acetazolamide has been researched along with Muscular Diseases in 9 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)
Muscular Diseases: Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hypokalaemic periodic paralysis (hypoPP) is the archetypal skeletal muscle channelopathy caused by dysfunction of one of two sarcolemmal ion channels, either the sodium channel Nav1." | 2.46 | Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis? ( Hanna, MG; Matthews, E, 2010) |
| "Hypokalemic periodic paralysis is a chronic condition characterized by sporadic attacks of weakness associated with acute hypokalemia." | 1.72 | The role of nephrologists in management of hypokalemic periodic paralysis: a case report. ( Li, J; Moten, S; Rauf, AA, 2022) |
| "Hyperkalemia was found in foals 1 and 4." | 1.28 | Respiratory stridor associated with polymyopathy suspected to be hyperkalemic periodic paralysis in four quarter horse foals. ( Child, G; Ingram, JT; Kiper, ML; MacAllister, CG; Stashak, TS; Tarr, S; Traub-Dargatz, JL, 1992) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (33.33) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 3 (33.33) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Li, J | 1 |
| Moten, S | 1 |
| Rauf, AA | 1 |
| Matthews, E | 2 |
| Hartley, L | 1 |
| Sud, R | 1 |
| Hanna, MG | 2 |
| Muntoni, F | 1 |
| Munot, P | 1 |
| Petzold, A | 1 |
| Luthert, PJ | 1 |
| Collin, JR | 1 |
| Plant, GT | 1 |
| PEARSON, CM | 1 |
| TURPIN, R | 1 |
| CAILLE, B | 1 |
| LAFOURCADE, J | 1 |
| BEBE, M | 1 |
| NAYRAC, P | 1 |
| WAROT, P | 1 |
| FOSSATI, P | 1 |
| MILBLED, G | 1 |
| MALAFOSSE, M | 1 |
| MEIGNIE, S | 1 |
| Tricarico, D | 1 |
| Lovaglio, S | 1 |
| Mele, A | 1 |
| Rotondo, G | 1 |
| Mancinelli, E | 1 |
| Meola, G | 1 |
| Camerino, DC | 1 |
| Schipperheyn, JJ | 1 |
| Buruma, OJ | 1 |
| Voogd, PJ | 1 |
| Traub-Dargatz, JL | 1 |
| Ingram, JT | 1 |
| Stashak, TS | 1 |
| Kiper, ML | 1 |
| Tarr, S | 1 |
| Child, G | 1 |
| MacAllister, CG | 1 |
1 review available for acetazolamide and Muscular Diseases
| Article | Year |
|---|---|
Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?
Topics: Acetazolamide; Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Channelopathies; Humans; | 2010 |
8 other studies available for acetazolamide and Muscular Diseases
| Article | Year |
|---|---|
The role of nephrologists in management of hypokalemic periodic paralysis: a case report.
Topics: Acetazolamide; Adult; Humans; Hypokalemia; Hypokalemic Periodic Paralysis; Male; Muscular Diseases; | 2022 |
Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathy.
Topics: Acetazolamide; Adolescent; Anticonvulsants; Calcium Channels, L-Type; Child; Female; Humans; Muscula | 2019 |
Recurrent ptosis due to myopathy of the levator palpebrae superioris.
Topics: Acetazolamide; Blepharoptosis; Carbonic Anhydrase Inhibitors; Eyelid Diseases; Female; Follow-Up Stu | 2010 |
THE PERIODIC PARALYSES: DIFFERENTIAL FEATURES AND PATHOLOGICAL OBSERVATIONS IN PERMANENT MYOPATHIC WEAKNESS.
Topics: Acetazolamide; Drug Therapy; Epinephrine; Humans; Hydrochlorothiazide; Hydrocortisone; Hyperkalemia; | 1964 |
[A FAMILIAL DISEASE PRESENTING IN CERTAIN SUBJECTS THE APPEARANCE OF EULENBURG'S PARAMYOTONIA AND RESEMBLING IN OTHERS HEREDITARY EPISODIC ADYNAMIA].
Topics: Acetazolamide; Adolescent; Blood; Child; Drug Therapy; Electromyography; Genetics, Medical; Humans; | 1964 |
Acetazolamide prevents vacuolar myopathy in skeletal muscle of K(+) -depleted rats.
Topics: Acetazolamide; Animals; Bendroflumethiazide; Carbonic Anhydrase Inhibitors; Cell Count; Dichlorphena | 2008 |
Hypokalaemic periodic paralysis and cardiomyopathy.
Topics: Acetazolamide; Adolescent; Adult; Cardiomyopathies; Echocardiography; Electrocardiography; Female; H | 1978 |
Respiratory stridor associated with polymyopathy suspected to be hyperkalemic periodic paralysis in four quarter horse foals.
Topics: Acetazolamide; Animals; Arytenoid Cartilage; Calcium; Electromyography; Fluid Therapy; Horse Disease | 1992 |