Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Identifieur interne :
003981 ( PascalFrancis/Corpus );
précédent :
003980;
suivant :
003982
Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Auteurs : A. E. HardingSource :
-
Movement disorders [ 0885-3185 ] ; 1989.
RBID : Pascal:90-0192170
Descripteurs français
English descriptors
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
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A08 | 01 | 1 | ENG | @1 Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what? |
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A11 | 01 | 1 | | @1 HARDING (A. E.) |
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A14 | 01 | | | @1 Inst. neurology @2 London @3 GBR @Z A11011000 |
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A20 | | | | @1 18-19 |
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A21 | | | | @1 1989 |
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A64 | | 1 | | @0 Movement disorders |
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A66 | 01 | | | @0 USA |
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C02 | 01 | X | | @0 002B17G |
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C03 | 01 | X | FRE | @0 Dyssynergie cérébelleuse myoclonique Hunt |
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C03 | 02 | X | FRE | @0 Epilepsie myoclonique familiale Unverricht Lundborg |
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C03 | 03 | X | FRE | @0 Ataxie |
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C03 | 04 | X | FRE | @0 Myoclonie |
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C03 | 05 | X | FRE | @0 Epilepsie |
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C03 | 06 | X | FRE | @0 Maladie dégénérative |
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C03 | 07 | X | FRE | @0 Maladie héréditaire |
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C03 | 08 | X | FRE | @0 Système nerveux pathologie |
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C03 | 09 | X | FRE | @0 Diagnostic différentiel |
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C03 | 10 | X | FRE | @0 Homme |
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C03 | 01 | X | ENG | @0 Dyssynergia cerebellia myoclonica |
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C03 | 02 | X | ENG | @0 Progressive myoclonus epilepsy |
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C03 | 03 | X | ENG | @0 Ataxia |
---|
C03 | 04 | X | ENG | @0 Myoclonus |
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C03 | 05 | X | ENG | @0 Epilepsy |
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C03 | 06 | X | ENG | @0 Degenerative disease |
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C03 | 07 | X | ENG | @0 Genetic disease |
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C03 | 08 | X | ENG | @0 Nervous system diseases |
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C03 | 09 | X | ENG | @0 Differential diagnostic |
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C03 | 10 | X | ENG | @0 Human |
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C03 | 01 | X | SPA | @0 Disinergía cerebelosa mioclónica Hunt |
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C03 | 02 | X | SPA | @0 Epilepsia mioclónica progresiva |
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C03 | 03 | X | SPA | @0 Ataxia |
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C03 | 04 | X | SPA | @0 Mioclonia |
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C03 | 05 | X | SPA | @0 Epilepsia |
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C03 | 06 | X | SPA | @0 Enfermedad degenerativa |
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C03 | 07 | X | SPA | @0 Enfermedad hereditaria |
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C03 | 08 | X | SPA | @0 Sistema nervioso patología |
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C03 | 09 | X | SPA | @0 Diagnóstico diferencial |
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C03 | 10 | X | SPA | @0 Hombre |
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N21 | | | | @1 903 |
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N82 | | | | @1 NBS |
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Format Inist (serveur)
NO : | PASCAL 90-0192170 INIST |
ET : | Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what? |
AU : | HARDING (A. E.) |
AF : | Inst. neurology/London/Royaume-Uni (A11011000) |
DT : | Publication en série; Niveau analytique |
SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1989; Vol. 4; No. 1; Pp. 18-19 |
LA : | Anglais |
CC : | 002B17G |
FD : | Dyssynergie cérébelleuse myoclonique Hunt; Epilepsie myoclonique familiale Unverricht Lundborg; Ataxie; Myoclonie; Epilepsie; Maladie dégénérative; Maladie héréditaire; Système nerveux pathologie; Diagnostic différentiel; Homme |
ED : | Dyssynergia cerebellia myoclonica; Progressive myoclonus epilepsy; Ataxia; Myoclonus; Epilepsy; Degenerative disease; Genetic disease; Nervous system diseases; Differential diagnostic; Human |
SD : | Disinergía cerebelosa mioclónica Hunt; Epilepsia mioclónica progresiva; Ataxia; Mioclonia; Epilepsia; Enfermedad degenerativa; Enfermedad hereditaria; Sistema nervioso patología; Diagnóstico diferencial; Hombre |
LO : | CNRS-20953 |
ID : | 90-0192170 |
Links to Exploration step
Pascal:90-0192170
Le document en format XML
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