Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study
Gespeichert in:
Veröffentlicht in: | Revista de neurologiá 2006-08, Vol.43 (4), p.251 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | spa |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 4 |
container_start_page | 251 |
container_title | Revista de neurologiá |
container_volume | 43 |
creator | García-Oguiza, A Miralbés-Terraza, S Calvo-Martín, M Labarta-Aizpun, J López-Pisón, J Marco-Tello, A Rebage, V |
description | |
format | Article |
fullrecord | <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_16883514</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16883514</sourcerecordid><originalsourceid>FETCH-pubmed_primary_168835143</originalsourceid><addsrcrecordid>eNqFjrsOgjAUQDtoBB-_YO4PmBRBg7PxMTmxk0u5QE0fpC1D_14GnZ3OcM5wFizlx4wfOM94wtbevzkv8uLCVyzJzmWZn7IiZdWLrMGACh7WKWnAR9M6qwnQeyskBmohWBhIS009KjKCxgFVBGFNJ52efROhJ0NBCvBhauOWLTtUnnZfbtj-fquuz8M4NXNfj05qdLH-beR_gw8wrj63</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>García-Oguiza, A ; Miralbés-Terraza, S ; Calvo-Martín, M ; Labarta-Aizpun, J ; López-Pisón, J ; Marco-Tello, A ; Rebage, V</creator><creatorcontrib>García-Oguiza, A ; Miralbés-Terraza, S ; Calvo-Martín, M ; Labarta-Aizpun, J ; López-Pisón, J ; Marco-Tello, A ; Rebage, V</creatorcontrib><identifier>ISSN: 0210-0010</identifier><identifier>PMID: 16883514</identifier><language>spa</language><publisher>Spain</publisher><subject>Adult ; Basal Cell Nevus Syndrome - complications ; Basal Cell Nevus Syndrome - diagnosis ; Basal Cell Nevus Syndrome - genetics ; Basal Cell Nevus Syndrome - pathology ; Base Sequence ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Molecular Sequence Data ; Mutation ; Nervous System Malformations - diagnosis ; Nervous System Malformations - etiology ; Nervous System Malformations - genetics ; Nervous System Malformations - pathology ; Patched Receptors ; Receptors, Cell Surface - genetics</subject><ispartof>Revista de neurologiá, 2006-08, Vol.43 (4), p.251</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16883514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García-Oguiza, A</creatorcontrib><creatorcontrib>Miralbés-Terraza, S</creatorcontrib><creatorcontrib>Calvo-Martín, M</creatorcontrib><creatorcontrib>Labarta-Aizpun, J</creatorcontrib><creatorcontrib>López-Pisón, J</creatorcontrib><creatorcontrib>Marco-Tello, A</creatorcontrib><creatorcontrib>Rebage, V</creatorcontrib><title>Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study</title><title>Revista de neurologiá</title><addtitle>Rev Neurol</addtitle><subject>Adult</subject><subject>Basal Cell Nevus Syndrome - complications</subject><subject>Basal Cell Nevus Syndrome - diagnosis</subject><subject>Basal Cell Nevus Syndrome - genetics</subject><subject>Basal Cell Nevus Syndrome - pathology</subject><subject>Base Sequence</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Nervous System Malformations - diagnosis</subject><subject>Nervous System Malformations - etiology</subject><subject>Nervous System Malformations - genetics</subject><subject>Nervous System Malformations - pathology</subject><subject>Patched Receptors</subject><subject>Receptors, Cell Surface - genetics</subject><issn>0210-0010</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFjrsOgjAUQDtoBB-_YO4PmBRBg7PxMTmxk0u5QE0fpC1D_14GnZ3OcM5wFizlx4wfOM94wtbevzkv8uLCVyzJzmWZn7IiZdWLrMGACh7WKWnAR9M6qwnQeyskBmohWBhIS009KjKCxgFVBGFNJ52efROhJ0NBCvBhauOWLTtUnnZfbtj-fquuz8M4NXNfj05qdLH-beR_gw8wrj63</recordid><startdate>20060816</startdate><enddate>20060816</enddate><creator>García-Oguiza, A</creator><creator>Miralbés-Terraza, S</creator><creator>Calvo-Martín, M</creator><creator>Labarta-Aizpun, J</creator><creator>López-Pisón, J</creator><creator>Marco-Tello, A</creator><creator>Rebage, V</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20060816</creationdate><title>Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study</title><author>García-Oguiza, A ; Miralbés-Terraza, S ; Calvo-Martín, M ; Labarta-Aizpun, J ; López-Pisón, J ; Marco-Tello, A ; Rebage, V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_168835143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>spa</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Basal Cell Nevus Syndrome - complications</topic><topic>Basal Cell Nevus Syndrome - diagnosis</topic><topic>Basal Cell Nevus Syndrome - genetics</topic><topic>Basal Cell Nevus Syndrome - pathology</topic><topic>Base Sequence</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Nervous System Malformations - diagnosis</topic><topic>Nervous System Malformations - etiology</topic><topic>Nervous System Malformations - genetics</topic><topic>Nervous System Malformations - pathology</topic><topic>Patched Receptors</topic><topic>Receptors, Cell Surface - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García-Oguiza, A</creatorcontrib><creatorcontrib>Miralbés-Terraza, S</creatorcontrib><creatorcontrib>Calvo-Martín, M</creatorcontrib><creatorcontrib>Labarta-Aizpun, J</creatorcontrib><creatorcontrib>López-Pisón, J</creatorcontrib><creatorcontrib>Marco-Tello, A</creatorcontrib><creatorcontrib>Rebage, V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Revista de neurologiá</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García-Oguiza, A</au><au>Miralbés-Terraza, S</au><au>Calvo-Martín, M</au><au>Labarta-Aizpun, J</au><au>López-Pisón, J</au><au>Marco-Tello, A</au><au>Rebage, V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study</atitle><jtitle>Revista de neurologiá</jtitle><addtitle>Rev Neurol</addtitle><date>2006-08-16</date><risdate>2006</risdate><volume>43</volume><issue>4</issue><spage>251</spage><pages>251-</pages><issn>0210-0010</issn><cop>Spain</cop><pmid>16883514</pmid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0210-0010 |
ispartof | Revista de neurologiá, 2006-08, Vol.43 (4), p.251 |
issn | 0210-0010 |
language | spa |
recordid | cdi_pubmed_primary_16883514 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Adult Basal Cell Nevus Syndrome - complications Basal Cell Nevus Syndrome - diagnosis Basal Cell Nevus Syndrome - genetics Basal Cell Nevus Syndrome - pathology Base Sequence Female Humans Infant Infant, Newborn Male Molecular Sequence Data Mutation Nervous System Malformations - diagnosis Nervous System Malformations - etiology Nervous System Malformations - genetics Nervous System Malformations - pathology Patched Receptors Receptors, Cell Surface - genetics |
title | Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T03%3A12%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Neonatal%20Gorlin%20syndrome%20associated%20to%20hemimegalencephaly%20confirmed%20by%20genetic%20study&rft.jtitle=Revista%20de%20neurologi%C3%A1&rft.au=Garc%C3%ADa-Oguiza,%20A&rft.date=2006-08-16&rft.volume=43&rft.issue=4&rft.spage=251&rft.pages=251-&rft.issn=0210-0010&rft_id=info:doi/&rft_dat=%3Cpubmed%3E16883514%3C/pubmed%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/16883514&rfr_iscdi=true |