Physician
Pediatric Hematology & Oncology
Dr. William Zinkham, MD
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William Zinkham practices Pediatric Hematology & Oncology. He studied medicine at Johns Hopkins University School of Medicine. Johns Hopkins University School of Medicine is one of the top medical schools in the US. Johns Hopkins University School of Medicine is ranked 3/29 in Research/PrimaryCare. Doctor William Zinkham, MD is a published doctor. He published 81 publications, including: 'Unstable hemoglobins and the selective hemolytic action of sulfonamides.'
Publications
- A note on studies of hemolysis in paroxysmal (cold) hemoglobinuria.
- A report on observations relative to paroxysmal cold hemoglobinuria.
- Observations on the mechanism of hemolysis in paroxysmal hemoglobinuria.
- Lactate Dehydrogenases in Human Testes.
- IN VITRO INTERCONVERSION OF 16-C-ESTRONE AND 16-C-ESTRADIOL-17beta BY ERYTHROCYTES FROM NORMAL SUBJECTS AND FROM SUBJECTS WITH A DEFICIENCY OF RED CELL GLUCOSE-6-PHOSP...
- In vitro erythrophagocytosis in acquired hemolytic anemia.
- HEMOGLOBIN ZUERICH; CLINICAL, CHEMICAL AND KINETIC STUDIES.
- AN UNUSUAL ISOZYME OF LACTATE DEHYDROGENASE IN MATURE TESTES: LOCALIZATION, ONTOGENY, AND KINETIC PROPERTIES.
- GENETIC CONTROL AND ONTOGENY OF LACTATE DEHYDROGENASE IN PIGEON TESTS.
- LACTATE DEHYDROGENASE IN PIGEON TESTES: GENETIC CONTROL BY THREE LOCI.
- LACTATE DEHYDROGENASE IN TESTIS: DISSOCIATION AND RECOMBINATION OF SUBUNITS.
- SEVERE INTRAVASCULAR HEMOLYSIS FOLLOWING SURGICAL REPAIR OF ENDOCARDIAL CUSHION DEFECTS.
- Peripheral blood and bilirubin values in normal full-term primaquine-sensitive Negro infants: effect of vitamin K.
- Metabolic abnormalities of erythrocytes from patients with congenital nonspherocytic hemolytic anemia.
- An in-vitro abnormality of glutathione metabolism in erythrocytes from normal newborns: mechanism and clinical significance.
- A defect of glutathione metabolism in erythrocytes from patients with a naphthalene-induced hemolytic anemia.
- A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism.
- A genetic study of a defect in glutathione metabolism of the erythrocyte.
- Some factors influencing the formation of L.E. cells; a method for enhancing L.E. cell production.
- Effect of erucic acid on platelets in patients with adrenoleukodystrophy.
- Henna: a potential cause of oxidative hemolysis and neonatal hyperbilirubinemia.
- Lorenzo's oil and thrombocytopenia in patients with adrenoleukodystrophy.
- Variable degrees of suppression of hemoglobin S synthesis in subjects with hemoglobin SS disease on a long-term transfusion regimen.
- Methylene blue-induced Heinz body hemolytic anemia.
- Prophylaxis and therapy with factor VII concentrate (human) immuno, vapor heated in patients with congenital factor VII deficiency: a summary of case reports.
- Carboxyhemoglobin levels in an unstable hemoglobin disorder (Hb Zürich): effect on phenotypic expression.
- Varicella-associated thrombocytopenia: clues to the etiology of childhood idiopathic thrombocytopenic purpura.
- Prognostic role of the intravenous urogram in children with acute leukemia.
- Testicular leukemic relapse: rate of regression and persistent disease after radiation therapy.
- Hemoglobin Cheverly: an unstable hemoglobin associated with chronic mild anemia.
- Unique sensitivity of Hb Zürich to oxidative injury by phenazopyridine: reversal of the effects by elevating carboxyhemoglobin levels in vivo and in vitro.
- Relation between variations in the phenotypic expression of an unstable hemoglobin disorder (hemoglobin Zürich) and carboxyhemoglobin levels.
- Abnormalities of the spleen and liver in patients with hemophilia.
- Gonadal function in two siblings with Fanconi''s anemia.
- Phenotypic variability in siblings with Farber disease.
