vigabatrin has been researched along with Genetic Predisposition in 4 studies
Excerpt | Relevance | Reference |
---|---|---|
"Proline dehydrogenase (PRODH), which degrades L-proline, resides within the schizophrenia-linked 22q11." | 3.83 | Cytosolic Accumulation of L-Proline Disrupts GABA-Ergic Transmission through GAD Blockade. ( Crabtree, GW; Gogos, JA; Gordon, JA; Park, AJ, 2016) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Madaan, P | 1 |
Negi, S | 1 |
Sharma, R | 1 |
Kaur, A | 1 |
Sahu, JK | 1 |
Chukwu, J | 1 |
Delanty, N | 1 |
Webb, D | 1 |
Cavalleri, GL | 1 |
Crabtree, GW | 1 |
Park, AJ | 1 |
Gordon, JA | 1 |
Gogos, JA | 1 |
Buoni, S | 1 |
Zannolli, R | 1 |
Waterham, H | 1 |
Wanders, R | 1 |
Fois, A | 1 |
1 review available for vigabatrin and Genetic Predisposition
Article | Year |
---|---|
Weight change, genetics and antiepileptic drugs.
Topics: Animals; Anticonvulsants; Epilepsy; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Huma | 2014 |
3 other studies available for vigabatrin and Genetic Predisposition
Article | Year |
---|---|
X-Linked ALG13 Gene Variant as a Cause of Epileptic Encephalopathy in Girls.
Topics: Brain; Exome; Female; Genetic Predisposition to Disease; Genetic Variation; Humans; India; Infant; M | 2019 |
Cytosolic Accumulation of L-Proline Disrupts GABA-Ergic Transmission through GAD Blockade.
Topics: Animals; Central Nervous System; Cytosol; Disease Models, Animal; Gamma Rhythm; gamma-Aminobutyric A | 2016 |
D-bifunctional protein deficiency associated with drug resistant infantile spasms.
Topics: 17-Hydroxysteroid Dehydrogenases; Anticonvulsants; Disease Progression; DNA Mutational Analysis; Dru | 2007 |