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Journal Articles

SF3B1, RUNX1 and TP53 Mutations Significantly Impact the Outcome of Patients with Lower-Risk Myelodysplastic Syndrome

Jose F. Falantes, Francisco J. Márquez-Malaver, Estrella Carrillo-Cruz, Rosario M Morales-Camacho, Concepción Prats-Martín, Teresa Caballero, Eduardo Rodriguez Arbolí, Ildefonso Espigado, Jose A. Perez-Simon

Blood (2022) 140 (Supplement 1): 6920–6922.

https://doi.org/10.1182/blood-2022-169372

Published: 2022

Journal Articles

Autosomal Recessive Congenital Dyserythropoietic Anemia Type III Is Caused By Mutations in the Centralspindlin RACGAP1 Component

Lídia Romero-Cortadellas, Gonzalo Hernández, Xènia Ferrer-Cortès, Veronica Venturi, Mireia Olivella, Concepción Pérez de Soto, Rosario M. Morales-Camacho, Ana Villegas, F. Ataulfo Gonzalez-Fernandez, Marta Morado, Santiago Pérez-Montero, Cristian Tornador, Mayka Sánchez

Blood (2021) 138 (Supplement 1): 847.

https://doi.org/10.1182/blood-2021-150097

Published: 2021

Journal Articles

Nuclear protrusion in dysplastic micromegakaryocytes

Laura Pérez-Ortega, Rosario M. Morales-Camacho

Blood (2019) 133 (10): 1164.

https://doi.org/10.1182/blood-2018-12-889451

Published: 2019

Journal Articles

Eosinophils with ring-shaped nuclei in a patient treated with adalimumab

Rosario M. Morales-Camacho, Concepción Prats-Martín

Blood (2019) 133 (1): 101.

https://doi.org/10.1182/blood-2018-09-877399

Published: 2019

Journal Articles

Internuclear bridging outside of primary myelodysplasia and congenital dyserythropoietic anemia

Javier Alberto Rojas-Martínez, Rosario M. Morales-Camacho

Blood (2018) 132 (2): 236.

https://doi.org/10.1182/blood-2018-05-849232

Published: 2018

Journal Articles

Circulating hypergranular neoplastic cells: not always leukemic promyelocytes

Concepción Prats-Martín, Rosario M. Morales-Camacho

Blood (2017) 130 (24): 2689.

https://doi.org/10.1182/blood-2017-08-803346

Published: 2017

NARROW

SF3B1, RUNX1 and TP53 Mutations Significantly Impact the Outcome of Patients with Lower-Risk Myelodysplastic Syndrome

Autosomal Recessive Congenital Dyserythropoietic Anemia Type III Is Caused By Mutations in the Centralspindlin RACGAP1 Component

Nuclear protrusion in dysplastic micromegakaryocytes

Eosinophils with ring-shaped nuclei in a patient treated with adalimumab

Internuclear bridging outside of primary myelodysplasia and congenital dyserythropoietic anemia

Circulating hypergranular neoplastic cells: not always leukemic promyelocytes

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ASH Publications

American Society of Hematology

SF3B1, RUNX1 and TP53 Mutations Significantly Impact the Outcome of Patients with Lower-Risk Myelodysplastic Syndrome

Autosomal Recessive Congenital Dyserythropoietic Anemia Type III Is Caused By Mutations in the Centralspindlin RACGAP1 Component

Nuclear protrusion in dysplastic micromegakaryocytes

Eosinophils with ring-shaped nuclei in a patient treated with adalimumab

Internuclear bridging outside of primary myelodysplasia and congenital dyserythropoietic anemia

Circulating hypergranular neoplastic cells: not always leukemic promyelocytes

Email alerts

ASH Publications

American Society of Hematology

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