Works matching IS 13518216 AND DT 2018 AND VI 24 AND IP 4

Results: 60

New Editor‐in‐Chief for Haemophilia!

Published in:: Haemophilia, 2018, v. 24, n. 4, p. 513, doi. 10.1111/hae.13599
Publication type:: Article

A changing haemophilia world: Opportunities and challenges for the Haemophilia journal.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 514, doi. 10.1111/hae.13602

By:

Hermans, Cedric

Publication type:

Article

Performance of next‐generation sequencing in the detection of large exon deletion in patients of haemophilia A.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e296, doi. 10.1111/hae.13584

By:

He, X.;
Xiong, Z.;
Shen, N.;
Lu, Y.;
Wang, X.

Publication type:

Article

rFIXFc for Immune Tolerance Induction in a Severe Hemophilia B Patient with an Inhibitor and Prior History of ITI Related Nephrotic Syndrome.

Published in:

2018

By:

Malec, Lynn;
Abshire, Thomas;
Jobe, Shawn;
White, Gilbert

Publication type:

Case Study

Unexpectedly high response to DDAVP in two patients with moderate haemophilia A.

Published in:

2018

By:

Polzella, P.;
Coutts, K.;
Bignell, P.;
Curry, N.

Publication type:

Case Study

A novel synonymous variant in the F8 gene, p.(Leu40=)/c.120C>A, likely causes mild haemophilia A.

Published in:

2018

By:

Inaba, H.;
Shinozawa, K.;
Fukutake, K.;
Amano, K.

Publication type:

Letter to the Editor

Surgical treatment of ruptured giant haemophilic pseudotumour complicated with infection: A case report and literature review.

Published in:

2018

By:

Feng, B.;
Li, Y. L.;
Jiang, C.;
Qiu, G. X.;
Weng, X. S.

Publication type:

Case Study

Successful immune tolerance in a young female with inhibitor and severe haemophilia A due to a complex genetic rearrangement.

Published in:

2018

By:

Zuccherato, L. W.;
Roberti, M. R. F.;
Jardim, L. L.;
Rezende, S. M.

Publication type:

Case Study

Continuous infusion of extended half‐life factor VIII (efmoroctocog alpha) for surgery in severe haemophilia A.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e280, doi. 10.1111/hae.13557

By:

Kremer Hovinga, I. C. L.;
Schutgens, R. E. G.;
van der Valk, P. R.;
van Vulpen, L. F. D.;
Mauser‐Bunschoten, E. P.;
Fischer, K.

Publication type:

Article

The combination of urinary CTX‐II and serum CS‐846: Promising biochemical markers to predict radiographic progression of haemophilic arthropathy—An exploratory study.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e278, doi. 10.1111/hae.13554

By:

Pulles, A. E.;
Mastbergen, S. C.;
Foppen, W.;
Schutgens, R. E. G.;
Lafeber, F. P. J. G.;
van Vulpen, L. F. D.

Publication type:

Article

Defining patient value in haemophilia care.

Published in:

2018

By:

van Balen, E. C.;
Gouw, S. C.;
Hazelzet, J. A.;
van der Bom, J. G.;
Cnossen, M. H.

Publication type:

Editorial

Recombinant activated factor VII in approved indications: Update on safety.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e275, doi. 10.1111/hae.13547

By:

Neufeld, E. J.;
Négrier, C.;
Benchikh el Fegoun, S.;
Cooper, D. L.;
Rojas‐Rios, A.;
Seremetis, S.

Publication type:

Article

Comment on: Interpreting data on inhibitor development from previously untreated patient studies, beware of premature conclusions.

Published in:

2018

By:

Liesner, Dr R. J.

Publication type:

Letter to the Editor

Haemophilia clinical care and research needs: Assessing priorities.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e270, doi. 10.1111/hae.13544

By:

Chowdary, P.;
Angchaisuksiri, P.;
Dimsits, J.;
Iorio, A.;
Kavakli, K.;
Lentz, S. R.;
Mahlangu, J.;
McCarthy, A.;
Kessler, C.

Publication type:

Article

Recombinant FVIIa therapy for heavy menstrual bleeding in patients with severe FV deficiency.

Published in:

2018

By:

Kaya, Z.

Publication type:

Case Study

Blood group O: A novel risk factor for increased postpartum blood loss?

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e207, doi. 10.1111/hae.13537

By:

Kahr, M. K.;
Franke, D.;
Brun, R.;
Wisser, J.;
Zimmermann, R.;
Haslinger, C.

Publication type:

Article

The viability and necessity of APRN‐led care models in the clinical management of haemophilia and other inherited bleeding and clotting disorders.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 563, doi. 10.1111/hae.13536

By:

Federizo, A.;
Shullick, M.;
Witkop, M.

Publication type:

Article

Choices of factor VIII products in previously untreated patients with haemophilia A: A global survey.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e266, doi. 10.1111/hae.13535

By:

Peyvandi, F.;
Palla, R.;
Franchi, C.;
Nobili, A.;
Rosendaal, F. R.;
Mannucci, P. M.

