Neurophysiological abnormalities in the Westphal variant of Huntington's disease
Identifieur interne :
002F21 ( PascalFrancis/Corpus );
précédent :
002F20;
suivant :
002F22
Neurophysiological abnormalities in the Westphal variant of Huntington's disease
Auteurs : R. Töpper ;
M. Schwarz ;
H. W. Lange ;
H. Hefter ;
J. NothSource :
-
Movement disorders [ 0885-3185 ] ; 1998.
RBID : Pascal:99-0011809
Descripteurs français
English descriptors
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 13 |
|---|
| A06 | | | | @2 6 |
|---|
| A08 | 01 | 1 | ENG | @1 Neurophysiological abnormalities in the Westphal variant of Huntington's disease |
|---|
| A11 | 01 | 1 | | @1 TÖPPER (R.) |
|---|
| A11 | 02 | 1 | | @1 SCHWARZ (M.) |
|---|
| A11 | 03 | 1 | | @1 LANGE (H. W.) |
|---|
| A11 | 04 | 1 | | @1 HEFTER (H.) |
|---|
| A11 | 05 | 1 | | @1 NOTH (J.) |
|---|
| A14 | 01 | | | @1 Department of Neurology, Technical University of Aachen @3 DEU @Z 1 aut. @Z 2 aut. @Z 5 aut. |
|---|
| A14 | 02 | | | @1 Neurological Therapy Center, Heinrich-Heine University @2 Düsseldorf @3 DEU @Z 3 aut. |
|---|
| A14 | 03 | | | @1 Department of Neurology, Heinrich-Heine University @2 Düsseldorf @3 DEU @Z 4 aut. |
|---|
| A20 | | | | @1 920-928 |
|---|
| A21 | | | | @1 1998 |
|---|
| A23 | 01 | | | @0 ENG |
|---|
| A43 | 01 | | | @1 INIST @2 20953 @5 354000071406360090 |
|---|
| A44 | | | | @0 0000 @1 © 1999 INIST-CNRS. All rights reserved. |
|---|
| A45 | | | | @0 43 ref. |
|---|
| A47 | 01 | 1 | | @0 99-0011809 |
|---|
| A60 | | | | @1 P |
|---|
| A61 | | | | @0 A |
|---|
| A64 | | 1 | | @0 Movement disorders |
|---|
| A66 | 01 | | | @0 USA |
|---|
| C02 | 01 | X | | @0 002B17G |
|---|
| C03 | 01 | X | FRE | @0 Chorée Huntington @5 01 |
|---|
| C03 | 01 | X | ENG | @0 Huntington disease @5 01 |
|---|
| C03 | 01 | X | SPA | @0 Corea Huntington @5 01 |
|---|
| C03 | 02 | X | FRE | @0 Potentiel évoqué somatosensoriel @5 04 |
|---|
| C03 | 02 | X | ENG | @0 Somatosensory evoked potential @5 04 |
|---|
| C03 | 02 | X | SPA | @0 Potencial evocado somatosensorial @5 04 |
|---|
| C03 | 03 | X | FRE | @0 Hypokinésie @5 07 |
|---|
| C03 | 03 | X | ENG | @0 Hypokinesia @5 07 |
|---|
| C03 | 03 | X | SPA | @0 Hipoquinesia @5 07 |
|---|
| C03 | 04 | X | FRE | @0 Etude cas @5 16 |
|---|
| C03 | 04 | X | ENG | @0 Case study @5 16 |
|---|
| C03 | 04 | X | SPA | @0 Estudio caso @5 16 |
|---|
| C03 | 05 | X | FRE | @0 Exploration @5 17 |
|---|
| C03 | 05 | X | ENG | @0 Exploration @5 17 |
|---|
| C03 | 05 | X | SPA | @0 Exploración @5 17 |
|---|
| C03 | 06 | X | FRE | @0 Homme @5 20 |
|---|
| C03 | 06 | X | ENG | @0 Human @5 20 |
|---|
| C03 | 06 | X | SPA | @0 Hombre @5 20 |
|---|
| C03 | 07 | X | FRE | @0 Mâle @5 21 |
|---|
| C03 | 07 | X | ENG | @0 Male @5 21 |
|---|
| C03 | 07 | X | SPA | @0 Macho @5 21 |
|---|
| C03 | 08 | X | FRE | @0 Forme clinique @5 23 |
|---|
| C03 | 08 | X | ENG | @0 Clinical form @5 23 |
|---|
| C03 | 08 | X | SPA | @0 Forma clínica @5 23 |
|---|
| C07 | 01 | X | FRE | @0 Système nerveux pathologie @5 37 |
|---|
| C07 | 01 | X | ENG | @0 Nervous system diseases @5 37 |
|---|
| C07 | 01 | X | SPA | @0 Sistema nervioso patología @5 37 |
|---|
| C07 | 02 | X | FRE | @0 Système nerveux central pathologie @5 38 |
|---|
| C07 | 02 | X | ENG | @0 Central nervous system disease @5 38 |
|---|
| C07 | 02 | X | SPA | @0 Sistema nervosio central patología @5 38 |
|---|
| C07 | 03 | X | FRE | @0 Encéphale pathologie @5 39 |
|---|
| C07 | 03 | X | ENG | @0 Cerebral disorder @5 39 |
|---|
| C07 | 03 | X | SPA | @0 Encéfalo patología @5 39 |
|---|
| C07 | 04 | X | FRE | @0 Extrapyramidal syndrome @5 40 |
|---|
| C07 | 04 | X | ENG | @0 Extrapyramidal syndrome @5 40 |
|---|
| C07 | 04 | X | SPA | @0 Extrapiramidal síndrome @5 40 |
|---|
