tyrosine has been researched along with Embryopathies in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (64.29) | 18.7374 |
| 1990's | 4 (28.57) | 18.2507 |
| 2000's | 1 (7.14) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dhondt, JL; Farriaux, JP; Largillière, C | 1 |
| Berger, R; Jansen, RP; Ploos van Amstel, JK; van den Berg, IE; Verjaal, M | 1 |
| Cederbaum, S; Gagné, R; Grenier, A; Jakobs, C; Laberge, C; Tanguay, RM | 1 |
| Brodie, SG; Kitoh, H; Lipson, M; Sifry-Platt, M; Wilcox, WR | 1 |
| Cho, S; McDonald, JD | 1 |
| al-Awadi, SA; al-Ghanim, MM; al-Najdi, K; el-Badramany, MH; Farag, TI; Girish, Y; Uma, R; Usha, R | 1 |
| Ampola, MG; Bailey, IV; Benacerraf, B; Doherty, LB; Levy, HL; Rohr, FJ; Waisbren, SE | 1 |
| Bélanger, L; Bélanger, M; Gourdeau, H; Larochelle, J | 1 |
| Farquhar, DL; Steven, F; Westwood, A | 1 |
| Boggs, DE | 1 |
| Chamove, AS; Harlow, HF; Kerr, GR; Waisman, HA | 1 |
| Howell, RR; Parmley, TH; Stevenson, RE; Thomas, GH | 1 |
| Anderson, JA; Fisch, RO; Walker, WA | 1 |
1 review(s) available for tyrosine and Embryopathies
| Article | Year |
|---|---|
Detection of inborn errors of metabolism.
Topics: Amino Acids; Amniocentesis; Calcium; Chromatography; Copper; Creatinine; Erythrocytes; Female; Fetal Diseases; Glycosaminoglycans; Humans; Indoles; Infant, Newborn; Keto Acids; Leukocytes; Mass Screening; Metabolism, Inborn Errors; Methods; Oxalates; Phenylketonurias; Pregnancy; Pyruvates; Tyrosine; Urine | 1971 |
13 other study(ies) available for tyrosine and Embryopathies
| Article | Year |
|---|---|
[The newborn infant of the phenylketonuric mother ].
Topics: Female; Fetal Diseases; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylketonurias; Pregnancy; Pregnancy Complications; Risk; Tyrosine | 1983 |
Prenatal diagnosis of type I hereditary tyrosinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Diseases in Twins; DNA Mutational Analysis; Female; Fetal Diseases; Humans; Pregnancy; Pregnancy, Multiple; Prenatal Diagnosis; Tyrosine | 1994 |
A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluid.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Cells, Cultured; DNA Mutational Analysis; Enzyme Inhibitors; Female; Fetal Diseases; Gas Chromatography-Mass Spectrometry; Heptanoates; Humans; Male; Predictive Value of Tests; Pregnancy; Pregnancy Trimester, Second; Prenatal Diagnosis; Tyrosine | 1996 |
Thanatophoric dysplasia type I with syndactyly.
Topics: Cysteine; Fetal Diseases; Humans; Male; Point Mutation; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndactyly; Thanatophoric Dysplasia; Tyrosine | 1998 |
Effect of maternal blood phenylalanine level on mouse maternal phenylketonuria offspring.
Topics: Abortion, Spontaneous; Animals; Disease Models, Animal; Embryonic and Fetal Development; Female; Fetal Diseases; Humans; Male; Mice; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Tyrosine | 2001 |
Late diagnosis of phenylketonuria in a Bedouin mother.
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 |
New England Maternal PKU Project: prospective study of untreated and treated pregnancies and their outcomes.
Topics: Adolescent; Adult; Female; Fetal Blood; Fetal Diseases; Humans; Infant, Newborn; Microcephaly; Patient Compliance; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Prenatal Diagnosis; Prognosis; Tyrosine | 1987 |
[New observations on fetal liver cirrhosis associated with hereditary tyrosinemia].
Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Female; Fetal Diseases; Guinea Pigs; Humans; Liver; Liver Cirrhosis; Pregnancy; Rats; S-Adenosylmethionine; Tyrosine | 1985 |
Preliminary report on inverse diurnal variation of phenylalanine: implications in maternal phenylketonuria.
Topics: Adult; Amino Acids; Circadian Rhythm; Female; Fetal Diseases; Humans; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine | 1985 |
[Cerebral damage of the infant due to intrauterine and postnatal under- and malnutrition (symposion by letter)].
Topics: Brain; Brain Diseases; Child Development; Embryonic and Fetal Development; Female; Fetal Diseases; Gestational Age; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature, Diseases; Labor, Induced; Maternal-Fetal Exchange; Nutrition Disorders; Placenta Diseases; Pregnancy; Tyrosine | 1974 |
"Fetal PKU:" the effect of maternal hyperphenylalaninemia during pregnancy in the rhesus monkey (Macaca mulatta).
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 |
Developmental changes in amino acid concentrations in human amniotic fluid: abnormal findings in maternal phenylketonuria.
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 |
Prenatal and postnatal developmental consequences of maternal phenylketonuria.
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 |