Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan
Identifieur interne :
000177 ( PascalFrancis/Curation );
précédent :
000176;
suivant :
000178
Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan
Auteurs : Sergei N. Illarioshkin [
Russie] ;
Irina A. Ivanova-Smolenskaya [
Russie] ;
Rahmatullo A. Rahmonov [
Russie] ;
Elena D. Markova [
Russie] ;
Giovanni Stevanin [
France] ;
Alexis Brice [
France]
Source :
-
Movement disorders [ 0885-3185 ] ; 2000.
RBID : Pascal:00-0480444
Descripteurs français
- Pascal (Inist)
- Tremblement,
Essentiel,
Hétérogénéité,
Gène,
Locus,
Génotype,
Liaison génétique,
Etude familiale,
Déterminisme génétique,
Biologie moléculaire,
Homme.
- Wicri :
English descriptors
- KwdEn :
- Essential,
Family study,
Gene,
Genetic determinism,
Genotype,
Heterogeneity,
Human,
Linkage,
Locus,
Molecular biology,
Tremor.
| pA |
| A01 | 01 | 1 | | @0 0885-3185 |
|---|
| A03 | | 1 | | @0 Mov. disord. |
|---|
| A05 | | | | @2 15 |
|---|
| A06 | | | | @2 5 |
|---|
| A08 | 01 | 1 | ENG | @1 Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan |
|---|
| A11 | 01 | 1 | | @1 ILLARIOSHKIN (Sergei N.) |
|---|
| A11 | 02 | 1 | | @1 IVANOVA-SMOLENSKAYA (Irina A.) |
|---|
| A11 | 03 | 1 | | @1 RAHMONOV (Rahmatullo A.) |
|---|
| A11 | 04 | 1 | | @1 MARKOVA (Elena D.) |
|---|
| A11 | 05 | 1 | | @1 STEVANIN (Giovanni) |
|---|
| A11 | 06 | 1 | | @1 BRICE (Alexis) |
|---|
| A14 | 01 | | | @1 Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences @2 Moscow @3 RUS @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. |
|---|
| A14 | 02 | | | @1 INSERM U289, Hôpital de la Salpêtrière @2 Paris @3 FRA @Z 5 aut. @Z 6 aut. |
|---|
| A20 | | | | @1 1020-1023 |
|---|
| A21 | | | | @1 2000 |
|---|
| A23 | 01 | | | @0 ENG |
|---|
| A43 | 01 | | | @1 INIST @2 20953 @5 354000091356830430 |
|---|
| A44 | | | | @0 0000 @1 © 2000 INIST-CNRS. All rights reserved. |
|---|
| A45 | | | | @0 17 ref. |
|---|
| A47 | 01 | 1 | | @0 00-0480444 |
|---|
| A60 | | | | @1 P |
|---|
| A61 | | | | @0 A |
|---|
| A64 | 01 | 1 | | @0 Movement disorders |
|---|
| A66 | 01 | | | @0 USA |
|---|
| C02 | 01 | X | | @0 002B17A01 |
|---|
| C03 | 01 | X | FRE | @0 Tremblement @5 01 |
|---|
| C03 | 01 | X | ENG | @0 Tremor @5 01 |
|---|
| C03 | 01 | X | SPA | @0 Temblor @5 01 |
|---|
| C03 | 02 | X | FRE | @0 Essentiel @5 02 |
|---|
| C03 | 02 | X | ENG | @0 Essential @5 02 |
|---|
| C03 | 02 | X | SPA | @0 Esencial @5 02 |
|---|
| C03 | 03 | X | FRE | @0 Hétérogénéité @5 04 |
|---|
| C03 | 03 | X | ENG | @0 Heterogeneity @5 04 |
|---|
| C03 | 03 | X | SPA | @0 Heterogeneidad @5 04 |
|---|
| C03 | 04 | X | FRE | @0 Gène @5 05 |
|---|
| C03 | 04 | X | ENG | @0 Gene @5 05 |
|---|
| C03 | 04 | X | SPA | @0 Gen @5 05 |
|---|
| C03 | 05 | X | FRE | @0 Locus @5 07 |
|---|
| C03 | 05 | X | ENG | @0 Locus @5 07 |
|---|
| C03 | 05 | X | SPA | @0 Locus @5 07 |
|---|
| C03 | 06 | X | FRE | @0 Génotype @5 08 |
|---|
| C03 | 06 | X | ENG | @0 Genotype @5 08 |
|---|
| C03 | 06 | X | SPA | @0 Genotipo @5 08 |
|---|
| C03 | 07 | X | FRE | @0 Liaison génétique @5 10 |
|---|
| C03 | 07 | X | ENG | @0 Linkage @5 10 |
|---|
| C03 | 07 | X | SPA | @0 Ligamiento genético @5 10 |
|---|
| C03 | 08 | X | FRE | @0 Etude familiale @5 17 |
|---|
