Head trauma in the haemophilic child and management in a paediatric emergency department: Descriptive study (English)
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In:
Haemophilia
;
24
, 4
;
e187-e193
;
2018
- Article (Journal) / Electronic Resource
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Title:Head trauma in the haemophilic child and management in a paediatric emergency department: Descriptive study
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Contributors:García Sánchez, P. ( author ) / Molina Gutiérrez, M. Á. ( author ) / Martín Sánchez, J. ( author ) / Inisterra Viu, L. ( author ) / García García, S. ( author ) / Rivas Pollmar, M. I. ( author ) / Martín Salces, M. ( author ) / Álvarez Román, M. T. ( author ) / Jiménez Yuste, V. ( author )
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Published in:Haemophilia ; 24, 4 ; e187-e193
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Publisher:
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Publication date:2018-07-01
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Size:7 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 24, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 505
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Issue Information| 2018
- 513
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New Editor‐in‐Chief for Haemophilia!| 2018
- 514
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A changing haemophilia world: Opportunities and challenges for the Haemophilia journalHermans, Cedric et al. | 2018
- 516
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Defining patient value in haemophilia carevan Balen, E. C. / Gouw, S. C. / Hazelzet, J. A. / van der Bom, J. G. / Cnossen, M. H. et al. | 2018
- 519
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Factor XI and pulmonary infectionsGailani, D. / Mohammed, B. M. / Cheng, Q. et al. | 2018
- 522
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Haemophilia commentary: The utility of BATsSholzberg, M. et al. | 2018
- 525
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The diagnostic accuracy of bleeding assessment tools for the identification of patients with mild bleeding disorders: A systematic reviewMoenen, F. C. J. I. / Nelemans, P. J. / Schols, S. E. M. / Schouten, H. C. / Henskens, Y. M. C. / Beckers, E. A. M. et al. | 2018
- 536
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Methodologies for data collection in congenital haemophilia with inhibitors (CHwI): critical assessment of the literature and lessons learned from recombinant factor VIIaKessler, C. M. / Benchikh el Fegoun, S. / Worster, A. et al. | 2018
- 548
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Total elbow arthroplasty in haemophiliaDale, T. M. / Saucedo, J. M. / Rodriguez‐Merchan, E. C. et al. | 2018
- 557
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Miracle of haemophilia drugs: Personal views about a few main playersMannucci, P. M. et al. | 2018
- 563
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The viability and necessity of APRN‐led care models in the clinical management of haemophilia and other inherited bleeding and clotting disordersFederizo, A. / Shullick, M. / Witkop, M. et al. | 2018
- 570
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Prophylactic bypassing agent use before and during immune tolerance induction in patients with haemophilia A and inhibitors to FVIIICarpenter, S. L. / Khair, K. / Gringeri, A. / Valentino, L. A. et al. | 2018
- 578
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Role of chromogenic assays in haemophilia A and B diagnosisBowyer, A. E. / Duncan, E. M. / Antovic, J. P. et al. | 2018
- 584
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Prospects for research in haemophilia with real‐world data—An analysis of German registry and secondary dataSchopohl, D. / Bidlingmaier, C. / Herzig, D. / Klamroth, R. / Kurnik, K. / Rublee, D. / Schramm, W. / Schwarzkopf, L. / Berger, K. et al. | 2018
- 595
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Long‐term tolerability, immunogenicity and efficacy of Nuwiq® (human‐cl rhFVIII) in children with severe haemophilia AKlukowska, A. / Szczepański, T. / Vdovin, V. / Knaub, S. / Bichler, J. / Jansen, M. / Dzhunova, I. / Liesner, R. J. et al. | 2018
- 604
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Clinical experience with moroctocog alfa (AF‐CC) in younger paediatric patients with severe haemophilia A: Two open‐label studiesRusen, L. / Kavakli, K. / Korth‐Bradley, J. / Huard, F. / Rendo, P. / Fuiman, J. / Baumann, J. A. / Smith, L. / Alvey, C. / Rupon, J. et al. | 2018
- 611
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Perioperative replacement therapy in haemophilia B: An appeal to “B” more preciseHazendonk, 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. et al. | 2018
- 619
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Individual thrombin generation and spontaneous bleeding rate during personalized prophylaxis with Nuwiq® (human‐cl rhFVIII) in previously treated patients with severe haemophilia ADargaud, Y. / Negrier, C. / Rusen, L. / Windyga, J. / Georgiev, P. / Bichler, J. / Solomon, C. / Knaub, S. / Lissitchkov, T. / Klamroth, R. et al. | 2018
