tyrosine and Cretinism

tyrosine has been researched along with Cretinism in 19 studies

Research

Studies (19)

TimeframeStudies, this research(%)All Research%
pre-199017 (89.47)18.7374
1990's0 (0.00)18.2507
2000's2 (10.53)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
KASSENAAR, AA; MEIJER, JW; STANBURY, JB; TERPSTRA, J1
BLOCK, RJ; KASSENAAR, AA; MANDL, RH; WERNER, SC1
JOB, JC; JOSEPH, R1
CHOUFOER, JC; KASSENAAR, AA; QUERIDO, A1
JANSSEN, MA; RICCABONA, G; STANBURY, JB1
BASTENIE, PA; DUMONT, JE; ERMANS, AM1
RICCABONA, G1
LINDEBOOM, GA; WIENER, JD1
de Vijlder, JJ1
Ieiri, T1
Hansen, JM; Siersbaek-Nielsen, K1
Dussault, JH; Gagné, R; Grenier, A; Laberge, C; Morissette, J1
Rigilano, JC; Stevens, MB; Wilson, CC1
Kawamura, M1
Abdelmoumene, N; Ait Hammou, N; Benmiloud, M1
Jones, B; Jones, JE; Lizarralde, G; Seal, US1
Stanbury, JB1
Delire, M; Orsini, A; Pierron, H1
Bisacchi, U; Guazzelli, R; Morabito, F; Strazzulla, G1

Reviews

3 review(s) available for tyrosine and Cretinism

ArticleYear
Primary congenital hypothyroidism: defects in iodine pathways.
    European journal of endocrinology, 2003, Volume: 149, Issue:4

    Topics: Animals; Congenital Hypothyroidism; Humans; Hypothyroidism; Iodides; Iodine; Iodoproteins; Mutation; Thyroglobulin; Thyroid Gland; Thyroid Hormones; Tyrosine

2003
[Defects in the coupling of iodotyrosyl residues].
    Nihon rinsho. Japanese journal of clinical medicine, 2006, May-28, Volume: Suppl 1

    Topics: Congenital Hypothyroidism; Diagnosis, Differential; Humans; Hydrogen Peroxide; Iodide Peroxidase; Iodine; Prognosis; Thyroglobulin; Thyroxine; Tyrosine

2006
Radioisotopes in the diagnosis of hypothyroid states, iodine deficiency, and thyroiditis.
    Nuclear-Medizin, 1965

    Topics: Adolescent; Blood Protein Disorders; Child, Preschool; Chile; Congenital Hypothyroidism; Congo; Deficiency Diseases; Diiodotyrosine; Humans; Hypothyroidism; Iodides; Iodine; Iodine Radioisotopes; Male; Metabolic Diseases; Peroxidases; Radionuclide Imaging; Serum Albumin; Thyroid Function Tests; Thyroid Gland; Thyroiditis; Tyrosine; Venezuela

1965

Other Studies

16 other study(ies) available for tyrosine and Cretinism

ArticleYear
The occurrence of mono- and di-iodotyrosine in the blood of a patient with congenital goiter.
    The Journal of clinical endocrinology and metabolism, 1955, Volume: 15, Issue:10

    Topics: Blood; Child; Congenital Hypothyroidism; Goiter; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Monoiodotyrosine; Thyroxine; Tyrosine

1955
Pathogenesis of a case of congenital goiter with abnormally high levels of SPI and with mono- and diiodotyrosine in the serum.
    The Journal of clinical endocrinology and metabolism, 1957, Volume: 17, Issue:7

    Topics: Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Infant, Newborn; Infant, Newborn, Diseases; Iodine; Tyrosine

1957
[Congenital hypothyroidism with anomaly of iodotyrosine condensation: familial incidence: physiopathological discussion].
    Archives francaises de pediatrie, 1958, Volume: 15, Issue:4

    Topics: Biochemical Phenomena; Congenital Hypothyroidism; Humans; Incidence; Monoiodotyrosine; Tyrosine

1958
The syndrome of congenital hypothyroidism with defective dehalogenation of iodotyrosines. Further observations and a discussion of the pathophysiology.
    The Journal of clinical endocrinology and metabolism, 1960, Volume: 20

    Topics: Congenital Hypothyroidism; Humans; Hypothyroidism; Monoiodotyrosine; Syndrome; Tyrosine

1960
Iodotyrosyl coupling defect in congenital hypothyroidism with goitre.
    Lancet (London, England), 1963, Apr-27, Volume: 1, Issue:7287