- Blood and bone-marrow findings in congenital rubella.
- The selective hemolytic action of drugs: clinical and mechanistic considerations.
- Thrombocytopenic purpura following rubella infection in children and adults.
- Polymorphism of lactate dehydrogenase isozymes in pigeons.
- Severe idiopathic pulmonary hemosiderosis in the absence of clinical or radiologic evidence of pulmonary disease.
- Linkage of lactate dehydrogenase B and C loci in pigeons.
- Indications for and complicatons of splenectomy in childhood.
- Malate dehydrogenase in Ascaris suum: characterization, ontogeny, and genetic control.
- Visceral larva migrans due to Toxocara as a cause of eosinophilia.
- The molecular size of lactate dehydrogenase isozymes in mature tests.
- Isozymes: biological and clinical significance.
- Lactate dehydrogenase isozymes of testis and sperm: biological and biochemical properties and genetic control.
- A unique form of lactate dehydrogenase in human sperm: biological and clinical significance.
- Hemoglobin Zürich. A third family presenting with hemolytic reactions to sulfonamides.
- In vivo aging of transfused erythrocytes and 2,3-diphosphoglycerate levels.
- Etiology and therapy of thrombocytopenia associated with sarcoidosis.
- Genetic control of lactate dehydrogenase synthesis in the somatic and gametic tissues of pigeons.
- A variant of lactate dehydrogenase in somatic tissues of pigeons: physicochemical properties and genetic control.
- Polymorphism of malate dehydrogenase in Ascaris suum.
- Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
- Homozygous protein C deficiency: observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy.
- Farber disease: pathologic diagnosis in sibs with phenotypic variability.
- Kasabach-Merritt syndrome: therapeutic considerations.
- Generalized venocentric lesions in the virus-associated hemophagocytic syndrome.
- Unstable hemoglobins: influence of environment on phenotypic expression of a genetic disorder.
- Hb Catonsville (glutamic acid inserted between Pro-37(C2)alpha and Thr-38(C3)alpha). Nonallelic gene conversion in the globin system?
- Thrombocytopenia absent radius syndrome associated with renal insufficiency.
- Twenty-nail dystrophy associated with hematologic abnormalities.
- Multifocal eosinophilic granuloma. Natural history, etiology and management.
- Demonstration of parasitism in tissues by electrophoretic definition of parasite enzymes in host tissues.
- Fever of unknown origin and the value of gallium-67 and technetium-99M for defining abnormality of the spleen: a case report.
- The University of Ibadan (Nigeria) exchange program.
- Unstable hemoglobins and the selective hemolytic action of sulfonamides.
- Hemoglobin SC, SS/GPhiladelphia and SOArab diseases diagnostic importance of an integrative analysis of clinical, hematologic and electrophoretic findings.
- Invasive aspergillosis.
- Observations on the rate and mechanism of hemolysis in individuals with Hb Zürich [His E7 (63)beta leads to Arg]: I. Concentrations of haptoglobin and hemopexin in the...
- Observations on the motile behavior of individual neutrophils from a patient with recurrent bacterial infections.
- Abnormalities of the peripheral blood as a presenting feature of immunodeficiency.
- Munchausen syndrome by proxy: definition of factitious bleeding in an infant by 51Cr labeling of erythrocytes.
- Observations on the rate and mechanism of hemolysis in individuals with Hb Zürich [His E7(63)beta leads to Arg]: II. Thermal denaturation of hemoglobin as a cause of a...
- Production of erythrocytes that contain fetal hemoglobin in anemia. Transient in vivo changes.
- Neurofibromatosis and leukemia.
- Visceral larva migrans. A review and reassessment indicating two forms of clinical expression: visceral and ocular.
- Changing erythrocyte populations in juvenile chronic myelocytic leukemia: evidence for disordered regulation.
- Elevation of pyrimidine enzyme activities in the RBC of patients with congenital hypoplastic anaemia and their parents.
Schools
Johns Hopkins University School of Medicine
Johns Hopkins Hospital
Childrens Hospital
Doctors Specialties
- Pediatric Hematology
- Oncology
Accepted Insurances
Education
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Johns Hopkins University -
Boston Children's Hospital -
Johns Hopkins University School of Medicine
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