalanine; Pregnancy; Up-Regulation

2019
Tyr204Phe and Val34Leu polymorphisms in two Brazilian ethnic groups and in patients with recurrent miscarriages.
    Fertility and sterility, 2004, Volume: 82, Issue:5

    Topics: Abortion, Habitual; Black People; Brazil; Factor XIII; Female; Humans; Leucine; Male; Phenylalanine; Polymorphism, Genetic; Pregnancy; Tyrosine; Valine; White People

2004
Congenital malformations in offspring of phenylketonuric mothers.
    Pediatrics, 1967, Volume: 40, Issue:1

    Topics: Abortion, Habitual; Adult; Birth Weight; Child; Child, Preschool; Congenital Abnormalities; Female; Heart Defects, Congenital; Hip Dislocation, Congenital; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications, Hematologic; Strabismus

1967
Late diagnosis of phenylketonuria in a Bedouin mother.
    American journal of medical genetics, 1992, Dec-01, Volume: 44, Issue:6

    Topics: Abortion, Habitual; Adult; Child, Preschool; Female; Fetal Diseases; Heart Defects, Congenital; Humans; Infant; Intellectual Disability; Male; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine

1992