Works matching IS 13518216 AND DT 2005 AND VI 11 AND IP 5

Results: 21

Stability of lyophilized and reconstituted plasma/albumin-free recombinant human factor VIII (ADVATE rAHF-PFM).
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 492, doi. 10.1111/j.1365-2516.2005.01128.x
By:
- Parti, R.;
- Schoppmann, A.;
- Lee, H.;
- Yang, L.
Publication type:
Article
Screening women with menorrhagia for underlying bleeding disorders: the utility of the platelet function analyser and bleeding time.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 497, doi. 10.1111/j.1365-2516.2005.01129.x
By:
- Philipp, C. S.;
- Miller, C. H.;
- Faiz, A.;
- Dilley, A.;
- Michaels, L. A.;
- Ayers, C.;
- Bachmann, G.;
- Dowling, N.;
- Saidi, P.
Publication type:
Article
Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 459, doi. 10.1111/j.1365-2516.2005.01134.x
By:
- Ghosh, K.;
- Nair, A. P.;
- Jijina, F.;
- Madkaikar, M.;
- Shetty, S.;
- Mohanty, D.
Publication type:
Article
National haemophilia programme development in the Republic of Georgia.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 529, doi. 10.1111/j.1365-2516.2005.01127.x
By:
- Kirtava, A.;
- Soucie, M.;
- Evatt, B.;
- Mdivinishvili, M.;
- Abashidze, M.;
- Iosava, G.
Publication type:
Article
Intracranial haemorrhages in French haemophilia patients (1991–2001): clinical presentation, management and prognosis factors for death.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 452, doi. 10.1111/j.1365-2516.2005.01090.x
By:
- Stieltjes, N.;
- Calvez, T.;
- Demiguel, V.;
- Torchet, M. F.;
- Briquel, M. E.;
- Fressinaud, E.;
- Claeyssens, S.;
- Coatmelec, B.;
- Chambost, H.
Publication type:
Article
Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 481, doi. 10.1111/j.1365-2516.2005.01121.x
By:
- Jayandharan, G.;
- Shaji, R. V.;
- Baidya, S.;
- Nair, S. C.;
- Chandy, M.;
- Srivastava, A.
Publication type:
Article
Discrepant factor VIII activity in a family with mild haemophilia A and Arg531His mutation using various FVIII assays and APTT reagents.
Published in:
2005
By:
- Lucía, J. F.;
- Aguilar, C.;
- Dobon, M.;
- Aznar, J. A.;
- Tizano, E.;
- Borés, C.;
- Cornudella, R.;
- Calvo, M. T.
Publication type:
Letter
Iliopsoas haemorrhage in patients with haemophilia: results from one centre.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 463, doi. 10.1111/j.1365-2516.2005.01123.x
By:
- Balkan, C.;
- Kavakli, K.;
- Karapinar, D.
Publication type:
Article
Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 438, doi. 10.1111/j.1365-2516.2005.01124.x
By:
- Dijk, K.;
- Fischer, K.;
- Bom, J. G.;
- Grobbee, D. E.;
- Berg, H. M.
Publication type:
Article
Spontaneous major bleeding in acquired factor X deficiency secondary to AL-amyloidosis.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 535, doi. 10.1111/j.1365-2516.2005.01125.x
By:
- Enjeti, A. K.;
- Walsh, M.;
- Seldon, M.
Publication type:
Article
Renal haemophilic pseudotumour.
Published in:
2005
By:
- Gürkan, E.;
- Öçal, F.
Publication type:
Letter
Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group.
Published in:
2005
By:
- Ludlam, C. A.;
- Mannucci, P. M.;
- Powderly, W. G.
Publication type:
Other
The use of a disability model in haemophilia research.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 472, doi. 10.1111/j.1365-2516.2005.01135.x
By:
- Genderen, F. R.;
- Meeteren, N. L. U.;
- Heijnen, L.;
- Berg, H. M.;
- Helders, P. J. M.
Publication type:
Article
A postmarketing surveillance study of the safety and efficacy of ReFacto® (St Louis-derived active substance) in patients with haemophilia A.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 444, doi. 10.1111/j.1365-2516.2005.01131.x
By:
- Smith, M. P.;
- Giangrande, P.;
- Pollman, H.;
- Littlewood, R.;
- Kollmer, C.;
- Feingold, J.
Publication type:
Article
Dental procedures in adult patients with hereditary bleeding disorders: 10 years experience in three Italian Hemophilia Centers.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 504, doi. 10.1111/j.1365-2516.2005.01132.x
By:
- Franchini, M.;
- Rossetti, G.;
- Tagliaferri, A.;
- Pattacini, C.;
- Pozzoli, D.;
- Lorenz, C.;
- Del Dot, L.;
- Ugolotti, G.;
- Dell'Aringa, C.;
- Gandini, G.
Publication type:
Article
Outcome of surgical concepts in haemophilic arthropathy of the hindfoot.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 468, doi. 10.1111/j.1365-2516.2005.01133.x
By:
- Panotopoulos, J.;
- Hanslik-Schnabel, B.;
- Wanivenhaus, A.;
- Trieb, K.
Publication type:
Article
Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 539, doi. 10.1111/j.1365-2516.2005.01137.x
By:
- Onland, W.;
- Böing, A. N.;
- Meijer, A. B.;
- Schaap, M. C. L.;
- Nieuwland, R.;
- Haasnoot, K.;
- Sturk, A.;
- Peters, M.
Publication type:
Article
Acquired haemophilia: management of bleeds and immune therapy to eradicate autoantibodies.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 510, doi. 10.1111/j.1365-2516.2005.01136.x
By:
- Holme, P. A.;
- Brosstad, F.;
- Tjønnfjord, G. E.
Publication type:
Article
Prevalence of conditions associated with human immunodeficiency and hepatitis virus infections among persons with haemophilia, 2001–2003.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 516, doi. 10.1111/j.1365-2516.2005.01138.x
By:
- Goedert, J. J.
Publication type:
Article
Ortner syndrome and haemophilia.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 548, doi. 10.1111/j.1365-2516.2005.01140.x
By:
- Hermans, C.;
- Manocha, S.;
- McLaughlin, J. E.;
- Lipman, M.;
- Lee, C. A.
Publication type:
Article
Major surgery in a severe haemophilia A patient with high titre inhibitor: use of the thrombin generation test in the therapeutic decision.
Published in:
Haemophilia, 2005, v. 11, n. 5, p. 552, doi. 10.1111/j.1365-2516.2005.01141.x
By:
- Dargaud, Y.;
- Lienhart, A.;
- Meunier, S.;
- Hequet, O.;
- Chavanne, H.;
- Chamouard, V.;
- Marin, S.;
- Negrier, C.
Publication type:
Article

