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Identifiant pérenne de la notice : 050850989Copier cet identifiant (PPN)
URI de l'entité : http://www.idref.fr/050850989/idCopier cet URI
Notice de type FMeSH

Point d'accès autorisé

Syndromes parkinsoniens

Variantes de point d'accès

Parkinsonian Syndrome
[Nom commun]
Parkinsonian Syndromes
[Nom commun]
Parkinsonian Diseases
[Nom commun]
Parkinsonism
[Nom commun]
Parkinsonisme
[Nom commun]
Troubles parkinsoniens
[Nom commun]
Autosomal Dominant Parkinsonism
[Nom commun]
Dominant Parkinsonism, Autosomal
[Nom commun]
Parkinsonism, Autosomal Dominant
[Nom commun]
Autosomal Recessive Juvenile Parkinson Disease
[Nom commun]
Juvenile Parkinson Disease, Autosomal Recessive
[Nom commun]
Juvenile Parkinsonism, Autosomal Recessive
[Nom commun]
Parkinsonism, Juvenile, Autosomal Recessive
[Nom commun]
Familial Parkinson Disease, Autosomal Recessive
[Nom commun]
Autosomal Recessive Juvenile Parkinsonism
[Nom commun]
Parkinson Disease 2, Autosomal Recessive Juvenile
[Nom commun]
Parkinsonism, Early-Onset, With Diurnal Fluctuation
[Nom commun]
Parkinson Disease, Juvenile, Autosomal Recessive
[Nom commun]
Parkinson Disease 2
[Nom commun]
Parkinson Disease Autosomal Recessive, Early Onset
[Nom commun]
Parkinsonism, Early Onset, with Diurnal Fluctuation
[Nom commun]
Chromosome 6-Linked Autosomal Recessive Parkinsonism
[Nom commun]
Chromosome 6 Linked Autosomal Recessive Parkinsonism
[Nom commun]
Parkinson Disease, Familial, Autosomal Recessive
[Nom commun]
Ramsay Hunt Paralysis Syndrome
[Nom commun]
Familial Juvenile Parkinsonism
[Nom commun]
Juvenile Parkinsonism, Familial
[Nom commun]
Parkinsonism, Familial Juvenile
[Nom commun]
Parkinsonism, Experimental
[Nom commun]
Experimental Parkinsonisms
[Nom commun]
Parkinsonisms, Experimental
[Nom commun]
Parkinson Disease, Experimental
[Nom commun]
Experimental Parkinsonism, MPTP-Induced
[Nom commun]
Experimental Parkinsonism, MPTP Induced
[Nom commun]
Parkinsonism, MPTP-Induced Experimental
[Nom commun]
MPTP-Induced Experimental Parkinsonism
[Nom commun]
MPTP Induced Experimental Parkinsonism
[Nom commun]
Experimental Parkinson Disease
[Nom commun]
Diseases, Experimental Parkinson
[Nom commun]
Experimental Parkinson Diseases
[Nom commun]
Parkinson Diseases, Experimental
[Nom commun]
Experimental Parkinsonism
[Nom commun]
Parkinsonism, Juvenile
[Nom commun]
Juvenile Parkinsonism
[Nom commun]
Juvenile Parkinsonisms
[Nom commun]
Parkinsonisms, Juvenile
[Nom commun]
Parkinson Disease, Juvenile
[Nom commun]
Juvenile Parkinson Disease
[Nom commun]
Autosomal Dominant Juvenile Parkinson Disease
[Nom commun]
Autosomal Dominant Juvenile Parkinsonism
[Nom commun]
Parkinsonism, Juvenile, Autosomal Dominant
[Nom commun]
Parkinson Disease, Autosomal Dominant. Juvenile
[Nom commun]
Parkinson Disease, Juvenile, Autosomal Dominant
[Nom commun]
Juvenile Parkinsonism, Autosomal Dominant
[Nom commun]
Juvenile Parkinson Disease, Autosomal Dominant
[Nom commun]
Autosomal Recessive Parkinsonism
[Nom commun]
Parkinsonism, Autosomal Recessive
[Nom commun]
Recessive Parkinsonism, Autosomal
[Nom commun]
Parkinsonisme autosomique dominant
[Nom commun]
Maladie de Parkinson juvénile autosomique récessive
[Nom commun]
Maladie de Parkinson précoce autosomique récessive
[Nom commun]
Paralysie de Hunt
[Nom commun]
Parkinsonisme familial juvénile
[Nom commun]
Parkinsonisme expérimental
[Nom commun]
Maladie de Parkinson expérimentale due au MPTP
[Nom commun]
Maladie de Parkinson expérimentale
[Nom commun]
Parkinsonisme induit par le MPTP
[Nom commun]
Syndrome parkinsonien induit par le MPTP
[Nom commun]
Parkinsonisme juvénile
[Nom commun]
Maladie de Parkinson juvénile
[Nom commun]
Maladie de Parkinson juvénile autosomique dominante
[Nom commun]
Maladie de Parkinson précoce autosomique dominante
[Nom commun]
Parkinsonisme autosomique récessif
[Nom commun]
Parkinsonisme
[Nom commun]
Troubles parkinsoniens
[Nom commun]

Informations

Note publique d''information : 
A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA

Note générale sur le champ d'application : 
Gen: prefer specifics; do not confuse entry term RAMSAY HUNT PARALYSIS SYNDROME with RAMSAY HUNT AURICULAR SYNDROME see HERPES ZOSTER OTICUS or RAMSAY HUNT CEREBELLAR SYNDROME see MYOCLONIC CEREBELLAR DYSSYNERGIA


Notice d'autorité liée

Dégénerescence striatonigrique

Point d'accès autorisé parallèle

Parkinsonian Disorders

Identifiants externes

Identifiant MeSH : mesD020734

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 / SU2000; for PARKINSONISM use PARKINSON DISEASE 1978-1999; for PARKINSONIAN SYNDROME use PARKINSON DISEASE, SECONDARY 1974-1999; for RAMSAY HUNT PARALYSIS SYNDROME use PARKINSON DISEASE 1992-1999

Informations sur la notice

Identifiant de la notice : 050850989
RCR créateur de la notice : 0001
Date de création : 03-11-1999
RCR dernier modificateur de la notice : 1999
Date de dernière modification : 26-11-2024 à 16 h 09

... Références liées : ...