4-aminopyridine has been researched along with Muscle Weakness in 7 studies
Muscle Weakness: A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251)
Excerpt | Relevance | Reference |
---|---|---|
"Thirteen subjects with amyotrophic lateral sclerosis and seven subjects with only a lower motor neuron syndrome." | 2.76 | Effects of 3-4 diaminopyridine (DAP) in motor neuron diseases. ( Bertorini, TE; Igarashi, M; Li, YD; Rashed, H; Tolley, EA; Zeno, M, 2011) |
"Fast channel congenital myasthenic syndromes are rare, but frequently result in severe weakness." | 1.38 | Clinical features in a series of fast channel congenital myasthenia syndrome. ( Bailey, S; Beeson, D; Carr, A; Jayawant, S; Lashley, D; McConville, J; Palace, J; Robb, S, 2012) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 1 (14.29) | 29.6817 |
2010's | 5 (71.43) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Thakkar, N | 1 |
Guptill, JT | 1 |
Aleš, K | 1 |
Jacobus, D | 1 |
Jacobus, L | 1 |
Peloquin, C | 1 |
Cohen-Wolkowiez, M | 1 |
Gonzalez, D | 1 |
Oh, SJ | 1 |
Morsch, M | 1 |
Reddel, SW | 1 |
Ghazanfari, N | 1 |
Toyka, KV | 1 |
Phillips, WD | 1 |
Bertorini, TE | 1 |
Rashed, H | 1 |
Zeno, M | 1 |
Tolley, EA | 1 |
Igarashi, M | 1 |
Li, YD | 1 |
Palace, J | 1 |
Lashley, D | 1 |
Bailey, S | 1 |
Jayawant, S | 1 |
Carr, A | 1 |
McConville, J | 1 |
Robb, S | 1 |
Beeson, D | 1 |
Morbiato, L | 1 |
Carli, L | 1 |
Johnson, EA | 1 |
Montecucco, C | 1 |
Molgó, J | 1 |
Rossetto, O | 1 |
Aisen, ML | 1 |
Sevilla, D | 1 |
Edelstein, L | 1 |
Blass, J | 1 |
3 trials available for 4-aminopyridine and Muscle Weakness
Article | Year |
---|---|
Population Pharmacokinetics/Pharmacodynamics of 3,4-Diaminopyridine Free Base in Patients With Lambert-Eaton Myasthenia.
Topics: 4-Aminopyridine; Adult; Aged; Aged, 80 and over; Amifampridine; Arylamine N-Acetyltransferase; Femal | 2017 |
Effects of 3-4 diaminopyridine (DAP) in motor neuron diseases.
Topics: 4-Aminopyridine; Adult; Aged; Aged, 80 and over; Amifampridine; Cross-Over Studies; Double-Blind Met | 2011 |
A double-blind placebo-controlled study of 3,4-diaminopyridine in amytrophic lateral sclerosis patients on a rehabilitation unit.
Topics: 4-Aminopyridine; Administration, Oral; Aged; Amifampridine; Amyotrophic Lateral Sclerosis; Cross-Ove | 1996 |
4 other studies available for 4-aminopyridine and Muscle Weakness
Article | Year |
---|---|
3,4-diaminopyridine in Lambert-Eaton myasthenic syndrome: Concerns regarding presentation of previous studies.
Topics: 4-Aminopyridine; Amifampridine; Humans; Lambert-Eaton Myasthenic Syndrome; Muscle Weakness; Potassiu | 2018 |
Pyridostigmine but not 3,4-diaminopyridine exacerbates ACh receptor loss and myasthenia induced in mice by muscle-specific kinase autoantibody.
Topics: 4-Aminopyridine; Amifampridine; Animals; Autoantibodies; Cholinesterase Inhibitors; Evoked Potential | 2013 |
Clinical features in a series of fast channel congenital myasthenia syndrome.
Topics: 4-Aminopyridine; Adult; Amifampridine; Child; Child, Preschool; Humans; Infant; Middle Aged; Muscle | 2012 |
Neuromuscular paralysis and recovery in mice injected with botulinum neurotoxins A and C.
Topics: 4-Aminopyridine; Amifampridine; Animals; Botulinum Toxins; Botulinum Toxins, Type A; Drug Resistance | 2007 |