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Identifiant pérenne de la notice : 040813053Copier cet identifiant (PPN)
Notice de type FMeSH

Point d'accès autorisé

Maladies du motoneurone

Variantes de point d'accès

Motor Neuron Diseases
[Nom commun]
Neuron Disease, Motor
[Nom commun]
Neuron Diseases, Motor
[Nom commun]
Motor System Disease
[Nom commun]
Motor System Diseases
[Nom commun]
Affections du neurone moteur
[Nom commun]
Maladie du motoneurone
[Nom commun]
Maladie du neurone moteur
[Nom commun]
Familial Motor Neuron Disease
[Nom commun]
Motor Neuron Disease, Familial
[Nom commun]
Lateral Sclerosis
[Nom commun]
Lateral Scleroses
[Nom commun]
Scleroses, Lateral
[Nom commun]
Sclerosis, Lateral
[Nom commun]
Primary Lateral Sclerosis
[Nom commun]
Lateral Scleroses, Primary
[Nom commun]
Lateral Sclerosis, Primary
[Nom commun]
Primary Lateral Scleroses
[Nom commun]
Scleroses, Primary Lateral
[Nom commun]
Sclerosis, Primary Lateral
[Nom commun]
Motor Neuron Disease, Upper
[Nom commun]
Upper Motor Neuron Disease
[Nom commun]
Motor Neuron Disease, Secondary
[Nom commun]
Secondary Motor Neuron Disease
[Nom commun]
Anterior Horn Cell Disease
[Nom commun]
Motor Neuron Disease, Lower
[Nom commun]
Lower Motor Neuron Disease
[Nom commun]
Maladie du neurone moteur d'origine familiale
[Nom commun]
Maladie du motoneurone d'origine familiale
[Nom commun]
Sclérose latérale primitive
[Nom commun]
SLP (Sclérose Latérale Primitive)
[Nom commun]
Maladie du motoneurone supérieur
[Nom commun]
Affection du motoneurone central
[Nom commun]
Affection du neurone moteur supérieur
[Nom commun]
Maladies du motoneurone secondaires
[Nom commun]
Affections secondaires du neurone moteur
[Nom commun]
Syndrome de la corne antérieure
[Nom commun]
Maladie du motoneurone inférieur
[Nom commun]
Affection du motoneurone spinal
[Nom commun]
Affection du neurone moteur inférieur
[Nom commun]
Maladie du motoneurone périphérique
[Nom commun]
Affections du neurone moteur
[Nom commun]
Maladie du motoneurone
[Nom commun]
Maladie du neurone moteur
[Nom commun]

Informations

Note publique d''information : 
Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)

Note générale sur le champ d'application : 
general or unspecified; prefer specifics

Point d'accès autorisé parallèle

Motor Neuron Disease

Identifiants externes

Identifiant MeSH : mesD016472

Utilisation dans FMeSH

Qualificatifs autorisés : DI / PS / IM / MI / DG / PP / RH / EN / ET / MO / EP / BL / CF / CI / CN / DH / DT / TH / PX / UR / VI / VE / HI / CL / EC / EM / GE / NU / RT / EH / PC / PA / ME / CO / SU92

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