Publication type:

Article

Prophylactic bypassing agent use before and during immune tolerance induction in patients with haemophilia A and inhibitors to FVIII.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 570, doi. 10.1111/hae.13534

By:

Carpenter, S. L.;
Khair, K.;
Gringeri, A.;
Valentino, L. A.

Publication type:

Article

Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutation.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e263, doi. 10.1111/hae.13532

By:

Pagliari, M. T.;
Baronciani, L.;
Stufano, F.;
Colpani, P.;
Siboni, S. M.;
Peyvandi, F.

Publication type:

Article

Utility of global hemostatic assays in the management of anticoagulation in a haemophilia patient.

Published in:

2018

By:

Wu, I. Q.;
Tan, C. W.;
Wong, W. H.;
Ng, H. J.

Publication type:

Letter to the Editor

Letter to the Editor of Haemophilia.

Published in:

2018

By:

Faber, J.‐C.

Publication type:

Letter to the Editor

The Kids' immune thrombocytopenia Tool is not suitable for assessing quality of life in children with platelet function disorders.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e259, doi. 10.1111/hae.13528

By:

Khair, Kate;
Holland, Michael

Publication type:

Article

Head trauma in the haemophilic child and management in a paediatric emergency department: Descriptive study.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e187, doi. 10.1111/hae.13526

By:

García Sánchez, P.;
Molina Gutiérrez, M. Á.;
Martín Sánchez, J.;
Inisterra Viu, L.;
García García, S.;
Rivas Pollmar, M. I.;
Martín Salces, M.;
Álvarez Román, M. T.;
Jiménez Yuste, V.

Publication type:

Article

Principles of haemophilia care: The Asia‐Pacific perspective.

Published in:

2018

By:

Burnouf, T.

Publication type:

Letter to the Editor

Principles of haemophilia care: The asia pacific perspective. Response.

Published in:

2018

By:

Dunkley, S.;
Lam, J. C. M.;
John, M. J.;
Wong, R. S. M.;
Tran, H.;
Yang, R.;
Nair, S. C.;
Shima, M.;
Street, A.;
Srivastava, A.

Publication type:

Letter to the Editor

Postpartum haemorrhage in an unselected cohort of carriers of haemophilia.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e256, doi. 10.1111/hae.13521

By:

Zwagemaker, A.;
Gouw, S. C.;
Valk, C.;
Ganzevoort, W.;
Coppens, M.;
Peters, M.

Publication type:

Article

Role of chromogenic assays in haemophilia A and B diagnosis.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 578, doi. 10.1111/hae.13520

By:

Bowyer, A. E.;
Duncan, E. M.;
Antovic, J. P.

Publication type:

Article

Miracle of haemophilia drugs: Personal views about a few main players.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 557, doi. 10.1111/hae.13519

By:

Mannucci, P. M.

Publication type:

Article

The Jamaican Haemophilia Registry: Describing the burden of disease.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e179, doi. 10.1111/hae.13517

By:

Wharfe, G.;
Buchner‐Daley, L.;
Gibson, T.;
Hilliard, P.;
Usuba, K.;
Abad, A.;
Boma‐Fischer, L.;
Bouskill, V.;
Floros, G.;
Lillicrap, D.;
Lowe, Y.;
Lowe, D.;
Palmer‐Mitchell, N.;
Rand, M. L.;
Teitel, J.;
Tuttle, A.;
Watson, A.;
White, R.;
Young, N. L.;
Blanchette, V. S.

Publication type:

Article

Low bone mineral density and associated factors in patients with haemophilia in Colombia.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e222, doi. 10.1111/hae.13516

By:

Sossa Melo, C. L.;
Wandurraga, E. A.;
Peña, A. M.;
Jiménez, S. I.;
Salazar, L. A.;
Ochoa, M. E.;
Luna‐Gonzalez, M. L.;
Ortiz, M. L.;
Morales, K.;
Ayala‐Castillo, M.;
Reyes, D. L.;
Chalela, C. M.

Publication type:

Article

Perspectives on haemophilia access in Brazil?

Published in:

2018

By:

Guedes, V. G.;
Thomas, S.;
Farrugia, A.;
Wachholz, P. A.;
Souza, S. A. L.

Publication type:

Letter to the Editor

Managing paediatric bleeding disorder patients undergoing surgical procedures: Leveraging the electronic medical record.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e173, doi. 10.1111/hae.13514

By:

Tarango, C.;
Dahale, D.;
Dodson, N.;
Otte, A.;
Schoettker, P. J.

Publication type:

Article

Immunotolerance approach to refractory CNS bleeding in a patient with congenital factor XIII deficiency and acquired alloantibody.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e252, doi. 10.1111/hae.13513

By:

Guzman, M. P.;
Alderuccio, J. P.;
Harrington, T.

Publication type:

Article

International collaboration is needed to reduce the risk for inhibitors in PUPs with severe haemophilia A.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e242, doi. 10.1111/hae.13512

By:

van den Berg, H. M.

Publication type:

Article

A case report on a multicentre cooperative rehabilitation programme for inhibitor‐positive patients with haemophilia A.

