phenytoin has been researched along with Amyotrophic Lateral Sclerosis in 2 studies
Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Anger, T | 1 |
Madge, DJ | 1 |
Mulla, M | 1 |
Riddall, D | 1 |
Cordonnier, M | 1 |
Delwaide, PJ | 1 |
1 review available for phenytoin and Amyotrophic Lateral Sclerosis
Article | Year |
---|---|
Medicinal chemistry of neuronal voltage-gated sodium channel blockers.
Topics: Amyotrophic Lateral Sclerosis; Analgesics; Anticonvulsants; Epilepsy; Humans; Ion Channel Gating; Mo | 2001 |
1 other study available for phenytoin and Amyotrophic Lateral Sclerosis
Article | Year |
---|---|
[Malignant and benign fasciculations. Apropos of a case of neuromyotonia].
Topics: Amyotrophic Lateral Sclerosis; Electromyography; Fasciculation; Female; Humans; Middle Aged; Movemen | 1979 |