thyroxine has been researched along with Autosomal Chromosome Disorders in 14 studies
Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We have studied the largest kindred with familial dysalbuminemic hyperthyroxinemia (FDH) thus far reported, comprising thirty-three blood relations in four generations and three of their spouses." | 7.67 | A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin. ( Braverman, LE; Etzkorn, JR; Ingbar, SH; Rajatanavin, R; Yabu, Y; Yeo, PP, 1987) |
| "The liver dysfunction was associated with hypothyroidism that resolved with thyroid hormone treatment." | 5.38 | Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome. ( Hara, T; Ihara, K; Ishimura, M; Ohga, S; Ohkubo, K, 2012) |
| "We have studied the largest kindred with familial dysalbuminemic hyperthyroxinemia (FDH) thus far reported, comprising thirty-three blood relations in four generations and three of their spouses." | 3.67 | A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin. ( Braverman, LE; Etzkorn, JR; Ingbar, SH; Rajatanavin, R; Yabu, Y; Yeo, PP, 1987) |
| " The affected family members were clinically euthyroid but all had goiters and markedly increased serum thyroid hormone levels: thyroxine (T4) = 21." | 3.66 | Familial thyroid hormone resistance. ( Barbato, AL; Brooks, MH; Collins, S; Garbincius, J; Hoffman, D; Neidballa, RG, 1981) |
| "The liver dysfunction was associated with hypothyroidism that resolved with thyroid hormone treatment." | 1.38 | Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome. ( Hara, T; Ihara, K; Ishimura, M; Ohga, S; Ohkubo, K, 2012) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 11 (78.57) | 18.7374 |
| 1990's | 2 (14.29) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (7.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ohkubo, K | 1 |
| Ihara, K | 1 |
| Ohga, S | 1 |
| Ishimura, M | 1 |
| Hara, T | 1 |
| Brooks, MH | 1 |
| Barbato, AL | 1 |
| Collins, S | 1 |
| Garbincius, J | 1 |
| Neidballa, RG | 1 |
| Hoffman, D | 1 |
| Jones, KL | 1 |
| Carey, DE | 1 |
| Khan, F | 1 |
| Verma, RS | 1 |
| Dosik, H | 1 |
| Warman, J | 1 |
| Hasen, J | 1 |
| Bartalos, M | 1 |
| Nilsson, C | 1 |
| Hansson, A | 1 |
| Nilsson, G | 1 |
| Thorpe-Beeston, JG | 1 |
| Nicolaides, KH | 1 |
| Gosden, CM | 1 |
| McGregor, AM | 1 |
| Grodum, E | 1 |
| Kvetny, J | 1 |
| Bollerslev, J | 1 |
| Yeo, PP | 1 |
| Yabu, Y | 1 |
| Etzkorn, JR | 1 |
| Rajatanavin, R | 1 |
| Braverman, LE | 1 |
| Ingbar, SH | 1 |
| Lizarralde, G | 1 |
| Jones, B | 1 |
| Seal, US | 1 |
| Jones, JE | 1 |
| Chopra, IJ | 1 |
| Solomon, DH | 1 |
| Ho, RS | 1 |
| Nishikawa, M | 1 |
| Ito, S | 1 |
| Sano, K | 1 |
| Nishioeda, Y | 1 |
| Nasako, Y | 1 |
| Cross, HE | 1 |
| Hollander, CS | 1 |
| Rimoin, DL | 1 |
| McKusick, VA | 1 |
| Kitlak, W | 1 |
| Gebert, P | 1 |
14 other studies available for thyroxine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome.
Topics: Child; Child, Preschool; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 18; Hep | 2012 |
Familial thyroid hormone resistance.
Topics: Adolescent; Adult; Child; Chromosome Aberrations; Chromosome Disorders; Female; Genes, Dominant; Goi | 1981 |
Brief clinical report: Graves disease in a patient with the del(18p) syndrome.
Topics: Adolescent; Autoimmune Diseases; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; | 1982 |
Primary amenorrhea in a black female with duplication and inversion of the secondary constriction regions of chromosome 9.
Topics: Adult; Amenorrhea; Androgens; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 | 1978 |
Dyshormonogenetic goitrous hypothyroidism in a patient with short arm deletion of E18 chromosome.
Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosome | 1975 |
Influence of thyroid hormones on satellite association in man and the origin of chromosome abnormalities.
Topics: Adult; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Chr | 1975 |
Thyroid function in fetuses with chromosomal abnormalities.
Topics: Chromosome Aberrations; Chromosome Disorders; Fetal Blood; Fetal Diseases; Gestational Age; Humans; | 1991 |
Decreased thyroid hormone-stimulated oxygen consumption and glucose uptake in mononuclear blood cells from patients with autosomal dominant osteopetrosis type I.
Topics: Adult; Aged; Blood Glucose; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Female; G | 1991 |
A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin.
Topics: Aged; Blood Protein Disorders; Chromosome Aberrations; Chromosome Disorders; Contraceptives, Oral; F | 1987 |
Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gel; Chromosome Aberrations; Chromosome | 1966 |
Competitive ligand-binding assay for measurement of thyronine-binding globulin (TBG).
Topics: Animals; Binding Sites; Cattle; Chromosome Aberrations; Chromosome Disorders; Dogs; Female; Graves D | 1972 |
A case of familial cystathioninuria with goiter and some anomalies.
Topics: Abnormalities, Multiple; Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Chr | 1970 |
Familial agoitrous cretinism accompanied by musclar hypertrophy.
Topics: Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Congenital Hypothyroidism; Fe | 1968 |
[Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
Topics: Adult; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Goit | 1968 |