Works matching IS 13518216 AND DT 2008 AND VI 14

Results: 283

Prevention of haemophilic arthropathy in haemophilic children with inhibitors.

Published in:

Haemophilia, 2008, v. 14, p. 1, doi. 10.1111/j.1365-2516.2008.01881.x

By:

RODRIGUEZ-MERCHAN, E. C.

Publication type:

Article

Haemophilic arthropathy: the importance of the earliest haemarthroses and consequences for treatment.

Published in:

Haemophilia, 2008, v. 14, p. 4, doi. 10.1111/j.1365-2516.2008.01882.x

By:

ROOSENDAAL, G.;
JANSEN, N. W. D.;
SCHUTGENS, R.;
LAFEBER, F. P. J. G.

Publication type:

Article

Prevention of arthropathy in haemophilia – intensive on-demand treatment, UK perspective.

Published in:

Haemophilia, 2008, v. 14, p. 11, doi. 10.1111/j.1365-2516.2008.01883.x

By:

LEE, C. A.

Publication type:

Article

Prevention of arthropathy in haemophilia: prophylaxis.

Published in:

Haemophilia, 2008, v. 14, p. 16, doi. 10.1111/j.1365-2516.2008.01884.x

By:

SANTAGOSTINO, E.;
MANCUSO, M. E.

Publication type:

Article

Articular status of haemophilia patients with inhibitors.

Published in:

Haemophilia, 2008, v. 14, p. 20, doi. 10.1111/j.1365-2516.2008.01885.x

By:

MORFINI, M.

Publication type:

Article

Prevention of arthropathy: may it be extrapolated from patients without inhibitors to patients with inhibitors?

Published in:

Haemophilia, 2008, v. 14, p. 23, doi. 10.1111/j.1365-2516.2008.01886.x

By:

HEDNER, U.

Publication type:

Article

Experiences in the prevention of arthropathy in haemophila patients with inhibitors.

Published in:

Haemophilia, 2008, v. 14, p. 28, doi. 10.1111/j.1365-2516.2008.01887.x

By:

JIMENEZ-YUSTE, V.;
RODRIGUEZ-MERCHAN, E. C.;
ALVAREZ, M. T.;
QUINTANA, M.;
MARTIN-SALCES, M.;
HERNANDEZ-NAVARRO, F.

Publication type:

Article

Clinical and echographical control protocol of haemarthrosis in haemophilia patients with inhibitors: evaluation of the efficacy of recombinant factor VIIa in the evolution process (EFFISEVEN protocol).

Published in:

Haemophilia, 2008, v. 14, p. 36, doi. 10.1111/j.1365-2516.2008.01888.x

By:

QUEROL, F.;
CORTINA, V.;
CID, A. R.;
HAYA, S.;
AZNAR, J. A.

Publication type:

Article

The role of rehabilitation and sports in haemophilia patients with inhibitors.

Published in:

Haemophilia, 2008, v. 14, p. 45, doi. 10.1111/j.1365-2516.2008.01889.x

By:

HEIJNEN, L.

Publication type:

Article

Synoviorthesis in haemophilia patients with inhibitors.

Published in:

Haemophilia, 2008, v. 14, p. 52, doi. 10.1111/j.1365-2516.2008.01890.x

By:

PASTA, G.;
MANCUSO, M. E.;
PERFETTO, O. S.;
SOLIMENO, L. P.

Publication type:

Article

Orthopaedic surgery in haemophilia patients with inhibitors as the last resort.

Published in:

Haemophilia, 2008, v. 14, p. 56, doi. 10.1111/j.1365-2516.2008.01891.x

By:

RODRIGUEZ-MERCHAN, E. C.;
QUINTANA, M.;
JIMENEZ-YUSTE, V.

Publication type:

Article

Prevention of haemophilic arthropathy during childhood. May common orthopaedic management be extrapolated from patients without inhibitors to patients with inhibitors?

Published in:

Haemophilia, 2008, v. 14, p. 68, doi. 10.1111/j.1365-2516.2008.01892.x

By:

RODRIGUEZ-MERCHAN, E. C.;
HEDNER, U.;
HEIJNEN, L.;
JIMENEZ-YUSTE, V.;
LEE, C. A.;
MORFINI, M.;
QUEROL, F.;
ROOSENDAAL, G.;
SANTAGOSTINO, E.;
SOLIMENO, L. P.

Publication type:

Article

von Willebrand’s disease: from discovery to therapy – milestones in the last 25 years.

Published in:

2008

By:

KREUZ, W.

Publication type:

Editorial

Haemate® P von Willebrand factor/factor VIII concentrate: 25 years of clinical experience.

Published in:

Haemophilia, 2008, v. 14, p. 3, doi. 10.1111/j.1365-2516.2008.01847.x

By:

SCHRAMM, W.

Publication type:

Article

Function of von Willebrand factor in haemostasis and thrombosis.

