“People can become really frustrated when trying to communicate, so if this app can make things easier that’s a really good thing,” says Matthew Hollis from theMotor Neurone Disease Association. There are currently limited options for people with ALS to communicate. The most common is t...
An individualised disease-specific letter expressing patient's wishes for their future care was offered to people with Amyotrophic Lateral Sclerosis (ALS) from 2001 to 2008. All patients attended a multidisciplinary ALS service where they were seen by a palliative physician. Each letter was developed...
In preclinical studies involving mice with an ALS gene mutation, the researchers saw that two months prior to ALS onset, monocytes in the spleen began exhibiting proinflammatory qualities. As disease onset loomed, there was an increase in cell-signaling molecules that directed monocytes to flood the...
Lenovo approached DeepBrain with an opportunity to create an avatar specifically focused on helping someone with a debilitating disease like ALS. With the assistance of the Scott Morgan Foundation and Lenovo, Erin visited the DeepBrain AI video studio in California, and the avatar creation...
Atkins R (1989): In Grief and Anger: Photographing People With AIDS. Aperture 144: 70–72 Google Scholar Ausst.-Kat. 1989: Witnesses: Against Our Vanishing, Artists Space, New York, 16.11.1989–6.1.1990. Google Scholar Barthes R (1990): Die Fotografie als Botschaft (1964). In: Ders. ...
In the United States, more than 5,600 people are diagnosed with ALS every year. In 90 to 95 percent of cases, there is no family history of the disease; it appears to occur randomly, with no clearly associated risk factors. Answer ALS’ research effort is “the single...
Taylor was diagnosed with ALS in the summer of 2023. Her career in botany, forestry, and related work in the wild was abruptly paused as she and her mother faced countless questions about the progression of the disease. The shock was especially potent given the disease primarily affects p...
“We can leave the mountain anytime we want but those with ALS are prisoners in their own body”-Alex Williams. People with ALS start losing their ability to move as the disease goes through their body. In the Book Tuesdays with Morrie by Mitch Albom Morrie Schwartz has ALS and he tries...
Almost all people with amyotrophic lateral sclerosis (ALS) experience a motor speech disorder, such as dysarthria, as the disease progresses. At some point, 80 to of people with ALS are unable to meet their daily communication needs using natural speech. Unfortunately, once intelligibility begins ...
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