alanine has been researched along with Congenital Hypothyroidism in 2 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Congenital Hypothyroidism: A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fricke-Otto, S | 1 |
| Pfarr, N | 1 |
| Mühlenberg, R | 1 |
| Pohlenz, J | 1 |
| Hayek, A | 1 |
2 other studies available for alanine and Congenital Hypothyroidism
| Article | Year |
|---|---|
Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V).
Topics: Adult; Alanine; Amino Acid Sequence; Base Sequence; Child; Congenital Hypothyroidism; Female; Homozy | 2005 |
Unimpaired gluconeogenesis in congenital hypothyroidism.
Topics: Alanine; Blood Glucose; Congenital Hypothyroidism; Glucagon; Gluconeogenesis; Humans; Hypothyroidism | 1979 |