| C03 | 08 | X | ENG | @0 Family study @5 17 |
|---|
| C03 | 08 | X | SPA | @0 Estudio familiar @5 17 |
|---|
| C03 | 09 | X | FRE | @0 Déterminisme génétique @5 18 |
|---|
| C03 | 09 | X | ENG | @0 Genetic determinism @5 18 |
|---|
| C03 | 09 | X | SPA | @0 Determinismo genético @5 18 |
|---|
| C03 | 10 | X | FRE | @0 Biologie moléculaire @5 19 |
|---|
| C03 | 10 | X | ENG | @0 Molecular biology @5 19 |
|---|
| C03 | 10 | X | SPA | @0 Biología molecular @5 19 |
|---|
| C03 | 11 | X | FRE | @0 Homme @5 20 |
|---|
| C03 | 11 | X | ENG | @0 Human @5 20 |
|---|
| C03 | 11 | X | SPA | @0 Hombre @5 20 |
|---|
| 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 Trouble neurologique @5 38 |
|---|
| C07 | 02 | X | ENG | @0 Neurological disorder @5 38 |
|---|
| C07 | 02 | X | SPA | @0 Trastorno neurológico @5 38 |
|---|
| C07 | 03 | X | FRE | @0 Mouvement involontaire @5 39 |
|---|
| C07 | 03 | X | ENG | @0 Involuntary movement @5 39 |
|---|
| C07 | 03 | X | SPA | @0 Movimiento involuntario @5 39 |
|---|
| C07 | 04 | X | FRE | @0 Maladie héréditaire @5 40 |
|---|
| C07 | 04 | X | ENG | @0 Genetic disease @5 40 |
|---|
| C07 | 04 | X | SPA | @0 Enfermedad hereditaria @5 40 |
|---|
| C07 | 05 | X | FRE | @0 Génétique @5 61 |
|---|
| C07 | 05 | X | ENG | @0 Genetics @5 61 |
|---|
| C07 | 05 | X | SPA | @0 Genética @5 61 |
|---|
| N21 | | | | @1 318 |
|---|
|
|---|
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Le document en format XML
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<author><name sortKey="Illarioshkin, Sergei N" sort="Illarioshkin, Sergei N" uniqKey="Illarioshkin S" first="Sergei N." last="Illarioshkin">Sergei N. Illarioshkin</name>
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<s2>Moscow</s2>
<s3>RUS</s3>
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<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
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</affiliation><author><name sortKey="Ivanova Smolenskaya, Irina A" sort="Ivanova Smolenskaya, Irina A" uniqKey="Ivanova Smolenskaya I" first="Irina A." last="Ivanova-Smolenskaya">Irina A. Ivanova-Smolenskaya</name>
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</inist:fA14><country>France</country>
</affiliation><author><name sortKey="Brice, Alexis" sort="Brice, Alexis" uniqKey="Brice A" first="Alexis" last="Brice">Alexis Brice</name>
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<idno type="RBID">Pascal:00-0480444</idno>
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<idno type="wicri:Area/PascalFrancis/Curation">000177</idno>
</publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan</title>
<author><name sortKey="Illarioshkin, Sergei N" sort="Illarioshkin, Sergei N" uniqKey="Illarioshkin S" first="Sergei N." last="Illarioshkin">Sergei N. Illarioshkin</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14><country>Russie</country>
</affiliation><author><name sortKey="Ivanova Smolenskaya, Irina A" sort="Ivanova Smolenskaya, Irina A" uniqKey="Ivanova Smolenskaya I" first="Irina A." last="Ivanova-Smolenskaya">Irina A. Ivanova-Smolenskaya</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14><country>Russie</country>
