Dr. James Arthur Warth MD
Hematologist-Pathologist | Hematology
1153 Center Street Suite 5950 Faulkner Jamaica Plain MA, 02130About
Dr. James Warth is a hematology pathologist practicing in Jamaica Plain, MA. Dr. Warth specializes in reviewing blood samples and interpreting laboratory results. These results give them an idea of whether certain diseases are malignant or not, in order for them to properly determine what exact treatment is needed. Hematology pathologists are normally experts in leukemia, lymphoma, anemia, hemophilia and many other blood diseases.
Education and Training
Tufts Univ Sch of Med, Boston Ma 1967
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Simultaneous occurrence of polycythemia vera and Waldenstrom macroglobulinemia: a case report and review of the literature.
- Nocardia asteroides-infected aneurysm of the aorta: case report and review of the literature.
- Warfarin-induced skin necrosis in a patient with heparin-induced thrombocytopenia: two diseases or one?
- Direct measurement of the internal viscosity of sickle erythrocytes as a function of cell density.
- Intraerythrocyte pH, pCO2 and the hexose monophosphate shunt.
- Intraerythrocyte pH, pCO2 and the hexose monophosphate shunt.
- Sequestrocytes: a manifestation of transcellular cross-bonding of the red cell membrane in sickle cell anemia.
- The risk of developing AIDS in hemophiliac and homosexual men.
- Altered amount and activity of superoxide dismutase in sickle cell anemia.
- The phosphoproteins of the sickle erythrocyte membrane.
- Elimination of the settling artifact in the nuclear magnetic resonance spectroscopy of living cells.
- Effect of zinc on hyperammonemia in sickle cell anemia subjects.
- Effect of zinc on hyperammonemia in sickle cell anemia subjects.
- Relationship of glutathione levels and Heinz body formation to irreversibly sickled cells in sickle cell anemia.
- Hypertension and a seizure following transfusion in an adult with sickle cell anemia.
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