Enzymatic Prenatal Diagnosis of Primary Hyperoxaluria Type 1: Potential and Limitations
Gespeichert in:
| Veröffentlicht in: | Journal of inherited metabolic disease 1989-01, Vol.12 (S2), p.286-288 |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 288 |
|---|---|
| container_issue | S2 |
| container_start_page | 286 |
| container_title | Journal of inherited metabolic disease |
| container_volume | 12 |
| creator | Danpure, C. J. Cooper, P. J. Jennings, P. R. Wise, P. J. Penketh, R. J. Rodeck, C. H. |
| description | |
| doi_str_mv | 10.1007/BF03335400 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79368244</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79368244</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3526-8f370d4352cd490a0947905c27a95f734dbf65d617c77dd2b5237ec2933882b33</originalsourceid><addsrcrecordid>eNp9kLtPwzAQxi0EKqWwsCNlQAxIgfMrjtmgD1pURIcixsh1HGSUR4kTQfjrSZWobEz3-t13ug-hcww3GEDcPsyAUsoZwAEaYi6oT4KAH6IhYIb9UHJ-jE6c-wAAGXI-QAPCMWFEDNHbNP9pMlVZ7a1Kk6tKpd7Eqve8cNZ5RdJ2babKxps3W1MW3yqtS6u8dVt5-M5bFZXJK9suqTz2ljazVatV5O4UHSUqdeasjyP0Opuux3N_-fK4GN8vfU05CfwwoQJi1uY6ZhIUSCYkcE2EkjwRlMWbJOBxgIUWIo7JhhMqjCaS0jAkG0pH6KrT3ZbFZ21cFWXWaZOmKjdF7SIhaRASxlrwugN1WThXmiTadp9FGKKdi9Gfiy180avWm8zEe7S3rZ1f9nPltEqTUuXauj0WcEko3mHQYV82Nc0_B6OnxfMESBjQX80DhfM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79368244</pqid></control><display><type>article</type><title>Enzymatic Prenatal Diagnosis of Primary Hyperoxaluria Type 1: Potential and Limitations</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Danpure, C. J. ; Cooper, P. J. ; Jennings, P. R. ; Wise, P. J. ; Penketh, R. J. ; Rodeck, C. H.</creator><creatorcontrib>Danpure, C. J. ; Cooper, P. J. ; Jennings, P. R. ; Wise, P. J. ; Penketh, R. J. ; Rodeck, C. H.</creatorcontrib><identifier>ISSN: 0141-8955</identifier><identifier>EISSN: 1573-2665</identifier><identifier>DOI: 10.1007/BF03335400</identifier><identifier>PMID: 2512427</identifier><identifier>CODEN: JIMDDP</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Alanine Transaminase - deficiency ; Alanine Transaminase - metabolism ; Biological and medical sciences ; Female ; Gynecology. Andrology. Obstetrics ; Humans ; Hyperoxaluria - diagnosis ; Liver - embryology ; Liver - enzymology ; Management. Prenatal diagnosis ; Medical sciences ; Pregnancy ; Pregnancy. Fetus. Placenta ; Prenatal Diagnosis ; Reference Values ; Transaminases</subject><ispartof>Journal of inherited metabolic disease, 1989-01, Vol.12 (S2), p.286-288</ispartof><rights>1989 SSIEM</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3526-8f370d4352cd490a0947905c27a95f734dbf65d617c77dd2b5237ec2933882b33</citedby><cites>FETCH-LOGICAL-c3526-8f370d4352cd490a0947905c27a95f734dbf65d617c77dd2b5237ec2933882b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6592317$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2512427$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Danpure, C. J.</creatorcontrib><creatorcontrib>Cooper, P. J.</creatorcontrib><creatorcontrib>Jennings, P. R.</creatorcontrib><creatorcontrib>Wise, P. J.</creatorcontrib><creatorcontrib>Penketh, R. J.</creatorcontrib><creatorcontrib>Rodeck, C. H.</creatorcontrib><title>Enzymatic Prenatal Diagnosis of Primary Hyperoxaluria Type 1: Potential and Limitations</title><title>Journal of inherited metabolic disease</title><addtitle>J Inherit Metab Dis</addtitle><subject>Alanine Transaminase - deficiency</subject><subject>Alanine Transaminase - metabolism</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Hyperoxaluria - diagnosis</subject><subject>Liver - embryology</subject><subject>Liver - enzymology</subject><subject>Management. Prenatal diagnosis</subject><subject>Medical sciences</subject><subject>Pregnancy</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>Prenatal Diagnosis</subject><subject>Reference Values</subject><subject>Transaminases</subject><issn>0141-8955</issn><issn>1573-2665</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLtPwzAQxi0EKqWwsCNlQAxIgfMrjtmgD1pURIcixsh1HGSUR4kTQfjrSZWobEz3-t13ug-hcww3GEDcPsyAUsoZwAEaYi6oT4KAH6IhYIb9UHJ-jE6c-wAAGXI-QAPCMWFEDNHbNP9pMlVZ7a1Kk6tKpd7Eqve8cNZ5RdJ2babKxps3W1MW3yqtS6u8dVt5-M5bFZXJK9suqTz2ljazVatV5O4UHSUqdeasjyP0Opuux3N_-fK4GN8vfU05CfwwoQJi1uY6ZhIUSCYkcE2EkjwRlMWbJOBxgIUWIo7JhhMqjCaS0jAkG0pH6KrT3ZbFZ21cFWXWaZOmKjdF7SIhaRASxlrwugN1WThXmiTadp9FGKKdi9Gfiy180avWm8zEe7S3rZ1f9nPltEqTUuXauj0WcEko3mHQYV82Nc0_B6OnxfMESBjQX80DhfM</recordid><startdate>19890101</startdate><enddate>19890101</enddate><creator>Danpure, C. J.