glycine and CADASIL
glycine has been researched along with CADASIL in 3 studies
CADASIL: A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146)
Research Excerpts
| Excerpt | Relevance | Reference |
|---|---|---|
| "CADASIL is an autosomal dominant arteriopathy characterised by diffuse white matter lesions and small subcortical infarcts on neuroimaging and a variable combination of recurrent cerebral ischaemic episodes, cognitive deficits, migraine with aura and psychiatric symptoms." | 1.34 | Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation. ( Cacchiò, G; Cavallaro, T; Fabrizi, GM; Ragno, M; Scarcella, M; Silvaggio, F; Taioli, F; Trojano, L, 2007) |
Research
Studies (3)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Pavlovic, AM | 1 |
| Dobricic, V | 1 |
| Semnic, R | 1 |
| Lackovic, V | 1 |
| Novakovic, I | 1 |
| Bajcetic, M | 1 |
| Sternic, N | 1 |
| Coto, E | 1 |
| Menéndez, M | 1 |
| Navarro, R | 1 |
| García-Castro, M | 1 |
| Alvarez, V | 1 |
| Ragno, M | 1 |
| Cacchiò, G | 1 |
| Fabrizi, GM | 1 |
| Scarcella, M | 1 |
| Silvaggio, F | 1 |
| Cavallaro, T | 1 |
| Taioli, F | 1 |
| Trojano, L | 1 |
Other Studies
3 other studies available for glycine and CADASIL
| Article | Year |
|---|---|
A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family.
Topics: Brain; CADASIL; Cysteine; Family Health; Female; Genetic Testing; Glycine; Humans; Magnetic Resonanc | 2013 |
A new de novo Notch3 mutation causing CADASIL.
Topics: Adult; CADASIL; Cysteine; DNA Mutational Analysis; Glycine; Humans; Magnetic Resonance Imaging; Male | 2006 |
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation.
Topics: Aged; CADASIL; Cystine; Exons; Family Health; Female; Glycine; Humans; Italy; Magnetic Resonance Ima | 2007 |