✦ LIBER ✦

Subacute Budd–Chiari syndrome associated with polycythemia vera and factor V Leiden mutation

✍ Scribed by S Simsek; R.V Verheesen; E.B Haagsma; J Lourens

Book ID: 117454110
Publisher: Elsevier Science
Year: 2000
Tongue: English
Weight: 337 KB
Volume: 57
Category: Article
ISSN: 0300-2977
DOI: 10.1016/s0300-2977(00)00046-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Fulminant Budd–Chiari syndrome associate

Fulminant Budd–Chiari syndrome associated with polycythemia rubra vera and factor V Leiden mutation

✍ Murat Akyildiz; Zeki Karasu; Hamad Dheir; Necla Osmanoglu; Sinan Akay; Tankut Il 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 64 KB

Budd-Chiari syndrome and factor V Leiden

Budd-Chiari syndrome and factor V Leiden mutation

✍ M-H. Denninger; K. Beldjord; F. Durand; C. Denie; D. Valla; M-C. Guillin; A.E.A. 📂 Article 📅 1995 🏛 The Lancet 🌐 English ⚖ 332 KB

Budd-Chiari Syndrome Associated with Vis

Budd-Chiari Syndrome Associated with Visceral Leishmaniasis and Factor V Leiden Mutation

✍ Emel Gürkan; Çağatay Ünsal; Fikri Başlamışlı; Didem Arslan 📂 Article 📅 2004 🏛 Springer US 🌐 English ⚖ 151 KB

Budd-Chiari Syndrome Related to Factor V

Budd-Chiari Syndrome Related to Factor V Leiden Mutation

✍ Joakim Delarive M.D.; Jean-Jacques Gonvers M.D. 📂 Article 📅 1998 🏛 Nature Publishing Group 🌐 English ⚖ 23 KB

Budd-chiari syndrome associated with fac

Budd-chiari syndrome associated with factor V leiden mutation: A report of 6 patients

✍ Hoffman, Ron ;Nimer, Assy ;Lanir, Naomi ;Brenner, Benjamin ;Baruch, Yaacov 📂 Article 📅 1999 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 56 KB

Budd-Chiari syndrome is characterized by hepatic venous outflow obstruction. Although myeloproliferative disorders are usually responsible for this severe thrombotic disorder, deficiency or dysfunction of the natural anticoagulants can be involved. Resistance to activated protein C caused by factor

Budd-Chiari syndrome with underlying hom

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations

✍ Kassem A. Barada; Cecilio R. Azar; Zaher K. Otrock; Ali T. Taher 📂 Article 📅 2005 🏛 Springer Japan 🌐 English ⚖ 90 KB