Page last updated: 2024-10-24

carbamazepine and Batten Turner Congenital Myopathy

carbamazepine has been researched along with Batten Turner Congenital Myopathy in 8 studies

Carbamazepine: A dibenzazepine that acts as a sodium channel blocker. It is used as an anticonvulsant for the treatment of grand mal and psychomotor or focal SEIZURES. It may also be used in the management of BIPOLAR DISORDER, and has analgesic properties.
carbamazepine : A dibenzoazepine that is 5H-dibenzo[b,f]azepine carrying a carbamoyl substituent at the azepine nitrogen, used as an anticonvulsant.

Research Excerpts

ExcerptRelevanceReference
"Both forms of myotonia congenita are attributable to mutations in the CLCN1 gene."1.36Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita. ( Duron, R; Holden, KR; Lyons, MJ; Molinero, I; Sangiuolo, F, 2010)
"Myotonia congenita is a rare disease of skeletal muscle characterized by painless myotonia, generalized muscular hypertrophy and a non-progressive course."1.33Myotonia congenita--a successful response to carbamazepine. ( Hyderi, A; Krishnamurthy, B; Ramachandra, NB; Savitha, MR, 2006)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's1 (12.50)18.2507
2000's3 (37.50)29.6817
2010's2 (25.00)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Fuseya, Y1
Ishikawa, N1
Sasaki, R1
Yamashita, H1
Desaphy, JF1
Carbonara, R1
Costanza, T1
Conte Camerino, D1
Lyons, MJ1
Duron, R1
Molinero, I1
Sangiuolo, F1
Holden, KR1
Savitha, MR1
Krishnamurthy, B1
Hyderi, A1
Ramachandra, NB1
Berardinelli, A1
Gorni, K1
Orcesi, S1
Sheela, SR1
Hahn, AF1
Parkes, AW1
Bolton, CF1
Stewart, SA1
Jusić, A1
Stimac, D1

Other Studies

8 other studies available for carbamazepine and Batten Turner Congenital Myopathy

ArticleYear
Teaching Video NeuroImage: Carbamazepine Improves Gait Initiation in Autosomal Recessive Myotonia Congenita.
    Neurology, 2022, 01-18, Volume: 98, Issue:3

    Topics: Carbamazepine; Chloride Channels; Electromyography; Gait; Genes, Recessive; Humans; Myotonia Congeni

2022
Preclinical evaluation of marketed sodium channel blockers in a rat model of myotonia discloses promising antimyotonic drugs.
    Experimental neurology, 2014, Volume: 255

    Topics: Animals; Carbamazepine; Disease Models, Animal; Flecainide; HEK293 Cells; Humans; Mexiletine; Muscle

2014
Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita.
    Pediatric neurology, 2010, Volume: 42, Issue:5

    Topics: Adolescent; Carbamazepine; Chloride Channels; Genes, Recessive; Humans; Male; Mutation; Myotonia Con

2010
Myotonia congenita--a successful response to carbamazepine.
    Indian journal of pediatrics, 2006, Volume: 73, Issue:5

    Topics: Carbamazepine; Child; Female; Humans; Myotonia Congenita; Neuromuscular Agents; Treatment Outcome

2006
Response to carbamazepine of recessive-type myotonia congenita.
    Muscle & nerve, 2000, Volume: 23, Issue:1

    Topics: Anticonvulsants; Carbamazepine; Child, Preschool; Humans; Male; Myotonia Congenita

2000
Myotonia congenita: response to carbamazepine.
    Indian pediatrics, 2000, Volume: 37, Issue:10

    Topics: Adolescent; Anticonvulsants; Carbamazepine; Child, Preschool; Female; Humans; Male; Myotonia Congeni

2000
Neuromyotonia in hereditary motor neuropathy.
    Journal of neurology, neurosurgery, and psychiatry, 1991, Volume: 54, Issue:3

    Topics: Adolescent; Anti-Arrhythmia Agents; Carbamazepine; Child; Electromyography; Female; Humans; Lidocain

1991
[Central genesis of dystrophia myotonica and Tegretal therapy].
    Fortschritte der Neurologie, Psychiatrie, und ihrer Grenzgebiete, 1972, Volume: 40, Issue:2

    Topics: Adult; Carbamazepine; Central Nervous System Diseases; Electromyography; Electrophysiology; Female;

1972