glycine has been researched along with Hemangioma, Cavernous, Central Nervous System in 1 studies
Hemangioma, Cavernous, Central Nervous System: A vascular anomaly composed of a collection of large, thin walled tortuous VEINS that can occur in any part of the central nervous system but lack intervening nervous tissue. Familial occurrence is common and has been associated with a number of genes mapped to 7q, 7p and 3q. Clinical features include SEIZURES; HEADACHE; STROKE; and progressive neurological deficit.
| 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 Hemangioma, Cavernous, 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 |