- 628
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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 NetworkHolm, E. / Carlsson, K. Steen / Lövdahl, S. / Lail, A. E. / Abshire, T. C. / Berntorp, E. et al. | 2018
- 634
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Factor XI deficiency is not associated with an increased risk of pneumonia and pneumonia‐related mortalitySalomon, O. / Preis, M. / Abu Shtaya, A. / Kotler, A. / Stein, N. / Saliba, W. et al. | 2018
- 641
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Intracranial haemorrhage in children with inherited bleeding disorders in the UK 2003‐2015: A national cohort studyChalmers, E. A. / Alamelu, J. / Collins, P. W. / Mathias, M. / Payne, J. / Richards, M. / Tunstall, O. / Williams, M. / Palmer, B. / Mumford, A. et al. | 2018
- 648
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“In vitro” correction of the severe factor V deficiency‐related coagulopathy by a novel plasma‐derived factor V concentrateBulato, C. / Novembrino, C. / Anzoletti, M. Boscolo / Spiezia, L. / Gavasso, S. / Berbenni, C. / Tagariello, G. / Farina, C. / Nardini, I. / Campello, E. et al. | 2018
- 657
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Pain and structural alterations in knee joints in patients with haemophiliaKrüger, S. / Hoffmeister, M. / Hilberg, T. et al. | 2018
- 667
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Postural control during a transition task in haemophilic children, adolescents and young adults with haemophilic ankle arthropathyDeschamps, K. / Staes, F. / Eerdekens, M. / Peerlinck, K. / Hermans, C. / Vandesande, J. / Lobet, S. et al. | 2018
- 675
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Measurement of B‐domain‐deleted ReFacto AF activity with a product‐specific standard is affected by choice of reagent and patient‐specific factorsJacquemin, M. / Vodolazkaia, A. / Toelen, J. / Schoeters, J. / Van Horenbeeck, I. / Vanlinthout, I. / Debasse, M. / Peerlinck, K. et al. | 2018
- 684
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Instructions for Authors| 2018
- e167
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Core outcome set for gene therapy in haemophilia: Results of the coreHEM multistakeholder projectIorio, A. / Skinner, M. W. / Clearfield, E. / Messner, D. / Pierce, G. F. / Witkop, M. / Tunis, S. / the coreHEM panel et al. | 2018
- e173
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Managing paediatric bleeding disorder patients undergoing surgical procedures: Leveraging the electronic medical recordTarango, C. / Dahale, D. / Dodson, N. / Otte, A. / Schoettker, P. J. et al. | 2018
- e179
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The Jamaican Haemophilia Registry: Describing the burden of diseaseWharfe, G. / Buchner‐Daley, L. / Gibson, T. / Hilliard, P. / Usuba, K. / Abad, A. / Boma‐Fischer, L. / Bouskill, V. / Floros, G. / Lillicrap, D. et al. | 2018
- e187
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Head trauma in the haemophilic child and management in a paediatric emergency department: Descriptive studyGarcía 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. et al. | 2018
- e194
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Desmopressin stimulation testing: Response to intravenous and intranasal formsMcCormick, M. C. / Siripong, N. / Cooper, J. D. et al. | 2018
- e199
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Goal Attainment Scaling for haemophilia (GAS‐Hēm): testing the feasibility of a new patient‐centric outcome measure in people with haemophiliaRoberts, J. C. / Lattimore, S. / Recht, M. / Jackson, S. / Gue, D. / Squire, S. / Robinson, K. S. / Price, V. / Denne, M. / Richardson, S. et al. | 2018
- e207
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Blood group O: A novel risk factor for increased postpartum blood loss?Kahr, M. K. / Franke, D. / Brun, R. / Wisser, J. / Zimmermann, R. / Haslinger, C. et al. | 2018
- e213
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Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohortsLassalle, F. / Marmontel, O. / Zawadzki, C. / Fretigny, M. / Bouvagnet, P. / Vinciguerra, C. et al. | 2018
- e222
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Low bone mineral density and associated factors in patients with haemophilia in ColombiaSossa 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. et al. | 2018
- e230
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Muscle function deterioration in patients with haemophilia: Prospective experience from Costa RicaSeuser, A. / Navarrete‐Duran, M. / Auerswald, G. / Mancuso, M. E. et al. | 2018
- e242
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International collaboration is needed to reduce the risk for inhibitors in PUPs with severe haemophilia Avan den Berg, H. M. et al. | 2018
- e243
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Principles of haemophilia care: The asia pacific perspective. ResponseDunkley, 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. et al. | 2018
- e245
