tiagabine hydrochloride has been researched along with Seizures in 3 studies
*Seizures: Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. [MeSH]
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andersen, KE; Huusfeldt, PO; Knutsen, LJ; Lau, J; Lundt, BF; Petersen, H; Suzdak, PD; Swedberg, MD; Sørensen, JL | 1 |
Andersen, KE; Huusfeldt, PO; Lau, J; Lundt, BF; Petersen, H; Suzdak, PD; Swedberg, MD; Sørensen, JL | 1 |
Arisawa, M; Hayakawa, W; Ide, S; Ito, Y; Katayama, T; Kawamura, S; Kobayashi, T; Masuda, E; Minami, M; Nakada, K; Shuto, S; Suemasa, A; Yamada, S; Yoshikawa, M | 1 |
3 other study(ies) available for tiagabine hydrochloride and Seizures
Article | Year |
---|---|
Synthesis of novel GABA uptake inhibitors. 4. Bioisosteric transformation and successive optimization of known GABA uptake inhibitors leading to a series of potent anticonvulsant drug candidates.
Topics: Animals; Anticonvulsants; Female; gamma-Aminobutyric Acid; In Vitro Techniques; Neurotransmitter Uptake Inhibitors; Nipecotic Acids; Rats; Seizures; Structure-Activity Relationship; Synaptosomes | 1999 |
Synthesis of novel gamma-aminobutyric acid (GABA) uptake inhibitors. 5.(1) Preparation and structure-activity studies of tricyclic analogues of known GABA uptake inhibitors.
Topics: Animals; Anticonvulsants; Antidepressive Agents, Tricyclic; Brain Chemistry; Carbolines; Convulsants; Female; gamma-Aminobutyric Acid; Mice; Neuroglia; Neurons; Neurotransmitter Uptake Inhibitors; Postural Balance; Rats; Seizures; Structure-Activity Relationship; Synaptosomes | 2001 |
Cyclopropane-based conformational restriction of GABA by a stereochemical diversity-oriented strategy: identification of an efficient lead for potent inhibitors of GABA transports.
Topics: Animals; Anticonvulsants; Brain; Cyclopropanes; GABA Modulators; GABA Plasma Membrane Transport Proteins; gamma-Aminobutyric Acid; Ligands; Mice; Protein Binding; Rats; Seizures; Stereoisomerism; Structure-Activity Relationship | 2013 |