Clinical implications of FLT3 mutations in pediatric AML
- Author
- MESHINCHI, Soheil; ALONZO, Todd A; RADICH, Jerald P; STIREWALT, Derek L; ZWAAN, Michel; ZIMMERMAN, Martin; REINHARDT, Dirk; KASPERS, Gertjan J. L; HEEREMA, Nyla A; GERBING, Robert; LANGE, Beverly J
[1] Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States
[2] Department of Pediatrics, University of Washington Medical Center, Seattle, United States
[3] University of Southern California Keck School of Medicine, Los Angeles, United States
[4] Department of Pediatric Hematology/Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, Netherlands
[5] Dutch Childhood Oncology Group, Rotterdam, Netherlands
[6] AML-BFM Study Group, Münster, Germany
[7] Department of Pediatric Hematology/Oncology, Vrije Universiteit (VU) University Medical Center, Amsterdam, Netherlands
[8] Dutch Childhood Oncology Group, Amsterdam, Netherlands
[9] Ohio State University, Columbus, United States
[10] Children's Hospital of Philadelphia, PA, United States
[11] Children's Oncology Group, Arcadia, CA, United States - Source
Blood. 2006, Vol 108, Num 12, pp 3654-3661, 8 p ; ref : 32 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)
- Enfant Gène onc cellulaire Génétique Mutation Pronostic Protooncogène Leucémie aiguë myéloblastique Récepteur tyrosine kinase FLT3 Homme Hémopathie maligne
- Keyword (en)
- Child C-Onc gene Genetics Mutation Prognosis Protooncogene Acute myelocytic leukemia Fms-like tyrosine kinase 3 Human Malignant hemopathy
- Keyword (es)
- Niño Gen onc celular Genética Mutación Pronóstico Protooncogen Leucemia mieloblástica Hombre Hemopatía maligna
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19B Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18318797
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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DOI
10.1182/blood-2006-03-009233 
https://dx.doi.org/10.1182/blood-2006-03-009233
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