Works matching IS 13518216 AND DT 2007 AND VI 13 AND IP 2

Results: 21

The coagulation laboratory needs to move out of the middle age.
Published in:
2007
By:
- LIPTON, R.
Publication type:
Letter
Percutaneous liver biopsy in adult haemophiliacs with hepatitis C virus: safety of outpatient procedure and impact of human immunodeficiency virus coinfection on the spectrum of liver disease.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 164, doi. 10.1111/j.1365-2516.2006.01322.x
By:
- STERLING, R. K.;
- LYONS, C. D.;
- STRAVITZ, R. T.;
- LUKETIC, V. A.;
- SANYAL, A. J.;
- CARR, M. E.;
- SMITH, T. J.;
- HACKNEY, M. H.;
- CONTOS, M. J.;
- MILLS, S. A.;
- KUHN, J. G.;
- NOLTE, M. E.;
- SHIFFMAN, M. L.
Publication type:
Article
Different clinical phenotype in triplets with haemophilia A.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 202, doi. 10.1111/j.1365-2516.2006.01396.x
By:
- BARNES, C.;
- BLANCHETTE, V.;
- LILLICRAP, D.;
- MANN, K.;
- STAIN, A. M.;
- LEGGO, J.;
- HILLIARD, P.;
- CARCAO, M.
Publication type:
Article
Factor VIII Inhibitor Associated with Peginterferon – A Follow Up.
Published in:
2007
By:
- HERMAN, C. H.;
- BOGGIO, L. N.;
- GREEN, D.
Publication type:
Letter
Is primary postpartum haemorrhage a good predictor of inherited bleeding disorders?
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 178, doi. 10.1111/j.1365-2516.2006.01413.x
By:
- KADIR, R. A.;
- KINGMAN, C. E. C.;
- CHI, C.;
- LEE, C. A.;
- ECONOMIDES, D. L.
Publication type:
Article
Hepatitis C virus genotypes among patients with thalassemia and inherited bleeding disorders in Markazi province, Iran.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 156, doi. 10.1111/j.1365-2516.2006.01415.x
By:
- SAMIMI-RAD, K.;
- SHAHBAZ, B.
Publication type:
Article
Efficacy, safety and tolerability of recombinant factor VIII (REFACTO®) in patients with haemophilia A: interim data from a postmarketing surveillance study in Germany and Austria.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 131, doi. 10.1111/j.1365-2516.2006.01416.x
By:
- POLLMANN, H.;
- EXTERNEST, D.;
- GANSER, A.;
- EIFRIG, B.;
- KREUZ, W.;
- LENK, H.;
- PABINGER, I.;
- SCHRAMM, W.;
- SCHWARZ, T. F.;
- ZIMMERMANN, R.;
- ZAVAZAVA, N.;
- OLDENBURG, J.;
- KLAMROTH, R.
Publication type:
Article
ReFacto®.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 124, doi. 10.1111/j.1365-2516.2006.01420.x
By:
- DI PAOLA, J.;
- SMITH, M. P.;
- KLAMROTH, R.;
- MANNUCCI, P. M.;
- KOLLMER, C.;
- FEINGOLD, J.;
- KESSLER, C.;
- POLLMANN, H.;
- MORFINI, M.;
- UDATA, C.;
- ROTHSCHILD, C.;
- HERMANS, C.;
- JANCO, R.
Publication type:
Article
Communicating about haemophilia within the family: the importance of context and of experience.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 189, doi. 10.1111/j.1365-2516.2006.01417.x
By:
- GREGORY, M.;
- BODDINGTON, P.;
- DIMOND, R.;
- ATKINSON, P.;
- CLARKE, A.;
- COLLINS, P.
Publication type:
Article
Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 149, doi. 10.1111/j.1365-2516.2006.01418.x
By:
- CHALMERS, E. A.;
- BROWN, S. A.;
- KEELING, D.;
- LIESNER, R.;
- RICHARDS, M.;
- STIRLING, D.;
- THOMAS, A.;
- VIDLER, V.;
- WILLIAMS, M. D.;
- YOUNG, D.
Publication type:
Article
Pharmacovigilance studies in haemophilia.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 121, doi. 10.1111/j.1365-2516.2006.01419.x
By:
- INGERSLEV, J.
Publication type:
Article
Successful concurrent triple surgery in an adolescent patient with haemophilia A and inhibitors treated with recombinant factor VIIa.
Published in:
2007
By:
- JANIC, D.;
- BRDAR, R.;
- KRISTIC, Z.;
- JOVANOVIC, N.;
- DOKMANOVIC, L.;
- RODIC, P.;
- PETRONIC, I.;
- ANTOVIC, J.
Publication type:
Letter
Inhibitor development in one patient and laboratory discrepancies in several families with both mild haemophilia and Arg531Cys mutation.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 206, doi. 10.1111/j.1365-2516.2006.01422.x
By:
- CID, A. R.;
- CASAÑA, P.;
- CABRERA, N.;
- HAYA, S.;
- CORTINA, V.;
- AZNAR, J. A.
Publication type:
Article
Multicentric giant cell tumours in an adolescent with haemophilia.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 199, doi. 10.1111/j.1365-2516.2006.01423.x
By:
- CHANG, C.-C.;
- CHANG, S.-T.;
- CHANG, H.-Y.;
- LIN, G.-M.;
- LAI, M.-H.;
- CHIANG, S.-L.
Publication type:
Article
32P colloid radiosynovectomy in treatment of chronic haemophilic synovitis: Iran experience.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 182, doi. 10.1111/j.1365-2516.2006.01424.x
By:
- MORTAZAVI, S. M. J.;
- ASADOLLAHI, S.;
- FARZAN, M.;
- SHAHRIARAN, S.;
- AGHILI, M.;
- IZADYAR, S.;
- LAK, M.
Publication type:
Article
Successful combination therapy of a proximal haemophilic pseudotumour with surgery, radiation and embolization in a child with mild haemophilia A.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 209, doi. 10.1111/j.1365-2516.2006.01425.x
By:
- AHUJA, S. P.;
- SIDONIO, R.;
- RAJ, A. B.;
- BERTOLONE, S. J.;
- SILVERMAN, C.;
- ANTEKEIER, D. P.;
- FALLAT, M. E.
Publication type:
Article
The haemophilic pseudotumour – surgical treatment by excision and filling the defect with calcium-phosphate cement granules.
Published in:
2007
By:
- MOHANTY, S. S.;
- BHASME, V. K.;
- GARG, H.;
- WARGANTIWAR, A.
Publication type:
Letter
Efficacy and safety of a high purity, double virus inactivated factor VIII/von Willebrand factor concentrate (Biostate®) in patients with von Willebrand disorder requiring invasive or surgical procedures.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 144, doi. 10.1111/j.1365-2516.2006.01430.x
By:
- SHORTT, J.;
- DUNKLEY, S.;
- RICKARD, K.;
- BAKER, R.;
- STREET, A.
Publication type:
Article
Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders.
Published in:
Haemophilia, 2007, v. 13, n. 2, p. 172, doi. 10.1111/j.1365-2516.2006.01431.x
By:
- SHETTY, S.;
- GHOSH, K.
Publication type:
Article
Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis.
Published in:
2007
By:
- TRIGUI, N.;
- FRÈRE, C.;
- D'ERCOLE, C.;
- CHAMBOST, H.;
- CHAPUIS, N.;
- POUYMAYOU, C.;
- MORANGE, P.;
- DE MAZANCOURT, P.
Publication type:
Letter
Blastocystis hominis colitis in a haemophilic patient as a cause of lower gastrointestinal bleeding.
Published in:
2007
By:
- LUCÍA, J. F.;
- AGUILAR, C.;
- BETRAN, A.
Publication type:
Letter