Published in:

Haemophilia, 2008, v. 14, p. 11, doi. 10.1111/j.1365-2516.2008.01848.x

By:

REININGER, A. J.

Publication type:

Article

Diagnosis of von Willebrand disease subtypes: implications for treatment.

Published in:

Haemophilia, 2008, v. 14, p. 27, doi. 10.1111/j.1365-2516.2008.01849.x

By:

BUDDE, U.

Publication type:

Article

Haemate® P/Humate-P® for the treatment of von Willebrand disease: considerations for use and clinical experience.

Published in:

Haemophilia, 2008, v. 14, p. 39, doi. 10.1111/j.1365-2516.2008.01850.x

By:

AUERSWALD, G.;
KREUZ, W.

Publication type:

Article

Prophylaxis in von Willebrand disease.

Published in:

Haemophilia, 2008, v. 14, p. 47, doi. 10.1111/j.1365-2516.2008.01851.x

By:

BERNTORP, E.

Publication type:

Article

Pathogen safety of plasma-derived products – Haemate® P/Humate-P®.

Published in:

Haemophilia, 2008, v. 14, p. 54, doi. 10.1111/j.1365-2516.2008.01852.x

By:

GRÖNER, A.

Publication type:

Article

Factor XI deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1183, doi. 10.1111/j.1365-2516.2008.01667.x

By:

GOMEZ, K.;
BOLTON-MAGGS, P.

Publication type:

Article

α2-Antiplasmin and its deficiency: fibrinolysis out of balance.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1250, doi. 10.1111/j.1365-2516.2008.01766.x

By:

CARPENTER, S. L.;
MATHEW, P.

Publication type:

Article

Hereditary haemorrhagic telangiectasia.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1269, doi. 10.1111/j.1365-2516.2008.01774.x

By:

SHARATHKUMAR, A. A.;
SHAPIRO, A.

Publication type:

Article

Protein S deficiency: a clinical perspective.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1222, doi. 10.1111/j.1365-2516.2008.01775.x

By:

TEN KATE, M. K.;
VAN DER MEER, J.

Publication type:

Article

Factor V deficiency: a concise review.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1164, doi. 10.1111/j.1365-2516.2008.01785.x

By:

HUANG, J. N.;
KOERPER, M. A.

Publication type:

Article

Plasminogen deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1261, doi. 10.1111/j.1365-2516.2008.01825.x

By:

MEHTA, R.;
SHAPIRO, A. D.

Publication type:

Article

Inherited antithrombin deficiency: a review.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1229, doi. 10.1111/j.1365-2516.2008.01830.x

By:

PATNAIK, M. M.;
MOLL, S.

Publication type:

Article

Rare inherited disorders of fibrinogen.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1151, doi. 10.1111/j.1365-2516.2008.01831.x

By:

ACHARYA, S. S.;
DIMICHELE, D. M.

Publication type:

Article

Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1159, doi. 10.1111/j.1365-2516.2008.01832.x

By:

MEEKS, S. L.;
ABSHIRE, T. C.

Publication type:

Article

Plasminogen activator inhibitor type 1 deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1255, doi. 10.1111/j.1365-2516.2008.01834.x

By:

MEHTA, R.;
SHAPIRO, A. D.

Publication type:

Article

Protein C deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1214, doi. 10.1111/j.1365-2516.2008.01838.x

By:

GOLDENBERG, N. A.;
MANCO-JOHNSON, M. J.

Publication type:

Article

Factor VII deficiency: defining the clinical picture and optimizing therapeutic options.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1170, doi. 10.1111/j.1365-2516.2008.01844.x

By:

LAPECORELLA, M.;
MARIANI, G.

Publication type:

Article

Combined FV and FVIII deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1201, doi. 10.1111/j.1365-2516.2008.01845.x

By:

SPREAFICO, M.;
PEYVANDI, F.

Publication type:

Article

Familial deficiency of vitamin K-dependent clotting factors.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1209, doi. 10.1111/j.1365-2516.2008.01853.x

By:

WESTON, B. W.;
MONAHAN, P. E.

Publication type:

Article

Diagnosis and treatment of inherited factor X deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1176, doi. 10.1111/j.1365-2516.2008.01856.x

By:

BROWN, D. L.;
KOUIDES, P. A.

Publication type:

Article

Factor XIII deficiency.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1190, doi. 10.1111/j.1365-2516.2008.01857.x

By:

HSIEH, L.;
NUGENT, D.

Publication type:

Article

Platelet function defects.

Published in:

Haemophilia, 2008, v. 14, n. 6, p. 1240, doi. 10.1111/j.1365-2516.2008.01898.x

By:

SIMON, D.;
KUNICKI, T.;
NUGENT, D.

Publication type:

Article

Infusion rates of recombinant FVIII-FS with PEGylated liposomes in haemophilia A.