Published in:

2018

By:

Kubota, M.;
Takedani, H.;
Ono, K.;
Noguchi, M.;
Nakata, A.;
Oka, T.

Publication type:

Case Study

Core outcome set for gene therapy in haemophilia: Results of the coreHEM multistakeholder project.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e167, doi. 10.1111/hae.13504

By:

Iorio, A.;
Skinner, M. W.;
Clearfield, E.;
Messner, D.;
Pierce, G. F.;
Witkop, M.;
Tunis, S.;
the coreHEM panel

Publication type:

Article

Factor XI and pulmonary infections.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 519, doi. 10.1111/hae.13503

By:

Gailani, D.;
Mohammed, B. M.;
Cheng, Q.

Publication type:

Article

Total elbow arthroplasty in haemophilia.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 548, doi. 10.1111/hae.13498

By:

Dale, T. M.;
Saucedo, J. M.;
Rodriguez‐Merchan, E. C.

Publication type:

Article

Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohorts.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. e213, doi. 10.1111/hae.13480

By:

Lassalle, F.;
Marmontel, O.;
Zawadzki, C.;
Fretigny, M.;
Bouvagnet, P.;
Vinciguerra, C.

Publication type:

Article

Haemophilia commentary: The utility of BATs.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 522, doi. 10.1111/hae.13487

By:

Sholzberg, M.

Publication type:

Article

The diagnostic accuracy of bleeding assessment tools for the identification of patients with mild bleeding disorders: A systematic review.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 525, doi. 10.1111/hae.13486

By:

Moenen, F. C. J. I.;
Nelemans, P. J.;
Schols, S. E. M.;
Schouten, H. C.;
Henskens, Y. M. C.;
Beckers, E. A. M.

Publication type:

Article

Postural control during a transition task in haemophilic children, adolescents and young adults with haemophilic ankle arthropathy.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 667, doi. 10.1111/hae.13484

By:

Deschamps, K.;
Staes, F.;
Eerdekens, M.;
Peerlinck, K.;
Hermans, C.;
Vandesande, J.;
Lobet, S.

Publication type:

Article

Methodologies for data collection in congenital haemophilia with inhibitors (CHwI): critical assessment of the literature and lessons learned from recombinant factor VIIa.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 536, doi. 10.1111/hae.13482

By:

Kessler, C. M.;
Benchikh el Fegoun, S.;
Worster, A.

Publication type:

Article

Individual thrombin generation and spontaneous bleeding rate during personalized prophylaxis with Nuwiq<sup>®</sup> (human‐cl rhFVIII) in previously treated patients with severe haemophilia A.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 619, doi. 10.1111/hae.13493

By:

Dargaud, Y.;
Negrier, C.;
Rusen, L.;
Windyga, J.;
Georgiev, P.;
Bichler, J.;
Solomon, C.;
Knaub, S.;
Lissitchkov, T.;
Klamroth, R.

Publication type:

Article

Bleeding‐related hospitalization in patients with von Willebrand disease and the impact of prophylaxis: Results from national registers in Sweden compared with normal controls and participants in the von Willebrand Disease Prophylaxis Network.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 628, doi. 10.1111/hae.13473

By:

Holm, E.;
Carlsson, K. Steen;
Lövdahl, S.;
Lail, A. E.;
Abshire, T. C.;
Berntorp, E.

Publication type:

Article

Pain and structural alterations in knee joints in patients with haemophilia.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 657, doi. 10.1111/hae.13472

By:

Krüger, S.;
Hoffmeister, M.;
Hilberg, T.

Publication type:

Article

Perioperative replacement therapy in haemophilia B: An appeal to “B” more precise.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 611, doi. 10.1111/hae.13469

By:

Hazendonk, H. C. A. M.;
Preijers, T.;
Liesner, R.;
Chowdary, P.;
Hart, D.;
Keeling, D.;
Driessens, M. H. E.;
Laros‐van Gorkom, B. A. P.;
van der Meer, F. J. M.;
Meijer, K.;
Fijnvandraat, K.;
Leebeek, F. W. G.;
Mathôt, R. A. A.;
Collins, P. W.;
Cnossen, M. H.

Publication type:

Article

Clinical experience with moroctocog alfa (AF‐CC) in younger paediatric patients with severe haemophilia A: Two open‐label studies.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 604, doi. 10.1111/hae.13466

By:

Rusen, L.;
Kavakli, K.;
Korth‐Bradley, J.;
Huard, F.;
Rendo, P.;
Fuiman, J.;
Baumann, J. A.;
Smith, L.;
Alvey, C.;
Rupon, J.

Publication type:

Article

“In vitro” correction of the severe factor V deficiency‐related coagulopathy by a novel plasma‐derived factor V concentrate.

Published in:

Haemophilia, 2018, v. 24, n. 4, p. 648, doi. 10.1111/hae.13465

By:

Bulato, C.;
Novembrino, C.;
Anzoletti, M. Boscolo;
Spiezia, L.;
Gavasso, S.;
Berbenni, C.;
Tagariello, G.;
Farina, C.;
Nardini, I.;
Campello, E.;
Peyvandi, F.;
Simioni, P.

Publication type:

Article