Works matching IS 13518216 AND DT 2005 AND VI 11 AND IP 5

Stability of lyophilized and reconstituted plasma/albumin-free recombinant human factor VIII (ADVATE rAHF-PFM).

Screening women with menorrhagia for underlying bleeding disorders: the utility of the platelet function analyser and bleeding time.

Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country.

National haemophilia programme development in the Republic of Georgia.

Intracranial haemorrhages in French haemophilia patients (1991–2001): clinical presentation, management and prognosis factors for death.

Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.

Discrepant factor VIII activity in a family with mild haemophilia A and <sup>Arg</sup>531<sup>His</sup> mutation using various FVIII assays and APTT reagents.

Iliopsoas haemorrhage in patients with haemophilia: results from one centre.

Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed.

Spontaneous major bleeding in acquired factor X deficiency secondary to AL-amyloidosis.

Renal haemophilic pseudotumour.

Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group.

The use of a disability model in haemophilia research.

A postmarketing surveillance study of the safety and efficacy of ReFacto<sup>®</sup> (St Louis-derived active substance) in patients with haemophilia A.

Dental procedures in adult patients with hereditary bleeding disorders: 10 years experience in three Italian Hemophilia Centers.

Outcome of surgical concepts in haemophilic arthropathy of the hindfoot.

Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family.

Acquired haemophilia: management of bleeds and immune therapy to eradicate autoantibodies.

Prevalence of conditions associated with human immunodeficiency and hepatitis virus infections among persons with haemophilia, 2001–2003.

Ortner syndrome and haemophilia.

Major surgery in a severe haemophilia A patient with high titre inhibitor: use of the thrombin generation test in the therapeutic decision.