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  2. ALS Functional Rating Scale - Revised - Wikipedia

    en.wikipedia.org/wiki/ALS_Functional_Rating...

    Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that typically affects adults around 54–67 [1] years of age, although anyone can be diagnosed with the disease. People diagnosed with ALS live on average 2–4 years after diagnosis due to the quick progression of the disease.

  3. ALS - Wikipedia

    en.wikipedia.org/wiki/ALS

    ALS can strike at any age, but its likelihood increases with age. [64] Most people who develop ALS are between the ages of 40 and 70, with an average age of 55 at the time of diagnosis. [65] ALS is 20% more common in men than women, [65] but this difference in sex distribution is no longer present in patients with onset after age 70. [64]

  4. List of people with motor neuron disease - Wikipedia

    en.wikipedia.org/wiki/List_of_people_with_motor...

    Astrophysicist Stephen Hawking, whose ALS was diagnosed in 1963, had the disease for 55 years, the longest recorded time one had the disease. He died at the age of 76 in 2018. The 11th century monk Hermann of Reichenau had a lifelong disease that is considered likely to have been ALS. This would make him one of the earliest known patients of ...

  5. Former MLB Pitcher Diagnosed With ALS At 55 - AOL

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    The post Former MLB Pitcher Diagnosed With ALS At 55 appeared first on The Spun. Skip to main content. Sign in. Mail. 24/7 Help. For premium support please call: 800-290-4726 more ways to reach us ...

  6. 30-year-old former NFL player announces ALS diagnosis via the ...

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  7. Motor neuron diseases - Wikipedia

    en.wikipedia.org/wiki/Motor_neuron_diseases

    About 95% of ALS patients have abnormalities in the nucleus-cytoplasmic localization in spinal motor neurons of TDP43. In TDP-43 depleted human neural stem cell-derived motor neurons, as well as in sporadic ALS patients' spinal cord specimens there is significant double-strand break accumulation and reduced levels of NHEJ.

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  9. Genetics of amyotrophic lateral sclerosis - Wikipedia

    en.wikipedia.org/wiki/Genetics_of_amyotrophic...

    [4] [5] ALS has an oligogenic mode of inheritance, meaning that mutations in two or more genes are required to cause disease. [6] C9orf72 is the most common gene associated with ALS, causing 40% of familial cases of ALS, as well as a small percentage of sporadic cases; [7] it also causes about 25% of familial cases of frontotemporal dementia. [6]