glycine has been researched along with Cavernous Angioma, Central Nervous System in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Familial cerebral cavernous malformation (CCM) exhibits autosomal dominant inheritance and is characterized by vascular disorders of the brain, which can lead to seizures, focal neurological deficits, hemorrhagic stroke, and migraine." | 1.32 | Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test. ( Dorcaratto, A; Ferrera, L; Garrè, C; Mareni, C; Marini, V; Origone, P; Viale, G, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Marini, V | 1 |
| Ferrera, L | 1 |
| Dorcaratto, A | 1 |
| Viale, G | 1 |
| Origone, P | 1 |
| Mareni, C | 1 |
| Garrè, C | 1 |
1 other study available for glycine and Cavernous Angioma, Central Nervous System
| Article | Year |
|---|---|
Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test.
Topics: Cysteine; DNA Mutational Analysis; Genetic Linkage; Glycine; Hemangioma, Cavernous, Central Nervous | 2003 |