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Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study. Commentary

Author
ABSHIRE, Thomas (Commentator (written text)) 1 ; GOUW, Samantha C2 3 ; VAN DER BOM, Johanna G4 ; AUERSWALD, Günter5 ; ETTINGHAUSEN, Carmen Escuriola6 ; TEDGARD, Ulf7 ; VAN DEN BERG, H. Marijke2
[1] Emory University and Children's Healthcare of Atlanta, United States
[2] Ven Creveldkliniek, University Medical Center Utrecht, Netherlands
[3] Department of Pediatrics, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands
[4] Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, Netherlands
[5] Prof Hess-Kinderklinik, Zentrum fur Kinderheilkunde und Jugendmedizin, Bremen, Germany
[6] Centre of Pediatrics III, Department of Hematology, Oncology and Haemostaseology, Johann-Wolfgang-Goethe University Hospital, Frankfurt AM Main, Germany
[7] Department of Pediatrics, University of Lund, University Hospital, Malmö, Sweden
CANAL Study Group
Source

Blood. 2007, Vol 109, Num 11 ; 4596, 4693-4697 [6 p.] ; ref : 45 ref

ISSN
0006-4971
Scientific domain
Medical oncology; Hematology
Publisher
The Americain Society of Hematology, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Développement produit Etude cohorte Etude comparative Facteur antihémophilique A Facteur coagulation Homme Hématologie Hémophilie A Inhibiteur Plasma sanguin Produit dérivé Protéine recombinante Coagulopathie Hémopathie Maladie héréditaire
Keyword (en)
Product development Cohort study Comparative study Factor VIII Coagulation factor Human Hematology Hemophilia A Inhibitor Blood plasma Derived product Recombinant protein Coagulopathy Hemopathy Genetic disease
Keyword (es)
Desarrollo producto Estudio cohorte Estudio comparativo Factor antihemofílico A Factor coagulación Hombre Hematología Hemofilia A Inhibidor Plasma sanguíneo Producto derivado Proteína recombinante Coagulopatía Hemopatía Enfermedad hereditaria
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19C Platelet diseases and coagulopathies

Discipline
Blood diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
18814923

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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