Cavernous Malformations of the Central Nervous System
Cerebral cavernous malformations occur in 0.5% of the population; 85% are sporadic, and 15% are familial or radiation-induced. Several genetic variants, including variants in CCM , drive their development.
Gespeichert in:
Veröffentlicht in: | The New England journal of medicine 2024-03, Vol.390 (11), p.1022-1028 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1028 |
---|---|
container_issue | 11 |
container_start_page | 1022 |
container_title | The New England journal of medicine |
container_volume | 390 |
creator | Smith, Edward R. |
description | Cerebral cavernous malformations occur in 0.5% of the population; 85% are sporadic, and 15% are familial or radiation-induced. Several genetic variants, including variants in
CCM
, drive their development. |
doi_str_mv | 10.1056/NEJMra2305116 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2956682600</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2956682600</sourcerecordid><originalsourceid>FETCH-LOGICAL-c351t-bb143532e99c59afc3b46368e9d9c39cc408f903b3b84fa865022350a2d384593</originalsourceid><addsrcrecordid>eNp10EtLAzEUBeAgiq3VpVsZEMHN6M2zyVKG-qKtC3U9ZNIEWyYzNZkp9N87fSgoeDd383E4HITOMdxg4OJ2OnqeBE0ocIzFAepjTmnKGIhD1AcgMmVDRXvoJMYFdIeZOkY9KtlwqKTqI57plQ1V3cZkoktXB6-beV3FpHZJ82GTzFZN0GUytWG1Qa_r2Fh_io6cLqM92_8Ber8fvWWP6fjl4Sm7G6eGctykRYEZ5ZRYpQxX2hlaMEGFtGqmDFXGMJBOAS1oIZnTUnAghHLQZNY15IoO0PUudxnqz9bGJvfzaGxZ6sp2bXKiuBCSCICOXv6hi7oNVdduqyQGtQ1Md8qEOsZgXb4Mc6_DOseQb_bMf-3Z-Yt9alt4O_vR3wN24GoHvI95ZRf-n6AvwVp5ZQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2956810959</pqid></control><display><type>article</type><title>Cavernous Malformations of the Central Nervous System</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>New England Journal of Medicine</source><creator>Smith, Edward R.</creator><contributor>Ropper, Allan H.</contributor><creatorcontrib>Smith, Edward R. ; Ropper, Allan H.</creatorcontrib><description>Cerebral cavernous malformations occur in 0.5% of the population; 85% are sporadic, and 15% are familial or radiation-induced. Several genetic variants, including variants in
CCM
, drive their development.</description><identifier>ISSN: 0028-4793</identifier><identifier>EISSN: 1533-4406</identifier><identifier>DOI: 10.1056/NEJMra2305116</identifier><identifier>PMID: 38477989</identifier><language>eng</language><publisher>United States: Massachusetts Medical Society</publisher><subject>CCM2 protein ; Cell division ; Central Nervous System ; Gadolinium ; Genetics ; Genetics General ; Hemorrhage ; Humans ; Hypotheses ; Kinases ; Magnetic resonance imaging ; Nervous system ; Neurology ; Neurosurgery ; Neurosurgery General ; Pathogenesis ; Pediatrics ; Pediatrics General ; Polymerization ; Radiation ; Radiation therapy ; Radiology ; Radiology General ; Seizures ; Surgery ; Surgery General</subject><ispartof>The New England journal of medicine, 2024-03, Vol.390 (11), p.1022-1028</ispartof><rights>Copyright © 2024 Massachusetts Medical Society. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-bb143532e99c59afc3b46368e9d9c39cc408f903b3b84fa865022350a2d384593</citedby><cites>FETCH-LOGICAL-c351t-bb143532e99c59afc3b46368e9d9c39cc408f903b3b84fa865022350a2d384593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.nejm.org/doi/pdf/10.1056/NEJMra2305116$$EPDF$$P50$$Gmms$$H</linktopdf><linktohtml>$$Uhttps://www.nejm.org/doi/full/10.1056/NEJMra2305116$$EHTML$$P50$$Gmms$$H</linktohtml><link.rule.ids>314,776,780,2746,2747,26082,27903,27904,52360,54042</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38477989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ropper, Allan H.</contributor><creatorcontrib>Smith, Edward R.</creatorcontrib><title>Cavernous Malformations of the Central Nervous System</title><title>The New England journal of medicine</title><addtitle>N Engl J Med</addtitle><description>Cerebral cavernous malformations occur in 0.5% of the population; 85% are sporadic, and 15% are familial or radiation-induced. Several genetic variants, including variants in
CCM
