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Movement Disorders (revue)

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Hereditary spastic paraplegia associated with dopa-responsive Parkinsonism

Identifieur interne : 001B39 ( PascalFrancis/Corpus ); précédent : 001B38; suivant : 001B40

Hereditary spastic paraplegia associated with dopa-responsive Parkinsonism

Auteurs : Federico Micheli ; Maria Graciela Cersosimo ; Carlos Zuniga Ramirez

Source :

RBID : Pascal:06-0289045

Descripteurs français

English descriptors

Abstract

A 47-year-old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 21
A06       @2 5
A08 01  1  ENG  @1 Hereditary spastic paraplegia associated with dopa-responsive Parkinsonism
A11 01  1    @1 MICHELI (Federico)
A11 02  1    @1 GRACIELA CERSOSIMO (Maria)
A11 03  1    @1 ZUNIGA RAMIREZ (Carlos)
A14 01      @1 Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José cle San Martín @2 Buenos Aires @3 ARG @Z 1 aut. @Z 2 aut. @Z 3 aut.
A20       @1 716-717
A21       @1 2006
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000142568210230
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 24 ref.
A47 01  1    @0 06-0289045
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 A 47-year-old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment.
C02 01  X    @0 002B17
C02 02  X    @0 002B17H
C02 03  X    @0 002B17G
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Paraplégie spasmodique héréditaire Strumpell Lorrain @5 02
C03 02  X  ENG  @0 Hereditary spastic paraplegia @5 02
C03 02  X  SPA  @0 Paraplejía espasmódica hereditaria Strumpell Lorrain @5 02
C03 03  X  FRE  @0 Parkinsonisme @2 NM @5 03
C03 03  X  ENG  @0 Parkinsonism @2 NM @5 03
C03 03  X  SPA  @0 Parkinson síndrome @2 NM @5 03
C03 04  X  FRE  @0 Paraparésie @5 04
C03 04  X  ENG  @0 Paraparesia @5 04
C03 04  X  SPA  @0 Paraparesia @5 04
C03 05  X  FRE  @0 Dopa @2 NK @2 FR @5 09
C03 05  X  ENG  @0 Dopa @2 NK @2 FR @5 09
C03 05  X  SPA  @0 Dopa @2 NK @2 FR @5 09
C03 06  X  FRE  @0 Lévodopa @2 NK @2 FR @5 10
C03 06  X  ENG  @0 Levodopa @2 NK @2 FR @5 10
C03 06  X  SPA  @0 Levodopa @2 NK @2 FR @5 10
C07 01  X  FRE  @0 Encéphale pathologie @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Maladie dégénérative @5 38
C07 02  X  ENG  @0 Degenerative disease @5 38
C07 02  X  SPA  @0 Enfermedad degenerativa @5 38
C07 03  X  FRE  @0 Maladie héréditaire @5 39
C07 03  X  ENG  @0 Genetic disease @5 39
C07 03  X  SPA  @0 Enfermedad hereditaria @5 39
C07 04  X  FRE  @0 Moelle épinière pathologie @5 40
C07 04  X  ENG  @0 Spinal cord disease @5 40
C07 04  X  SPA  @0 Médula espinal patología @5 40
C07 05  X  FRE  @0 Système nerveux central pathologie @5 41
C07 05  X  ENG  @0 Central nervous system disease @5 41
C07 05  X  SPA  @0 Sistema nervosio central patología @5 41
C07 06  X  FRE  @0 Trouble moteur @5 42
C07 06  X  ENG  @0 Motor system disorder @5 42
C07 06  X  SPA  @0 Trastorno motor @5 42
C07 07  X  FRE  @0 Trouble neurologique @5 43
C07 07  X  ENG  @0 Neurological disorder @5 43
C07 07  X  SPA  @0 Trastorno neurológico @5 43
C07 08  X  FRE  @0 Parésie @5 44
C07 08  X  ENG  @0 Paresis @5 44
C07 08  X  SPA  @0 Paresia @5 44
N21       @1 184
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 06-0289045 INIST
ET : Hereditary spastic paraplegia associated with dopa-responsive Parkinsonism
AU : MICHELI (Federico); GRACIELA CERSOSIMO (Maria); ZUNIGA RAMIREZ (Carlos)
AF : Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José cle San Martín/Buenos Aires/Argentine (1 aut., 2 aut., 3 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 5; Pp. 716-717; Bibl. 24 ref.
LA : Anglais
EA : A 47-year-old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment.
CC : 002B17; 002B17H; 002B17G
FD : Système nerveux pathologie; Paraplégie spasmodique héréditaire Strumpell Lorrain; Parkinsonisme; Paraparésie; Dopa; Lévodopa
FG : Encéphale pathologie; Maladie dégénérative; Maladie héréditaire; Moelle épinière pathologie; Système nerveux central pathologie; Trouble moteur; Trouble neurologique; Parésie
ED : Nervous system diseases; Hereditary spastic paraplegia; Parkinsonism; Paraparesia; Dopa; Levodopa
EG : Cerebral disorder; Degenerative disease; Genetic disease; Spinal cord disease; Central nervous system disease; Motor system disorder; Neurological disorder; Paresis
SD : Sistema nervioso patología; Paraplejía espasmódica hereditaria Strumpell Lorrain; Parkinson síndrome; Paraparesia; Dopa; Levodopa
LO : INIST-20953.354000142568210230
ID : 06-0289045

Links to Exploration step

Pascal:06-0289045

Le document en format XML

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<AF>Parkinson's Disease and Movement Disorders Unit, Hospital de Clínicas José cle San Martín/Buenos Aires/Argentine (1 aut., 2 aut., 3 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 5; Pp. 716-717; Bibl. 24 ref.</SO>
<LA>Anglais</LA>
<EA>A 47-year-old patient with hereditary spastic paraplegia and parkinsonian features is reported. Treatment with levodopa led to marked improvement in his neurological status and quality of life. However, several years later he developed motor fluctuations and dyskinesias. The latter promptly remitted with amantadine treatment.</EA>
<CC>002B17; 002B17H; 002B17G</CC>
<FD>Système nerveux pathologie; Paraplégie spasmodique héréditaire Strumpell Lorrain; Parkinsonisme; Paraparésie; Dopa; Lévodopa</FD>
<FG>Encéphale pathologie; Maladie dégénérative; Maladie héréditaire; Moelle épinière pathologie; Système nerveux central pathologie; Trouble moteur; Trouble neurologique; Parésie</FG>
<ED>Nervous system diseases; Hereditary spastic paraplegia; Parkinsonism; Paraparesia; Dopa; Levodopa</ED>
<EG>Cerebral disorder; Degenerative disease; Genetic disease; Spinal cord disease; Central nervous system disease; Motor system disorder; Neurological disorder; Paresis</EG>
<SD>Sistema nervioso patología; Paraplejía espasmódica hereditaria Strumpell Lorrain; Parkinson síndrome; Paraparesia; Dopa; Levodopa</SD>
<LO>INIST-20953.354000142568210230</LO>
<ID>06-0289045</ID>
</server>
</inist>
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