Works matching IS 13518216 AND DT 2007 AND VI 13 AND IP 2

The coagulation laboratory needs to move out of the middle age.

Percutaneous liver biopsy in adult haemophiliacs with hepatitis C virus: safety of outpatient procedure and impact of human immunodeficiency virus coinfection on the spectrum of liver disease.

Different clinical phenotype in triplets with haemophilia A.

Factor VIII Inhibitor Associated with Peginterferon – A Follow Up.

Is primary postpartum haemorrhage a good predictor of inherited bleeding disorders?

Hepatitis C virus genotypes among patients with thalassemia and inherited bleeding disorders in Markazi province, Iran.

Efficacy, safety and tolerability of recombinant factor VIII (REFACTO<sup>®</sup>) in patients with haemophilia A: interim data from a postmarketing surveillance study in Germany and Austria.

ReFacto®.

Communicating about haemophilia within the family: the importance of context and of experience.

Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A.

Pharmacovigilance studies in haemophilia.

Successful concurrent triple surgery in an adolescent patient with haemophilia A and inhibitors treated with recombinant factor VIIa.

Inhibitor development in one patient and laboratory discrepancies in several families with both mild haemophilia and Arg531Cys mutation.

Multicentric giant cell tumours in an adolescent with haemophilia.

<sup>32</sup>P colloid radiosynovectomy in treatment of chronic haemophilic synovitis: Iran experience.

Successful combination therapy of a proximal haemophilic pseudotumour with surgery, radiation and embolization in a child with mild haemophilia A.

The haemophilic pseudotumour – surgical treatment by excision and filling the defect with calcium-phosphate cement granules.

Efficacy and safety of a high purity, double virus inactivated factor VIII/von Willebrand factor concentrate (Biostate<sup>®</sup>) in patients with von Willebrand disorder requiring invasive or surgical procedures.

Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders.

Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis.

Blastocystis hominis colitis in a haemophilic patient as a cause of lower gastrointestinal bleeding.