How the imaging investigation of EAST syndrome points towards the future of radiological multi‐parametric phenotyping of a genetic disease
This commentary is on the original article by Cross et al. on pages 846–856 of this issue.
Gespeichert in:
| Veröffentlicht in: | Developmental medicine and child neurology 2013-09, Vol.55 (9), p.783-784 |
|---|---|
| 1. Verfasser: | |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 784 |
|---|---|
| container_issue | 9 |
| container_start_page | 783 |
| container_title | Developmental medicine and child neurology |
| container_volume | 55 |
| creator | Stivaros, Stavros |
| description | This commentary is on the original article by Cross et al. on pages 846–856 of this issue. |
| doi_str_mv | 10.1111/dmcn.12189 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1419340118</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1419340118</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3299-eb102437262b2a0dcf7f7d825bf0449419f7a39adddccac7bddd2582b51602bc3</originalsourceid><addsrcrecordid>eNp9kMFO2zAYgK0JNArbZQ8w-YgmBWzHTeIjKgUmdXAYO0eO_Sd4SuzMdqh62wNw4Bl5krkt44gvtuTP3y9_CH2h5Iymda4HZc8oo5X4gGaUFyKrSi4O0IwQyjJaMHaEjkP4TQjJizn_iI5YLhgnFZ2hpxu3xvEBsBlkZ2yHjX2EEE0no3EWuxYvL37e47Cx2rsB8OiMjQFHt5Zeh93LdoqThy3qpTaud51RssfD1Efz8vd5lF4OEL1ReHwA6-Jm3M5JuMQdWIjpQpsAMsAndNjKPsDn1_0E_bpa3i9ustXd9ffFxSpTORMig4YSxvOSFaxhkmjVlm2pKzZvWsK54FS0pcyF1ForJVXZpAObV6yZ04KwRuUn6HTvHb37M6Xv1oMJCvpeWnBTqGlS5JxQWiX02x5V3oXgoa1Hn1L5TU1Jva1fb-vXu_oJ_vrqnZoB9Bv6P3cC6B5Ymx4276jqyx-L2730H9rtk90</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1419340118</pqid></control><display><type>article</type><title>How the imaging investigation of EAST syndrome points towards the future of radiological multi‐parametric phenotyping of a genetic disease</title><source>MEDLINE</source><source>Wiley Online Library Free Content</source><source>Access via Wiley Online Library</source><creator>Stivaros, Stavros</creator><creatorcontrib>Stivaros, Stavros</creatorcontrib><description>This commentary is on the original article by Cross et al. on pages 846–856 of this issue.</description><identifier>ISSN: 0012-1622</identifier><identifier>EISSN: 1469-8749</identifier><identifier>DOI: 10.1111/dmcn.12189</identifier><identifier>PMID: 23924081</identifier><language>eng</language><publisher>England</publisher><subject>Central Nervous System - abnormalities ; Developmental Disabilities - etiology ; Female ; Hearing Loss, Sensorineural - diagnosis ; Hearing Loss, Sensorineural - therapy ; Humans ; Intellectual Disability - diagnosis ; Intellectual Disability - therapy ; Magnetic Resonance Imaging ; Male ; Potassium Channels, Inwardly Rectifying - genetics ; Seizures - diagnosis ; Seizures - therapy</subject><ispartof>Developmental medicine and child neurology, 2013-09, Vol.55 (9), p.783-784</ispartof><rights>2013 Mac Keith Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3299-eb102437262b2a0dcf7f7d825bf0449419f7a39adddccac7bddd2582b51602bc3</citedby><cites>FETCH-LOGICAL-c3299-eb102437262b2a0dcf7f7d825bf0449419f7a39adddccac7bddd2582b51602bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fdmcn.12189$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fdmcn.12189$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,1434,27926,27927,45576,45577,46411,46835</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23924081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stivaros, Stavros</creatorcontrib><title>How the imaging investigation of EAST syndrome points towards the future of radiological multi‐parametric phenotyping of a genetic disease</title><title>Developmental medicine and child neurology</title><addtitle>Dev Med Child Neurol</addtitle><description>This commentary is on the original article by Cross et al. on pages 846–856 of this issue.