Professor of Medicine
Hematology
Dr. Gregory J. Kato, MD
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Gregory Kato is an expert in the field of Hematology. He studied medicine at George Washington University School of Medicine. George Washington University School of Medicine has a rank of 67 in research and a 0 in primary care Gregory Kato is a published doctor as well. He has 98 publications published. The latest was: Elevated Transpulmonary Gradient and Cardiac Magnetic Resonance-Derived Right Ventricular Remodeling Predict Poor Outcomes in Sickle Cell Disease.
Publications
- Elevated Transpulmonary Gradient and Cardiac Magnetic Resonance-Derived Right Ventricular Remodeling Predict Poor Outcomes in Sickle Cell Disease.
- Kinetics of sickle cell biorheology and implications for painful vasoocclusive crisis.
- Iron, inflammation, and early death in adults with sickle cell disease.
- Management of patients with sickle cell disease.
- Prominent role of platelets in the formation of circulating neutrophil-red cell heterocellular aggregates in sickle cell anemia.
- Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide.
- Defective nitric oxide metabolism in sickle cell disease.
- Sleep disturbance, depression and pain in adults with sickle cell disease.
- Imaging flow cytometry documents incomplete resistance of human sickle F-cells to ex vivo hypoxia-induced sickling.
- Reply: Practice Guideline for Pulmonary Hypertension in Sickle Cell: Direct Evidence Needed before Universal Adoption.
- Elevated sphingosine-1-phosphate promotes sickling and sickle cell disease progression.
- Computed tomography correlates with cardiopulmonary hemodynamics in pulmonary hypertension in adults with sickle cell disease.
- Heme-bound iron activates placenta growth factor in erythroid cells via erythroid Krüppel-like factor.
- Abnormal pulmonary function and associated risk factors in children and adolescents with sickle cell anemia.
- Therapeutic Strategies to Alter the Oxygen Affinity of Sickle Hemoglobin.
- No NO means yes to sickle red cell adhesion.
- An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease.
- Mechanisms of hemolysis-associated platelet activation.
- Imaging flow cytometry for automated detection of hypoxia-induced erythrocyte shape change in sickle cell disease.
- Microvascular oxygen consumption during sickle cell pain crisis.
- A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia.
- A Retrospective Review of Acupuncture Use for the Treatment of Pain in Sickle Cell Disease Patients: Descriptive Analysis From a Single Institution.
- Thrombospondin-1 inhibits ADAMTS13 activity in sickle cell disease.
- A fluorescence method to detect and quantitate sterol esterification by lecithin:cholesterol acyltransferase.
- Effect of Extended-Release Niacin on Serum Lipids and on Endothelial Function in Adults With Sickle Cell Anemia and Low High-Density Lipoprotein Cholesterol Levels.
- Extensive Ex Vivo Expansion of Functional Human Erythroid Precursors Established from Umbilical Cord Blood Cells by Defined Factors.
- Lactate dehydrogenase and hemolysis in sickle cell disease.
- Vasculopathy, inflammation and blood flow in leg ulcers of patients with sickle cell anemia.
- Circulating blood endothelial nitric oxide synthase contributes to the regulation of systemic blood pressure and nitrite homeostasis.
- Liver stiffness increases acutely during sickle cell vaso-occlusive crisis.
- Genetic determinants of haemolysis in sickle cell anaemia.
- Clinical correlates of acute pulmonary events in children and adolescents with sickle cell disease.
- Leg Ulcers in Sickle Cell Disease: Current Patterns and Practices.
- Circulating endothelial progenitor cells in adults with sickle cell disease.
- Imaging flow cytometry for morphologic and phenotypic characterization of rare circulating endothelial cells.
- Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidin.
- Characterizing non-linear dependencies among pairs of clinical variables and imaging data.
- Hemodynamic Predictors of Mortality in Adults with Sickle Cell Disease.
- Understanding the erythrocyte storage lesion.
- Anemia, age, desaturation, and impaired neurocognition in sickle cell anemia.
- Infrared imaging of nitric oxide-mediated blood flow in human sickle cell disease.
- A systematic comparison and evaluation of high density exon arrays and RNA-seq technology used to unravel the peripheral blood transcriptome of sickle cell disease.
- Infusion of hemolyzed red blood cells within peripheral blood stem cell grafts in patients with and without sickle cell disease.
- TRV: A physiological biomarker in sickle cell disease.
- High-Density Lipoprotein Cholesterol Efflux, Nitration of Apolipoprotein A-I, and Endothelial Function in Obese Women.
- Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.
- NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.
- Ancestry of African Americans with sickle cell disease.
- Anti-haemolytic effect of senicapoc and decrease in NT-proBNP in adults with sickle cell anaemia.
- Priapism in Sickle-Cell Disease: A Hematologist's Perspective.
- Predictors of osteoclast activity in sickle cell disease patients.
- Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacity.
- Laboratory and echocardiography markers in sickle cell patients with leg ulcers.
- Increased pulmonary pressures and myocardial wall stress in children with severe malaria.
- Pulmonary hypertension and NO in sickle cell.
- Diastolic dysfunction in sickle cell.
- High levels of placenta growth factor in sickle cell disease promote pulmonary hypertension.
- Hydroxyurea-induced expression of glutathione peroxidase 1 in red blood cells of individuals with sickle cell anemia.
- Relationship of erythropoietin, fetal hemoglobin, and hydroxyurea treatment to tricuspid regurgitation velocity in children with sickle cell disease.
- Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions.
- Prospective echocardiography assessment of pulmonary hypertension and its potential etiologies in children with sickle cell disease.
- Improvement in hemolysis and pulmonary arterial systolic pressure in adult patients with sickle cell disease during treatment with hydroxyurea.
- Haptoglobin halts hemoglobin's havoc.
- Proteomic identification of altered apolipoprotein patterns in pulmonary hypertension and vasculopathy of sickle cell disease.
- Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease.
- Evolution of novel small-molecule therapeutics targeting sickle cell vasculopathy.
- Prevalence and risk factors for pulmonary artery systolic hypertension among sickle cell disease patients in Nigeria.
- Corticosteroids and increased risk of readmission after acute chest syndrome in children with sickle cell disease.
- Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain.
- Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease.
- Severe pulmonary hypertension in an adolescent with sickle cell disease.
- Sickle cell disease and pulmonary hypertension in Africa: a global perspective and review of epidemiology, pathophysiology, and management.
- Novel small molecule therapeutics for sickle cell disease: nitric oxide, carbon monoxide, nitrite, and apolipoprotein A-I.
- A network model to predict the risk of death in sickle cell disease.
- Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin.
- Diastolic dysfunction is an independent risk factor for death in patients with sickle cell disease.
- Cerebrovascular disease associated with sickle cell pulmonary hypertension.
- Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sick...
- Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension, and mortality in sickle cell disease.
- Hemolysis-associated pulmonary hypertension in thalassemia.
- Cardiopulmonary complications of sickle cell disease: role of nitric oxide and hemolytic anemia.
- Images in clinical medicine. Tumor pseudosyncytiae.
- Inhibition of PDE4 phosphodiesterase activity induces growth suppression, apoptosis, glucocorticoid sensitivity, p53, and p21(WAF1/CIP1) proteins in human acute lympho...
- Elevated Pulse Pressure is Associated with Hemolysis, Proteinuria and Chronic Kidney Disease in Sickle Cell Disease.
- Severe painful vaso-occlusive crises and mortality in a contemporary adult sickle cell anemia cohort study.
- Expression of Regulatory Platelet MicroRNAs in Patients with Sickle Cell Disease.
- Risk factors for death in 632 patients with sickle cell disease in the United States and United kingdom.
- Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
- Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents ...
- Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia).
- Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia.
- The proteome of sickle cell disease: insights from exploratory proteomic profiling.
- Nitric oxide for inhalation in the acute treatment of sickle cell pain crisis: a randomized controlled trial.
- Apolipoprotein A-I and serum amyloid A plasma levels are biomarkers of acute painful episodes in patients with sickle cell disease.
- NT-proBNP as a marker of cardiopulmonary status in sickle cell anaemia in Africa.
- Effects of a single sickling event on the mechanical fragility of sickle cell trait erythrocytes.
- Lipid levels in sickle-cell disease associated with haemolytic severity, vascular dysfunction and pulmonary hypertension.
Schools
G Washington Univ Sch Med amp Hlth Sci
Children39s Hospital Los Angeles
Johns Hopkins Hospital
Conditions Treated
- Pancytopenia
Doctors Specialties
- Hematology
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Card PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Community Blue PPO
- Choice Care PPO
- MultiPlan PPO
- PHCS Network PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- UPMC PPO
Education
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Johns Hopkins University -
Children's Hospital of Los Angeles -
George Washington University School of Medicine
Hospital
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UPMC Presbyterian Shadyside
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1578504767 |
| Last Name Of The Provider | KATO |
| First Name Of The Provider | GREGORY |
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