La maladie de Parkinson au Canada (serveur d'exploration)

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Genome-wide scan for Parkinson's disease: The genePD Study

Identifieur interne : 000113 ( PascalFrancis/Curation ); précédent : 000112; suivant : 000114

Genome-wide scan for Parkinson's disease: The genePD Study

Auteurs : A. L. Destefano [États-Unis] ; L. I. Golbe [États-Unis] ; M. H. Mark [États-Unis] ; A. M. Lazzarini [États-Unis] ; N. E. Maher [États-Unis] ; M. Saint-Hilaire [États-Unis] ; R. G. Feldman [États-Unis] ; M. Guttman [États-Unis] ; R. L. Watts [États-Unis] ; O. Suchowersky [Canada] ; A. L. Lafontaine [Canada] ; N. Labelle [Canada] ; M. F. Lew [États-Unis] ; C. H. Waters [États-Unis] ; J. H. Growdon [États-Unis] ; C. Singer [États-Unis] ; L. J. Currie [États-Unis] ; G. F. Wooten [États-Unis] ; P. Vieregge [Allemagne] ; P. P. Pramstaller [Italie] ; C. Klein [Allemagne] ; J. P. Hubble [États-Unis] ; M. Stacy [États-Unis] ; E. Montgomery [États-Unis] ; M. E. Macdonald [États-Unis] ; J. F. Gusella [États-Unis] ; R. H. Myers [États-Unis]

Source :

RBID : Pascal:02-0020721

Descripteurs français

English descriptors

Abstract

Article abstract-A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine β-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.
pA  
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A03   1    @0 Neurology
A05       @2 57
A06       @2 6
A08 01  1  ENG  @1 Genome-wide scan for Parkinson's disease: The genePD Study
A11 01  1    @1 DESTEFANO (A. L.)
A11 02  1    @1 GOLBE (L. I.)
A11 03  1    @1 MARK (M. H.)
A11 04  1    @1 LAZZARINI (A. M.)
A11 05  1    @1 MAHER (N. E.)
A11 06  1    @1 SAINT-HILAIRE (M.)
A11 07  1    @1 FELDMAN (R. G.)
A11 08  1    @1 GUTTMAN (M.)
A11 09  1    @1 WATTS (R. L.)
A11 10  1    @1 SUCHOWERSKY (O.)
A11 11  1    @1 LAFONTAINE (A. L.)
A11 12  1    @1 LABELLE (N.)
A11 13  1    @1 LEW (M. F.)
A11 14  1    @1 WATERS (C. H.)
A11 15  1    @1 GROWDON (J. H.)
A11 16  1    @1 SINGER (C.)
A11 17  1    @1 CURRIE (L. J.)
A11 18  1    @1 WOOTEN (G. F.)
A11 19  1    @1 VIEREGGE (P.)
A11 20  1    @1 PRAMSTALLER (P. P.)
A11 21  1    @1 KLEIN (C.)
A11 22  1    @1 HUBBLE (J. P.)
A11 23  1    @1 STACY (M.)
A11 24  1    @1 MONTGOMERY (E.)
A11 25  1    @1 MACDONALD (M. E.)
A11 26  1    @1 GUSELLA (J. F.)
A11 27  1    @1 MYERS (R. H.)
A14 01      @1 Department of Neurology, Boston University Schools of Medicine and of Public Health @2 Boston, MA @3 USA @Z 1 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 27 aut.
A14 02      @1 Department of Epidemiology and Biostatistics, Boston University Schools of Medicine and of Public Health @2 Boston, MA @3 USA @Z 1 aut.
A14 03      @1 Department of Neurology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School @2 New Brunswick @3 USA @Z 2 aut. @Z 3 aut. @Z 4 aut.
A14 04      @1 Division of Neurology, Department of Medicine, University of Toronto, @2 Ontario @3 USA @Z 8 aut.
A14 05      @1 Department of Neurology, Emory University School of Medicine @2 Atlanta, GA @3 USA @Z 9 aut.
A14 06      @1 Departments of Clinical Neurosciences and Medical Genetics, University of Calgary @2 Alberta @3 CAN @Z 10 aut. @Z 11 aut. @Z 12 aut.
A14 07      @1 Department of Neurology, University of Southern California @2 Los Angeles @3 USA @Z 13 aut. @Z 14 aut.
A14 08      @1 Department of Neurology, Massachusetts General Hospital, Harvard Medical School @2 Boston, MA @3 USA @Z 15 aut. @Z 25 aut. @Z 26 aut.
A14 09      @1 Department of Neurology, University of Miami @2 FL @3 USA @Z 16 aut.
A14 10      @1 Department of Neurology, University of Virginia Health System @2 Charlottesville @3 USA @Z 17 aut. @Z 18 aut.
A14 11      @1 Department of Neurology, Medical University of Lübeck @3 DEU @Z 19 aut. @Z 21 aut.
A14 12      @1 Department of Neurology, General Regional Hospital Bolzano @3 ITA @Z 20 aut.
A14 13      @1 Department of Neurology, Ohio State University @2 Columbus @3 USA @Z 22 aut.
A14 14      @1 Department of Neurology, Barrow Clinic @2 Phoenix, AZ @3 USA @Z 23 aut.
A14 15      @1 Departments of Neurology and Neuroscience, Cleveland Clinic Foundation @2 OH @3 USA @Z 24 aut.
A20       @1 1124-1126
A21       @1 2001
A23 01      @0 ENG
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C01 01    ENG  @0 Article abstract-A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine β-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.
C02 01  X    @0 002B17G
C03 01  X  FRE  @0 Parkinson maladie @5 01
C03 01  X  ENG  @0 Parkinson disease @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @5 01
C03 02  X  FRE  @0 Idiopathique @5 02
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C03 02  X  SPA  @0 Idiopático @5 02
C03 03  X  FRE  @0 Liaison génétique @5 04
C03 03  X  ENG  @0 Linkage @5 04
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C03 04  X  FRE  @0 Chromosome C9 @5 07
C03 04  X  ENG  @0 Chromosome C9 @5 07
C03 04  X  SPA  @0 Cromosoma C9 @5 07
C03 05  X  FRE  @0 Etude familiale @5 16
C03 05  X  ENG  @0 Family study @5 16
C03 05  X  SPA  @0 Estudio familiar @5 16
C03 06  X  FRE  @0 Exploration @5 17
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C07 01  X  SPA  @0 Sistema nervioso patología @5 37
C07 02  X  FRE  @0 Système nerveux central pathologie @5 38
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C07 02  X  SPA  @0 Sistema nervosio central patología @5 38
C07 03  X  FRE  @0 Encéphale pathologie @5 39
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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 Génétique @5 45
C07 06  X  ENG  @0 Genetics @5 45
C07 06  X  SPA  @0 Genética @5 45
N21       @1 007