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Principles of haemophilia care: The Asia‐Pacific perspective.Burnouf, T. et al. | 2018
- e246
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Letter to the Editor of HaemophiliaFaber, J.‐C. et al. | 2018
- e248
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A case report on a multicentre cooperative rehabilitation programme for inhibitor‐positive patients with haemophilia AKubota, M. / Takedani, H. / Ono, K. / Noguchi, M. / Nakata, A. / Oka, T. et al. | 2018
- e252
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Immunotolerance approach to refractory CNS bleeding in a patient with congenital factor XIII deficiency and acquired alloantibodyGuzman, M. P. / Alderuccio, J. P. / Harrington, T. et al. | 2018
- e255
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Perspectives on haemophilia access in Brazil?Guedes, V. G. / Thomas, S. / Farrugia, A. / Wachholz, P. A. / Souza, S. A. L. et al. | 2018
- e256
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Postpartum haemorrhage in an unselected cohort of carriers of haemophiliaZwagemaker, A. / Gouw, S. C. / Valk, C. / Ganzevoort, W. / Coppens, M. / Peters, M. et al. | 2018
- e259
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The Kids' immune thrombocytopenia Tool is not suitable for assessing quality of life in children with platelet function disordersKhair, Kate / Holland, Michael et al. | 2018
- e261
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Utility of global hemostatic assays in the management of anticoagulation in a haemophilia patientWu, I. Q. / Tan, C. W. / Wong, W. H. / Ng, H. J. et al. | 2018
- e263
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Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutationPagliari, M. T. / Baronciani, L. / Stufano, F. / Colpani, P. / Siboni, S. M. / Peyvandi, F. et al. | 2018
- e266
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Choices of factor VIII products in previously untreated patients with haemophilia A: A global surveyPeyvandi, F. / Palla, R. / Franchi, C. / Nobili, A. / Rosendaal, F. R. / Mannucci, P. M. et al. | 2018
- e269
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Recombinant FVIIa therapy for heavy menstrual bleeding in patients with severe FV deficiencyKaya, Z. et al. | 2018
- e270
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Haemophilia clinical care and research needs: Assessing prioritiesChowdary, P. / Angchaisuksiri, P. / Dimsits, J. / Iorio, A. / Kavakli, K. / Lentz, S. R. / Mahlangu, J. / McCarthy, A. / Kessler, C. et al. | 2018
- e273
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Comment on: Interpreting data on inhibitor development from previously untreated patient studies, beware of premature conclusionsLiesner, Dr R.J et al. | 2018
- e275
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Recombinant activated factor VII in approved indications: Update on safetyNeufeld, E. J. / Négrier, C. / Benchikh el Fegoun, S. / Cooper, D. L. / Rojas‐Rios, A. / Seremetis, S. et al. | 2018
- e278
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The combination of urinary CTX‐II and serum CS‐846: Promising biochemical markers to predict radiographic progression of haemophilic arthropathy—An exploratory studyPulles, A. E. / Mastbergen, S. C. / Foppen, W. / Schutgens, R. E. G. / Lafeber, F. P. J. G. / van Vulpen, L. F. D. et al. | 2018
- e280
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Continuous infusion of extended half‐life factor VIII (efmoroctocog alpha) for surgery in severe haemophilia AKremer Hovinga, I. C. L. / Schutgens, R. E. G. / van der Valk, P. R. / van Vulpen, L. F. D. / Mauser‐Bunschoten, E. P. / Fischer, K. et al. | 2018
- e283
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Successful immune tolerance in a young female with inhibitor and severe haemophilia A due to a complex genetic rearrangementZuccherato, L. W. / Roberti, M. R. F. / Jardim, L. L. / Rezende, S. M. et al. | 2018
- e286
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Surgical treatment of ruptured giant haemophilic pseudotumour complicated with infection: A case report and literature reviewFeng, B. / Li, Y. L. / Jiang, C. / Qiu, G. X. / Weng, X. S. et al. | 2018
- e289
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A novel synonymous variant in the F8 gene, p.(Leu40=)/c.120C>A, likely causes mild haemophilia AInaba, H. / Shinozawa, K. / Fukutake, K. / Amano, K. et al. | 2018
- e292
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Unexpectedly high response to DDAVP in two patients with moderate haemophilia APolzella, P. / Coutts, K. / Bignell, P. / Curry, N. et al. | 2018
- e294
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rFIXFc for Immune Tolerance Induction in a Severe Hemophilia B Patient with an Inhibitor and Prior History of ITI Related Nephrotic SyndromeMalec, Lynn / Abshire, Thomas / Jobe, Shawn / White, Gilbert et al. | 2018
- e296
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Performance of next‐generation sequencing in the detection of large exon deletion in patients of haemophilia AHe, X. / Xiong, Z. / Shen, N. / Lu, Y. / Wang, X. et al. | 2018