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100. Reprogramming HSC-derived erythroid cells for lysosomal enzyme production leads to visceral and CNS cross-correction in mice with MPS type I

Molecular genetics and metabolism, 2010-02, Vol.99 (2), p.S28

2010

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801 Overexpression of human TLR8 induces bone marrow dysfunction and severe anemia in lupus- prone mice

Lupus science & medicine, 2024-05, Vol.11 (Suppl 2), p.A67-A69

2024

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Acquired Hemolytic Anemias

Concise Guide to Hematology, 2018, p.67-79

Kalfa, Theodosia A.

2018

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Activation of HIF-2a-EPO Axis in Kidney or Liver Is Sufficient to Drive Erythrocytosis in a Novel Inducible HIF-2a Transgenic Mouse Model

Blood, 2015-12, Vol.126 (23), p.931-931

2015

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Activation of Pyruvate Kinase-R with Etavopivat (FT-4202) Is Well Tolerated, Improves Anemia, and Decreases Intravascular Hemolysis in Patients with Sickle Cell Disease Treated for up to 12 Weeks

Blood, 2021-11, Vol.138 (Supplement 1), p.9-9

2021

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Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency

American journal of hematology, 2019-01, Vol.94 (1), p.149-161

2019

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Altered erythropoiesis in newborns with congenital heart disease

Pediatric research, 2022-02, Vol.91 (3), p.606-611

2022

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Altered phosphorylation of cytoskeleton proteins in sickle red blood cells: The role of protein kinase C, Rac GTPases, and reactive oxygen species

Blood cells, molecules, & diseases, 2010-06, Vol.45 (1), p.41-45

2010

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Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients

Human mutation, 2018-03, Vol.39 (3), p.389-393

2018

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Alu-Element Insertion in Pklr Gene As a Novel Cause of Severe Hereditary Nonspherocytic Hemolytic Anemia

Blood, 2015-12, Vol.126 (23), p.3349-3349

2015

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Analysis of Erythropoiesis Using Imaging Flow Cytometry

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1698, p.175

2018

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Anchoring at an island to relieve stress

Blood, 2011-01, Vol.117 (3), p.748-749

Kalfa, Theodosia A.

2011

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Angiotensin Signaling Is Essential for Stress Erythropoiesis but Results in Retention of Dysfunctional Mitochondria in Erythrocytes That Generate Excessive Reactive Oxygen Species

Blood, 2020-11, Vol.136 (Supplement 1), p.31-32

2020

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Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab

British journal of haematology, 2016-11, Vol.175 (4), p.744-747

2016

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

Cell reports (Cambridge), 2022-07, Vol.40 (2), p.111072-111072, Article 111072

2022

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Autoimmune Hemolytic Anemia in the Pediatric Setting

Journal of clinical medicine, 2021-01, Vol.10 (2), p.216

2021

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Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia

Frontiers in physiology, 2021-03, Vol.12, p.636609-636609

2021

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Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Frontiers in hematology, 2024-03, Vol.3

2024

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Cation Leak in Red Blood Cells of Patients with Wiskott-Aldrich Syndrome Leads to Non-Immunologic Hemolysis

Blood, 2014-12, Vol.124 (21), p.1338-1338

2014

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Cdc42 critically regulates the balance between myelopoiesis and erythropoiesis

Blood, 2007-12, Vol.110 (12), p.3853-3861

2007

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Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

Blood, 2016-12, Vol.128 (22), p.2446-2446

2016

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Change in Expressional Profile of KCl Cotransporter Genes during Human Erythroid Differentiation

Blood, 2007-11, Vol.110 (11), p.1709-1709

2007

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Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients

Scientific reports, 2021-04, Vol.11 (1), p.7909-7909, Article 7909

2021

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100. Reprogramming HSC-derived erythroid cells for lysosomal enzyme production leads to visceral and CNS cross-correction in mice with MPS type I

801 Overexpression of human TLR8 induces bone marrow dysfunction and severe anemia in lupus- prone mice

Acquired Hemolytic Anemias

Activation of HIF-2a-EPO Axis in Kidney or Liver Is Sufficient to Drive Erythrocytosis in a Novel Inducible HIF-2a Transgenic Mouse Model

Activation of Pyruvate Kinase-R with Etavopivat (FT-4202) Is Well Tolerated, Improves Anemia, and Decreases Intravascular Hemolysis in Patients with Sickle Cell Disease Treated for up to 12 Weeks

Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency

Altered erythropoiesis in newborns with congenital heart disease

Altered phosphorylation of cytoskeleton proteins in sickle red blood cells: The role of protein kinase C, Rac GTPases, and reactive oxygen species

Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients

Alu-Element Insertion in Pklr Gene As a Novel Cause of Severe Hereditary Nonspherocytic Hemolytic Anemia

Analysis of Erythropoiesis Using Imaging Flow Cytometry

Anchoring at an island to relieve stress

Angiotensin Signaling Is Essential for Stress Erythropoiesis but Results in Retention of Dysfunctional Mitochondria in Erythrocytes That Generate Excessive Reactive Oxygen Species

Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab

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

Autoimmune Hemolytic Anemia in the Pediatric Setting

Automated Oxygen Gradient Ektacytometry: A Novel Biomarker in Sickle Cell Anemia

Base editing of haematopoietic stem cells rescues sickle cell disease in mice

Base editing of hematopoietic stem cells rescues sickle cell disease in mice

Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Cation Leak in Red Blood Cells of Patients with Wiskott-Aldrich Syndrome Leads to Non-Immunologic Hemolysis

Cdc42 critically regulates the balance between myelopoiesis and erythropoiesis

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

Change in Expressional Profile of KCl Cotransporter Genes during Human Erythroid Differentiation

Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients

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