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Article

Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians - 1 Aug 2009

Politou Marianna, Gialeraki Argyri, Salamalekis Georgios, Markatos Christos, Merkouri Efrosyni, Travlou Anthi, Salamalekis Emmanouil, Skarpas Panagiotis

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PMID: 19479640
DOI: 10.1080/14767050802609783

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Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation.PMID 19479640Read ↗

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HELLP Syndrome—Holistic Insight into PathophysiologySemantic proximity Read ↗

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Sweet's syndrome in a woman with a prothrombin gene (G20210A) mutation.Semantic proximity Read ↗

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.Semantic proximity Read ↗

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.Semantic proximity Read ↗

[Budd-Chiari Syndrome in a patient with essential thrombocytopenia carrier of the prothrombin gene mutation G2021A].Semantic proximity Read ↗

Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.Semantic proximity Read ↗

What is the clinical relevance of the prothrombin G20210A mutation?Semantic proximity Read ↗

Molecular and Functional Analysis of the Human Prothrombinase Gene (HFGL2) and Its Role in Viral HepatitisSemantic proximity Read ↗

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

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