Page last updated: 2024-10-24

celecoxib and Spinal Muscular Atrophies of Childhood

celecoxib has been researched along with Spinal Muscular Atrophies of Childhood in 1 studies

Spinal Muscular Atrophies of Childhood: A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)

Research

Studies (1)

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 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Farooq, F1
Abadía-Molina, F1
MacKenzie, D1
Hadwen, J1
Shamim, F1
O'Reilly, S1
Holcik, M1
MacKenzie, A1

Other Studies

1 other study available for celecoxib and Spinal Muscular Atrophies of Childhood

ArticleYear
Celecoxib increases SMN and survival in a severe spinal muscular atrophy mouse model via p38 pathway activation.
    Human molecular genetics, 2013, Sep-01, Volume: 22, Issue:17

    Topics: Adolescent; Animals; Brain; Celecoxib; Cells, Cultured; Child; Child, Preschool; Disease Models, Ani

2013