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Publisher: Wiley-Blackwell

Volume 15, Number 6, November 2009

Mosaics and haemophilia
pp. 1181-1186(6)
Authors: KASPER, C. K.; BUZIN, C. H.

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Functional roles of the factor VIII B domain
pp. 1187-1196(10)
Author: PIPE, S. W.

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Emerging clinical concerns in the ageing haemophilia patient
pp. 1197-1209(13)
Authors: KONKLE, B. A.; KESSLER, C.; ALEDORT, L.; ANDERSEN, J.; FOGARTY, P.; KOUIDES, P.; QUON, D.; RAGNI, M.; ZAKARIJA, A.; EWENSTEIN, B.

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Changing patterns of bleeding in patients with severe haemophilia A
pp. 1210-1214(5)
Authors: STEPHENSEN, D.; TAIT, R. C.; BRODIE, N.; COLLINS, P.; CHEAL, R.; KEELING, D.; MELTON, K.; DOLAN, G.; HAYE, H.; HAYMAN, E.; WINTER, M.

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Efficacy assessment of a new clotting factor concentrate in haemophilia A patients, including prophylactic treatment
pp. 1215-1218(4)
Authors: DEN UIJL, I.; MAUSER-BUNSCHOTEN, E. P.; ROOSENDAAL, G.; SCHUTGENS, R.; FISCHER, K.

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Polymorphism in factor VII gene modifies phenotype of severe haemophilia
pp. 1228-1236(9)
Authors: JAYANDHARAN, G. R.; NAIR, S. C.; POONNOOSE, P. M.; THOMAS, R.; JOHN, J.; KESHAV, S. K.; CHERIAN, R. S.; DEVADARISHINI, M.; LAKSHMI, K. M.; SHAJI, R. V.; VISWABANDYA, A.; GEORGE, B.; MATHEWS, V.; CHANDY, M.; SRIVASTAVA, A.

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Pharmacokinetic study of a high-purity factor IX concentrate (Factor IX Grifols®) with a 6-month follow up in previously treated patients with severe haemophilia B
pp. 1243-1248(6)
Authors: AZNAR, J. A.; CABRERA, N.; MATYSIAK, M.; ZAWILSKA, K.; GERCHEVA, L.; ANTONOV, A.; MONTAÑÉS, M.; PÁEZ, A. M.; LISSITCHKOV, T.

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Elimination capacity of a TSE-model agent in the manufacturing process of Alphanate®/Fanhdi®, a human factor VIII/VWF complex concentrate
pp. 1249-1257(9)
Authors: DIEZ, J. M.; CABALLERO, S.; BELDA, F. J.; OTEGUI, M.; GAJARDO, R.; JORQUERA, J. I.

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Undetected factor VIII in a patient with type 3 von Willebrands disease mistaken as severe haemophilia A
pp. 1258-1261(4)
Authors: MULLAH-ALI, A. M.; CHAN, A. K.; LILLICRAP, D.; DECKER, K.; SEROSKI, W.; MOFFAT, K.; WALKER, I.; PAI, M. K.

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Ethanol lock therapy for the treatment of catheter-related infections in haemophilia patients
pp. 1267-1271(5)
Authors: RAJPURKAR, M.; BOLDT-MACDONALD, K.; MCLENON, R.; CALLAGHAN, M. U.; CHITLUR, M.; LUSHER, J. M.; BECKER, C.

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Monthly recombinant tissue plasminogen activator administration to implantable central venous access devices decreases infections in children with haemophilia
pp. 1272-1280(9)
Authors: JENG, M. R.; O’BRIEN, M.; WONG, W.; ZOLAND, J.; LEA, J.; TANG, N.; GLADER, B.

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Sites of initial bleeding episodes, mode of delivery and age of diagnosis in babies with haemophilia diagnosed before the age of 2 years: a report from The Centers for Disease Control and Prevention’s (CDC) Universal Data Collection (UDC) project
pp. 1281-1290(10)
Authors: KULKARNI, R.; SOUCIE, J. M.; LUSHER, J.; PRESLEY, R.; SHAPIRO, A.; GILL, J.; MANCO-JOHNSON, M.; KOERPER, M.; MATHEW, P.; ABSHIRE, T.; DIMICHELE, D.; HOOTS, K.; JANCO, R.; NUGENT, D.; GERAGHTY, S.; EVATT, B.

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Gynaecological and obstetrical problems in women with different bleeding disorders
pp. 1291-1299(9)
Authors: SIBONI, S. M.; SPREAFICO, M.; CALÒ, L.; MAINO, A.; SANTAGOSTINO, E.; FEDERICI, A. B.; PEYVANDI, F.

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Profiling of factor VIII mutations in Korean haemophilia A
pp. 1311-1317(7)
Authors: HWANG, S. H.; KIM, M. J.; LIM, J. A.; KIM, H. C.; KIM, H. S.

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The national registry of haemophilia A and B in Spain: results from a census of patients
pp. 1327-1330(4)
Authors: AZNAR, J. A.; ABAD-FRANCH, L.; CORTINA, V. R.; MARCO, P.

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The new age of haemophilia
pp. 1330-1331(2)
Authors: LAMBING, A.; KACHALSKY, E.

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Successful liver surgery in a haemophilia patient with high titre factor VIII inhibitor
pp. 1332-1333(2)
Authors: JONES, A. E.; ROY, A.; ARMSTRONG, T.; REES, M.; WELSH, F. K.

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Acquired factor VIII inhibitor in patient infected with HIV: a casual association or a prone immunological setting?
pp. 1334-1335(2)
Authors: MIGLIORE, E.; ALLIONE, A.; DUTTO, L.; BERNARDI, E.; VETTORAZZI, L. A.; RICCA, M.; TARTAGLINO, B.; RAPEZZI, D.; GRASSO, M.

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Non-catheter related internal jugular vein thrombosis in a patient with severe haemophilia A
pp. 1339-1340(2)
Authors: RAO, A. A. N.; KUMAR, R.; ARTEAGA, G. M.; GALARDY, P. J.; RODRIGUEZ, V.

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Type IIb von Willebrand disease with angiodysplasias and refractory gastrointestinal bleeding successfully treated with thalidomide
pp. 1340-1342(3)
Authors: NOMIKOU, E.; TSEVRENIS, V.; GAFOU, A.; BELLIA, M.; THEODOSSIADES, G.

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Clinical variability of haemophilia A and B in Mexican families by factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T/A1298C
pp. 1342-1345(4)
Authors: LÓPEZ-JIMÉNEZ, J. J.; BELTRÁN-MIRANDA, C. P.; MANTILLA-CAPACHO, J. M.; ESPARZA-FLORES, M. A.; LÓPEZ GONZÁLEZ, L. C.; JALOMA-CRUZ, A. R.

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Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand gene
pp. 1346-1348(3)
Authors: ACQUILA, M.; BOTTINI, F.; DI DUCA, M.; VIJZELAAR, R.; MOLINARI, A. C.; BICOCCHI, M. P.

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Effect of the F8 mutation c.1538-2A>T on pre-mRNA splicing
pp. 1348-1350(3)
Authors: LAURIE, A. D.; SMITH, M. P.

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Pregnancy in a patient with severe factor X deficiency
pp. 1351-1353(3)
Authors: MAMOPOULOS, A.; VAKALOPOULOU, S.; LEFKOU, E.; FILELI, A.; GARIPIDOU, V.; MAVROMATIDIS, G.; DINAS, K.; KARAGIANNIS, V.

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