Associate Professor, Departments of Laboratory Medicine and Pediatrics, Yale University
Pathology
Dr. Jeanne E. Hendrickson, MD
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Jeanne Hendrickson practices Pathology. She graduated from Emory University School of Medicine. Emory University School of Medicine is ranked 23 in research and 42 in primary care medicine Jeanne Hendrickson is a published MD. She has 37 papers published. The most current publication "Erythrophagocytosis by plasmacytoid dendritic cells and monocytes is enhanced during inflammation." She is registered with Medicare.
Publications
- Erythrophagocytosis by plasmacytoid dendritic Cells and monocytes is enhanced during inflammation.
- Measuring the influence of blood component infusion rate on recipient vital signs.
- Impact of red blood cell alloimmunization on Sickle cell disease mortality: a case series.
- Immune parameter analysis of children with sickle cell disease on hydroxycarbamide or chronic transfusion therapy.
- Factors Influencing RBC Alloimmunization: Lessons Learned from Murine Models.
- Blood transfusion transmission of the tick-borne relapsing fever spirochete Borrelia miyamotoi in mice.
- The ethics of a proposed study of hematopoietic stem cell transplant for children with "less severe" Sickle cell disease.
- Red Blood Cell Alloimmunization Mitigation Strategies.
- Antigen Modulation Confers Protection to Red Blood Cells from Antibody through Fcγ Receptor Ligation.
- A novel role for C3 in antibody-induced red blood Cell clearance and antigen modulation.
- Antibodies of undetermined significance: nuisance or near miss?
- Transfusion of murine red blood Cells expressing the human KEL glycoprotein induces clinically significant alloantibodies.
- Frequency of glucose-6-phosphate dehydrogenase-deficient red blood Cell units in a metropolitan transfusion service.
- Initiation and Regulation of Complement during Hemolytic Transfusion Reactions.
- Generation of transgenic mice with antithetical KEL1 and KEL2 human blood group antigens on red blood Cells.
- Implementation of a pediatric trauma massive transfusion protocol: one institution's experience.
- Transfusion in the absence of inflammation induces antigen specific tolerance to murine RBCs.
- Transfusion of human volunteers with older, stored red blood Cells produces extravascular hemolysis and circulating non-transferrin-bound iron.
- Coagulopathy is Prevalent and Associated with Adverse Outcomes in Transfused Pediatric Trauma Patients.
- Alloimmunization to transfused HOD red blood cells is not increased in mice with Sickle cell disease.
- Transfusion of fresh murine red blood Cells reverses adverse effects of older stored red blood Cells.
- Rapid clearance of transfused murine red blood Cells is associated with recipient cytokine storm and enhanced alloimmunogenicity.
- Polycythemia in an infant secondary to granulocyte transfusions.
- Transfusion of red blood Cells after prolonged storage produces harmful effects that are mediated by iron and inflammation.
- Regulation of primary alloantibody response through antecedent exposure to a microbial T-Cell epitope.
- Storage of murine red blood Cells enhances alloantibody responses to an erythroid-specific model antigen.
- The spleen plays a central role in primary humoral alloimmunization to transfused mHEL red blood Cells.
- A novel mouse model of red blood Cell storage and posttransfusion in vivo survival.
- The role of inflammation in alloimmunization to antigens on transfused red blood Cells.
- Discrete Toll-like receptor agonists have differential effects on alloimmunization to transfused red blood Cells.
- Inflammation enhances consumption and presentation of transfused RBC antigens by dendritic Cells.
- Recipient inflammation affects the frequency and magnitude of immunization to transfused red blood Cells.
- Neonatal transfusions.
- Use of mouse models to study the mechanisms and consequences of RBC clearance.
- MHC II on transfused murine blood is not required for alloimmunization against MHC I.
- Alloimmunization against RBC or PLT antigens is independent of TRIM21 expression in a murine model.
Schools
Emory University School Of Medicine
Procedures Preformed
- Plasmapheresis
Conditions Treated
- Anemia
- Coagulation Disorders (incl. Hemophilia)
- Immune Thrombocytopenic Purpura (ITP)
- Neutropenia
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Doctors Specialties
- Pathology
Accepted Insurances
Education
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Emory University -
Emory University School of Medicine
Hospital
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Yale-New Haven Hospital
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1326005059 |
| Last Name Of The Provider | HENDRICKSON |
| First Name Of The Provider | JEANNE |
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