acetazolamide has been researched along with Dysarthosis in 6 studies
Acetazolamide: One of the CARBONIC ANHYDRASE INHIBITORS that is sometimes effective against absence seizures. It is sometimes useful also as an adjunct in the treatment of tonic-clonic, myoclonic, and atonic seizures, particularly in women whose seizures occur or are exacerbated at specific times in the menstrual cycle. However, its usefulness is transient often because of rapid development of tolerance. Its antiepileptic effect may be due to its inhibitory effect on brain carbonic anhydrase, which leads to an increased transneuronal chloride gradient, increased chloride current, and increased inhibition. (From Smith and Reynard, Textbook of Pharmacology, 1991, p337)
Excerpt | Relevance | Reference |
---|---|---|
"Treatment with acetazolamide resulted in complete abolition of the attacks." | 5.30 | Acetazolamide-responsive hereditary paroxysmal ataxia: report of a family. ( Jeon, BS; Kim, HJ, 1998) |
"Treatment with acetazolamide 250 mg daily, completely abolished the attacks in both patients." | 5.27 | [Familial paroxysmal ataxia responsive to acetazolamide]. ( Aimard, G; Devic, M; Trillet, M; Ventre, JJ; Vighetto, A, 1983) |
"Dystonia is potentially included as a further part of the phenotype spectrum of CACNA1A gene mutations." | 1.42 | Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine. ( Beyer, A; Kinder, S; Ossig, C; Smitka, M; Storch, A; von der Hagen, M; Wienecke, M, 2015) |
"Treatment with acetazolamide resulted in complete abolition of the attacks." | 1.30 | Acetazolamide-responsive hereditary paroxysmal ataxia: report of a family. ( Jeon, BS; Kim, HJ, 1998) |
"Acute intermittent familial ataxia is a rare disorder with autosomal dominant inheritance and unknown etiology which usually in childhood or adolescence." | 1.29 | [Acute intermittent familial ataxia: report of a new family]. ( Aparicio-Meix, JM; Lorenzo-Sanz, G; Pérez-Rodríguez, MJ, 1996) |
"Treatment with acetazolamide 250 mg daily, completely abolished the attacks in both patients." | 1.27 | [Familial paroxysmal ataxia responsive to acetazolamide]. ( Aimard, G; Devic, M; Trillet, M; Ventre, JJ; Vighetto, A, 1983) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 3 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Pramila, PJ | 1 |
Mannam, P | 1 |
Chacko, AG | 1 |
Benjamin, RN | 1 |
Kinder, S | 1 |
Ossig, C | 1 |
Wienecke, M | 1 |
Beyer, A | 1 |
von der Hagen, M | 1 |
Storch, A | 1 |
Smitka, M | 1 |
Aimard, G | 1 |
Vighetto, A | 1 |
Trillet, M | 1 |
Ventre, JJ | 1 |
Devic, M | 1 |
Pérez-Rodríguez, MJ | 1 |
Lorenzo-Sanz, G | 1 |
Aparicio-Meix, JM | 1 |
Kim, HJ | 1 |
Jeon, BS | 1 |
Onofrj, M | 1 |
Thomas, A | 1 |
6 other studies available for acetazolamide and Dysarthosis
Article | Year |
---|---|
Progressive midbrain clefts after head trauma and decompressive surgery: a report of two patients.
Topics: Acetazolamide; Ataxia; Blepharoptosis; Brain Diseases; Brain Injuries, Diffuse; Carbonic Anhydrase I | 2021 |
Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine.
Topics: Acetazolamide; Age of Onset; Calcium Channels; Carbonic Anhydrase Inhibitors; Cerebellar Ataxia; Chi | 2015 |
[Familial paroxysmal ataxia responsive to acetazolamide].
Topics: Acetazolamide; Adult; Ataxia; Blood Glucose; Diagnosis, Differential; Dysarthria; Electrooculography | 1983 |
[Acute intermittent familial ataxia: report of a new family].
Topics: Acetazolamide; Adult; Ataxia; Carbonic Anhydrase Inhibitors; Child; Dysarthria; Female; Humans; Male | 1996 |
Acetazolamide-responsive hereditary paroxysmal ataxia: report of a family.
Topics: Acetazolamide; Adult; Ataxia; Dysarthria; Female; Humans; Male; Middle Aged; Nystagmus, Pathologic; | 1998 |
Acetazolamide-responsive periodic ataxia induced by amiodarone.
Topics: Acetazolamide; Aged; Amiodarone; Anti-Arrhythmia Agents; Anticonvulsants; Ataxia; Dysarthria; Humans | 1999 |