| [The use of recombinant activated factor VII in the treatment of gastrointestinal bleeding following acetylsalicylic acid therapy in a surgical patient] [English Abstract, Journal Article]
Srp Arh Celok Lek 2008 Sep.:240-5.
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| Mahieu S, Contini MD, González M, et al.
MELATONIN REDUCES OXIDATIVE DAMAGE INDUCED BY ALUMINIUM IN RAT KIDNEY. [JOURNAL ARTICLE]
Toxicol Lett 2009 Jun 15.
Abstract | Full Citation |
| Sterns RH, Nigwekar SU, Hix JK
The treatment of hyponatremia. [Journal Article]
Semin Nephrol 2009 May; 29(3):282-99.
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| Shestopalova LV, Lavrinenko VA, Shkurupiy VA, et al.
Involvement of interstitial structures of the kidney into hydrosmotic effect of vasopressin (morphofunctional study). [Journal Article]
Bull Exp Biol Med 2008 Dec; 146(6):682-6.
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| Sucker C, Michiels JJ, Zotz RB
Causes, Etiology and Diagnosis of Acquired von Willebrand Disease: A Prospective Diagnostic Workup to Establish the Most Effective Therapeutic Strategies. [JOURNAL ARTICLE]
Acta Haematol 2009; 121(2-3):177-182.
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| Michiels JJ, van Vliet HH, Berneman Z, et al.
Managing Patients with von Willebrand Disease Type 1, 2 and 3 with Desmopressin and von Willebrand Factor-Factor VIII Concentrate in Surgical Settings. [JOURNAL ARTICLE]
Acta Haematol 2009; 121(2-3):167-176.
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| Michiels JJ, van Vliet HH
Dominant von Willebrand Disease Type 2A Groups I and II due to Missense Mutations in the A2 Domain of the von Willebrand Factor Gene: Diagnosis and Management. [JOURNAL ARTICLE]
Acta Haematol 2009; 121(2-3):154-166.
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| Gadisseur A, van der Planken M, Schroyens W, et al.
Dominant von Willebrand Disease Type 2M and 2U Are Variable Expressions of One Distinct Disease Entity Caused by Loss-of-Function Mutations in the A1 Domain of the von Willebrand Factor Gene. [JOURNAL ARTICLE]
Acta Haematol 2009; 121(2-3):145-153.
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| Hermans C, Batlle J
Autosomal dominant von Willebrand disease type 2M. [Journal Article, Research Support, Non-U.S. Gov't]
Acta Haematol 2009; 121(2-3):139-44.
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| Gadisseur A, Berneman Z, Schroyens W, et al.
Laboratory Diagnosis of von Willebrand Disease Type 1/2E (2A Subtype IIE), Type 1 Vicenza and Mild Type 1 Caused by Mutations in the D3, D4, B1-B3 and C1-C2 Domains of the von Willebrand Factor Gene. Role of von Willebrand Factor Multimers and the von Willebrand Factor Propeptide/Antigen Ratio. [JOURNAL ARTICLE]
Acta Haematol 2009; 121(2-3):128-138.
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