</affiliation><author><name sortKey="Rahmonov, Rahmatullo A" sort="Rahmonov, Rahmatullo A" uniqKey="Rahmonov R" first="Rahmatullo A." last="Rahmonov">Rahmatullo A. Rahmonov</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14><country>Russie</country>
</affiliation><author><name sortKey="Markova, Elena D" sort="Markova, Elena D" uniqKey="Markova E" first="Elena D." last="Markova">Elena D. Markova</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14><country>Russie</country>
</affiliation><author><name sortKey="Stevanin, Giovanni" sort="Stevanin, Giovanni" uniqKey="Stevanin G" first="Giovanni" last="Stevanin">Giovanni Stevanin</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>INSERM U289, Hôpital de la Salpêtrière</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14><country>France</country>
</affiliation><author><name sortKey="Brice, Alexis" sort="Brice, Alexis" uniqKey="Brice A" first="Alexis" last="Brice">Alexis Brice</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>INSERM U289, Hôpital de la Salpêtrière</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14><country>France</country>
</affiliation><series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2000">2000</date>
</imprint><seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Essential</term>
<term>Family study</term>
<term>Gene</term>
<term>Genetic determinism</term>
<term>Genotype</term>
<term>Heterogeneity</term>
<term>Human</term>
<term>Linkage</term>
<term>Locus</term>
<term>Molecular biology</term>
<term>Tremor</term>
</keywords><keywords scheme="Pascal" xml:lang="fr"><term>Tremblement</term>
<term>Essentiel</term>
<term>Hétérogénéité</term>
<term>Gène</term>
<term>Locus</term>
<term>Génotype</term>
<term>Liaison génétique</term>
<term>Etude familiale</term>
<term>Déterminisme génétique</term>
<term>Biologie moléculaire</term>
<term>Homme</term>
</keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
</keywords><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0885-3185</s0>
</fA01><fA03 i2="1"><s0>Mov. disord.</s0>
</fA03><fA08 i1="01" i2="1" l="ENG"><s1>Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan</s1>
</fA08><fA11 i1="01" i2="1"><s1>ILLARIOSHKIN (Sergei N.)</s1>
</fA11><fA11 i1="02" i2="1"><s1>IVANOVA-SMOLENSKAYA (Irina A.)</s1>
</fA11><fA11 i1="03" i2="1"><s1>RAHMONOV (Rahmatullo A.)</s1>
</fA11><fA11 i1="04" i2="1"><s1>MARKOVA (Elena D.)</s1>
</fA11><fA11 i1="05" i2="1"><s1>STEVANIN (Giovanni)</s1>
</fA11><fA11 i1="06" i2="1"><s1>BRICE (Alexis)</s1>
</fA11><fA14 i1="01"><s1>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences</s1>
<s2>Moscow</s2>
<s3>RUS</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14><fA14 i1="02"><s1>INSERM U289, Hôpital de la Salpêtrière</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14><fA20><s1>1020-1023</s1>
</fA20><fA21><s1>2000</s1>
</fA21><fA23 i1="01"><s0>ENG</s0>
</fA23><fA43 i1="01"><s1>INIST</s1>
<s2>20953</s2>
<s5>354000091356830430</s5>
</fA43><fA44><s0>0000</s0>
<s1>© 2000 INIST-CNRS. All rights reserved.</s1>
</fA44><fA45><s0>17 ref.</s0>
</fA45><fA47 i1="01" i2="1"><s0>00-0480444</s0>
</fA47><fA64 i1="01" i2="1"><s0>Movement disorders</s0>
</fA64><fA66 i1="01"><s0>USA</s0>
</fA66><fC02 i1="01" i2="X"><s0>002B17A01</s0>
</fC02><fC03 i1="01" i2="X" l="FRE"><s0>Tremblement</s0>
