MovDisordV3, PascalFrancis, Checkpoint, bibRecord, 001617

Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions

Identifieur interne : 001617 ( PascalFrancis/Checkpoint ); précédent : 001616; suivant : 001618

Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions

Auteurs : Robert A. Wilcox [Australie] ; Andrew Churchyard [Australie] ; Henrik H. Dahl [Australie] ; Wendy M. Hutchison [Australie] ; Denise M. Kirby [Australie] ; Dominic Thyagarajan [Australie]

Source :

Movement disorders [ 0885-3185 ] ; 2007.

RBID : Pascal:07-0314961

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Parkinsonisme, Délétion, Cytopathie mitochondriale, Parkinson maladie, Ophtalmoplégie, Lévodopa, DNA mitochondrial, Chronique, Neuropathie, Réponse multiple.

English descriptors

KwdEn :
- Chronic, Deletion, Levodopa, Mitochondrial DNA, Mitochondrial disorder, Nervous system diseases, Neuropathy, Ophthalmoplegia, Parkinson disease, Parkinsonism.

Abstract

We report a patient with an autosomal dominant chronic progressive external ophthalmoplegia phenotype associated with multiple mtDNA deletions in muscle from a family in which linkage analysis excluded mutations in DNA polymerase (POLG), adenine nucleotide translocase (ANT-1) or C10orf2 (Twinkle). She presented with prominent Parkinsonism characterized by prolonged benefit from levodopa (L-dopa) and the later development of L-dopa induced dyskinesias and motor fluctuations. Thus L-dopa responsiveness, L-dopa induced dyskinesias and motor fluctuations may also occur in atypical Parkinsonism of mitochondrial disease, just as they may in multiple system atrophy.

Affiliations:

Australie

Links toward previous steps (curation, corpus...)

to stream PascalFrancis, to step Corpus: 001662
to stream PascalFrancis, to step Curation: 001659

