Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome
Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are prima...
Gespeichert in:
Veröffentlicht in: | British journal of ophthalmology 1986-10, Vol.70 (10), p.782-796 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 796 |
---|---|
container_issue | 10 |
container_start_page | 782 |
container_title | British journal of ophthalmology |
container_volume | 70 |
creator | Runge, P Calver, D Marshall, J Taylor, D |
description | Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are primarily affected. |
doi_str_mv | 10.1136/bjo.70.10.782 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1040828</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77150399</sourcerecordid><originalsourceid>FETCH-LOGICAL-b510t-b42fd9982e468097a408db60214caf723e9146a62947dc4897b6184f3e04d8383</originalsourceid><addsrcrecordid>eNqFkUuP0zAUhS0EGsrAkiVSJBBik-JXfO0NElMBA-oMGx5Ly3GcqUsSFzsZTf49rlqVx4aVfXU-3XuODkJPCV4SwsTrehuWkP94CZLeQwvChSwpBnUfLTDGUBIiyEP0KKVtHqkgcIbOGICUgi3Q9aVPY9iZcRO6cDMXoS16Pwa7CUMTvekKOx_kuTBDU4wbV6zNFN1gXXkVwlBeeNd0RZozHnr3GD1oTZfck-N7jr6-f_dldVmuP3_4uHq7LuuK4LGsOW0bpSR12SxWYDiWTS0wJdyaFihzKscwgioOjeVSQS2I5C1zmDeSSXaO3hz27qa6d411wxhNp3fR9ybOOhiv_1YGv9E34VYTnE_R_YKXxwUx_JxcGnXvk3VdZwYXpqQBSIWZUhl8_g-4DVMccjhNADAmQuEqU-WBsjGkFF17skKw3tekc00a8H7MNWX-2Z_-T_Sxl6y_OOomWdO10QzWpxMGilac8N9nc4nu7iSb-EMLYFDp628rfbG6It_Vp7Xep3514Ot--x-HvwA0UbZ7</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1770016905</pqid></control><display><type>article</type><title>Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Runge, P ; Calver, D ; Marshall, J ; Taylor, D</creator><creatorcontrib>Runge, P ; Calver, D ; Marshall, J ; Taylor, D</creatorcontrib><description>Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are primarily affected.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjo.70.10.782</identifier><identifier>PMID: 3778863</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Biological and medical sciences ; Child ; Child, Preschool ; Complex syndromes ; Female ; Humans ; Laurence-Moon Syndrome - pathology ; Male ; Medical genetics ; Medical sciences ; Microscopy, Electron ; Mitochondria - ultrastructure ; Pedigree ; Photoreceptor Cells - ultrastructure ; Pigment Epithelium of Eye - ultrastructure ; Retina - ultrastructure ; Retinal Degeneration - genetics ; Retinal Degeneration - pathology</subject><ispartof>British journal of ophthalmology, 1986-10, Vol.70 (10), p.782-796</ispartof><rights>1987 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Oct 1986</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b510t-b42fd9982e468097a408db60214caf723e9146a62947dc4897b6184f3e04d8383</citedby><cites>FETCH-LOGICAL-b510t-b42fd9982e468097a408db60214caf723e9146a62947dc4897b6184f3e04d8383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1040828/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1040828/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7925414$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3778863$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Runge, P</creatorcontrib><creatorcontrib>Calver, D</creatorcontrib><creatorcontrib>Marshall, J</creatorcontrib><creatorcontrib>Taylor, D</creatorcontrib><title>Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><description>Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are primarily affected.</description><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Complex syndromes</subject><subject>Female</subject><subject>Humans</subject><subject>Laurence-Moon Syndrome - pathology</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Mitochondria - ultrastructure</subject><subject>Pedigree</subject><subject>Photoreceptor Cells - ultrastructure</subject><subject>Pigment Epithelium of Eye - ultrastructure</subject><subject>Retina - ultrastructure</subject><subject>Retinal Degeneration - genetics</subject><subject>Retinal Degeneration - pathology</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkUuP0zAUhS0EGsrAkiVSJBBik-JXfO0NElMBA-oMGx5Ly3GcqUsSFzsZTf49rlqVx4aVfXU-3XuODkJPCV4SwsTrehuWkP94CZLeQwvChSwpBnUfLTDGUBIiyEP0KKVtHqkgcIbOGICUgi3Q9aVPY9iZcRO6cDMXoS16Pwa7CUMTvekKOx_kuTBDU4wbV6zNFN1gXXkVwlBeeNd0RZozHnr3GD1oTZfck-N7jr6-f_dldVmuP3_4uHq7LuuK4LGsOW0bpSR12SxWYDiWTS0wJdyaFihzKscwgioOjeVSQS2I5C1zmDeSSXaO3hz27qa6d411wxhNp3fR9ybOOhiv_1YGv9E34VYTnE_R_YKXxwUx_JxcGnXvk3VdZwYXpqQBSIWZUhl8_g-4DVMccjhNADAmQuEqU-WBsjGkFF17skKw3tekc00a8H7MNWX-2Z_-T_Sxl6y_OOomWdO10QzWpxMGilac8N9nc4nu7iSb-EMLYFDp628rfbG6It_Vp7Xep3514Ot--x-HvwA0UbZ7</recordid><startdate>19861001</startdate><enddate>19861001</enddate><creator>Runge, P</creator><creator>Calver, D</creator><creator>Marshall, J</creator><creator>Taylor, D</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19861001</creationdate><title>Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome</title><author>Runge, P ; Calver, D ; Marshall, J ; Taylor, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b510t-b42fd9982e468097a408db60214caf723e9146a62947dc4897b6184f3e04d8383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Complex syndromes</topic><topic>Female</topic><topic>Humans</topic><topic>Laurence-Moon Syndrome - pathology</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Mitochondria - ultrastructure</topic><topic>Pedigree</topic><topic>Photoreceptor Cells - ultrastructure</topic><topic>Pigment Epithelium of Eye - ultrastructure</topic><topic>Retina - ultrastructure</topic><topic>Retinal Degeneration - genetics</topic><topic>Retinal Degeneration - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Runge, P</creatorcontrib><creatorcontrib>Calver, D</creatorcontrib><creatorcontrib>Marshall, J</creatorcontrib><creatorcontrib>Taylor, D</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</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 Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Runge, P</au><au>Calver, D</au><au>Marshall, J</au><au>Taylor, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome</atitle><jtitle>British journal of ophthalmology</jtitle><addtitle>Br J Ophthalmol</addtitle><date>1986-10-01</date><risdate>1986</risdate><volume>70</volume><issue>10</issue><spage>782</spage><epage>796</epage><pages>782-796</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><coden>BJOPAL</coden><abstract>Clinical and histopathological studies of two patients with distinctly different inherited juvenile retinal dystrophies indicate that the ocular defect in mitochondrial cytopathy involves the underlying pigment epithelium, whereas in the Laurence-Moon-Biedl syndrome the photoreceptor cells are primarily affected.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>3778863</pmid><doi>10.1136/bjo.70.10.782</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0007-1161 |
ispartof | British journal of ophthalmology, 1986-10, Vol.70 (10), p.782-796 |
issn | 0007-1161 1468-2079 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1040828 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Biological and medical sciences Child Child, Preschool Complex syndromes Female Humans Laurence-Moon Syndrome - pathology Male Medical genetics Medical sciences Microscopy, Electron Mitochondria - ultrastructure Pedigree Photoreceptor Cells - ultrastructure Pigment Epithelium of Eye - ultrastructure Retina - ultrastructure Retinal Degeneration - genetics Retinal Degeneration - pathology |
title | Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T02%3A36%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Histopathology%20of%20mitochondrial%20cytopathy%20and%20the%20Laurence-Moon-Biedl%20syndrome&rft.jtitle=British%20journal%20of%20ophthalmology&rft.au=Runge,%20P&rft.date=1986-10-01&rft.volume=70&rft.issue=10&rft.spage=782&rft.epage=796&rft.pages=782-796&rft.issn=0007-1161&rft.eissn=1468-2079&rft.coden=BJOPAL&rft_id=info:doi/10.1136/bjo.70.10.782&rft_dat=%3Cproquest_pubme%3E77150399%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1770016905&rft_id=info:pmid/3778863&rfr_iscdi=true |