Page 1 | Search Results | Blood | American Society of Hematology

1-19 of 19

Sort by

Sort Order Select

Journal Articles

Refractory Cytopenia in Childhood Under Watch and Wait Strategy: Safe until Adulthood?

Beatrice Drexler, Stephan Schwarz-Furlan, Irith Baumann, Martina Rudelius, Peter Noellke, Dirk Lebrecht, Senthilkumar Ramamoorthy, Natalia Rotari, Axel Karow, Shinsuke Hirabayashi, Marcin Wlodarski, Fabian Beier, Yvonne Lisa Behrens, Gudrun Göhring, Reinhard Kalb, Brigitte Strahm, Miriam Erlacher, Charlotte Marie Niemeyer, Ayami Yoshimi

Blood (2024) 144 (Supplement 1): 1835.

https://doi.org/10.1182/blood-2024-209722

Published: 2024

Journal Articles

UBTF tandem Duplications Account for a Third of Advanced Pediatric MDS without Genetic Predisposition to Myeloid Neoplasia

Blood (2022) 140 (Supplement 1): 1355–1356.

https://doi.org/10.1182/blood-2022-159002

Published: 2022

Journal Articles

The Fanconi Anemia-Associated Protein NIPA Is Essential for the Nuclear Abundance of FANCD2

Blood (2019) 134 (Supplement_1): 3741.

https://doi.org/10.1182/blood-2019-125973

Published: 2019

Journal Articles

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Blood (2017) 130 (Supplement 1): 2449.

https://doi.org/10.1182/blood.V130.Suppl_1.2449.2449

Published: 2017

Journal Articles

Constitutional SAMD9L Mutations Cause Familial Myelodisplastic Syndrome with Monosomy 7 and Stable Revertant Mosaicism

Blood (2017) 130 (Supplement 1): 1672.

https://doi.org/10.1182/blood.V130.Suppl_1.1672.1672

Published: 2017

Journal Articles

Impact of Somatic Mutations on the Outcome of Children and Adolescents with Therapy-Related Myelodysplastic Syndrome

Blood (2016) 128 (22): 3162.

https://doi.org/10.1182/blood.V128.22.3162.3162

Published: 2016

Journal Articles

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents

Blood (2016) 127 (11): 1387–1397.

https://doi.org/10.1182/blood-2015-09-669937

Published: 2016

Includes: Supplemental data

Journal Articles

Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes

Blood (2015) 126 (23): 1662.

https://doi.org/10.1182/blood.V126.23.1662.1662

Published: 2015

Journal Articles

Bone Marrow Immunophenotyping By Flow Cytometry in Refractory Cytopenia of Childhood

Anna M. Aalbers, Marry M. van den Heuvel-Eibrink, Irith Baumann, Michael Dworzak, MD, Henrik Hasle, MD, Franco Locatelli, Barbara De Moerloose, Markus Schmugge, Ester Mejstrikova, MD, PhD, Michaela Novakova, Marco Zecca, MD, C. Michel Zwaan, Jeroen G. te Marvelde, Anton W Langerak, Jacques J.M. van Dongen, Rob Pieters, Charlotte Niemeyer, Vincent H.J. van der Velden, PhD

Blood (2014) 124 (21): 1916.

https://doi.org/10.1182/blood.V124.21.1916.1916

Published: 2014

Journal Articles

Unexpected High Frequency of GATA2 Mutations in Children with Non-Familial MDS and Monosomy 7

Blood (2012) 120 (21): 1699.

https://doi.org/10.1182/blood.V120.21.1699.1699

Published: 2012

Journal Articles

Recurrent 6pLOH Is the Most Common Somatic Lesion in Refractory Cytopenia of Childhood and Occurs Very Infrequently in Severe Aplastic Anemia

Marcin W Wlodarski, Shinsuke Hirabayashi, Brigitte Strahm, Sandra Urbaniak, Brigitte Schlegelberger, Ingrid Furlan, Alexandra Fischer, Wilfried Truckenmüller, Ayami Yoshimi-Noellke, Peter Noellke, Irith Baumann, Charlotte M Niemeyer

Blood (2012) 120 (21): 644.

https://doi.org/10.1182/blood.V120.21.644.644

Published: 2012

Journal Articles

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

Blood (2012) 119 (11): e96–e99.

https://doi.org/10.1182/blood-2011-12-395087

Published: 2012

Journal Articles

High Incidence of Fanconi Anemia in Patients with a Morphological Picture Consistent with Refractory Cytopenia of Childhood

Ayami Yoshimi, MD, PhD,, Charlotte M. Niemeyer, MD, Irith Baumann, M.D., Stephan Schwarz-Furlan, MD, Detlev Schindler, MD, Wolfram Ebell, MD, Brigitte Strahm, MD

Blood (2011) 118 (21): 2780.

https://doi.org/10.1182/blood.V118.21.2780.2780

Published: 2011

Journal Articles

Mutations of the Spliceosome Complex Genes Occur In Adult Patients but Are Very Rare In Children with Myeloid Neoplasia

