Movement Disorders (revue)

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Pyramidal tract degeneration in multiple system atrophy : The relevance of magnetization transfer imaging

Identifieur interne : 001801 ( PascalFrancis/Corpus ); précédent : 001800; suivant : 001802

Pyramidal tract degeneration in multiple system atrophy : The relevance of magnetization transfer imaging

Auteurs : Antonio José Da Rocha ; Antonio Carlos Martins Jr Maia ; Carlos Jorge Da Silva ; Flavio Tulio Braga ; Nelson Paes Diniz Fortes Ferreira ; Orlando Graziani Povoas Barsottini ; Henrique Ballalai Ferraz

Source :

RBID : Pascal:07-0133251

Descripteurs français

English descriptors

Abstract

The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism, cerebellar ataxia, and cortico-spinal tract dysfunction. Although the diagnosis of definite MSA requires pathological confirmation, magnetic resonance imaging (MRI) studies have been shown to contribute to the diagnosis of MSA. Although pyramidal tract dysfunction is frequent in MSA patients, signs of pyramidal tract involvement are controversially demonstrated by MRI. We evaluated the pyramidal involvement in 10 patients (7 women) with clinically probable MSA, detecting the presence of spasticity, hyperreflexia, and Babinski sign, as well as demonstrating degeneration of the pyramidal tract and primary motor cortex by MRI in all of them. Our article also discusses key radiological features of this syndrome. In MSA, pyramidal tract involvement seems to be more frequent than previously thought, and the clinicoradiological correlation between pyramidal tract dysfunction and degeneration may contribute to the understanding of the clinical hallmarks of MSA. MRI may also add information regarding the differential diagnosis of this syndrome.

