glutamic acid has been researched along with Congenital Adrenal Hyperplasia in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Grötzinger, J; Holterhus, PM; Krone, N; Riepe, FG; Schwarz, HP; Sippell, WG | 1 |
| Latronico, AC; Marui, S; Mendonca, BB; Russell, AJ; Sutcliffe, RG; Torrealba, IM | 1 |
2 other study(ies) available for glutamic acid and Congenital Adrenal Hyperplasia
| Article | Year |
|---|---|
Congenital adrenal hyperplasia due to 11-hydroxylase deficiency--insights from two novel CYP11B1 mutations (p.M92X, p.R453Q).
Topics: Adrenal Hyperplasia, Congenital; Animals; Arginine; Base Sequence; Chlorocebus aethiops; COS Cells; DNA Mutational Analysis; Glutamic Acid; Humans; Infant; Male; Methionine; Models, Molecular; Mutation, Missense; Pedigree; Polymorphism, Single Nucleotide; Steroid 11-beta-Hydroxylase; Transfection | 2009 |
A novel homozygous nonsense mutations E135* in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. Online.
Topics: 3-Hydroxysteroid Dehydrogenases; Adrenal Hyperplasia, Congenital; Female; Glutamic Acid; Homozygote; Humans; Infant, Newborn; Mutation, Missense; Salts | 1998 |