</creator><creator>Cooper, P. J.</creator><creator>Jennings, P. R.</creator><creator>Wise, P. J.</creator><creator>Penketh, R. J.</creator><creator>Rodeck, C. H.</creator><general>Springer Netherlands</general><general>Springer</general><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>7X8</scope></search><sort><creationdate>19890101</creationdate><title>Enzymatic Prenatal Diagnosis of Primary Hyperoxaluria Type 1: Potential and Limitations</title><author>Danpure, C. J. ; Cooper, P. J. ; Jennings, P. R. ; Wise, P. J. ; Penketh, R. J. ; Rodeck, C. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3526-8f370d4352cd490a0947905c27a95f734dbf65d617c77dd2b5237ec2933882b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Alanine Transaminase - deficiency</topic><topic>Alanine Transaminase - metabolism</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Hyperoxaluria - diagnosis</topic><topic>Liver - embryology</topic><topic>Liver - enzymology</topic><topic>Management. Prenatal diagnosis</topic><topic>Medical sciences</topic><topic>Pregnancy</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>Prenatal Diagnosis</topic><topic>Reference Values</topic><topic>Transaminases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Danpure, C. J.</creatorcontrib><creatorcontrib>Cooper, P. J.</creatorcontrib><creatorcontrib>Jennings, P. R.</creatorcontrib><creatorcontrib>Wise, P. J.</creatorcontrib><creatorcontrib>Penketh, R. J.</creatorcontrib><creatorcontrib>Rodeck, C. H.</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Journal of inherited metabolic disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Danpure, C. J.</au><au>Cooper, P. J.</au><au>Jennings, P. R.</au><au>Wise, P. J.</au><au>Penketh, R. J.</au><au>Rodeck, C. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatic Prenatal Diagnosis of Primary Hyperoxaluria Type 1: Potential and Limitations</atitle><jtitle>Journal of inherited metabolic disease</jtitle><addtitle>J Inherit Metab Dis</addtitle><date>1989-01-01</date><risdate>1989</risdate><volume>12</volume><issue>S2</issue><spage>286</spage><epage>288</epage><pages>286-288</pages><issn>0141-8955</issn><eissn>1573-2665</eissn><coden>JIMDDP</coden><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>2512427</pmid><doi>10.1007/BF03335400</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0141-8955 |
| ispartof | Journal of inherited metabolic disease, 1989-01, Vol.12 (S2), p.286-288 |
| issn | 0141-8955 1573-2665 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_79368244 |
| source | MEDLINE; SpringerLink Journals |
| subjects | Alanine Transaminase - deficiency Alanine Transaminase - metabolism Biological and medical sciences Female Gynecology. Andrology. Obstetrics Humans Hyperoxaluria - diagnosis Liver - embryology Liver - enzymology Management. Prenatal diagnosis Medical sciences Pregnancy Pregnancy. Fetus. Placenta Prenatal Diagnosis Reference Values Transaminases |
| title | Enzymatic Prenatal Diagnosis of Primary Hyperoxaluria Type 1: Potential and Limitations |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T06%3A58%3A59IST&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=Enzymatic%20Prenatal%20Diagnosis%20of%20Primary%20Hyperoxaluria%20Type%201:%20Potential%20and%20Limitations&rft.jtitle=Journal%20of%20inherited%20metabolic%20disease&rft.au=Danpure,%20C.%20J.&rft.date=1989-01-01&rft.volume=12&rft.issue=S2&rft.spage=286&rft.epage=288&rft.pages=286-288&rft.issn=0141-8955&rft.eissn=1573-2665&rft.coden=JIMDDP&rft_id=info:doi/10.1007/BF03335400&rft_dat=%3Cproquest_cross%3E79368244%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=79368244&rft_id=info:pmid/2512427&rfr_iscdi=true |