Theodosia Kalfa

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Cincinnati Children's Hospital Medical Center

United States

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Theodosia Kalfa is a Professor at Cincinnati Children's Hospital Medical Center. Her research focuses on hematology, particularly in the areas of anemia, neutropenia, and erythropoiesis, as evidenced by her recent publications. She has investigated various blood disorders, including childhood myelofibrosis and hereditary spherocytic pyropoikilocytosis. Dr. Kalfa's work also extends to the molecular mechanisms underlying hemolytic anemia and the effects of chromatin remodeling on erythroblast function.

Recent Grants

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The Role of Erythroblastic Islands in Anemia of Inflammation

Open Date: 2020-04-01

Close Date: 2024-03-31

Grant: Close

Rho GTPases in Terminal Erythroid Maturation

Open Date: 2012-09-26

Close Date: 2017-06-30

Grant: Close

Rac1 and Rac2 Guanosine Triphosphatases in Erythroid Function and Differentiation

Open Date: 2008-02-11

Close Date: 2012-11-30

Articles (13)

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2025

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2025

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (2)

Wenying Zhang

department of pediatrics university of cincinnati college of medicine cincinnati ohio usa

UNITED STATES

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Ran An

Assistant Professor

University of Houston

UNITED STATES

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Theodosia Kalfa

Research Interests

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Recent Grants

Articles (13)

G-CSF resistance of ELANE-mutant neutropenia depends on SERF1-containing truncated–neutrophil elastase aggregates

Three‐generation female cohort with macrocytic anemia and iron overload

Rapid measurement of hemoglobin-oxygen dissociation by leveraging Bohr effect and Soret band bathochromic shift

Hemolytic anemia and macrothrombocytopenia: A lipid problem?

Pediatric myelofibrosis due to compound heterozygous MPIG6B mutations in a patient of European ancestry

Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis

Erythroblastic islands foster granulopoiesis in parallel to terminal erythropoiesis.

Altered erythropoiesis in newborns with congenital heart disease

Autism-associated chromatin remodeler CHD8 regulates erythroblast cytokinesis and fine-tunes the balance of Rho GTPase signaling

Etavopivat, a Pyruvate Kinase Activator in Red Blood Cells, for the Treatment of Sickle Cell Disease

M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling

MPN-024 Hypereosinophilic Syndrome: A Catastrophic Pediatric Case

Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening

Collaborators (2)

Wenying Zhang

Ran An

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