amyotrophic lateral sclerosis

The latest CME article July 2018: “Assessment of bulbar function in amyotrophic lateral sclerosis: validation of a self-report scale” is online! Please log-in and browse to the LEARN  section on the EAN Website and answer the questions! All e-learning activities… Continue Reading

For February 2018, we have selected: Feneberg E, Oeckl P, Steinacker P, et al. Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis. Neurology 2018;90:e22-30. doi:10.1212/WNL.0000000000004761. Amyotrophic lateral sclerosis (ALS) is a devastating neurological disorder affecting motor neurons. The course of the disease is progressive with life span of 3 to 5 years from the onset of the symptoms.

or August 2017, we have selected: The Writing Group on behalf of the Edaravone (MCI-186) ALS 19 Study Group. Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomized, double-blind, placebo-controlled trial. Lancet Neurol 2017;16:505-512. There is evidence that oxidative stress induced by free radicals is a key factor of progression in amyotrophic lateral sclerosis (ALS).

As in the previous year, EANpages asked EAN committee members, panel chairs, and invited speakers  which session one should not miss at the upcoming congress in Amsterdam 2017. Please find their answers below! Mark Braschinsky , speaker at the Case… Continue Reading

As in the previous year, EANpages asked EAN committee members, panel chairs, and invited speakers  which session one should not miss at the upcoming congress in Amsterdam 2017. Please find their answers below!

For December 2016 we have selected: Gonzales-Bermejo J, Morélot-Panzini C, Tanguy M-L, et al.  Early diaphragm pacing in patients with amyotrophic lateral sclerosis (RespiStimALS): a randomized controlled triple-blind trial. Lancet Neurol 2016:15;1217-1227. The main cause of death in patients with amyotrophic lateral sclerosis (ALS) is related to respiratory failure. It has been hypothesized that diaphragm pacing (a technique that induces diaphragm contraction through the stimulation of the phrenic nerve) could slow the progression of respiratory muscle weakness, and increase alveolar ventilation and lung compliance in ALS patients.