Budd-Chiari Syndrome in a Patient Heterozygous for Both Factor V Leiden and the G20210a Mutation on the Prothrombin Gene
| dc.authorscopusid | 7005791514 | |
| dc.authorscopusid | 7006604555 | |
| dc.authorscopusid | 7101974609 | |
| dc.authorscopusid | 8591611800 | |
| dc.authorwosid | Arslan, Şükrü/Abc-4250-2021 | |
| dc.contributor.author | Oner, A.F. | |
| dc.contributor.author | Arslan, S. | |
| dc.contributor.author | Caksen, H. | |
| dc.contributor.author | Ceylan, A. | |
| dc.date.accessioned | 2025-05-10T17:05:21Z | |
| dc.date.available | 2025-05-10T17:05:21Z | |
| dc.date.issued | 1999 | |
| dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
| dc.department-temp | Oner A.F., Yuzuncii Yil University, Faculty of Medicine, Department of Pediatric Hematology, 65200 Van, Turkey; Arslan S., Yuzuncii Yil University, Faculty of Medicine, Department of Pediatric Hematology, 65200 Van, Turkey; Caksen H., Yuzuncii Yil University, Faculty of Medicine, Department of Pediatric Hematology, 65200 Van, Turkey; Ceylan A., Yuzuncii Yil University, Faculty of Medicine, Department of Pediatric Hematology, 65200 Van, Turkey | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.1055/s-0037-1614397 | |
| dc.identifier.endpage | 1367 | en_US |
| dc.identifier.issn | 0340-6245 | |
| dc.identifier.issue | 4 | en_US |
| dc.identifier.pmid | 10544935 | |
| dc.identifier.pmid | 10544935 | |
| dc.identifier.scopus | 2-s2.0-0032827641 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 1366 | en_US |
| dc.identifier.uri | https://doi.org/10.1055/s-0037-1614397 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14720/6301 | |
| dc.identifier.volume | 82 | en_US |
| dc.identifier.wos | WOS:000083145000037 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | Schattauer GmbH | en_US |
| dc.relation.ispartof | Thrombosis and Haemostasis | en_US |
| dc.relation.publicationcategory | Diğer | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | Budd-Chiari Syndrome in a Patient Heterozygous for Both Factor V Leiden and the G20210a Mutation on the Prothrombin Gene | en_US |
| dc.type | Letter | en_US |