phenylalanine and Embryopathies

phenylalanine has been researched along with Embryopathies in 31 studies

Research

Studies (31)

Timeframe	Studies, this research(%)	All Research%
pre-1990	21 (67.74)	18.7374
1990's	7 (22.58)	18.2507
2000's	3 (9.68)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bailey, I; Brereton, H; Gennaccaro, M; Gleason, S; Goss, B; Lesperance, E; Levy, H; Moseley, K; Munier, A; Rohr, F; Singh, R; Sullivan, D; Tonyes, L; Vespa, H; Waisbren, S	1
Arakawa, T; Dancis, J; Hutzler, J; Morikawa, T; Tada, K; Wada, Y	1
Dhont, JL; Farriaux, JP	1
Clow, CL; Scriver, CR	1
Lenke, RR; Levy, HL	1
Stroud, HW; Tenbrinck, MS	1
Matthieu, JM	1
Peat, B	1
Azen, C; Hanley, W; Koch, R; Levy, HL; Matalon, R; Rouse, B	1
Dhondt, JL; Farriaux, JP; Lacombe, A; Largillière, C; Puech, F; Valat, S	1
Bachman, RP; Buist, N; Geraghty, MT; Hanley, WB; Isaacs, J; O'Flynn, ME; Platt, LD; Rhead, WJ; Seidlitz, G; Tishler, B	1
Kesby, G	1
Hall, JG	1
Cho, S; McDonald, JD	1
Besana, R; Calcagni, L; Giovannini, M; Magnoni, D; Riva, E	1
Pantarotta, MF; Pecorari, D; Zunino, P	1
al-Awadi, SA; al-Ghanim, MM; al-Najdi, K; el-Badramany, MH; Farag, TI; Girish, Y; Uma, R; Usha, R	1
Carey, WF; Pollard, AC	1
Brenton, DP	1
Lowitzer, AC	1
Freedman, M	1
Erbe, RW; Ghavami, M; Levy, HL	1
Ampola, MG; Bailey, IV; Benacerraf, B; Doherty, LB; Levy, HL; Rohr, FJ; Waisbren, SE	1
Farquhar, DL; Steven, F; Westwood, A	1
Hansen, H	1
Blyumina, MG	1
Chamove, AS; Harlow, HF; Kerr, GR; Waisman, HA	1
Ballester, L; Callens, G; Callens, M; Duquennoy, C; Gaudier, B; Ponté, C	1
Howell, RR; Parmley, TH; Stevenson, RE; Thomas, GH	1
Egorov, NS; Khokhlov, AP	1
Anderson, JA; Fisch, RO; Walker, WA	1

Reviews

3 review(s) available for phenylalanine and Embryopathies

Article	Year
Phenylketonuria and other phenylalanine hydroxylation mutants in man. Annual review of genetics, 1980, Volume: 14 Topics: Alleles; Amino Acid Metabolism, Inborn Errors; Animals; Biopterins; Dihydropteridine Reductase; Female; Fetal Diseases; Gene Frequency; Genetic Carrier Screening; Heterozygote; Humans; Hydroxylation; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pregnancy; Pregnancy Complications; Rats	1980
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case finding. American journal of obstetrics and gynecology, 1999, Volume: 180, Issue:4 Topics: Adolescent; Adult; Female; Fetal Diseases; Humans; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Outcome; Prenatal Diagnosis; Retrospective Studies	1999
Maternal phenylketonuria: cause for concern among women with PKU. Research in developmental disabilities, 1987, Volume: 8, Issue:1 Topics: Female; Fetal Diseases; Humans; Infant, Newborn; Intellectual Disability; Intelligence; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1987

Trials

2 trial(s) available for phenylalanine and Embryopathies

Article	Year
The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings. Journal of inherited metabolic disease, 2004, Volume: 27, Issue:2 Topics: Female; Fetal Diseases; Gestational Age; Humans; Patient Compliance; Peer Group; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Prenatal Care; Program Evaluation; Social Support	2004
The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993. American journal of diseases of children (1960), 1993, Volume: 147, Issue:11 Topics: Adolescent; Adult; Anthropometry; Energy Intake; Female; Fetal Diseases; Follow-Up Studies; Humans; Infant; Infant, Newborn; Intelligence Tests; Morbidity; Neonatal Screening; North America; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Outcome; Prenatal Diagnosis; Prospective Studies	1993

Article

Year

The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings.

Journal of inherited metabolic disease, 2004, Volume: 27, Issue:2

Topics: Female; Fetal Diseases; Gestational Age; Humans; Patient Compliance; Peer Group; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Prenatal Care; Program Evaluation; Social Support

2004

The North American Collaborative Study of Maternal Phenylketonuria. Status report 1993.

