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  2. Experimental treatment pushed by ALS patients gets day ... - AOL

    www.aol.com/news/experimental-treatment-pushed...

    Experimental treatment pushed by ALS patients gets day before FDA, but agency unconvinced it works. MATTHEW PERRONE. September 25, 2023 at 12:44 PM.

  3. ALS - Wikipedia

    en.wikipedia.org/wiki/ALS

    ALS is the most common ... for the treatment of SOD1-associated ALS. ... A 2017 review concluded that mexiletine is safe and effective for treating cramps in ALS ...

  4. Project ALS - Wikipedia

    en.wikipedia.org/wiki/Project_ALS

    Project ALS is a non-profit organization whose mission is to identify and support leading scientific research toward the first effective treatments and a cure for ALS. Founded in 1998 by Jenifer Estess , Valerie Estess, Meredith Estess, and Julianne Hoffenberg, Project ALS recruits scientists and doctors to work together toward a better ...

  5. ALS Therapy Development Institute - Wikipedia

    en.wikipedia.org/wiki/ALS_Therapy_Development...

    The institute has raised and spent more than $100 million on research into effective treatments for ALS and practices open-source science. [19] After the discovery that the multiple sclerosis drug Gilenya might also be a treatment for ALS, the Institute enrolled 30 people in a Phase 2A clinical trial the drug in 2013, though it did not progress further.

  6. FDA advisers vote against experimental ALS treatment ... - AOL

    www.aol.com/news/fda-advisers-vote-against...

    Federal health advisers voted overwhelmingly against an experimental treatment for Lou Gehrig’s disease at a Wednesday meeting prompted by years of patient efforts seeking access to the unproven ...

  7. Watch: After generations of loss, UW Health patient ... - AOL

    www.aol.com/news/watch-generations-loss-uw...

    13 WREX News reports on Michelle Francis’ journey from a late diagnosis of ALS — or amyotrophic lateral sclerosis — […] The post Watch: After generations of loss, UW Health patient ...

  8. Amyotrophic lateral sclerosis research - Wikipedia

    en.wikipedia.org/wiki/Amyotrophic_lateral...

    The most studied model for ALS is the rodent, mouse model, which provide the most complex representation of nervous system that is considered the closest in mimicking human nervous system. [4] In this model, the phenotype, and genotype characteristics can be studied and controlled.

  9. Riluzole - Wikipedia

    en.wikipedia.org/wiki/Riluzole

    Riluzole is a medication used to treat amyotrophic lateral sclerosis (ALS) and other motor neuron diseases. Riluzole delays the onset of ventilator-dependence or tracheostomy in some people and may increase survival by two to three months. [5] Riluzole is available in tablet and liquid form.

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