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Identifiant pérenne de la notice : 040661245Copier cet identifiant (PPN)
Notice de type FMeSH

Point d'accès autorisé

Sclérose latérale amyotrophique

Variantes de point d'accès

Amyotrophic Lateral Sclerosis
[Nom commun]
Sclerosis, Amyotrophic Lateral
[Nom commun]
ALS - Amyotrophic Lateral Sclerosis
[Nom commun]
ALS Amyotrophic Lateral Sclerosis
[Nom commun]
Gehrig's Disease
[Nom commun]
Gehrig Disease
[Nom commun]
Gehrigs Disease
[Nom commun]
Lou Gehrig Disease
[Nom commun]
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
[Nom commun]
Lou Gehrig's Disease
[Nom commun]
Lou-Gehrigs Disease
[Nom commun]
Disease, Lou-Gehrigs
[Nom commun]
Charcot Disease
[Nom commun]
Amyotrophic Lateral Sclerosis With Dementia
[Nom commun]
Dementia With Amyotrophic Lateral Sclerosis
[Nom commun]
Amyotrophic Lateral Sclerosis, Guam Form
[Nom commun]
Guam Disease
[Nom commun]
Disease, Guam
[Nom commun]
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1
[Nom commun]
Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1
[Nom commun]
Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam
[Nom commun]
Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam
[Nom commun]
Guam Form of Amyotrophic Lateral Sclerosis
[Nom commun]
Association de sclérose latérale amyotrophique, de maladie de Parkinson et de démence de l'ile de Guam
[Nom commun]
Association de sclérose latérale amyotrophique, de maladie de Parkinson et de démence de type 1
[Nom commun]
Démence avec sclérose latérale amyotrophique
[Nom commun]
Maladie de Charcot
[Nom commun]
Maladie de Gehrig
[Nom commun]
Maladie de Guam
[Nom commun]
Maladie de l'ile de Guam
[Nom commun]
Maladie de Lou Gehrig
[Nom commun]
Sclérose latérale amyotrophique avec démence
[Nom commun]
Sclérose latérale amyotrophique de l'ile de Guam
[Nom commun]
Sclérose latérale amyotrophique de l'île de Guam
[Nom commun]
SLA (Sclérose Latérale Amyotrophique)
[Nom commun]
Syndrome de Guam
[Nom commun]
Syndrome de l'ile de Guam
[Nom commun]

Informations

Note publique d''information : 
A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)

Point d'accès autorisé parallèle

Amyotrophic Lateral Sclerosis

Identifiants externes

Identifiant MeSH : mesD000690

Utilisation dans FMeSH

Qualificatifs autorisés : BL / CF / CI / CL / CO / CN / DI / DH / DT / EC / EM / EN / EH / ET / GE / HI / IM / ME / MI / MO / NU / EP / PS / PA / PP / PC / PX / RT / RH / SU / TH / UR / VE / VI / DG

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