fomesafen has been researched along with Muscular Atrophy, Spinal in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (10.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 7 (70.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Barthez, MA; Best, H; Deleuze, JF; Ghorab, K; Guyant-Marechal, L; Ha, Y; Hernandorena, X; Laroche-Raynaud, C; Lia, AS; Mao, R; Masson, C; Nectoux, J; Nelson, I; Pedespan, JM; Si, Y; Swoboda, KJ; Toutain, A; Viollet, LM | 1 |
| Goswami, JN; Sahu, JK; Singhi, P | 1 |
| Muntoni, F; Zhou, H | 1 |
| Calderó, J; Dachs, E; Esquerda, JE; Hereu, M; Piedrafita, L | 1 |
| Carey, JC; Gappmaier, E; Johnson, BA; Krosschell, KJ; Lane, RH; Lewelt, A; Lopes, P; Marcus, RL; Stoddard, GJ; Swoboda, KJ; Viazzo-Trussell, D; Viollet, L; Weng, C; White, AT; Xue, M | 1 |
| Arnold, W; Burghes, AH; Corlett, KM; Kolb, SJ; Li, J; McGovern, VL; Rutkove, SB; Sanchez, B | 1 |
| Henderson, CE; Kariya, S; Li, DK; Liu, D; Lutz, CM; Monani, UR; Murphy, AJ; Osborne, MA; Patruni, S; Pellizzoni, L; Rojas, J; Valenzuela, DM; Winberg, ML | 1 |
| Bartalucci, A; Biagioni, F; Ferrucci, M; Fornai, F; Fulceri, F; Paparelli, S; Pasquali, L; Ruffoli, R | 1 |
| KUZUO, N; MIYATA, Y; SUMI, T; UETANE, S; WAKE, K | 1 |
| Antonini, G; Ceschin, V; Cruccu, G; Gragnani, F; Morino, S; Pennisi, EM; Romaniello, A; Santoro, L | 1 |
1 trial(s) available for fomesafen and Muscular Atrophy, Spinal
| Article | Year |
|---|---|
Sensory involvement in spinal-bulbar muscular atrophy (Kennedy's disease).
Topics: Aged; Electrodiagnosis; Electromyography; Evoked Potentials; Hereditary Sensory and Motor Neuropathy; Humans; Male; Middle Aged; Muscular Atrophy, Spinal; Nerve Fibers, Myelinated; Neural Conduction; Reflex; Sural Nerve; Trigeminal Ganglion | 2000 |
9 other study(ies) available for fomesafen and Muscular Atrophy, Spinal
| Article | Year |
|---|---|
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies.
Topics: Adolescent; Adult; Child; Child, Preschool; Cytoplasmic Dyneins; Female; Heterozygote; Humans; Lower Extremity; Male; Middle Aged; Motor Neurons; Muscle, Skeletal; Muscular Atrophy, Spinal; Mutation, Missense; Pedigree; Phenotype; Reflex; Upper Extremity | 2020 |
Spinal Muscular Atrophy with Preserved Deep Tendon Reflexes.
Topics: Humans; Muscular Atrophy, Spinal; Reflex; Tendons | 2018 |
Morpholino-Mediated Exon Inclusion for SMA.
Topics: Alternative Splicing; Animals; Animals, Newborn; Biopsy; Disease Models, Animal; Exons; Gene Expression Regulation; Male; Mice; Mice, Transgenic; Morpholinos; Motor Neurons; Muscle, Skeletal; Muscular Atrophy, Spinal; Neuromuscular Junction; Reflex; RNA Splicing; Survival of Motor Neuron 2 Protein | 2018 |
Chronic treatment with lithium does not improve neuromuscular phenotype in a mouse model of severe spinal muscular atrophy.
Topics: Animals; Blotting, Western; Cell Count; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; Image Processing, Computer-Assisted; Immunohistochemistry; In Situ Nick-End Labeling; Lithium Chloride; Mice; Mice, Transgenic; Motor Neurons; Muscle, Skeletal; Muscular Atrophy, Spinal; Mutation; Oncogene Protein v-akt; Phenotype; Postural Balance; Psychomotor Performance; Reflex; Spinal Cord; Survival of Motor Neuron 1 Protein | 2013 |
Resistance strength training exercise in children with spinal muscular atrophy.
Topics: Adolescent; Child; Child, Preschool; Female; Humans; Male; Motor Activity; Muscle Strength; Muscle, Skeletal; Muscular Atrophy, Spinal; Reflex; Reproducibility of Results; Resistance Training; Treatment Outcome | 2015 |
The neuromuscular impact of symptomatic SMN restoration in a mouse model of spinal muscular atrophy.
Topics: Animals; Animals, Newborn; Atrophy; Disease Models, Animal; Electric Impedance; Genetic Therapy; Longitudinal Studies; Mice, Transgenic; Muscle, Skeletal; Muscular Atrophy, Spinal; Myography; Oligonucleotides, Antisense; Reflex; Survival Analysis | 2016 |
Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy.
Topics: Alleles; Animals; Cloning, Molecular; Crosses, Genetic; Disease Models, Animal; Extremities; Humans; Mice; Motor Neurons; Muscular Atrophy, Spinal; Phenotype; Reflex; Survival of Motor Neuron 1 Protein; Synapses; Treatment Outcome | 2011 |
Motor neuron pathology and behavioral alterations at late stages in a SMA mouse model.
Topics: Animals; Cell Size; Disease Models, Animal; Disease Progression; Humans; Mice; Mice, Knockout; Mice, Transgenic; Motor Activity; Motor Neurons; Muscle Weakness; Muscular Atrophy, Spinal; Nerve Degeneration; Reflex; Rotarod Performance Test; Spinal Cord; Survival of Motor Neuron 1 Protein; Survival of Motor Neuron 2 Protein | 2012 |
[A CASE OF RAPIDLY PROGRESSIVE MUSCULAR ATROPHY].
Topics: Muscular Atrophy; Muscular Atrophy, Spinal; Nervous System Physiological Phenomena; Pathology; Reflex | 1963 |