The Asp620Asn Mutation in VPS35 Is Not a Common Cause of Familial Parkinson's Disease
Identifieur interne :
000171 ( PascalFrancis/Corpus );
précédent :
000170;
suivant :
000172
The Asp620Asn Mutation in VPS35 Is Not a Common Cause of Familial Parkinson's Disease
Auteurs : Ilaria Guella ;
Giulia Solda ;
Roberto Cilia ;
Gianni Pezzoli ;
Rosanna Asselta ;
Stefano Duga ;
Stefano GoldwurmSource :
-
Movement disorders [ 0885-3185 ] ; 2012.
RBID : Pascal:12-0248770
Descripteurs français
English descriptors
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
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A08 | 01 | 1 | ENG | @1 The Asp620Asn Mutation in VPS35 Is Not a Common Cause of Familial Parkinson's Disease |
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A11 | 01 | 1 | | @1 GUELLA (Ilaria) |
---|
A11 | 02 | 1 | | @1 SOLDA (Giulia) |
---|
A11 | 03 | 1 | | @1 CILIA (Roberto) |
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A11 | 04 | 1 | | @1 PEZZOLI (Gianni) |
---|
A11 | 05 | 1 | | @1 ASSELTA (Rosanna) |
---|
A11 | 06 | 1 | | @1 DUGA (Stefano) |
---|
A11 | 07 | 1 | | @1 GOLDWURM (Stefano) |
---|
A14 | 01 | | | @1 Dipartimento di Biologia e Genetica per le Scienze Mediche, Università degli Studi di Milano @2 Milan @3 ITA @Z 1 aut. @Z 2 aut. @Z 5 aut. @Z 6 aut. |
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A14 | 02 | | | @1 Parkinson Institute, Istituti Clinici di Perfezionamento @2 Milan @3 ITA @Z 3 aut. @Z 4 aut. @Z 7 aut. |
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A20 | | | | @1 800-801 |
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A43 | 01 | | | @1 INIST @2 20953 @5 354000507771510290 |
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A44 | | | | @0 0000 @1 © 2012 INIST-CNRS. All rights reserved. |
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C03 | 02 | X | FRE | @0 Pathologie du système nerveux @5 02 |
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C03 | 02 | X | ENG | @0 Nervous system diseases @5 02 |
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C03 | 02 | X | SPA | @0 Sistema nervioso patología @5 02 |
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C03 | 03 | X | FRE | @0 Mutation @5 09 |
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C03 | 03 | X | ENG | @0 Mutation @5 09 |
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C03 | 03 | X | SPA | @0 Mutación @5 09 |
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C03 | 04 | X | FRE | @0 Maladie familiale @2 NM @5 10 |
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C03 | 04 | X | ENG | @0 Familial disease @2 NM @5 10 |
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C03 | 04 | X | SPA | @0 Enfermedad familiar @2 NM @5 10 |
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C07 | 01 | X | FRE | @0 Pathologie de l'encéphale @5 37 |
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C07 | 01 | X | ENG | @0 Cerebral disorder @5 37 |
---|
C07 | 01 | X | SPA | @0 Encéfalo patología @5 37 |
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C07 | 02 | X | FRE | @0 Syndrome extrapyramidal @5 38 |
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C07 | 02 | X | ENG | @0 Extrapyramidal syndrome @5 38 |
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C07 | 02 | X | SPA | @0 Extrapiramidal síndrome @5 38 |
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C07 | 03 | X | FRE | @0 Maladie dégénérative @5 39 |
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C07 | 03 | X | ENG | @0 Degenerative disease @5 39 |
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C07 | 03 | X | SPA | @0 Enfermedad degenerativa @5 39 |
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C07 | 04 | X | FRE | @0 Pathologie du système nerveux central @5 40 |
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C07 | 04 | X | ENG | @0 Central nervous system disease @5 40 |
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C07 | 04 | X | SPA | @0 Sistema nervosio central patología @5 40 |
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N21 | | | | @1 191 |
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N44 | 01 | | | @1 OTO |
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N82 | | | | @1 OTO |
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|
Format Inist (serveur)
NO : | PASCAL 12-0248770 INIST |
ET : | The Asp620Asn Mutation in VPS35 Is Not a Common Cause of Familial Parkinson's Disease |
AU : | GUELLA (Ilaria); SOLDA (Giulia); CILIA (Roberto); PEZZOLI (Gianni); ASSELTA (Rosanna); DUGA (Stefano); GOLDWURM (Stefano) |
AF : | Dipartimento di Biologia e Genetica per le Scienze Mediche, Università degli Studi di Milano/Milan/Italie (1 aut., 2 aut., 5 aut., 6 aut.); Parkinson Institute, Istituti Clinici di Perfezionamento/Milan/Italie (3 aut., 4 aut., 7 aut.) |
DT : | Publication en série; Correspondance, lettre; Niveau analytique |
SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2012; Vol. 27; No. 6; Pp. 800-801; Bibl. 6 ref. |
LA : | Anglais |
CC : | 002B17; 002B17G |
FD : | Maladie de Parkinson; Pathologie du système nerveux; Mutation; Maladie familiale |
FG : | Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central |
ED : | Parkinson disease; Nervous system diseases; Mutation; Familial disease |
EG : | Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease |
SD : | Parkinson enfermedad; Sistema nervioso patología; Mutación; Enfermedad familiar |
LO : | INIST-20953.354000507771510290 |
ID : | 12-0248770 |
Links to Exploration step
Pascal:12-0248770
Le document en format XML
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<server><NO>PASCAL 12-0248770 INIST</NO>
<ET>The Asp620Asn Mutation in VPS35 Is Not a Common Cause of Familial Parkinson's Disease</ET>
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<AF>Dipartimento di Biologia e Genetica per le Scienze Mediche, Università degli Studi di Milano/Milan/Italie (1 aut., 2 aut., 5 aut., 6 aut.); Parkinson Institute, Istituti Clinici di Perfezionamento/Milan/Italie (3 aut., 4 aut., 7 aut.)</AF>
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