E. Hellström Lindberg

Familial platelet disorder due to germline exonic deletions in RUNX1: a diagnostic challenge with distinct alterations of the transcript isoform equilibrium

L. Cavelier, E. Kuchinskaya, V. Ljungström, 2022, Leukemia & lymphoma.

SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts.

P. Campbell, M. Cazzola, E. Papaemmanuil, 2015, Blood.

Apoptosis in refractory anaemia with ringed sideroblasts is initiated at the stem cell level and associated with increased activation of caspases

Bengt Fadeel, Boris Zhivotovsky, B. Zhivotovsky, 2001, British journal of haematology.

Postazacitidine clone size predicts long-term outcome of patients with myelodysplastic syndromes and related myeloid neoplasms

S. Miyano, T. Naoe, E. Papaemmanuil, 2023, Blood Advances.

SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts.

P. Campbell, M. Cazzola, E. Papaemmanuil, 2015, Blood.