Published in:

2008

By:

MARTINOWITZ, U.;
LALEZARI, S.;
LUBOSHITZ, J.;
LUBETSKY, A.;
SPIRA, J.

Publication type:

Letter

The role of physiotherapy after total knee arthroplasty in patients with haemophilia.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 989, doi. 10.1111/j.1365-2516.2008.01748.x

By:

LOBET, S.;
PENDEVILLE, E.;
DALZELL, R.;
DEFALQUE, A.;
LAMBERT, C.;
POTHEN, D.;
HERMANS, C.

Publication type:

Article

Prophylaxis with recombinant factor VIIa for the management of bleeding episodes during immune tolerance treatment in a boy with severe haemophilia A and high-response inhibitors.

Published in:

2008

By:

BLATNY, J.;
KOHLEROVA, S.;
ZAPLETAL, O.;
FIAMOLI, V.;
PENKA, M.;
SMITH, O.

Publication type:

Letter

Putting the shoe on the wrong foot: a reply to Ponder and Srivastava.

Published in:

2008

By:

KIMMELMAN, J.

Publication type:

Letter

The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 1082, doi. 10.1111/j.1365-2516.2008.01779.x

By:

HUSSEIN, I. R.;
EL-BESHLAWY, A.;
SALEM, A.;
MOSAAD, R.;
ZAGHLOUL, N.;
RAGAB, L.;
FAYEK, H.;
GABER, K.;
EL-EKIABI, M.

Publication type:

Article

Use of recombinant factor VIIa for hip replacement surgery in a patient with severe factor XI deficiency and drug-induced platelet defect.

Published in:

2008

By:

DEMPFLE, C.-E.;
FRIETSCH, T.;
HOFFMANN, T.;
AHMAD-NEJAD, P.;
NEUMAIER, M.;
BORGGREFE, M.

Publication type:

Letter

One-stage and chromogenic FVIII:C assay discrepancy in mild haemophilia A and the relationship with the mutation and bleeding phenotype.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 1049, doi. 10.1111/j.1365-2516.2008.01781.x

By:

CID, A. R.;
CALABUIG, M.;
CORTINA, V.;
CASAÑA, P.;
HAYA, S.;
MORET, A.;
CABRERA, N.;
AZNAR, J. A.

Publication type:

Article

Clinical efficacy in bleeding and surgery in von Willebrand patients treated with Fanhdi® a highly purified, doubly inactivated FVIII/VWF concentrate.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 963, doi. 10.1111/j.1365-2516.2008.01784.x

By:

HERNANDEZ-NAVARRO, F.;
QUINTANA, M.;
JIMENEZ-YUSTE, V.;
ALVAREZ, M. T.;
FERNANDEZ-MORATA, R.

Publication type:

Article

Skewed X chromosome inactivation in fraternal female twins results in moderately severe and mild haemophilia B.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 1088, doi. 10.1111/j.1365-2516.2008.01786.x

By:

OKUMURA, K.;
FUJIMORI, Y.;
TAKAGI, A.;
MURATE, T.;
OZEKI, M.;
YAMAMOTO, K.;
KATSUMI, A.;
MATSUSHITA, T.;
NAOE, T.;
KOJIMA, T.

Publication type:

Article

Efficacy of different doses of recombinant activated factor VII in the treatment of haemophilia children with inhibitor.

Published in:

2008

By:

CHUANSUMRIT, A.;
SIRACHAINAN, N.;
PAKAKASAMA, S.;
SUEBSANGAD, A.;
CHOTSUPPAKARN, S.;
WONGWERAWATTANAKOON, P.

Publication type:

Letter

Structural analysis of factor IX protein variants to predict functional aberration causing haemophilia B.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 1076, doi. 10.1111/j.1365-2516.2008.01788.x

By:

MUKHERJEE, S.;
SAHA, A.;
BISWAS, P.;
MANDAL, C.;
RAY, K.

Publication type:

Article

The use of a psychological intervention to increase adherence during factor administration in a child with haemophilia.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 939, doi. 10.1111/j.1365-2516.2008.01789.x

By:

PENICA, S.;
WILLIAMS, K. E.

Publication type:

Article

Necrotizing enterocolitis as a result of postcircumcision bleeding in a neonate with haemophilia A.

Published in:

2008

By:

DUNN, A. L.

Publication type:

Letter

Effects of secondary prophylaxis started in adolescent and adult haemophiliacs.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 945, doi. 10.1111/j.1365-2516.2008.01791.x

By:

TAGLIAFERRI, A.;
FRANCHINI, M.;
COPPOLA, A.;
RIVOLTA, G. F.;
SANTORO, C.;
ROSSETTI, G.;
FEOLA, G.;
ZANON, E.;
DRAGANI, A.;
IANNACCARO, P.;
RADOSSI, P.;
MANNUCCI, P. M.

Publication type:

Article