, drive their development.</description><subject>CCM2 protein</subject><subject>Cell division</subject><subject>Central Nervous System</subject><subject>Gadolinium</subject><subject>Genetics</subject><subject>Genetics General</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Kinases</subject><subject>Magnetic resonance imaging</subject><subject>Nervous system</subject><subject>Neurology</subject><subject>Neurosurgery</subject><subject>Neurosurgery General</subject><subject>Pathogenesis</subject><subject>Pediatrics</subject><subject>Pediatrics General</subject><subject>Polymerization</subject><subject>Radiation</subject><subject>Radiation therapy</subject><subject>Radiology</subject><subject>Radiology General</subject><subject>Seizures</subject><subject>Surgery</subject><subject>Surgery General</subject><issn>0028-4793</issn><issn>1533-4406</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp10EtLAzEUBeAgiq3VpVsZEMHN6M2zyVKG-qKtC3U9ZNIEWyYzNZkp9N87fSgoeDd383E4HITOMdxg4OJ2OnqeBE0ocIzFAepjTmnKGIhD1AcgMmVDRXvoJMYFdIeZOkY9KtlwqKTqI57plQ1V3cZkoktXB6-beV3FpHZJ82GTzFZN0GUytWG1Qa_r2Fh_io6cLqM92_8Ber8fvWWP6fjl4Sm7G6eGctykRYEZ5ZRYpQxX2hlaMEGFtGqmDFXGMJBOAS1oIZnTUnAghHLQZNY15IoO0PUudxnqz9bGJvfzaGxZ6sp2bXKiuBCSCICOXv6hi7oNVdduqyQGtQ1Md8qEOsZgXb4Mc6_DOseQb_bMf-3Z-Yt9alt4O_vR3wN24GoHvI95ZRf-n6AvwVp5ZQ</recordid><startdate>20240314</startdate><enddate>20240314</enddate><creator>Smith, Edward R.</creator><general>Massachusetts Medical Society</general><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>0TZ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K0Y</scope><scope>LK8</scope><scope>M0R</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20240314</creationdate><title>Cavernous Malformations of the Central Nervous System</title><author>Smith, Edward R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-bb143532e99c59afc3b46368e9d9c39cc408f903b3b84fa865022350a2d384593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>CCM2 protein</topic><topic>Cell division</topic><topic>Central Nervous System</topic><topic>Gadolinium</topic><topic>Genetics</topic><topic>Genetics General</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Kinases</topic><topic>Magnetic resonance imaging</topic><topic>Nervous system</topic><topic>Neurology</topic><topic>Neurosurgery</topic><topic>Neurosurgery General</topic><topic>Pathogenesis</topic><topic>Pediatrics</topic><topic>Pediatrics General</topic><topic>Polymerization</topic><topic>Radiation</topic><topic>Radiation therapy</topic><topic>Radiology</topic><topic>Radiology General</topic><topic>Seizures</topic><topic>Surgery</topic><topic>Surgery General</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Edward R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>New England Journal of Medicine</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>The New England journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Edward R.</au><au>Ropper, Allan H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cavernous Malformations of the Central Nervous System</atitle><jtitle>The New England journal of medicine</jtitle><addtitle>N Engl J Med</addtitle><date>2024-03-14</date><risdate>2024</risdate><volume>390</volume><issue>11</issue><spage>1022</spage><epage>1028</epage><pages>1022-1028</pages><issn>0028-4793</issn><eissn>1533-4406</eissn><abstract>Cerebral cavernous malformations occur in 0.5% of the population; 85% are sporadic, and 15% are familial or radiation-induced. Several genetic variants, including variants in
CCM
, drive their development.</abstract><cop>United States</cop><pub>Massachusetts Medical Society</pub><pmid>38477989</pmid><doi>10.1056/NEJMra2305116</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-4793 |
ispartof | The New England journal of medicine, 2024-03, Vol.390 (11), p.1022-1028 |
issn | 0028-4793 1533-4406 |
language | eng |
recordid | cdi_proquest_miscellaneous_2956682600 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; New England Journal of Medicine |
subjects | CCM2 protein Cell division Central Nervous System Gadolinium Genetics Genetics General Hemorrhage Humans Hypotheses Kinases Magnetic resonance imaging Nervous system Neurology Neurosurgery Neurosurgery General Pathogenesis Pediatrics Pediatrics General Polymerization Radiation Radiation therapy Radiology Radiology General Seizures Surgery Surgery General |
title | Cavernous Malformations of the Central Nervous System |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T18%3A37%3A15IST&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=Cavernous%20Malformations%20of%20the%20Central%20Nervous%20System&rft.jtitle=The%20New%20England%20journal%20of%20medicine&rft.au=Smith,%20Edward%20R.&rft.date=2024-03-14&rft.volume=390&rft.issue=11&rft.spage=1022&rft.epage=1028&rft.pages=1022-1028&rft.issn=0028-4793&rft.eissn=1533-4406&rft_id=info:doi/10.1056/NEJMra2305116&rft_dat=%3Cproquest_cross%3E2956682600%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=2956810959&rft_id=info:pmid/38477989&rfr_iscdi=true |