Publisher: Wiley-Blackwell

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Volume 15, Number 4, July 2009

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Measuring patient-reported outcomes in haemophilia clinical research
pp. 843-852(10)
Authors: GLOBE, D.; YOUNG, N. L.; VON MACKENSEN, S.; BULLINGER, M.; WASSERMAN, J.

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Co-morbidity in the ageing haemophilia patient: the down side of increased life expectancy
pp. 853-863(11)
Authors: MAUSER-BUNSCHOTEN, E. P.; FRANSEN VAN DE PUTTE, D. E.; SCHUTGENS, R. E. G.

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The role of selective angiographic embolization of the musculo-skeletal system in haemophilia
pp. 864-868(5)
Authors: RODRIGUEZ-MERCHAN, E. C.; JIMENEZ-YUSTE, V.

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Clinical evaluation of moroctocog alfa (AF-CC), a new generation of B-domain deleted recombinant factor VIII (BDDrFVIII) for treatment of haemophilia A: demonstration of safety, efficacy, and pharmacokinetic equivalence to full-length recombinant factor VIII
pp. 869-880(12)
Authors: RECHT, M.; NEMES, L.; MATYSIAK, M.; MANCO-JOHNSON, M.; LUSHER, J.; SMITH, M.; MANNUCCI, P.; HAY, C.; ABSHIRE, T.; O’BRIEN, A.; HAYWARD, B.; UDATA, C.; ROTH, D.A.; ARKIN, S.

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Survival in a cohort of patients with haemophilia at the haemophilia care center in Vienna, Austria, from 1983 to 2006
pp. 888-893(6)
Authors: REITTER, S.; WALDHOER, T.; VUTUC, C.; LECHNER, K.; PABINGER, I.

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Comorbidities and bleeding pattern in elderly haemophilia A patients
pp. 894-899(6)
Authors: MIESBACH, W.; ALESCI, S.; KREKELER, S.; SEIFRIED, E.

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Concomitant infusion of low doses of rFVIIa and FEIBA in haemophilia patients with inhibitors
pp. 904-910(7)
Authors: MARTINOWITZ, U.; LIVNAT, T.; ZIVELIN, A.; KENET, G.

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Health-related quality of life and productivity impact in haemophilia patients with inhibitors
pp. 911-917(7)
Authors: BROWN, T. M.; LEE, W. C.; JOSHI, A. V.; PASHOS, C. L.

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Bleeding symptoms and laboratory correlation in patients with severe von Willebrand disease
pp. 918-925(8)
Authors: METJIAN, A. D.; WANG, C.; SOOD, S. L.; CUKER, A.; PETERSON, S. M.; SOUCIE, J. M.; KONKLE, B. A.

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Complications of hysterectomy in women with von Willebrand disease
pp. 926-931(6)
Authors: JAMES, A. H.; MYERS, E. R.; COOK, C.; PIETROBON, R.

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Factor VIII mutations in 42 Moldovan haemophilia A families, including 12 that are novel
pp. 942-951(10)
Authors: SIROCOVA, N.; TSOUREA, V.; VICOL, M.; BARBACAR, N.; NAKAYA, S. M.; THOMPSON, A. R.; PRATT, K. P.

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Treatment of ischaemic heart disease in haemophilia patients: an institutional guideline
pp. 952-958(7)
Authors: SCHUTGENS, R. E. G.; TUINENBURG, A.; ROOSENDAAL, G.; GUYOMI, S. Hoseyni; MAUSER-BUNSCHOTEN, E. P.

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The application of bypassing-agent prophylaxis in haemophilia A patients with inhibitors: a meeting report
pp. 959-965(7)
Authors: VALENTINO, L. A.; CARCAO, M.; MATHEW, P.; LEISSINGER, C. A.; BERNTORP, E.; BLANCHETTE, V.; ESCURIOLA-ETTINGSHAUSEN, C.; EWENSTEIN, B.; EWING, N.; GRINGERI, A.; HOOTS, W. K.; NEGRIER, C.

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Efficacy and safety evaluation of sucrose-formulated recombinant factor VIII for Taiwanese patients with haemophilia A
pp. 968-970(3)
Authors: YOUNG, J.-H.; LIU, H.-C.; HSUEH, E.-J.; HUANG, M.-L.; PENG, C.-T.; CHEN, R.-L.; MAAS-ENRIQUEZ, M.; ACHILLES, K.

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Discordant haemophilia A in male siblings due to a de novo mutation on a familial missense mutant allele
pp. 971-972(2)
Authors: KENTSIS, A.; ANEWALT, R.; GANGULY, A.; ALLEN, J. B.; NEUFELD, E. J.

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Application of the isokinetic test to quantify knee muscle strength in haemophiliac patients
pp. 973-975(3)
Authors: DAUTY, M.; BRESSON, C.; TROSSAERT, M.

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Hetastarch haemophilia
pp. 976-979(4)
Authors: NEPARIDZE, N.; KRIZ, N.; ORNSTEIN, D. L.

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Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosis
pp. 980-982(3)
Authors: ERLACHER, M.; HEISS, J.; HAINMANN, I.; UHL, M.; BUDDE, U.; OLDENBURG, J.; IVASKEVICIUS, V.; AL-JAMALI, J.; ZAJONC, H.; SUPERTI-FURGA, A.; ZIEGER, B.

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