Progressive dystonia in Mohr-Tranebjaerg syndrome with cochlear implant and deep brain stimulation.
Identifieur interne : 000061 ( France/Analysis ); précédent : 000060; suivant : 000062Progressive dystonia in Mohr-Tranebjaerg syndrome with cochlear implant and deep brain stimulation.
Auteurs : Laura Cif [France] ; Victoria Gonzalez ; Sara Garcia-Ptacek ; Syril James ; Julien Boetto ; Anne Seychelles ; Thomas Roujeau ; Ana Maria Moura De Ribeiro ; Martine Sillon ; Michel Mondain ; Philippe CoubesSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- Child, Preschool, Cochlear Implants, Deaf-Blind Disorders (complications), Deaf-Blind Disorders (diagnosis), Deaf-Blind Disorders (genetics), Deaf-Blind Disorders (therapy), Deep Brain Stimulation (methods), Dystonia (complications), Dystonia (diagnosis), Dystonia (genetics), Dystonia (therapy), Globus Pallidus (physiology), Humans, Intellectual Disability (complications), Intellectual Disability (diagnosis), Intellectual Disability (genetics), Intellectual Disability (therapy), Male, Membrane Transport Proteins (genetics), Optic Atrophy (complications), Optic Atrophy (diagnosis), Optic Atrophy (genetics), Optic Atrophy (therapy), Tomography, X-Ray Computed.
- MESH :
- chemical , genetics : Membrane Transport Proteins.
- complications : Deaf-Blind Disorders, Dystonia, Intellectual Disability, Optic Atrophy.
- diagnosis : Deaf-Blind Disorders, Dystonia, Intellectual Disability, Optic Atrophy.
- genetics : Deaf-Blind Disorders, Dystonia, Intellectual Disability, Optic Atrophy.
- methods : Deep Brain Stimulation.
- physiology : Globus Pallidus.
- therapy : Deaf-Blind Disorders, Dystonia, Intellectual Disability, Optic Atrophy.
- Child, Preschool, Cochlear Implants, Humans, Male, Tomography, X-Ray Computed.
DOI: 10.1002/mds.25519
PubMed: 23801560
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream PubMed, to step Checkpoint: 000839
- to stream Ncbi, to step Merge: 003C14
- to stream Ncbi, to step Curation: 003C14
- to stream Ncbi, to step Checkpoint: 003C14
- to stream Main, to step Merge: 000822
- to stream Main, to step Curation: 000822
- to stream Main, to step Exploration: 000822
- to stream France, to step Extraction: 000061
Links to Exploration step
pubmed:23801560Le document en format XML
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<author><name sortKey="Gonzalez, Victoria" sort="Gonzalez, Victoria" uniqKey="Gonzalez V" first="Victoria" last="Gonzalez">Victoria Gonzalez</name>
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<author><name sortKey="Garcia Ptacek, Sara" sort="Garcia Ptacek, Sara" uniqKey="Garcia Ptacek S" first="Sara" last="Garcia-Ptacek">Sara Garcia-Ptacek</name>
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<author><name sortKey="James, Syril" sort="James, Syril" uniqKey="James S" first="Syril" last="James">Syril James</name>
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<author><name sortKey="Boetto, Julien" sort="Boetto, Julien" uniqKey="Boetto J" first="Julien" last="Boetto">Julien Boetto</name>
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<author><name sortKey="Seychelles, Anne" sort="Seychelles, Anne" uniqKey="Seychelles A" first="Anne" last="Seychelles">Anne Seychelles</name>
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<author><name sortKey="Roujeau, Thomas" sort="Roujeau, Thomas" uniqKey="Roujeau T" first="Thomas" last="Roujeau">Thomas Roujeau</name>
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<author><name sortKey="Moura De Ribeiro, Ana Maria" sort="Moura De Ribeiro, Ana Maria" uniqKey="Moura De Ribeiro A" first="Ana Maria" last="Moura De Ribeiro">Ana Maria Moura De Ribeiro</name>
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<author><name sortKey="Coubes, Philippe" sort="Coubes, Philippe" uniqKey="Coubes P" first="Philippe" last="Coubes">Philippe Coubes</name>
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<author><name sortKey="Boetto, Julien" sort="Boetto, Julien" uniqKey="Boetto J" first="Julien" last="Boetto">Julien Boetto</name>
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<author><name sortKey="Seychelles, Anne" sort="Seychelles, Anne" uniqKey="Seychelles A" first="Anne" last="Seychelles">Anne Seychelles</name>
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<author><name sortKey="Roujeau, Thomas" sort="Roujeau, Thomas" uniqKey="Roujeau T" first="Thomas" last="Roujeau">Thomas Roujeau</name>
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<term>Deaf-Blind Disorders (diagnosis)</term>
<term>Deaf-Blind Disorders (genetics)</term>
<term>Deaf-Blind Disorders (therapy)</term>
<term>Deep Brain Stimulation (methods)</term>
<term>Dystonia (complications)</term>
<term>Dystonia (diagnosis)</term>
<term>Dystonia (genetics)</term>
<term>Dystonia (therapy)</term>
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<term>Intellectual Disability (diagnosis)</term>
<term>Intellectual Disability (genetics)</term>
<term>Intellectual Disability (therapy)</term>
<term>Male</term>
<term>Membrane Transport Proteins (genetics)</term>
<term>Optic Atrophy (complications)</term>
<term>Optic Atrophy (diagnosis)</term>
<term>Optic Atrophy (genetics)</term>
<term>Optic Atrophy (therapy)</term>
<term>Tomography, X-Ray Computed</term>
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<term>Dystonia</term>
<term>Intellectual Disability</term>
<term>Optic Atrophy</term>
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<term>Dystonia</term>
<term>Intellectual Disability</term>
<term>Optic Atrophy</term>
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<term>Dystonia</term>
<term>Intellectual Disability</term>
<term>Optic Atrophy</term>
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<name sortKey="Moura De Ribeiro, Ana Maria" sort="Moura De Ribeiro, Ana Maria" uniqKey="Moura De Ribeiro A" first="Ana Maria" last="Moura De Ribeiro">Ana Maria Moura De Ribeiro</name>
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