| C07 | 05 | X | FRE | @0 Maladie dégénérative @5 41 |
|---|
| C07 | 05 | X | ENG | @0 Degenerative disease @5 41 |
|---|
| C07 | 05 | X | SPA | @0 Enfermedad degenerativa @5 41 |
|---|
| C07 | 06 | X | FRE | @0 Maladie héréditaire @5 42 |
|---|
| C07 | 06 | X | ENG | @0 Genetic disease @5 42 |
|---|
| C07 | 06 | X | SPA | @0 Enfermedad hereditaria @5 42 |
|---|
| C07 | 07 | X | FRE | @0 Electrodiagnostic @5 45 |
|---|
| C07 | 07 | X | ENG | @0 Electrodiagnosis @5 45 |
|---|
| C07 | 07 | X | SPA | @0 Electrodiagnóstico @5 45 |
|---|
| C07 | 08 | X | FRE | @0 Trouble moteur @5 53 |
|---|
| C07 | 08 | X | ENG | @0 Motor system disorder @5 53 |
|---|
| C07 | 08 | X | SPA | @0 Trastorno motor @5 53 |
|---|
| N21 | | | | @1 004 |
|---|
|
|---|
Format Inist (serveur)
| NO : | PASCAL 99-0011809 INIST |
|---|
| ET : | Neurophysiological abnormalities in the Westphal variant of Huntington's disease |
|---|
| AU : | TÖPPER (R.); SCHWARZ (M.); LANGE (H. W.); HEFTER (H.); NOTH (J.) |
|---|
| AF : | Department of Neurology, Technical University of Aachen/Allemagne (1 aut., 2 aut., 5 aut.); Neurological Therapy Center, Heinrich-Heine University/Düsseldorf/Allemagne (3 aut.); Department of Neurology, Heinrich-Heine University/Düsseldorf/Allemagne (4 aut.) |
|---|
| DT : | Publication en série; Niveau analytique |
|---|
| SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1998; Vol. 13; No. 6; Pp. 920-928; Bibl. 43 ref. |
|---|
| LA : | Anglais |
|---|
| CC : | 002B17G |
|---|
| FD : | Chorée Huntington; Potentiel évoqué somatosensoriel; Hypokinésie; Etude cas; Exploration; Homme; Mâle; Forme clinique |
|---|
| FG : | Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Maladie héréditaire; Electrodiagnostic; Trouble moteur |
|---|
| ED : | Huntington disease; Somatosensory evoked potential; Hypokinesia; Case study; Exploration; Human; Male; Clinical form |
|---|
| EG : | Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease; Electrodiagnosis; Motor system disorder |
|---|
| SD : | Corea Huntington; Potencial evocado somatosensorial; Hipoquinesia; Estudio caso; Exploración; Hombre; Macho; Forma clínica |
|---|
| LO : | INIST-20953.354000071406360090 |
|---|
| ID : | 99-0011809 |
|---|
Links to Exploration step
Pascal:99-0011809
Le document en format XML
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<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
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<s5>354000071406360090</s5>
</fA43><fA44><s0>0000</s0>
<s1>© 1999 INIST-CNRS. All rights reserved.</s1>
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</fA45><fA47 i1="01" i2="1"><s0>99-0011809</s0>
</fA47><fA64 i2="1"><s0>Movement disorders</s0>
</fA64><fA66 i1="01"><s0>USA</s0>
</fA66><fC02 i1="01" i2="X"><s0>002B17G</s0>
</fC02><fC03 i1="01" i2="X" l="FRE"><s0>Chorée Huntington</s0>
<s5>01</s5>
</fC03><fC03 i1="01" i2="X" l="ENG"><s0>Huntington disease</s0>
<s5>01</s5>
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<s5>01</s5>
</fC03><fC03 i1="02" i2="X" l="FRE"><s0>Potentiel évoqué somatosensoriel</s0>
<s5>04</s5>
</fC03><fC03 i1="02" i2="X" l="ENG"><s0>Somatosensory evoked potential</s0>
<s5>04</s5>
</fC03><fC03 i1="02" i2="X" l="SPA"><s0>Potencial evocado somatosensorial</s0>
<s5>04</s5>
</fC03><fC03 i1="03" i2="X" l="FRE"><s0>Hypokinésie</s0>
<s5>07</s5>
</fC03><fC03 i1="03" i2="X" l="ENG"><s0>Hypokinesia</s0>
<s5>07</s5>
</fC03><fC03 i1="03" i2="X" l="SPA"><s0>Hipoquinesia</s0>
<s5>07</s5>
</fC03><fC03 i1="04" i2="X" l="FRE"><s0>Etude cas</s0>
<s5>16</s5>
</fC03><fC03 i1="04" i2="X" l="ENG"><s0>Case study</s0>
<s5>16</s5>
</fC03><fC03 i1="04" i2="X" l="SPA"><s0>Estudio caso</s0>
<s5>16</s5>
</fC03><fC03 i1="05" i2="X" l="FRE"><s0>Exploration</s0>
<s5>17</s5>
</fC03><fC03 i1="05" i2="X" l="ENG"><s0>Exploration</s0>
