glycocyamine has been researched along with Abnormalities, Multiple in 2 studies
glycocyamine: RN given refers to parent cpd; structure
guanidinoacetate : A monocarboxylic acid anion that is the conjugate base of guanidinoacetic acid, obtained by deprotonation of the carboxy group.
guanidinoacetic acid : The N-amidino derivative of glycine.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Nasrallah, F | 1 |
| Kraoua, I | 1 |
| Joncquel-Chevalier Curt, M | 1 |
| Bout, MA | 1 |
| Taieb, SH | 1 |
| Feki, M | 1 |
| Khouja, N | 1 |
| Briand, G | 1 |
| Kaabachi, N | 1 |
| Caldeira Araújo, H | 1 |
| Smit, W | 1 |
| Verhoeven, NM | 1 |
| Salomons, GS | 1 |
| Silva, S | 1 |
| Vasconcelos, R | 1 |
| Tomás, H | 1 |
| Tavares de Almeida, I | 1 |
| Jakobs, C | 1 |
| Duran, M | 1 |
2 other studies available for glycocyamine and Abnormalities, Multiple
| Article | Year |
|---|---|
Guanidinoacetate methyltransferase (GAMT) deficiency in two Tunisian siblings: clinical and biochemical features.
Topics: Abnormalities, Multiple; Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Hi | 2012 |
Guanidinoacetate methyltransferase deficiency identified in adults and a child with mental retardation.
Topics: Abnormalities, Multiple; Adult; Alleles; Amino Acid Metabolism, Inborn Errors; Child; Creatinine; DN | 2005 |