threonine has been researched along with Congenital Hypothyroidism in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cabrol, S; Carré, A; Castanet, M; Cerqueira, TL; Chevrier, L; De Roux, N; Guillot, L; Léger, J; Polak, M; Puel, O; Queinnec, C; Ramos, HE; Szinnai, G; Tron, E | 1 |
1 other study(ies) available for threonine and Congenital Hypothyroidism
Article | Year |
---|---|
Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations.
Topics: Blotting, Western; Chromatography; Congenital Hypothyroidism; Cross-Sectional Studies; Female; France; Genetic Testing; Humans; Infant, Newborn; Isoleucine; Kidney; Male; Mutagenesis; Mutation; Neonatal Screening; Paired Box Transcription Factors; PAX8 Transcription Factor; Pedigree; Phenotype; Radionuclide Imaging; Threonine; Thyroid Dysgenesis; Thyrotropin; Transcriptional Activation; Ultrasonography | 2014 |