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                             20 results found
no title author magazine year volume issue page(s) type
1 Anasarca improved by extracorporeal ultrafiltration through an internal shunt in a case of severe haemophilia B with inhibitor and steroid-resistant nephrotic syndrome SATOMURA, A.
2006
12 1 p. 103-105
article
2 A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families FANG, Y.
2006
12 1 p. 62-67
article
3 Canadian multi-institutional survey of immune tolerance therapy (ITT) – experience with the use of recombinant factor VIII for ITT BARNES, C.
2006
12 1 p. 1-6
article
4 Compliance with treatment and understanding of own disease in patients with severe and moderate haemophilia LINDVALL, K.
2006
12 1 p. 47-51
article
5 Congenital factor VII deficiency: therapy with recombinant activated factor VII – a critical appraisal MARIANI, G.
2006
12 1 p. 19-27
article
6 Considerations in the evaluation of haemophilia patients for short-term prophylactic therapy: a paediatric and adult case study LUCHTMAN-JONES, L.
2006
12 1 p. 82-86
article
7 Cost minimization model for treatment of minor bleeding episodes in inhibitor patients – methodological issues SEREMETIS, S.
2006
12 1 p. 108-109
article
8 Deep vein thrombosis in a patient with severe haemophilia A KASHYAP, R.
2006
12 1 p. 87-89
article
9 Haemophilia in Poland WINDYGA, J.
2006
12 1 p. 52-57
article
10 Hepatitis C at the Israeli National Hemophilia Center MAOR, Y.
2006
12 1 p. 68-74
article
11 Higher recovery of factor VIII (FVIII) with intermediate FVIII/von Willebrand factor concentrate than with recombinant FVIII in a haemophilia A patient with an inhibitor INOUE, T.
2006
12 1 p. 110-113
article
12 Inhibitor challenges in the paediatric setting SIEGER, L.
2006
12 1 p. 106-107
article
13 Long-term evaluation of radioisotope synovectomy with Yttrium 90 for chronic synovitis in Turkish haemophiliacs: Izmir experience KAVAKLI, K.
2006
12 1 p. 28-35
article
14 Long-term prophylaxis with intermediate-purity factor VIII concentrate (Haemate P) in a patient with type 3 von Willebrand disease and recurrent gastrointestinal bleeding COPPOLA, A.
2006
12 1 p. 90-94
article
15 Measuring patients’ perceptions on their functional abilities: validation of the Haemophilia Activities List GENDEREN, F. R.
2006
12 1 p. 36-46
article
16 Needles and needleless devices for infusion of anti-haemophilic factor concentrate: impact on protein structure and function PRABHU, S.
2006
12 1 p. 58-61
article
17 Practice patterns in haemophilia A therapy – global progress towards optimal care GERAGHTY, S.
2006
12 1 p. 75-81
article
18 Rituximab for congenital haemophiliacs with inhibitors: a Canadian experience CARCAO, M.
2006
12 1 p. 7-18
article
19 Rituximab in the treatment of high responding inhibitors in severe haemophilia A MOSCHOVI, M.
2006
12 1 p. 95-99
article
20 Successful induction of immune tolerance by continuous infusion of recombinant factor VIII in a haemophilia A patient with high-inhibitor titres TAMURA, K.
2006
12 1 p. 100-102
article
                             20 results found
 
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