EXTENSION OF THE CLINICAL SPECTRUM OF DANON DISEASE
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Veröffentlicht in: | Neurology 2008-04, Vol.70 (16), p.1358-1359 |
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container_title | Neurology |
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creator | VAN DER KOOI, A. J VAN LANGEN, I. M DE VISSER, M ARONICA, E VAN DOOM, P. A WOKKE, J. H. J BRUSSE, E LANGERHORST, C. T BERGIN, P DEKKER, L. R. C DIT DEPREZ, R. H. Lekanne |
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doi_str_mv | 10.1212/01.wnl.0000309219.61785.b3 |
format | Article |
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J ; VAN LANGEN, I. M ; DE VISSER, M ; ARONICA, E ; VAN DOOM, P. A ; WOKKE, J. H. J ; BRUSSE, E ; LANGERHORST, C. T ; BERGIN, P ; DEKKER, L. R. C ; DIT DEPREZ, R. H. Lekanne</creator><creatorcontrib>VAN DER KOOI, A. J ; VAN LANGEN, I. M ; DE VISSER, M ; ARONICA, E ; VAN DOOM, P. A ; WOKKE, J. H. J ; BRUSSE, E ; LANGERHORST, C. T ; BERGIN, P ; DEKKER, L. R. C ; DIT DEPREZ, R. H. Lekanne</creatorcontrib><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/01.wnl.0000309219.61785.b3</identifier><identifier>PMID: 18413590</identifier><identifier>CODEN: NEURAI</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Female ; Glycogen Storage Disease Type IIb - genetics ; Glycogen Storage Disease Type IIb - pathology ; Humans ; Lysosomal Membrane Proteins - genetics ; Lysosomal-Associated Membrane Protein 2 ; Male ; Medical sciences ; Middle Aged ; Mutation, Missense - genetics ; Neurology</subject><ispartof>Neurology, 2008-04, Vol.70 (16), p.1358-1359</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-b2d33fcb5f2e350dc9dafaa79468547df27195d54ac7a0754beacfcd44f424ee3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20274000$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18413590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>VAN DER KOOI, A. J</creatorcontrib><creatorcontrib>VAN LANGEN, I. M</creatorcontrib><creatorcontrib>DE VISSER, M</creatorcontrib><creatorcontrib>ARONICA, E</creatorcontrib><creatorcontrib>VAN DOOM, P. A</creatorcontrib><creatorcontrib>WOKKE, J. H. J</creatorcontrib><creatorcontrib>BRUSSE, E</creatorcontrib><creatorcontrib>LANGERHORST, C. T</creatorcontrib><creatorcontrib>BERGIN, P</creatorcontrib><creatorcontrib>DEKKER, L. R. C</creatorcontrib><creatorcontrib>DIT DEPREZ, R. H. Lekanne</creatorcontrib><title>EXTENSION OF THE CLINICAL SPECTRUM OF DANON DISEASE</title><title>Neurology</title><addtitle>Neurology</addtitle><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Female</subject><subject>Glycogen Storage Disease Type IIb - genetics</subject><subject>Glycogen Storage Disease Type IIb - pathology</subject><subject>Humans</subject><subject>Lysosomal Membrane Proteins - genetics</subject><subject>Lysosomal-Associated Membrane Protein 2</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation, Missense - genetics</subject><subject>Neurology</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1LwzAUhoMobk7_ghRB71rz2TTeja5zhdmJ7WB3IU0TmHQfNhviv7d1xZ2bc3Ge9z3wAPCAYIAwws8QBd_bOoDtECgwEkGIeMSCklyAIWI49EOCV5dgCCGOfBLxaABunPuEsD1ycQ0GKKKIMAGHgCSrIsnydJF5i6lXzBIvnqdZGo_nXv6exMXH8q07TMZZS0zSPBnnyS24sqp25q7fI7CcJkU88-eL1y7pa0L5wS9xRYjVJbPYEAYrLSplleKChhGjvLKYI8EqRpXmCnJGS6O01RWllmJqDBmBp1Pvvtl9HY07yM3aaVPXamt2RydDgSAhEWvBlxOom51zjbFy36w3qvmRCMpOmYRItsrkWZn8UyZL0obv-y_HcmOqc7R31AKPPaCcVrVt1Fav3T-HIea06_0FR8hwfA</recordid><startdate>20080415</startdate><enddate>20080415</enddate><creator>VAN DER KOOI, A. 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source | MEDLINE; Alma/SFX Local Collection; Journals@Ovid Complete |
subjects | Adolescent Adult Aged Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Female Glycogen Storage Disease Type IIb - genetics Glycogen Storage Disease Type IIb - pathology Humans Lysosomal Membrane Proteins - genetics Lysosomal-Associated Membrane Protein 2 Male Medical sciences Middle Aged Mutation, Missense - genetics Neurology |
title | EXTENSION OF THE CLINICAL SPECTRUM OF DANON DISEASE |
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