Ghent University Academic Bibliography

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Mark
Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents

Marcin W Wlodarski, Shinsuke Hirabayashi, Victor Pastor, Jan Starý, Henrik Hasle, Riccardo Masetti, Michael Dworzak, Markus Schmugge, Marry van den Heuvel-Eibrink, Marek Ussowicz, et al.

(2016) BLOOD. 127(11). p.1387-1397
Mark
Clonal mutational landscape of childhood myelodysplastic syndromes

Emilia J Kozyra, Shinsuke Hirabayashi, Victor Bengt Pastor Loyola, Bartlomiej Przychodzen, Axel Karow, Albert Catala, Barbara De Moerloose (UGent) , Michael Dworzak, Henrik Hasle, Riccardo Masetti, et al.

(2015) BLOOD. 126(23).
Mark
Somatic genetic and epigenetic architecture of myelodysplastic syndromes arising from GATA2 deficiency

Victor Bengt Pastor Loyola, Shinsuke Hirabayashi, Sandra Pohl, Emilia J Kozyra, Albert Catala, Barbara De Moerloose (UGent) , Marek Dworzak, Henrik Hasle, Riccardo Masetti, Markus Schmugge, et al.

(2015) BLOOD. 126(23).
Mark
Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

Shinsuke Hirabayashi, Christian Flotho, Jessica Moetter, Michael Heuser, Henrik Hasle, Bernd Gruhn, Thomas Klingebiel, Felicitas Thol, Brigitte Schlegelberger, Irith Baumann, et al.

(2012) BLOOD. 119(11). p.e96-e99
Mark
Mutations of the spliceosome complex genes occur in adult patients but are very rare in children with myeloid neoplasia

Shinsuke Hirabayashi, Jessica Moetter, Kenichi Yoshida, Michael Heuser, Henrik Hasle, Alexandra Fischer, Brigitte Strahm, Brigitte Schlegelberger, Irith Baumann, Felicitas Thol, et al.

(2011) 53rd ASH annual meeting and exposition : abstracts, program and personal scheduler.
Mark
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 (UGent) , Jan Stary, et al.

(2010) BLOOD. 116(21). p.1633-1634

Academic Bibliography

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

Clonal mutational landscape of childhood myelodysplastic syndromes

Somatic genetic and epigenetic architecture of myelodysplastic syndromes arising from GATA2 deficiency

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

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

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