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Publications by Roberto R. Capela de Matos
An Uncommon T(9;11)(p24;q22) With Monoallelic Loss of ATM and KMT2A Genes in a Child With Myelodysplastic Syndrome/Acute Myeloid Leukemia Who Evolved From Fanconi Anemia
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Related publications
Myelodysplastic Syndrome/Acute Myeloid Leukemia Evolving From Aplastic Anemia: Efficacy of Hematopoietic Stem Cell Transplantation
Cellular Therapy and Transplantation
Transplantation
Molecular Medicine
Rare Cytogenetic Abnormalities in Acute Myeloid Leukemia Transformed From Fanconi Anemia – A Case Report
BMC Research Notes
Biochemistry
Medicine
Genetics
Molecular Biology
Myeloid Leukemia With T(7;21)(p22;q22) and 5q Deletion
Oncology Reports
Medicine
Cancer Research
Oncology
Acute Myeloid Leukemia After Myelodysplastic Syndrome and Failure of Therapy With Hypomethylating Agents: An Emerging Entity With a Poor Prognosis
Clinical Lymphoma, Myeloma and Leukemia
Cancer Research
Oncology
Hematology
Myelodysplastic Syndrome, Juvenile Myelomonocytic Leukemia, and Acute Myeloid Leukemia Associated With Complete or Partial Monosomy 7
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Allogeneic Stem Cell Transplantation Outcomes in Acute Myeloid Leukemia Patients With T(8;21)(q22;q22) in First Remission According to Conditioning Regimen
Biology of Blood and Marrow Transplantation
Transplantation
Hematology
Pattern Associated Leukemia Immunophenotypes and Measurable Disease Detection in Acute Myeloid Leukemia or Myelodysplastic Syndrome With Mutated NPM1
Cytometry Part B - Clinical Cytometry
Forensic Medicine
Pathology
Histology
Cell Biology
Management of Differentiation Syndrome in an Elderly Patient With Acute Promyelocytic Leukemia Who Subsequently Developed Refractory Anemia With Ring Sideroblasts
Leukemia and Lymphoma
Cancer Research
Oncology
Hematology
Abrogation of RUNX1 Gene Expression in De Novo Myelodysplastic Syndrome With T(4;21)(q21;q22)
Haematologica
Hematology
