Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease, is a neurodegenerative neuromuscular disease that results in the progressive loss of motor neurons that control voluntary muscles. ALS is the most common type of motor neuron disease. Early symptoms of ALS include stiff muscles, muscle twitches, and gradual increasing weakness and muscle wasting. Limb-onset ALS begins with weakness in the arms or legs, while bulbar-onset ALS begins with difficulty speaking or swallowing. Half of the people with ALS develop at least mild difficulties with thinking and behavior, and about 15% develop frontotemporal dementia. Most people experience pain. The affected muscles are responsible for chewing food, speaking, and walking. Motor neuron loss continue
academic discipline
death place
differential diagnosis
known for
medical cause
Wikipage disambiguates
A-L-SA.L.S.ALSALSODALS (disease)AlsAmiotrophic lateral sclerosisAmyoltrophic lateral sclerosisAmyotrophic Lateral SclerosisAmyotrophic Lateral Sclerosis (Lou Gehrig's Disease)Amyotrophic lateral schlerosisAmyotrophic lateral sclerosis, type 4Amyotrophic laterial sclerosisAmyotrophic sclerosisAmyotropic lateral sclerosisAmytrophic lateral sclerosisAnterior horn cell diseaseBulbar-onset ALSBunina bodiesExtraocular muscles and ALSFALSFTD-ALSFTD–ALSFamilial amyotrophic lateral sclerosisGehrig's diseaseJuvenile ALSJuvenile amyotrophic lateral sclerosisLateral sclerosisLimb-onset ALSLou Garrig's diseaseLou Garrig diseaseLou Gehrig'sLou Gehrig's DiseaseLou Gehrig's diseaseLou Gehrig DiseaseLou Gehrig diseaseLou Gehrigs diseaseLou Gehrig’s DiseaseLou Gehrig’s diseaseLou Gerhig's disease
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cause
Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease, is a neurodegenerative neuromuscular disease that results in the progressive loss of motor neurons that control voluntary muscles. ALS is the most common type of motor neuron disease. Early symptoms of ALS include stiff muscles, muscle twitches, and gradual increasing weakness and muscle wasting. Limb-onset ALS begins with weakness in the arms or legs, while bulbar-onset ALS begins with difficulty speaking or swallowing. Half of the people with ALS develop at least mild difficulties with thinking and behavior, and about 15% develop frontotemporal dementia. Most people experience pain. The affected muscles are responsible for chewing food, speaking, and walking. Motor neuron loss continue
has abstract
A esclerose lateral amiotrófic ...... ação pública sobre a condição.
@pt
Alboko esklerosi amiotrofikoa ...... xiegitasunagatik hiltzen dira.
@eu
Amyotrofe laterale sclerose of ...... mde honkballer die eraan leed.
@nl
Amyotrofická laterální skleróz ...... ly zatím dostatečně objasněny.
@cs
Amyotrofisk lateralskleros (AL ...... er hjärtat längre orkar pumpa.
@sv
Amyotrophic lateral sclerosis ...... ic awareness of the condition.
@en
H αμυοτροφική πλευρική σκλήρυν ...... ος επιστήμονας Στήβεν Χόκινγκ.
@el
L'esclerosi lateral amiotròfic ...... de la bufeta i els intestins.
@ca
La esclerosis lateral amiotróf ...... en el alivio de los síntomas.
@es
La sclerosi laterale amiotrofi ...... nni Papini, deceduto nel 1956.
@it
DiseasesDB
eMedicine subject
neuro
@en
eMedicine topic
14
@en
geneReviewsId
geneReviewsName
Amyotrophic lateral sclerosis
@en
ICD10
ICD9
medical diagnosis
MedlinePlus
MeSH ID
OMIM id
treatment
Wikipage page ID
19.375.577
page length (characters) of wiki page
Wikipage revision ID
1.025.854.238
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caption
An MRI of the brain with incre ...... tent with the diagnosis of ALS
@en
causes
Unknown , inherited
@en
diagnosis
Suspected as based on symptoms and supported by MRI
@en
DiseasesDB
eMedicineSubj
neuro
@en
eMedicineTopic
field
frequency
GeneReviewsName
Amyotrophic lateral sclerosis
@en
GeneReviewsNBK
NBK1450
@en
ICD
MedlinePlus
MeshID
D000690
@en
name
@en
Amyotrophic lateral sclerosis
@en
OMIM
onset
Orphanet
prognosis
-1.262304E8
Scholia
Q206901
@en
symptoms
Early: Stiff muscles, muscle twitches, gradual increasing weakness
@en
Later: Difficulty in speaking, swallowing, and breathing; respiratory failure
@en
synonyms
Charcot's disease;
@en
Lou Gehrig's disease;
@en
motor neurone disease
@en
treatment
wikiPageUsesTemplate
wordnet_type
subject
hypernym
comment
A esclerose lateral amiotrófic ...... ão, e, por fim, da respiração.
@pt
Alboko esklerosi amiotrofikoa ...... eritasunen artean ohikoena da.
@eu
Amyotrofe laterale sclerose of ...... mde honkballer die eraan leed.
@nl
Amyotrofická laterální skleróz ...... ly zatím dostatečně objasněny.
@cs
Amyotrofisk lateralskleros (AL ...... er hjärtat längre orkar pumpa.
@sv
Amyotrophic lateral sclerosis ...... ng. Motor neuron loss continue
@en
H αμυοτροφική πλευρική σκλήρυν ...... ι γνωστή θεραπεία για τη νόσο.
@el
L'esclerosi lateral amiotròfic ...... rt d'aquest tipus de neurones.
@ca
La esclerosis lateral amiotróf ...... os pioneros de la neurología).
@es
La sclerosi laterale amiotrofi ...... e, infine, della respirazione.
@it
label
Alboko esklerosi amiotrofiko
@eu
Amiotrofa lateralsklerozo
@eo
Amyotrofe laterale sclerose
@nl
Amyotrofická laterální skleróza
@cs
Amyotrofisk lateralskleros
@sv
Amyotrophe Lateralsklerose
@de
Amyotrophic lateral sclerosis
@en
Esclerose lateral amiotrófica
@pt
Esclerosi lateral amiotròfica
@ca
Esclerosis lateral amiotrófica
@es