American journal of diseases of children (1960), 1993, Volume: 147, Issue:11

Topics: Adolescent; Adult; Anthropometry; Energy Intake; Female; Fetal Diseases; Follow-Up Studies; Humans; Infant; Infant, Newborn; Intelligence Tests; Morbidity; Neonatal Screening; North America; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Outcome; Prenatal Diagnosis; Prospective Studies

1993

Other Studies

26 other study(ies) available for phenylalanine and Embryopathies

Article	Year
Hypervalinemia. A defect in valine transamination. Pediatrics, 1967, Volume: 39, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Asian People; Carbon Isotopes; Child, Preschool; Female; Fetal Diseases; Humans; Intellectual Disability; Isoleucine; Japan; Keto Acids; Leucine; Leukocytes; Methionine; Phenylalanine; Placenta; Pregnancy; Transaminases; Valine	1967
[Hyperphenylalaninemia in 1983]. Revue medicale de Bruxelles, 1983, Volume: 4, Issue:4 Topics: Biopterins; Female; Fetal Diseases; Humans; Infant, Newborn; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Pregnancy; Pregnancy Complications	1983
Maternal phenylketonuria--results of dietary therapy. American journal of obstetrics and gynecology, 1982, Mar-01, Volume: 142, Issue:5 Topics: Adult; Female; Fetal Diseases; Heart Defects, Congenital; Humans; Infant, Newborn; Intellectual Disability; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1982
Normal infant born to a mother with phenylketonuria. JAMA, 1982, Apr-16, Volume: 247, Issue:15 Topics: Adult; Child, Preschool; Female; Fetal Diseases; Follow-Up Studies; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Pregnancy Trimester, First	1982
[Maternal phenylketonuria: a misdiagnosed cause of embryopathy or fetal disease]. Revue medicale de la Suisse romande, 1994, Volume: 114, Issue:10 Topics: Female; Fetal Diseases; Humans; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Teratogens	1994
Pregnancy complicated by maternal phenylketonuria. The Australian & New Zealand journal of obstetrics & gynaecology, 1993, Volume: 33, Issue:2 Topics: Female; Fetal Diseases; Humans; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Retrospective Studies	1993
[Embryofetopathy of the newborn infant of a phenylketonuric mother. A diagnosis not to be missed]. Journal de gynecologie, obstetrique et biologie de la reproduction, 1993, Volume: 22, Issue:1 Topics: Adult; Female; Fetal Diseases; Fetal Growth Retardation; Heart Septal Defects; Humans; Infant, Newborn; Intellectual Disability; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1993
Repeated adverse fetal outcome in pregnancy complicated by uncontrolled maternal phenylketonuria. Journal of paediatrics and child health, 1999, Volume: 35, Issue:5 Topics: Adult; Female; Fetal Diseases; Humans; Intellectual Disability; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Syndrome	1999
When is careless conception a form of child abuse? Lessons from maternal phenylketonuria. The Journal of pediatrics, 2000, Volume: 136, Issue:1 Topics: Adolescent; Adult; Embryonic and Fetal Development; Female; Fetal Diseases; Heart Defects, Congenital; Humans; Infant; Maternal Behavior; Microcephaly; Phenylalanine; Phenylketonurias; Physician-Patient Relations; Preconception Care; Pregnancy; Pregnancy Complications	2000
Effect of maternal blood phenylalanine level on mouse maternal phenylketonuria offspring. Molecular genetics and metabolism, 2001, Volume: 74, Issue:4 Topics: Abortion, Spontaneous; Animals; Disease Models, Animal; Embryonic and Fetal Development; Female; Fetal Diseases; Humans; Male; Mice; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Tyrosine	2001
[Maternal hyperphenylalaninemia as a cause of embryo-fetal disease. Review of literature and clinical contribution]. Minerva pediatrica, 1979, Apr-30, Volume: 31, Issue:8 Topics: Abnormalities, Multiple; Female; Fetal Death; Fetal Diseases; Humans; Infant, Newborn; Male; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1979
[Problem of maternal phenylketonuria]. Minerva ginecologica, 1975, Volume: 27, Issue:12 Topics: Female; Fetal Diseases; Fetus; Humans; Infant, Newborn; Male; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1975
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
