Page last updated: 2024-08-18

tecnazene and Batten Turner Congenital Myopathy

tecnazene has been researched along with Batten Turner Congenital Myopathy in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Gardberg, M; Hackman, P; Jokela, M; Kiiski, K; Lehtokari, VL; Pelin, K; Sagath, L; Udd, B; Välipakka, S; Vihola, A; Wallgren-Pettersson, C1
Kim, DS; Kim, HS; Lee, CH; Park, YE; Shin, JH1

Other Studies

2 other study(ies) available for tecnazene and Batten Turner Congenital Myopathy

ArticleYear
Congenital asymmetric distal myopathy with hemifacial weakness caused by a heterozygous large de novo mosaic deletion in nebulin.
    Neuromuscular disorders : NMD, 2021, Volume: 31, Issue:6

    Topics: Adult; Biopsy; Distal Myopathies; Exons; Facial Muscles; Female; Finland; Heterozygote; Humans; Mosaicism; Muscle Proteins; Muscle Weakness; Mutation; Myotonia Congenita; Pedigree; Sequence Deletion

2021
Characterization of congenital myopathies at a Korean neuromuscular center.
    Muscle & nerve, 2018, Volume: 58, Issue:2

    Topics: Adolescent; Adult; Age of Onset; Child; Child, Preschool; Dynamin II; Dynamins; Female; Humans; Infant; Male; Muscle Fibers, Skeletal; Muscle Proteins; Mutation; Myopathies, Nemaline; Myopathies, Structural, Congenital; Myopathy, Central Core; Myotonia Congenita; Republic of Korea; Retrospective Studies; Ryanodine Receptor Calcium Release Channel; Treatment Outcome; Young Adult

2018