Compounds > tyrosine

tyrosine and Abnormalities, Congenital

tyrosine has been researched along with Abnormalities, Congenital in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19906 (60.00)18.7374
1990's1 (10.00)18.2507
2000's2 (20.00)29.6817
2010's1 (10.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blau, N; Dill, P; Jakobs, C; Schneider, J; Tekin, M; Thöny, B; Trachsel, D; Weber, P1
Devi, RR; Vijayalakshmi, P1
Levy, HL; Waisbren, SE1
Acosta, PB; Blaskovics, M; Cloud, H; Lis, E; Stroud, H; Wenz, E1
Basler, K; Cooper, JA; Kussick, SJ1
Bianchi, N; Boulat, O; Matthieu, JM1
Barton, SJ; Magenis, RE1
Hsia, DY1
Howell, RR; Parmley, TH; Stevenson, RE; Thomas, GH1
Anderson, JA; Fisch, RO; Walker, WA1

Reviews

1 review(s) available for tyrosine and Abnormalities, Congenital

ArticleYear
Phenylketonuria and its variants.
    Progress in medical genetics, 1970, Volume: 7

    Topics: Adult; Child, Preschool; Congenital Abnormalities; Female; Gene Frequency; Growth Disorders; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Middle Aged; Mixed Function Oxygenases; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine

1970

Other Studies

9 other study(ies) available for tyrosine and Abnormalities, Congenital

ArticleYear
Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM).
    Molecular genetics and metabolism, 2011, Volume: 104, Issue:3

    Topics: Base Sequence; Child; Codon, Nonsense; Congenital Abnormalities; Congenital Microtia; Dihydroxyphenylalanine; DNA Primers; Ear; Ear, Inner; Electroencephalography; Epilepsy; Fibroblast Growth Factor 3; Folate Receptor 1; Folic Acid Deficiency; Humans; Levodopa; Male; Molecular Sequence Data; Pyridoxal Phosphate; Radiography; Sequence Analysis, DNA; Skull; Syndrome; Tooth Abnormalities; Tyrosine

2011
Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
    Molecular vision, 2006, Mar-23, Volume: 12

    Topics: Adult; Arginine; Case-Control Studies; Cataract; Child; Congenital Abnormalities; Connexins; Cornea; Eye Proteins; Genes, Dominant; Glutamic Acid; Glutamine; Humans; India; Middle Aged; Mutation; Mutation, Missense; Myopia; Phenotype; Tyrosine

2006
Effects of untreated maternal phenylketonuria and hyperphenylalaninemia on the fetus.
    The New England journal of medicine, 1983, Nov-24, Volume: 309, Issue:21

    Topics: Abortion, Spontaneous; Birth Weight; Body Weight; Child; Child, Preschool; Congenital Abnormalities; Female; Fetal Blood; Fetus; Humans; Infant; Infant, Newborn; Intellectual Disability; Intelligence; Male; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine

1983
Nutrition in pregnancy of women with hyperphenylalaninemia.
    Journal of the American Dietetic Association, 1982, Volume: 80, Issue:5

    Topics: Abortion, Spontaneous; Congenital Abnormalities; Female; Fetal Death; Fetal Growth Retardation; Humans; Intellectual Disability; Maternal-Fetal Exchange; Phenylalanine; Phenylketonurias; Pregnancy; Tyrosine

1982
Ras1-dependent signaling by ectopically-expressed Drosophila src gene product in the embryo and developing eye.
    Oncogene, 1993, Volume: 8, Issue:10

    Topics: Animals; Base Sequence; Congenital Abnormalities; Drosophila; Drosophila Proteins; Enhancer Elements, Genetic; Eye; Female; Genes, Lethal; Genes, ras; Hot Temperature; Male; Microscopy, Electron, Scanning; Molecular Sequence Data; Mutation; Phenotype; Phosphorylation; Protein-Tyrosine Kinases; Proto-Oncogene Proteins; Tyrosine

1993
[Maternal phenylketonuria].
    Revue medicale de la Suisse romande, 2001, Volume: 121, Issue:4

    Topics: Adult; Congenital Abnormalities; Diet, Protein-Restricted; Energy Intake; Female; Fetal Growth Retardation; Gestational Age; Humans; Nutritional Requirements; Phenylalanine; Phenylketonuria, Maternal; Pregnancy; Prenatal Care; Risk Factors; Tyrosine

2001
Delineation of human prometaphase paracentromeric regions using sequential GTG- and C-banding.
    Cytogenetics and cell genetics, 1987, Volume: 45, Issue:3-4

    Topics: Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Centromere; Chromosome Banding; Chromosomes; Chromosomes, Human; Congenital Abnormalities; Female; Haploidy; Humans; Karyotyping; Lymphocytes; Male; Metaphase; Tyrosine; X Chromosome; Y Chromosome

1987
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
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