Blood (2011) 118 (21): 2797.

https://doi.org/10.1182/blood.V118.21.2797.2797

Published: 2011

Journal Articles

Refractory Cytopenia In Childhood (RCC) with Normal Karyotype Is Unlikely to Progress to Advanced MDS Under a Watch and Wait Strategy

Shinsuke Hirabayashi, Brigitte Strahm, Stephan Schwarz, Marco Zecca, Markus Schmugge, Michael Dworzak, Marry van den Heuvel-Eibrink, Henrik Hasle, Barbara De Moerloose, Jan Stary, Dorota Wojcik, Ingrid Furlan, Franco Locatelli, Irith Baumann, Charlotte M Niemeyer

Blood (2010) 116 (21): 4007.

https://doi.org/10.1182/blood.V116.21.4007.4007

Published: 2010

Journal Articles

Immunosuppressive therapy for aplastic anemia in children: a more severe disease predicts better survival

Monika Führer, Udo Rampf, Irith Baumann, Andreas Faldum, Charlotte Niemeyer, Gritta Janka-Schaub, Wilhelm Friedrich, Wolfram Ebell, Arndt Borkhardt, Christine Bender-Goetze, for the German/Austrian Aplastic Anemia Working Group

Blood (2005) 106 (6): 2102–2104.

https://doi.org/10.1182/blood-2005-03-0874

Published: 2005

Journal Articles

Bone Marrow Transplantation and Immunosuppressive Therapy in Children with Aplastic Anemia: Data from a Prospective Multinational Trial in Germany, Austria and Switzerland.

Monika M. Fuehrer, MD, Udo Rampf, MD, Charlotte M. Niemeyer, MD, Andreas Faldum, PhD, Irith Baumann, MD, Wilhelm Friedrich, MD, Wolfram Ebell, MD, Arndt Borkhardt, MD, Christine Bender-Goetze, MD

Blood (2004) 104 (11): 1439.

https://doi.org/10.1182/blood.V104.11.1439.1439

Published: 2004

Journal Articles

Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7

Gabriela Kardos, Irith Baumann, S. Jane Passmore, Franco Locatelli, Henrik Hasle, Kirk R. Schultz, Jan Starý, Annette Schmitt-Graeff, Alexandra Fischer, Jochen Harbott, Judith M. Chessells, Ian Hann, Susanna Fenu, Angelo Cantú Rajnoldi, Gitte Kerndrup, Elisabeth van Wering, Tim Rogge, Peter Nöllke, Charlotte M. Niemeyer

Blood (2003) 102 (6): 1997–2003.

https://doi.org/10.1182/blood-2002-11-3444

Published: 2003

Journal Articles

Expression of the recombination-activating genes in extrafollicular lymphocytes but no apparent reinduction in germinal center reactions in human tonsils

Nadine Meru, Andreas Jung, Irith Baumann, Gerald Niedobitek

Blood (2002) 99 (2): 531–537.

https://doi.org/10.1182/blood.V99.2.531

Published: 2002

NARROW

Refractory Cytopenia in Childhood Under Watch and Wait Strategy: Safe until Adulthood?

UBTF tandem Duplications Account for a Third of Advanced Pediatric MDS without Genetic Predisposition to Myeloid Neoplasia

The Fanconi Anemia-Associated Protein NIPA Is Essential for the Nuclear Abundance of FANCD2

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Constitutional SAMD9L Mutations Cause Familial Myelodisplastic Syndrome with Monosomy 7 and Stable Revertant Mosaicism

Impact of Somatic Mutations on the Outcome of Children and Adolescents with Therapy-Related Myelodysplastic Syndrome

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents

Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes

Bone Marrow Immunophenotyping By Flow Cytometry in Refractory Cytopenia of Childhood

Unexpected High Frequency of GATA2 Mutations in Children with Non-Familial MDS and Monosomy 7

Recurrent 6pLOH Is the Most Common Somatic Lesion in Refractory Cytopenia of Childhood and Occurs Very Infrequently in Severe Aplastic Anemia

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

High Incidence of Fanconi Anemia in Patients with a Morphological Picture Consistent with Refractory Cytopenia of Childhood

Mutations of the Spliceosome Complex Genes Occur In Adult Patients but Are Very Rare In Children with Myeloid Neoplasia

Refractory Cytopenia In Childhood (RCC) with Normal Karyotype Is Unlikely to Progress to Advanced MDS Under a Watch and Wait Strategy

Immunosuppressive therapy for aplastic anemia in children: a more severe disease predicts better survival

Bone Marrow Transplantation and Immunosuppressive Therapy in Children with Aplastic Anemia: Data from a Prospective Multinational Trial in Germany, Austria and Switzerland.

Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7

Expression of the recombination-activating genes in extrafollicular lymphocytes but no apparent reinduction in germinal center reactions in human tonsils

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only