Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1476-5551
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies ; volume:35 ; number:11 ; day:10 ; month:3 ; year:2021 ; pages:3304-3308 ; date:11.2021
Leukemia ; 35, Heft 11 (10.3.2021), 3304-3308, 11.2021
- Creator
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Decker, Melanie
Lammens, Tim
Ferster, Alina
Erlacher, Miriam
Yoshimi-Nöllke, Ayami
Niemeyer, Charlotte
Ernst, Martijn P. T.
Raaijmakers, Marc H. G. P.
Duployez, Nicolas
Flaum, Andreas
Steinemann, Doris
Schlegelberger, Brigitte
Illig, Thomas
Ripperger, Tim
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41375-021-01200-w
- URN
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urn:nbn:de:101:1-2023010420594175681532
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Decker, Melanie
- Lammens, Tim
- Ferster, Alina
- Erlacher, Miriam
- Yoshimi-Nöllke, Ayami
- Niemeyer, Charlotte
- Ernst, Martijn P. T.
- Raaijmakers, Marc H. G. P.
- Duployez, Nicolas
- Flaum, Andreas
- Steinemann, Doris
- Schlegelberger, Brigitte
- Illig, Thomas
- Ripperger, Tim
- SpringerLink (Online service)
Other Objects (12)
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
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Case report: Lomustine overdose in a 15-year-old, healthy adolescent—a prescription failure
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
Transient apoptosis inhibition by Bcl-xL overexpression during hematopoietic stem cell transplantation
Current treatment of juvenile myelomonocytic leukemia
Practical considerations for diagnosis and management of patients and carriers
Pädiatrische Hämatologie und Onkologie
Comprehensive assessments and related interventions to enhance the long-term outcomes of child, adolescent and young adult cancer survivors - presentation of the CARE for CAYA-Program study protocol and associated literature review
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure
Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia
GFI136N as a therapeutic and prognostic marker for myelodysplastic syndrome
Familial platelet disorders with a predisposition to acute myelogenous leukaemia: a RUNX1 update
Case report: Lomustine overdose in a 15-year-old, healthy adolescent—a prescription failure
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
Transient apoptosis inhibition by Bcl-xL overexpression during hematopoietic stem cell transplantation
Current treatment of juvenile myelomonocytic leukemia
Practical considerations for diagnosis and management of patients and carriers
Pädiatrische Hämatologie und Onkologie
Comprehensive assessments and related interventions to enhance the long-term outcomes of child, adolescent and young adult cancer survivors - presentation of the CARE for CAYA-Program study protocol and associated literature review
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure
Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia
GFI136N as a therapeutic and prognostic marker for myelodysplastic syndrome
Familial platelet disorders with a predisposition to acute myelogenous leukaemia: a RUNX1 update