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Statements

Subject Item
dbr:Amyotrophic_lateral_sclerosis
dbo:wikiPageWikiLink
dbr:ALS_Functional_Rating_Scale_-_Revised
Subject Item
dbr:ALS_Functional_Rating_Scale_-_Revised
rdfs:label
ALS Functional Rating Scale - Revised
rdfs:comment
Amyotrophic Lateral Sclerosis (ALS), is a neurodegenerative disease that typically affects adults around 54-67 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. The progression and severity of ALS is rated by doctors on the ALS Functional Rating Scale, which has been revised and is referred to as ALSFRS-R.
dct:subject
dbc:Neurology_articles_needing_expert_attention dbc:Neurology dbc:Amyotrophic_lateral_sclerosis dbc:Medical_scales
dbo:wikiPageID
55676424
dbo:wikiPageRevisionID
1112966206
dbo:wikiPageWikiLink
dbr:Vital_capacity dbc:Medical_scales dbc:Amyotrophic_lateral_sclerosis dbr:Bulbar-onset_ALS dbr:Amyotrophic_lateral_sclerosis dbr:Clinical_trial dbc:Neurology dbc:Neurology_articles_needing_expert_attention dbr:Limb-onset_ALS
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dbo:abstract
Amyotrophic Lateral Sclerosis (ALS), is a neurodegenerative disease that typically affects adults around 54-67 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. The progression and severity of ALS is rated by doctors on the ALS Functional Rating Scale, which has been revised and is referred to as ALSFRS-R.
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wikipedia-en:ALS_Functional_Rating_Scale_-_Revised?oldid=1112966206&ns=0
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11215
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wikipedia-en:ALS_Functional_Rating_Scale_-_Revised
Subject Item
dbr:Spinal_and_bulbar_muscular_atrophy
dbo:wikiPageWikiLink
dbr:ALS_Functional_Rating_Scale_-_Revised
Subject Item
wikipedia-en:ALS_Functional_Rating_Scale_-_Revised
foaf:primaryTopic
dbr:ALS_Functional_Rating_Scale_-_Revised