<s5>17</s5>
</fC03><fC03 i1="05" i2="X" l="SPA"><s0>Exploración</s0>
<s5>17</s5>
</fC03><fC03 i1="06" i2="X" l="FRE"><s0>Homme</s0>
<s5>20</s5>
</fC03><fC03 i1="06" i2="X" l="ENG"><s0>Human</s0>
<s5>20</s5>
</fC03><fC03 i1="06" i2="X" l="SPA"><s0>Hombre</s0>
<s5>20</s5>
</fC03><fC03 i1="07" i2="X" l="FRE"><s0>Mâle</s0>
<s5>21</s5>
</fC03><fC03 i1="07" i2="X" l="ENG"><s0>Male</s0>
<s5>21</s5>
</fC03><fC03 i1="07" i2="X" l="SPA"><s0>Macho</s0>
<s5>21</s5>
</fC03><fC03 i1="08" i2="X" l="FRE"><s0>Forme clinique</s0>
<s5>23</s5>
</fC03><fC03 i1="08" i2="X" l="ENG"><s0>Clinical form</s0>
<s5>23</s5>
</fC03><fC03 i1="08" i2="X" l="SPA"><s0>Forma clínica</s0>
<s5>23</s5>
</fC03><fC07 i1="01" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07><fC07 i1="01" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07><fC07 i1="01" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07><fC07 i1="02" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>38</s5>
</fC07><fC07 i1="02" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>38</s5>
</fC07><fC07 i1="02" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>38</s5>
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<s5>39</s5>
</fC07><fC07 i1="03" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07><fC07 i1="03" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07><fC07 i1="04" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07><fC07 i1="04" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07><fC07 i1="04" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07><fC07 i1="05" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07><fC07 i1="05" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07><fC07 i1="05" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07><fC07 i1="06" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>42</s5>
</fC07><fC07 i1="06" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>42</s5>
</fC07><fC07 i1="06" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>42</s5>
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<s5>45</s5>
</fC07><fC07 i1="07" i2="X" l="ENG"><s0>Electrodiagnosis</s0>
<s5>45</s5>
</fC07><fC07 i1="07" i2="X" l="SPA"><s0>Electrodiagnóstico</s0>
<s5>45</s5>
</fC07><fC07 i1="08" i2="X" l="FRE"><s0>Trouble moteur</s0>
<s5>53</s5>
</fC07><fC07 i1="08" i2="X" l="ENG"><s0>Motor system disorder</s0>
<s5>53</s5>
</fC07><fC07 i1="08" i2="X" l="SPA"><s0>Trastorno motor</s0>
<s5>53</s5>
</fC07><fN21><s1>004</s1>
</fN21><server><NO>PASCAL 99-0011809 INIST</NO>
<ET>Neurophysiological abnormalities in the Westphal variant of Huntington's disease</ET>
<AU>TÖPPER (R.); SCHWARZ (M.); LANGE (H. W.); HEFTER (H.); NOTH (J.)</AU>
<AF>Department of Neurology, Technical University of Aachen/Allemagne (1 aut., 2 aut., 5 aut.); Neurological Therapy Center, Heinrich-Heine University/Düsseldorf/Allemagne (3 aut.); Department of Neurology, Heinrich-Heine University/Düsseldorf/Allemagne (4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1998; Vol. 13; No. 6; Pp. 920-928; Bibl. 43 ref.</SO>
<LA>Anglais</LA>
<CC>002B17G</CC>
<FD>Chorée Huntington; Potentiel évoqué somatosensoriel; Hypokinésie; Etude cas; Exploration; Homme; Mâle; Forme clinique</FD>
<FG>Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Maladie héréditaire; Electrodiagnostic; Trouble moteur</FG>
<ED>Huntington disease; Somatosensory evoked potential; Hypokinesia; Case study; Exploration; Human; Male; Clinical form</ED>
<EG>Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease; Electrodiagnosis; Motor system disorder</EG>
<SD>Corea Huntington; Potencial evocado somatosensorial; Hipoquinesia; Estudio caso; Exploración; Hombre; Macho; Forma clínica</SD>
<LO>INIST-20953.354000071406360090</LO>
<ID>99-0011809</ID>
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