</description><subject>Central Nervous System - abnormalities</subject><subject>Developmental Disabilities - etiology</subject><subject>Female</subject><subject>Hearing Loss, Sensorineural - diagnosis</subject><subject>Hearing Loss, Sensorineural - therapy</subject><subject>Humans</subject><subject>Intellectual Disability - diagnosis</subject><subject>Intellectual Disability - therapy</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Potassium Channels, Inwardly Rectifying - genetics</subject><subject>Seizures - diagnosis</subject><subject>Seizures - therapy</subject><issn>0012-1622</issn><issn>1469-8749</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFO2zAYgK0JNArbZQ8w-YgmBWzHTeIjKgUmdXAYO0eO_Sd4SuzMdqh62wNw4Bl5krkt44gvtuTP3y9_CH2h5Iymda4HZc8oo5X4gGaUFyKrSi4O0IwQyjJaMHaEjkP4TQjJizn_iI5YLhgnFZ2hpxu3xvEBsBlkZ2yHjX2EEE0no3EWuxYvL37e47Cx2rsB8OiMjQFHt5Zeh93LdoqThy3qpTaud51RssfD1Efz8vd5lF4OEL1ReHwA6-Jm3M5JuMQdWIjpQpsAMsAndNjKPsDn1_0E_bpa3i9ustXd9ffFxSpTORMig4YSxvOSFaxhkmjVlm2pKzZvWsK54FS0pcyF1ForJVXZpAObV6yZ04KwRuUn6HTvHb37M6Xv1oMJCvpeWnBTqGlS5JxQWiX02x5V3oXgoa1Hn1L5TU1Jva1fb-vXu_oJ_vrqnZoB9Bv6P3cC6B5Ymx4276jqyx-L2730H9rtk90</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Stivaros, Stavros</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201309</creationdate><title>How the imaging investigation of EAST syndrome points towards the future of radiological multi‐parametric phenotyping of a genetic disease</title><author>Stivaros, Stavros</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3299-eb102437262b2a0dcf7f7d825bf0449419f7a39adddccac7bddd2582b51602bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Central Nervous System - abnormalities</topic><topic>Developmental Disabilities - etiology</topic><topic>Female</topic><topic>Hearing Loss, Sensorineural - diagnosis</topic><topic>Hearing Loss, Sensorineural - therapy</topic><topic>Humans</topic><topic>Intellectual Disability - diagnosis</topic><topic>Intellectual Disability - therapy</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Potassium Channels, Inwardly Rectifying - genetics</topic><topic>Seizures - diagnosis</topic><topic>Seizures - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stivaros, Stavros</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental medicine and child neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stivaros, Stavros</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>How the imaging investigation of EAST syndrome points towards the future of radiological multi‐parametric phenotyping of a genetic disease</atitle><jtitle>Developmental medicine and child neurology</jtitle><addtitle>Dev Med Child Neurol</addtitle><date>2013-09</date><risdate>2013</risdate><volume>55</volume><issue>9</issue><spage>783</spage><epage>784</epage><pages>783-784</pages><issn>0012-1622</issn><eissn>1469-8749</eissn><abstract>This commentary is on the original article by Cross et al. on pages 846–856 of this issue.</abstract><cop>England</cop><pmid>23924081</pmid><doi>10.1111/dmcn.12189</doi><tpages>2</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0012-1622 |
| ispartof | Developmental medicine and child neurology, 2013-09, Vol.55 (9), p.783-784 |
| issn | 0012-1622 1469-8749 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1419340118 |
| source | MEDLINE; Wiley Online Library Free Content; Access via Wiley Online Library |
| subjects | Central Nervous System - abnormalities Developmental Disabilities - etiology Female Hearing Loss, Sensorineural - diagnosis Hearing Loss, Sensorineural - therapy Humans Intellectual Disability - diagnosis Intellectual Disability - therapy Magnetic Resonance Imaging Male Potassium Channels, Inwardly Rectifying - genetics Seizures - diagnosis Seizures - therapy |
| title | How the imaging investigation of EAST syndrome points towards the future of radiological multi‐parametric phenotyping of a genetic disease |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T07%3A59%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=How%20the%20imaging%20investigation%20of%20EAST%20syndrome%20points%20towards%20the%20future%20of%20radiological%20multi%E2%80%90parametric%20phenotyping%20of%20a%20genetic%20disease&rft.jtitle=Developmental%20medicine%20and%20child%20neurology&rft.au=Stivaros,%20Stavros&rft.date=2013-09&rft.volume=55&rft.issue=9&rft.spage=783&rft.epage=784&rft.pages=783-784&rft.issn=0012-1622&rft.eissn=1469-8749&rft_id=info:doi/10.1111/dmcn.12189&rft_dat=%3Cproquest_cross%3E1419340118%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1419340118&rft_id=info:pmid/23924081&rfr_iscdi=true |