    Topics: Congenital Hypothyroidism; Goiter; Humans; Hypothyroidism; Iodine; Thyroid Gland; Thyronines; Tyrosine

1963
THYROID FUNCTION IN A GOITER ENDEMIC. V. MECHANISM OF THYROID FAILURE IN THE UELE ENDEMIC CRETINS.
    The Journal of clinical endocrinology and metabolism, 1963, Volume: 23

    Topics: Chromatography; Congenital Hypothyroidism; Congo; Diiodotyrosine; Goiter; Iodides; Iodine Isotopes; Metabolism; Saliva; Thiocyanates; Thyroid Function Tests; Thyrotropin; Thyroxine; Triiodothyronine; Tyrosine

1963
[IOSINE-TYROSYL COUPLING DEFECT IN CONGENITAL HYPOTHYROIDISM WITH GOITER].
    Klinische Medizin; osterreichische Zeitschrift fur wissenschaftliche und praktische Medizin, 1964, Volume: 19

    Topics: Child; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Hypothyroidism; Iodine; Iodine Isotopes; Metabolism; Thyroglobulin; Thyronines; Tyrosine

1964
THE POSSIBLE OCCURRENCE OF TWO INBORN ERRORS OF IODINE METABOLISM IN ONE PATIENT.
    Acta endocrinologica, 1964, Volume: 47

    Topics: Adolescent; Child; Congenital Hypothyroidism; Diiodotyrosine; Electrophoresis; Goiter; Humans; Iodides; Iodine; Metabolism, Inborn Errors; Thyroglobulin; Thyroid Function Tests; Thyroxine; Triiodothyronine; Tyrosine; Urine

1964
Thyroid function and plasma tyrosine in the neonatal period.
    Acta paediatrica Scandinavica, 1967, Volume: 56, Issue:2

    Topics: Adult; Blood; Congenital Hypothyroidism; Female; Humans; Infant, Newborn; Infant, Premature; Myxedema; Pregnancy; Thyroid Diseases; Thyroid Function Tests; Thyroid Gland; Thyroxine; Tyrosine; Umbilical Cord

1967
[Hereditary metabolic diseases in Quebec: blood screening].
    L'union medicale du Canada, 1980, Volume: 109, Issue:4

    Topics: Congenital Hypothyroidism; Humans; Infant, Newborn; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Quebec; Tyrosine

1980
State screening for metabolic disorders in newborns.
    American family physician, 1988, Volume: 37, Issue:4

    Topics: Adrenal Hyperplasia, Congenital; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Biotinidase; Congenital Hypothyroidism; Cystic Fibrosis; Galactosemias; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine; United States

1988
[Laboratory examinations for inborn errors of metabolism].
    Rinsho byori. The Japanese journal of clinical pathology, 1986, Volume: 34, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Chromatography, Gas; Computers; Congenital Hypothyroidism; Galactosemias; Gas Chromatography-Mass Spectrometry; Homocystinuria; Humans; Japan; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine

1986
Association of peroxidase enzyme defect and low thyroglobulin content in a case of endemic cretinism.
    Journal of endocrinological investigation, 1985, Volume: 8, Issue:3

    Topics: Adult; Chromatography, DEAE-Cellulose; Congenital Hypothyroidism; Female; Humans; Iodide Peroxidase; Iodine; Kinetics; Peroxidases; Proteins; Thyroglobulin; Thyroid Function Tests; Thyroid Gland; Tyrosine

1985
Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
    The Journal of clinical endocrinology and metabolism, 1966, Volume: 26, Issue:11

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gel; Chromosome Aberrations; Chromosome Disorders; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Immunodiffusion; Iodine Radioisotopes; Male; Mosaicism; Thyroglobulin; Thyroid Function Tests; Thyroxine; Triiodothyronine; Tyrosine; Ultracentrifugation

1966
[Hypothyroidism due to iodotyrosine deiodase deficiency. Results after 7 years of treatment with iodine].
    Marseille medical, 1969, Volume: 106, Issue:1

    Topics: Child; Child, Preschool; Congenital Hypothyroidism; Humans; Hypothyroidism; Infant; Iodine; Male; Monoiodotyrosine; Thyroid Hormones; Time Factors; Tyrosine

1969
[Testing for serum iodotyrosines in a case of infantilism without obvious signs of hypothyroidism].
    Rivista di clinica pediatrica, 1966, Volume: 78, Issue:3

    Topics: Adolescent; Child; Chromatography, Thin Layer; Congenital Hypothyroidism; Dwarfism; Dwarfism, Pituitary; Humans; Hypogonadism; Male; Tyrosine

1966