Page last updated: 2024-10-18
glycine and CADASILM
glycine has been researched along with CADASILM in 3 studies
CADASILM: A subvariety of CADASIL characterized by the high frequency of MIGRAINE. The acronym stands for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts, Leukoencephalopathy, and Migraine.
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 CADASILM
| 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 |