| Conţinutul numărului revistei |
| Articolul precedent |
| Articolul urmator |
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 944 12 |
| Ultima descărcare din IBN: 2023-10-27 13:02 |
 SM ISO690:2012SAGAIDAC, Irina, DRAGAN, Mariana. Trombofiliile ereditare - cauze ale pierderilor recurente de sarcină. In: Analele Ştiinţifice ale USMF „N. Testemiţanu”, 2011, nr. 5(12), pp. 64-68. ISSN 1857-1719. |
| EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
| Analele Ştiinţifice ale USMF „N. Testemiţanu” | ||||||
| Numărul 5(12) / 2011 / ISSN 1857-1719 | ||||||
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| Pag. 64-68 | ||||||
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| Rezumat | ||||||
Hereditary thrombophilia as cause of recurrent pregnancy loss
Thrombophilia includes all conditions associated with increased susceptibility to
thrombosis (both arterial and venous). During pregnancy a number of hereditary thrombophilia
causes recurrent pregnancy loss: antithrombin III deficiency, deficiency of protein C and S,
mutation of factor V Leiden, and gene mutations G20210A and МТНFR C677T
(Hyperhomocysteinemia). |
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Dublin Core Export
<?xml version='1.0' encoding='utf-8'?> <oai_dc:dc xmlns:dc='http://purl.org/dc/elements/1.1/' xmlns:oai_dc='http://www.openarchives.org/OAI/2.0/oai_dc/' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xsi:schemaLocation='http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd'> <dc:creator>Sagaidac, I.V.</dc:creator> <dc:creator>Dragan, M.</dc:creator> <dc:date>2011-12-01</dc:date> <dc:description xml:lang='en'>Hereditary thrombophilia as cause of recurrent pregnancy loss Thrombophilia includes all conditions associated with increased susceptibility to thrombosis (both arterial and venous). During pregnancy a number of hereditary thrombophilia causes recurrent pregnancy loss: antithrombin III deficiency, deficiency of protein C and S, mutation of factor V Leiden, and gene mutations G20210A and МТНFR C677T (Hyperhomocysteinemia).</dc:description> <dc:description xml:lang='ro'>Trombofilia include totalitatea afecţiunilor asociate cu o susceptibilitate crescută la tromboze (atât arteriale, cât si venoase). În timpul sarcinii un șir de trombofilii ereditare condiționează pierderile recurente de sarcină : deficitul antitrombinei III, deficitul proteinei C, deficitul proteinei S, mutația factorului V Leiden şi mutaţia G20210A, mutația genei МТНFR C677T (Hiperhomocisteinemia).</dc:description> <dc:source>Analele Ştiinţifice ale USMF „N. Testemiţanu” 12 (5) 64-68</dc:source> <dc:title>Trombofiliile ereditare - cauze ale pierderilor recurente de sarcină</dc:title> <dc:type>info:eu-repo/semantics/article</dc:type> </oai_dc:dc>
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