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Pascal:02-0020721

Le document en format XML

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<s1>Department of Neurology, Massachusetts General Hospital, Harvard Medical School</s1>
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<s1>Department of Neurology, University of Southern California</s1>
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<s1>Department of Neurology, Ohio State University</s1>
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<title level="j" type="main">Neurology</title>
<title level="j" type="abbreviated">Neurology</title>
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<title level="j" type="main">Neurology</title>
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<term>Chromosome C9</term>
<term>Exploration</term>
<term>Family study</term>
<term>Human</term>
<term>Idiopathic</term>
<term>Linkage</term>
<term>Parkinson disease</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Parkinson maladie</term>
<term>Idiopathique</term>
<term>Liaison génétique</term>
<term>Chromosome C9</term>
<term>Etude familiale</term>
<term>Exploration</term>
<term>Homme</term>
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<div type="abstract" xml:lang="en">Article abstract-A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine β-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.</div>
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<s2>New Brunswick</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>Division of Neurology, Department of Medicine, University of Toronto,</s1>
<s2>Ontario</s2>
<s3>USA</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>Department of Neurology, Emory University School of Medicine</s1>
<s2>Atlanta, GA</s2>
<s3>USA</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="06">
<s1>Departments of Clinical Neurosciences and Medical Genetics, University of Calgary</s1>
<s2>Alberta</s2>
<s3>CAN</s3>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
<sZ>12 aut.</sZ>
</fA14>
<fA14 i1="07">
<s1>Department of Neurology, University of Southern California</s1>
<s2>Los Angeles</s2>
<s3>USA</s3>
<sZ>13 aut.</sZ>
<sZ>14 aut.</sZ>
</fA14>
<fA14 i1="08">
<s1>Department of Neurology, Massachusetts General Hospital, Harvard Medical School</s1>
<s2>Boston, MA</s2>
<s3>USA</s3>
<sZ>15 aut.</sZ>
<sZ>25 aut.</sZ>
<sZ>26 aut.</sZ>
</fA14>
<fA14 i1="09">
<s1>Department of Neurology, University of Miami</s1>
<s2>FL</s2>
<s3>USA</s3>
<sZ>16 aut.</sZ>
</fA14>
<fA14 i1="10">
<s1>Department of Neurology, University of Virginia Health System</s1>
<s2>Charlottesville</s2>
<s3>USA</s3>
<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
</fA14>
<fA14 i1="11">
<s1>Department of Neurology, Medical University of Lübeck</s1>
<s3>DEU</s3>
<sZ>19 aut.</sZ>
<sZ>21 aut.</sZ>
</fA14>
<fA14 i1="12">
<s1>Department of Neurology, General Regional Hospital Bolzano</s1>
<s3>ITA</s3>
<sZ>20 aut.</sZ>
</fA14>
<fA14 i1="13">
<s1>Department of Neurology, Ohio State University</s1>
<s2>Columbus</s2>
<s3>USA</s3>
<sZ>22 aut.</sZ>
</fA14>
<fA14 i1="14">
<s1>Department of Neurology, Barrow Clinic</s1>
<s2>Phoenix, AZ</s2>
<s3>USA</s3>
<sZ>23 aut.</sZ>
</fA14>
<fA14 i1="15">
<s1>Departments of Neurology and Neuroscience, Cleveland Clinic Foundation</s1>
<s2>OH</s2>
<s3>USA</s3>
<sZ>24 aut.</sZ>
</fA14>
<fA20>
<s1>1124-1126</s1>
</fA20>
<fA21>
<s1>2001</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>6345</s2>
<s5>354000099211080390</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2002 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>10 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>02-0020721</s0>
</fA47>
<fA60>
<s1>P</s1>
<s3>CC</s3>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Neurology</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Article abstract-A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine β-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B17G</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Parkinson maladie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Parkinson disease</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Parkinson enfermedad</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Idiopathique</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Idiopathic</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Idiopático</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Liaison génétique</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Linkage</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Ligamiento genético</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Chromosome C9</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Chromosome C9</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Cromosoma C9</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Etude familiale</s0>
<s5>16</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Family study</s0>
<s5>16</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Estudio familiar</s0>
<s5>16</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Exploration</s0>
<s5>17</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Exploration</s0>
<s5>17</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Exploración</s0>
<s5>17</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Homme</s0>
<s5>20</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Human</s0>
<s5>20</s5>
</fC03>
<fC03 i1="07" 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>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>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<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>Génétique</s0>
<s5>45</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Genetics</s0>
<s5>45</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Genética</s0>
<s5>45</s5>
</fC07>
<fN21>
<s1>007</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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