<s5>01</s5>
</fC03><fC03 i1="01" i2="X" l="ENG"><s0>Tremor</s0>
<s5>01</s5>
</fC03><fC03 i1="01" i2="X" l="SPA"><s0>Temblor</s0>
<s5>01</s5>
</fC03><fC03 i1="02" i2="X" l="FRE"><s0>Essentiel</s0>
<s5>02</s5>
</fC03><fC03 i1="02" i2="X" l="ENG"><s0>Essential</s0>
<s5>02</s5>
</fC03><fC03 i1="02" i2="X" l="SPA"><s0>Esencial</s0>
<s5>02</s5>
</fC03><fC03 i1="03" i2="X" l="FRE"><s0>Hétérogénéité</s0>
<s5>04</s5>
</fC03><fC03 i1="03" i2="X" l="ENG"><s0>Heterogeneity</s0>
<s5>04</s5>
</fC03><fC03 i1="03" i2="X" l="SPA"><s0>Heterogeneidad</s0>
<s5>04</s5>
</fC03><fC03 i1="04" i2="X" l="FRE"><s0>Gène</s0>
<s5>05</s5>
</fC03><fC03 i1="04" i2="X" l="ENG"><s0>Gene</s0>
<s5>05</s5>
</fC03><fC03 i1="04" i2="X" l="SPA"><s0>Gen</s0>
<s5>05</s5>
</fC03><fC03 i1="05" i2="X" l="FRE"><s0>Locus</s0>
<s5>07</s5>
</fC03><fC03 i1="05" i2="X" l="ENG"><s0>Locus</s0>
<s5>07</s5>
</fC03><fC03 i1="05" i2="X" l="SPA"><s0>Locus</s0>
<s5>07</s5>
</fC03><fC03 i1="06" i2="X" l="FRE"><s0>Génotype</s0>
<s5>08</s5>
</fC03><fC03 i1="06" i2="X" l="ENG"><s0>Genotype</s0>
<s5>08</s5>
</fC03><fC03 i1="06" i2="X" l="SPA"><s0>Genotipo</s0>
<s5>08</s5>
</fC03><fC03 i1="07" i2="X" l="FRE"><s0>Liaison génétique</s0>
<s5>10</s5>
</fC03><fC03 i1="07" i2="X" l="ENG"><s0>Linkage</s0>
<s5>10</s5>
</fC03><fC03 i1="07" i2="X" l="SPA"><s0>Ligamiento genético</s0>
<s5>10</s5>
</fC03><fC03 i1="08" i2="X" l="FRE"><s0>Etude familiale</s0>
<s5>17</s5>
</fC03><fC03 i1="08" i2="X" l="ENG"><s0>Family study</s0>
<s5>17</s5>
</fC03><fC03 i1="08" i2="X" l="SPA"><s0>Estudio familiar</s0>
<s5>17</s5>
</fC03><fC03 i1="09" i2="X" l="FRE"><s0>Déterminisme génétique</s0>
<s5>18</s5>
</fC03><fC03 i1="09" i2="X" l="ENG"><s0>Genetic determinism</s0>
<s5>18</s5>
</fC03><fC03 i1="09" i2="X" l="SPA"><s0>Determinismo genético</s0>
<s5>18</s5>
</fC03><fC03 i1="10" i2="X" l="FRE"><s0>Biologie moléculaire</s0>
<s5>19</s5>
</fC03><fC03 i1="10" i2="X" l="ENG"><s0>Molecular biology</s0>
<s5>19</s5>
</fC03><fC03 i1="10" i2="X" l="SPA"><s0>Biología molecular</s0>
<s5>19</s5>
</fC03><fC03 i1="11" i2="X" l="FRE"><s0>Homme</s0>
<s5>20</s5>
</fC03><fC03 i1="11" i2="X" l="ENG"><s0>Human</s0>
<s5>20</s5>
</fC03><fC03 i1="11" i2="X" l="SPA"><s0>Hombre</s0>
<s5>20</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>Trouble neurologique</s0>
<s5>38</s5>
</fC07><fC07 i1="02" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>38</s5>
</fC07><fC07 i1="02" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>38</s5>
</fC07><fC07 i1="03" i2="X" l="FRE"><s0>Mouvement involontaire</s0>
<s5>39</s5>
</fC07><fC07 i1="03" i2="X" l="ENG"><s0>Involuntary movement</s0>
<s5>39</s5>
</fC07><fC07 i1="03" i2="X" l="SPA"><s0>Movimiento involuntario</s0>
<s5>39</s5>
</fC07><fC07 i1="04" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>40</s5>
</fC07><fC07 i1="04" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>40</s5>
</fC07><fC07 i1="04" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>40</s5>
</fC07><fC07 i1="05" i2="X" l="FRE"><s0>Génétique</s0>
<s5>61</s5>
</fC07><fC07 i1="05" i2="X" l="ENG"><s0>Genetics</s0>
<s5>61</s5>
</fC07><fC07 i1="05" i2="X" l="SPA"><s0>Genética</s0>
<s5>61</s5>
</fC07><fN21><s1>318</s1>
</fN21>
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