Links to Exploration step

Pascal:07-0314961

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions</title>
<author><name sortKey="Wilcox, Robert A" sort="Wilcox, Robert A" uniqKey="Wilcox R" first="Robert A." last="Wilcox">Robert A. Wilcox</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Flinders Medical Centre</s1>
<s2>SA</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>SA</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Churchyard, Andrew" sort="Churchyard, Andrew" uniqKey="Churchyard A" first="Andrew" last="Churchyard">Andrew Churchyard</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Cabini Medical Centre</s1>
<s2>Malvern, Victoria</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Cabini Medical Centre</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Dahl, Henrik H" sort="Dahl, Henrik H" uniqKey="Dahl H" first="Henrik H." last="Dahl">Henrik H. Dahl</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Parkville, Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Hutchison, Wendy M" sort="Hutchison, Wendy M" uniqKey="Hutchison W" first="Wendy M." last="Hutchison">Wendy M. Hutchison</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Parkville, Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Kirby, Denise M" sort="Kirby, Denise M" uniqKey="Kirby D" first="Denise M." last="Kirby">Denise M. Kirby</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Parkville, Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Thyagarajan, Dominic" sort="Thyagarajan, Dominic" uniqKey="Thyagarajan D" first="Dominic" last="Thyagarajan">Dominic Thyagarajan</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Flinders Medical Centre</s1>
<s2>SA</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>SA</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">07-0314961</idno>
<date when="2007">2007</date>
<idno type="stanalyst">PASCAL 07-0314961 INIST</idno>
<idno type="RBID">Pascal:07-0314961</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">001662</idno>
<idno type="wicri:Area/PascalFrancis/Curation">001659</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">001617</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions</title>
<author><name sortKey="Wilcox, Robert A" sort="Wilcox, Robert A" uniqKey="Wilcox R" first="Robert A." last="Wilcox">Robert A. Wilcox</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Flinders Medical Centre</s1>
<s2>SA</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>SA</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Churchyard, Andrew" sort="Churchyard, Andrew" uniqKey="Churchyard A" first="Andrew" last="Churchyard">Andrew Churchyard</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Cabini Medical Centre</s1>
<s2>Malvern, Victoria</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Cabini Medical Centre</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Dahl, Henrik H" sort="Dahl, Henrik H" uniqKey="Dahl H" first="Henrik H." last="Dahl">Henrik H. Dahl</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Parkville, Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Hutchison, Wendy M" sort="Hutchison, Wendy M" uniqKey="Hutchison W" first="Wendy M." last="Hutchison">Wendy M. Hutchison</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Parkville, Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Kirby, Denise M" sort="Kirby, Denise M" uniqKey="Kirby D" first="Denise M." last="Kirby">Denise M. Kirby</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>Parkville, Melbourne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Thyagarajan, Dominic" sort="Thyagarajan, Dominic" uniqKey="Thyagarajan D" first="Dominic" last="Thyagarajan">Dominic Thyagarajan</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Flinders Medical Centre</s1>
<s2>SA</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
<country>Australie</country>
<wicri:noRegion>SA</wicri:noRegion>
</affiliation>
</author>
</analytic>
<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="2007">2007</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chronic</term>
<term>Deletion</term>
<term>Levodopa</term>
<term>Mitochondrial DNA</term>
<term>Mitochondrial disorder</term>
<term>Nervous system diseases</term>
<term>Neuropathy</term>
<term>Ophthalmoplegia</term>
<term>Parkinson disease</term>
<term>Parkinsonism</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Parkinsonisme</term>
<term>Délétion</term>
<term>Cytopathie mitochondriale</term>
<term>Parkinson maladie</term>
<term>Ophtalmoplégie</term>
<term>Lévodopa</term>
<term>DNA mitochondrial</term>
<term>Chronique</term>
<term>Neuropathie</term>
<term>Réponse multiple</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We report a patient with an autosomal dominant chronic progressive external ophthalmoplegia phenotype associated with multiple mtDNA deletions in muscle from a family in which linkage analysis excluded mutations in DNA polymerase (POLG), adenine nucleotide translocase (ANT-1) or C10orf2 (Twinkle). She presented with prominent Parkinsonism characterized by prolonged benefit from levodopa (L-dopa) and the later development of L-dopa induced dyskinesias and motor fluctuations. Thus L-dopa responsiveness, L-dopa induced dyskinesias and motor fluctuations may also occur in atypical Parkinsonism of mitochondrial disease, just as they may in multiple system atrophy.</div>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0885-3185</s0>
</fA01>
<fA03 i2="1"><s0>Mov. disord.</s0>
</fA03>
<fA05><s2>22</s2>
</fA05>
<fA06><s2>7</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>WILCOX (Robert A.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>CHURCHYARD (Andrew)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>DAHL (Henrik H.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>HUTCHISON (Wendy M.)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>KIRBY (Denise M.)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>THYAGARAJAN (Dominic)</s1>
</fA11>
<fA14 i1="01"><s1>Department of Neurology, Flinders Medical Centre</s1>
<s2>SA</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Cabini Medical Centre</s1>
<s2>Malvern, Victoria</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Department of Paediatrics, The Murdoch Childrens Research Institute and University of Melbourne, Royal Children's Hospital</s1>
<s2>Parkville, Melbourne</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA20><s1>1020-1023</s1>
</fA20>
<fA21><s1>2007</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>20953</s2>
<s5>354000149881420190</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2007 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>13 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>07-0314961</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Movement disorders</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>We report a patient with an autosomal dominant chronic progressive external ophthalmoplegia phenotype associated with multiple mtDNA deletions in muscle from a family in which linkage analysis excluded mutations in DNA polymerase (POLG), adenine nucleotide translocase (ANT-1) or C10orf2 (Twinkle). She presented with prominent Parkinsonism characterized by prolonged benefit from levodopa (L-dopa) and the later development of L-dopa induced dyskinesias and motor fluctuations. Thus L-dopa responsiveness, L-dopa induced dyskinesias and motor fluctuations may also occur in atypical Parkinsonism of mitochondrial disease, just as they may in multiple system atrophy.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B17</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B17F</s0>
</fC02>
<fC02 i1="03" i2="X"><s0>002B17G</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Parkinsonisme</s0>
<s2>NM</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Parkinsonism</s0>
<s2>NM</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Parkinson síndrome</s0>
<s2>NM</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Délétion</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Deletion</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Deleción</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Cytopathie mitochondriale</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Mitochondrial disorder</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Citopatía mitocondrial</s0>
<s2>NM</s2>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Parkinson maladie</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Parkinson disease</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Parkinson enfermedad</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Ophtalmoplégie</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Ophthalmoplegia</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Oftalmoplejía</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Lévodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Levodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Levodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>DNA mitochondrial</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Mitochondrial DNA</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>DNA mitocondrial</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Chronique</s0>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Chronic</s0>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Crónico</s0>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Neuropathie</s0>
<s5>12</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Neuropathy</s0>
<s5>12</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Neuropatía</s0>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Réponse multiple</s0>
<s4>INC</s4>
<s5>86</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Enzymopathie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Enzymopathy</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Enzimopatía</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Métabolisme pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Metabolic diseases</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Metabolismo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>43</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Oculomotricité syndrome</s0>
<s5>44</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Oculomotor syndrome</s0>
<s5>44</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Oculomotricidad síndrome</s0>
<s5>44</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Oeil pathologie</s0>
<s5>45</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Eye disease</s0>
<s5>45</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Ojo patología</s0>
<s5>45</s5>
</fC07>
<fN21><s1>204</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
<affiliations><list><country><li>Australie</li>
</country>
</list>
<tree><country name="Australie"><noRegion><name sortKey="Wilcox, Robert A" sort="Wilcox, Robert A" uniqKey="Wilcox R" first="Robert A." last="Wilcox">Robert A. Wilcox</name>
</noRegion>
<name sortKey="Churchyard, Andrew" sort="Churchyard, Andrew" uniqKey="Churchyard A" first="Andrew" last="Churchyard">Andrew Churchyard</name>
<name sortKey="Dahl, Henrik H" sort="Dahl, Henrik H" uniqKey="Dahl H" first="Henrik H." last="Dahl">Henrik H. Dahl</name>
<name sortKey="Hutchison, Wendy M" sort="Hutchison, Wendy M" uniqKey="Hutchison W" first="Wendy M." last="Hutchison">Wendy M. Hutchison</name>
<name sortKey="Kirby, Denise M" sort="Kirby, Denise M" uniqKey="Kirby D" first="Denise M." last="Kirby">Denise M. Kirby</name>
<name sortKey="Thyagarajan, Dominic" sort="Thyagarajan, Dominic" uniqKey="Thyagarajan D" first="Dominic" last="Thyagarajan">Dominic Thyagarajan</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PascalFrancis/Checkpoint

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001617 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Checkpoint/biblio.hfd -nk 001617 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    PascalFrancis
   |étape=   Checkpoint
   |type=    RBID
   |clé=     Pascal:07-0314961
   |texte=   Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions
}}

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions

Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri