Myelodysplastic syndromes: 2023 update on diagnosis, risk‐stratification, and management

G Garcia‐Manero - American journal of hematology, 2023 - Wiley Online Library
Disease overview The myelodysplastic syndromes (MDS) are a very heterogeneous group
of myeloid disorders characterized by peripheral blood cytopenias and increased risk of …

Genetics of MDS

S Ogawa - Blood, The Journal of the American Society of …, 2019 - ashpublications.org
Our knowledge about the genetics of myelodysplastic syndromes (MDS) and related
myeloid disorders has been dramatically improved during the past decade, in which …

TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML

OK Weinberg, A Siddon, YF Madanat, J Gagan… - Blood …, 2022 - ashpublications.org
A subset of myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) show
complex karyotype (CK), and these cases include a relatively high proportion of cases of …

The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia

AS Sperling, CJ Gibson, BL Ebert - Nature Reviews Cancer, 2017 - nature.com
Myelodysplastic syndrome (MDS) is a clonal disease that arises from the expansion of
mutated haematopoietic stem cells. In a spectrum of myeloid disorders ranging from clonal …

Frequent pathway mutations of splicing machinery in myelodysplasia

K Yoshida, M Sanada, Y Shiraishi, D Nowak, Y Nagata… - Nature, 2011 - nature.com
Myelodysplastic syndromes and related disorders (myelodysplasia) are a heterogeneous
group of myeloid neoplasms showing deregulated blood cell production with evidence of …

Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet

L Malcovati, E Hellström-Lindberg… - Blood, The Journal …, 2013 - ashpublications.org
Within the myelodysplastic syndrome (MDS) work package of the European LeukemiaNet,
an Expert Panel was selected according to the framework elements of the National Institutes …

Clinical effect of point mutations in myelodysplastic syndromes

R Bejar, K Stevenson, O Abdel-Wahab… - … England Journal of …, 2011 - Mass Medical Soc
Background Myelodysplastic syndromes are clinically heterogeneous disorders
characterized by clonal hematopoiesis, impaired differentiation, peripheral-blood …

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7

S Narumi, N Amano, T Ishii, N Katsumata, K Muroya… - Nature …, 2016 - nature.com
Adrenal hypoplasia is a rare, life-threatening congenital disorder. Here we define a new
form of syndromic adrenal hypoplasia, which we propose to term MIRAGE (myelodysplasia …

Myelodysplastic syndromes: 2018 update on diagnosis, risk‐stratification and management

G Montalban‐Bravo… - American journal of …, 2018 - Wiley Online Library
Disease overview The myelodysplastic syndromes (MDS) are a very heterogeneous group
of myeloid disorders characterized by peripheral blood cytopenias and increased risk of …

New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an …

J Schanz, H Tüchler, F Solé, M Mallo, E Luno… - Journal of clinical …, 2012 - ascopubs.org
Purpose The karyotype is a strong independent prognostic factor in myelodysplastic
syndromes (MDS). Since the implementation of the International Prognostic Scoring System …