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 22
A06       @2 2
A08 01  1  ENG  @1 Pyramidal tract degeneration in multiple system atrophy : The relevance of magnetization transfer imaging
A11 01  1    @1 DA ROCHA (Antonio José)
A11 02  1    @1 MAIA (Antonio Carlos Martins JR)
A11 03  1    @1 DA SILVA (Carlos Jorge)
A11 04  1    @1 TULIO BRAGA (Flavio)
A11 05  1    @1 PAES DINIZ FORTES FERREIRA (Nelson)
A11 06  1    @1 GRAZIANI POVOAS BARSOTTINI (Orlando)
A11 07  1    @1 BALLALAI FERRAZ (Henrique)
A14 01      @1 Centro de Medicina Diagnóstica Fleury, Setor de Neuroradiologia @2 Sao Paulo @3 BRA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut.
A14 02      @1 Medimagem Hospital Beneficiência Portuguesa, Setor de Neuroradiologia @2 Sao Paulo @3 BRA @Z 5 aut.
A14 03      @1 Department of Neurology, Universidade Federal de Sao Paulo @2 Sao Paulo @3 BRA @Z 6 aut. @Z 7 aut.
A20       @1 238-244
A21       @1 2007
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000145528070160
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 41 ref.
A47 01  1    @0 07-0133251
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism, cerebellar ataxia, and cortico-spinal tract dysfunction. Although the diagnosis of definite MSA requires pathological confirmation, magnetic resonance imaging (MRI) studies have been shown to contribute to the diagnosis of MSA. Although pyramidal tract dysfunction is frequent in MSA patients, signs of pyramidal tract involvement are controversially demonstrated by MRI. We evaluated the pyramidal involvement in 10 patients (7 women) with clinically probable MSA, detecting the presence of spasticity, hyperreflexia, and Babinski sign, as well as demonstrating degeneration of the pyramidal tract and primary motor cortex by MRI in all of them. Our article also discusses key radiological features of this syndrome. In MSA, pyramidal tract involvement seems to be more frequent than previously thought, and the clinicoradiological correlation between pyramidal tract dysfunction and degeneration may contribute to the understanding of the clinical hallmarks of MSA. MRI may also add information regarding the differential diagnosis of this syndrome.
C02 01  X    @0 002B17
C02 02  X    @0 002B17F
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 Dégénérescence @5 02
C03 02  X  ENG  @0 Degeneration @5 02
C03 02  X  SPA  @0 Degeneración @5 02
C03 03  X  FRE  @0 Atrophie multisystématisée @2 NM @5 03
C03 03  X  ENG  @0 Multiple system atrophy @2 NM @5 03
C03 03  X  SPA  @0 Atrofia multisistematizada @2 NM @5 03
C03 04  X  FRE  @0 Parkinsonisme @2 NM @5 04
C03 04  X  ENG  @0 Parkinsonism @2 NM @5 04
C03 04  X  SPA  @0 Parkinson síndrome @2 NM @5 04
C03 05  X  FRE  @0 Faisceau pyramidal @5 09
C03 05  X  ENG  @0 Pyramidal tract @5 09
C03 05  X  SPA  @0 Fascículo piramidal @5 09
C03 06  X  FRE  @0 Aimantation @5 10
C03 06  X  ENG  @0 Magnetization @5 10
C03 06  X  SPA  @0 Imanación @5 10
C03 07  X  FRE  @0 Imagerie RMN @5 11
C03 07  X  ENG  @0 Nuclear magnetic resonance imaging @5 11
C03 07  X  SPA  @0 Imaginería RMN @5 11
C07 01  X  FRE  @0 Système nerveux central @5 37
C07 01  X  ENG  @0 Central nervous system @5 37
C07 01  X  SPA  @0 Sistema nervioso central @5 37
C07 02  X  FRE  @0 Voie motrice pyramidale @5 38
C07 02  X  ENG  @0 Pyramidal motor pathway @5 38
C07 02  X  SPA  @0 Vía motora piramidal @5 38
N21       @1 085
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 07-0133251 INIST
ET : Pyramidal tract degeneration in multiple system atrophy : The relevance of magnetization transfer imaging
AU : DA ROCHA (Antonio José); MAIA (Antonio Carlos Martins JR); DA SILVA (Carlos Jorge); TULIO BRAGA (Flavio); PAES DINIZ FORTES FERREIRA (Nelson); GRAZIANI POVOAS BARSOTTINI (Orlando); BALLALAI FERRAZ (Henrique)
AF : Centro de Medicina Diagnóstica Fleury, Setor de Neuroradiologia/Sao Paulo/Brésil (1 aut., 2 aut., 3 aut., 4 aut.); Medimagem Hospital Beneficiência Portuguesa, Setor de Neuroradiologia/Sao Paulo/Brésil (5 aut.); Department of Neurology, Universidade Federal de Sao Paulo/Sao Paulo/Brésil (6 aut., 7 aut.)
DT : Publication en série; Courte communication, note brève; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 2; Pp. 238-244; Bibl. 41 ref.
LA : Anglais
EA : The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism, cerebellar ataxia, and cortico-spinal tract dysfunction. Although the diagnosis of definite MSA requires pathological confirmation, magnetic resonance imaging (MRI) studies have been shown to contribute to the diagnosis of MSA. Although pyramidal tract dysfunction is frequent in MSA patients, signs of pyramidal tract involvement are controversially demonstrated by MRI. We evaluated the pyramidal involvement in 10 patients (7 women) with clinically probable MSA, detecting the presence of spasticity, hyperreflexia, and Babinski sign, as well as demonstrating degeneration of the pyramidal tract and primary motor cortex by MRI in all of them. Our article also discusses key radiological features of this syndrome. In MSA, pyramidal tract involvement seems to be more frequent than previously thought, and the clinicoradiological correlation between pyramidal tract dysfunction and degeneration may contribute to the understanding of the clinical hallmarks of MSA. MRI may also add information regarding the differential diagnosis of this syndrome.
CC : 002B17; 002B17F; 002B17G
FD : Système nerveux pathologie; Dégénérescence; Atrophie multisystématisée; Parkinsonisme; Faisceau pyramidal; Aimantation; Imagerie RMN
FG : Système nerveux central; Voie motrice pyramidale
ED : Nervous system diseases; Degeneration; Multiple system atrophy; Parkinsonism; Pyramidal tract; Magnetization; Nuclear magnetic resonance imaging
EG : Central nervous system; Pyramidal motor pathway
SD : Sistema nervioso patología; Degeneración; Atrofia multisistematizada; Parkinson síndrome; Fascículo piramidal; Imanación; Imaginería RMN
LO : INIST-20953.354000145528070160
ID : 07-0133251

