Page last updated: 2024-10-31

nocodazole and Muscular Atrophy, Spinal

nocodazole has been researched along with Muscular Atrophy, Spinal in 2 studies

Muscular Atrophy, Spinal: A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)

Research

Studies (2)

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

Authors

AuthorsStudies
Sferra, A1
Baillat, G1
Rizza, T1
Barresi, S1
Flex, E1
Tasca, G1
D'Amico, A1
Bellacchio, E1
Ciolfi, A1
Caputo, V1
Cecchetti, S1
Torella, A1
Zanni, G1
Diodato, D1
Piermarini, E1
Niceta, M1
Coppola, A1
Tedeschi, E1
Martinelli, D1
Dionisi-Vici, C1
Nigro, V1
Dallapiccola, B1
Compagnucci, C1
Tartaglia, M1
Haase, G1
Bertini, E1
Lefebvre, S1
Burlet, P1
Viollet, L1
Bertrandy, S1
Huber, C1
Belser, C1
Munnich, A1

Other Studies

2 other studies available for nocodazole and Muscular Atrophy, Spinal

ArticleYear
TBCE Mutations Cause Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy.
    American journal of human genetics, 2016, Oct-06, Volume: 99, Issue:4

    Topics: Adolescent; Age of Onset; Animals; Brain Diseases; Child; Female; Fibroblasts; Heterozygote; Homozyg

2016
A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy.
    Human molecular genetics, 2002, May-01, Volume: 11, Issue:9

    Topics: Animals; Antineoplastic Agents; Cell Nucleolus; Cells, Cultured; COS Cells; Cyclic AMP Response Elem

2002