Literature DB >> 20112006

[4-Aminopyridine (Fampridine). A new attempt for the symptomatic treatment of multiple sclerosis].

L Husseini1, V I Leussink, B C Kieseier, H-P Hartung.   

Abstract

Mobility limitation is a frequent clinical symptom of multiple sclerosis (MS) that poses a therapeutic challenge. For years results of animal experiments and clinical experience have indicated that the potassium channel blocker 4-aminopyridine improves axonal excitatory circuits and thus muscular strength in demyelinating diseases. A recently conducted randomized, placebo-controlled, multicenter phase 3 clinical trial in MS patients was able to show that an oral sustained-release formulation of 4-aminopyridine (Fampridine-SR) represents a suitable agent for treatment of walking disability in MS patients.This overview presents the study data and discusses the value of 4-aminopyridine for the symptomatic treatment of MS as a neurofunctional modifier of this disabling disease.

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Year:  2010        PMID: 20112006     DOI: 10.1007/s00115-009-2902-2

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  46 in total

1.  Walking capacities in multiple sclerosis measured by global positioning system odometer.

Authors:  A Créange; I Serre; M Levasseur; D Audry; A Nineb; D Boërio; T Moreau; P Maison
Journal:  Mult Scler       Date:  2007-01-29       Impact factor: 6.312

2.  Fampridine for MS responders: clinically relevant or hypothesis generating?

Authors:  Richard J Kryscio
Journal:  Neurology       Date:  2008-07-30       Impact factor: 9.910

Review 3.  Seizures in patients with multiple sclerosis: epidemiology, pathophysiology and management.

Authors:  Brendan J Kelley; Moses Rodriguez
Journal:  CNS Drugs       Date:  2009-10       Impact factor: 5.749

4.  Fatigue in progressive multiple sclerosis: results of a randomized, double-blind, placebo-controlled, crossover trial of oral 4-aminopyridine.

Authors:  P M Rossini; P Pasqualetti; C Pozzilli; M G Grasso; E Millefiorini; A Graceffa; G A Carlesimo; G Zibellini; C Caltagirone
Journal:  Mult Scler       Date:  2001-12       Impact factor: 6.312

5.  Symptomatic treatment of multiple sclerosis. Multiple Sclerosis Therapy Consensus Group (MSTCG) of the German Multiple Sclerosis Society.

Authors:  T Henze; P Rieckmann; K V Toyka
Journal:  Eur Neurol       Date:  2006-09-08       Impact factor: 1.710

6.  Pharmacokinetics and safety of multiple oral doses of sustained-release 4-aminopyridine (Fampridine-SR) in subjects with chronic, incomplete spinal cord injury.

Authors:  Keith C Hayes; Patrick J Potter; Jane T Hsieh; Mitchell A Katz; Andrew R Blight; Ron Cohen
Journal:  Arch Phys Med Rehabil       Date:  2004-01       Impact factor: 3.966

7.  Poisoning with 4-aminopyridine: report of three cases.

Authors:  D A Spyker; C Lynch; J Shabanowitz; J A Sinn
Journal:  Clin Toxicol       Date:  1980-06       Impact factor: 4.467

8.  Effects of 4-aminopyridine in patients with multiple sclerosis.

Authors:  R E Jones; J R Heron; D H Foster; R S Snelgar; R J Mason
Journal:  J Neurol Sci       Date:  1983 Aug-Sep       Impact factor: 3.181

9.  4-Aminopyridine in multiple sclerosis: prolonged administration.

Authors:  D Stefoski; F A Davis; W E Fitzsimmons; S S Luskin; J Rush; G W Parkhurst
Journal:  Neurology       Date:  1991-09       Impact factor: 9.910

10.  Atypical presentation of 4-aminopyridine overdose.

Authors:  T A Pickett; R Enns
Journal:  Ann Emerg Med       Date:  1996-03       Impact factor: 5.721

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  1 in total

1.  [Multiple sclerosis: updates on pathogenesis and treatment: report from the 9th MS Symposium held by the German Multiple Sclerosis Society].

Authors:  R Hohlfeld; K V Toyka
Journal:  Nervenarzt       Date:  2011-08       Impact factor: 1.214

  1 in total

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