Links to Exploration step

Pascal:07-0133251

Le document en format XML

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<div type="abstract" xml:lang="en">The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism, cerebellar ataxia, and cortico-spinal tract dysfunction. Although the diagnosis of definite MSA requires pathological confirmation, magnetic resonance imaging (MRI) studies have been shown to contribute to the diagnosis of MSA. Although pyramidal tract dysfunction is frequent in MSA patients, signs of pyramidal tract involvement are controversially demonstrated by MRI. We evaluated the pyramidal involvement in 10 patients (7 women) with clinically probable MSA, detecting the presence of spasticity, hyperreflexia, and Babinski sign, as well as demonstrating degeneration of the pyramidal tract and primary motor cortex by MRI in all of them. Our article also discusses key radiological features of this syndrome. In MSA, pyramidal tract involvement seems to be more frequent than previously thought, and the clinicoradiological correlation between pyramidal tract dysfunction and degeneration may contribute to the understanding of the clinical hallmarks of MSA. MRI may also add information regarding the differential diagnosis of this syndrome.</div>
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<s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Dégénérescence</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Degeneration</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Degeneración</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Atrophie multisystématisée</s0>
<s2>NM</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Multiple system atrophy</s0>
<s2>NM</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Atrofia multisistematizada</s0>
<s2>NM</s2>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Parkinsonisme</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Parkinsonism</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Parkinson síndrome</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Faisceau pyramidal</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Pyramidal tract</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Fascículo piramidal</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Aimantation</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Magnetization</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Imanación</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Imagerie RMN</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Nuclear magnetic resonance imaging</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Imaginería RMN</s0>
<s5>11</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Système nerveux central</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Central nervous system</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Sistema nervioso central</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Voie motrice pyramidale</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Pyramidal motor pathway</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Vía motora piramidal</s0>
<s5>38</s5>
</fC07>
<fN21>
<s1>085</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 07-0133251 INIST</NO>
<ET>Pyramidal tract degeneration in multiple system atrophy : The relevance of magnetization transfer imaging</ET>
<AU>DA ROCHA (Antonio José); MAIA (Antonio Carlos Martins JR); DA SILVA (Carlos Jorge); TULIO BRAGA (Flavio); PAES DINIZ FORTES FERREIRA (Nelson); GRAZIANI POVOAS BARSOTTINI (Orlando); BALLALAI FERRAZ (Henrique)</AU>
<AF>Centro de Medicina Diagnóstica Fleury, Setor de Neuroradiologia/Sao Paulo/Brésil (1 aut., 2 aut., 3 aut., 4 aut.); Medimagem Hospital Beneficiência Portuguesa, Setor de Neuroradiologia/Sao Paulo/Brésil (5 aut.); Department of Neurology, Universidade Federal de Sao Paulo/Sao Paulo/Brésil (6 aut., 7 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 2; Pp. 238-244; Bibl. 41 ref.</SO>
<LA>Anglais</LA>
<EA>The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism, cerebellar ataxia, and cortico-spinal tract dysfunction. Although the diagnosis of definite MSA requires pathological confirmation, magnetic resonance imaging (MRI) studies have been shown to contribute to the diagnosis of MSA. Although pyramidal tract dysfunction is frequent in MSA patients, signs of pyramidal tract involvement are controversially demonstrated by MRI. We evaluated the pyramidal involvement in 10 patients (7 women) with clinically probable MSA, detecting the presence of spasticity, hyperreflexia, and Babinski sign, as well as demonstrating degeneration of the pyramidal tract and primary motor cortex by MRI in all of them. Our article also discusses key radiological features of this syndrome. In MSA, pyramidal tract involvement seems to be more frequent than previously thought, and the clinicoradiological correlation between pyramidal tract dysfunction and degeneration may contribute to the understanding of the clinical hallmarks of MSA. MRI may also add information regarding the differential diagnosis of this syndrome.</EA>
<CC>002B17; 002B17F; 002B17G</CC>
<FD>Système nerveux pathologie; Dégénérescence; Atrophie multisystématisée; Parkinsonisme; Faisceau pyramidal; Aimantation; Imagerie RMN</FD>
<FG>Système nerveux central; Voie motrice pyramidale</FG>
<ED>Nervous system diseases; Degeneration; Multiple system atrophy; Parkinsonism; Pyramidal tract; Magnetization; Nuclear magnetic resonance imaging</ED>
<EG>Central nervous system; Pyramidal motor pathway</EG>
<SD>Sistema nervioso patología; Degeneración; Atrofia multisistematizada; Parkinson síndrome; Fascículo piramidal; Imanación; Imaginería RMN</SD>
<LO>INIST-20953.354000145528070160</LO>
<ID>07-0133251</ID>
</server>
</inist>
</record>

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