Microvillar enzymes in amniotic fluid. Considerations for the prenatal diagnosis of cystic fibrosis. The Medical journal of Australia, 1986, Jan-20, Volume: 144, Issue:2 Topics: Alkaline Phosphatase; Amniotic Fluid; Congenital Abnormalities; Cystic Fibrosis; Female; Fetal Diseases; gamma-Glutamyltransferase; Homoarginine; Humans; Infant, Newborn; Isoenzymes; Phenylalanine; Pregnancy; Pregnancy Trimester, First; Pregnancy Trimester, Second; Prenatal Diagnosis; Risk	1986
Maternal phenylketonuria. European journal of clinical nutrition, 1989, Volume: 43 Suppl 1 Topics: Brain Diseases; Cohort Studies; Embryonic and Fetal Development; Female; Fetal Diseases; Humans; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Pregnancy Outcome	1989
Consumption of aspartame by heterozygotes for phenylketonuria. The Journal of pediatrics, 1987, Volume: 110, Issue:4 Topics: Aspartame; Dipeptides; Female; Fetal Diseases; Heterozygote; Humans; Phenylalanine; Phenylketonurias; Pregnancy	1987
Prevention of fetal damage through dietary control of maternal hyperphenylalaninemia. Clinical obstetrics and gynecology, 1986, Volume: 29, Issue:3 Topics: Adolescent; Animals; Child; Child, Preschool; Female; Fetal Diseases; Follow-Up Studies; Humans; Infant; Infant, Newborn; Intellectual Disability; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1986
New England Maternal PKU Project: prospective study of untreated and treated pregnancies and their outcomes. The Journal of pediatrics, 1987, Volume: 110, Issue:3 Topics: Adolescent; Adult; Female; Fetal Blood; Fetal Diseases; Humans; Infant, Newborn; Microcephaly; Patient Compliance; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Prenatal Diagnosis; Prognosis; Tyrosine	1987
Preliminary report on inverse diurnal variation of phenylalanine: implications in maternal phenylketonuria. Human nutrition. Applied nutrition, 1985, Volume: 39, Issue:3 Topics: Adult; Amino Acids; Circadian Rhythm; Female; Fetal Diseases; Humans; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1985
Risk of fetal damage in maternal phenylketonuria. The Journal of pediatrics, 1973, Volume: 83, Issue:3 Topics: Brain Damage, Chronic; Diet Therapy; Female; Fetal Diseases; Humans; Infant, Newborn; Intellectual Disability; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications	1973
The role of heterozygosity of women with respect to the phenylketonuria gene in the origin of spontaneous abortions and disturbances of intrauterine fetal development. Soviet genetics, 1974, May-01, Volume: 8, Issue:3 Topics: Abortion, Spontaneous; Bone and Bones; Chromatography, Paper; Congenital Abnormalities; Female; Fetal Diseases; Heterozygote; Humans; Phenylalanine; Phenylketonurias; Pregnancy	1974
"Fetal PKU:" the effect of maternal hyperphenylalaninemia during pregnancy in the rhesus monkey (Macaca mulatta). Pediatrics, 1968, Volume: 42, Issue:1 Topics: Amino Acids; Animals; Animals, Newborn; Birth Weight; Diet; Female; Fetal Diseases; Haplorhini; Humans; Intellectual Disability; Learning; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Serine; Tyrosine	1968
[Delayed intrauterine growth with microcephaly in 3 children born of a hyperphenylalaninemic mother]. Annales de pediatrie, 1972, Volume: 19, Issue:4 Topics: Abortion, Spontaneous; Adult; Child; Child, Preschool; Congenital Abnormalities; Diet Therapy; Female; Fetal Diseases; Growth Disorders; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Microcephaly; Pedigree; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications, Hematologic	1972
Developmental changes in amino acid concentrations in human amniotic fluid: abnormal findings in maternal phenylketonuria. American journal of obstetrics and gynecology, 1971, Volume: 111, Issue:1 Topics: Adult; Amino Acids; Amniotic Fluid; Chromatography; Congenital Abnormalities; Female; Fetal Diseases; Gestational Age; Humans; Infant, Newborn; Intellectual Disability; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1971
[Excretion of phenylacetylglutamine in the newborn with birth trauma, intrauterine hypotrophy and hemolytic disease]. Pediatriia, 1968, Volume: 6 Topics: Birth Injuries; Congenital Abnormalities; Erythroblastosis, Fetal; Female; Fetal Diseases; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylalanine; Pregnancy	1968
Prenatal and postnatal developmental consequences of maternal phenylketonuria. Pediatrics, 1966, Volume: 37, Issue:6 Topics: Adult; Birth Weight; Congenital Abnormalities; Female; Fetal Diseases; Humans; Infant, Newborn; Intellectual Disability; Male; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1966