Physician
Hematology
Dr. Virgil F. Fairbanks, MD
|
|
Give Review
Dr. Virgil F. Fairbanks practices Hematology. He went to medical school at University of Michigan Medical School. Dr. Virgil F. Fairbanks has written publications. He has 101 publications published with PubMed. The lastest paper is: 'Routine erythrocyte measurements in diagnosis of iron-deficiency anemia and thalassemia minor.'
Publications
- Red cell mass and plasma volume measurements in polycythemia: evaluation of performance and practical utility.
- Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
- Three new hemoglobin variants with abnormal oxygen affinity: Hb Saratoga Springs [alpha40(C5)Lys --> Asn (alpha1)], Hb Santa Clara [beta97(FG4)His --> Asn], and Hb Spa...
- Three new variants of the alpha1-globin gene without clinical or hematologic effects: Hb Hagerstown [alpha44(CE2)Pro-->Ala (alpha1)]; Hb Buffalo [alpha89(FG1)His-->Gln...
- Four new beta chain hemoglobin variants without clinical or hematological effects: Hb San Bruno [beta39(C5)Gln-->His]; Hb Fort Dodge [beta93(F9)Cys-Tyr]; Hb Rhode Isla...
- Flow cytometric measurement of hemoglobin F in RBCs: diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-hPF...
- Four new variants of the alpha2-globin gene without clinical or hematologic effects: Hb Park Ridge [alpha9(alpha7)Asn-->Lys (alpha2)], Hb Norton [alpha72(EF1)His--&...
- Recognition and management of hereditary hemochromatosis.
- Myeloproliferative Disease: Polycythemia Vera: The Packed Cell Volume and The Curious Logic of The Red Cell Mass.
- Chromosomal constitution in glucose-6-phosphatate-dehydrogenase deficiency.
- Autoimmunity in the Lambert-Eaton myasthenic syndrome.
- Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
- Screening for hemochromatosis: a cost-effectiveness study based on 12,258 patients.
- Prevalence of anemia in medical practice: community versus referral patients.
- Hb Washtenaw [ beta 11(A8)Val-->Phe]: an electrophorectically silent, unstable, low oxygen affinity variant associated with anemia and chronic cyanosis.
- Can hematology reference intervals be derived from hospitalized patients' data?
- Homozygous hemoglobin E mimics beta-thalassemia minor without anemia or hemolysis: hematologic, functional, and biosynthetic studies of first North American cases.
- A pitfall in hemoglobin electrophoresis. Artefactual minor unstable hemoglobin results from improper specimen handling.
- Glucose-6-phosphate dehydrogenase variants: reexamination of G6PD Chicago and Cornell and a new variant (G6PD Pea Ridge) resembling G6PD Chicago.
- Nonequivalence of automated and manual hematocrit and erythrocytic indices.
- Effect on hemoglobin A1 of rapid normalization of glycemia with an artificial endocrine pancreas.
- Hemosiderosis in a dialysis patient: treatment with hemofiltration and deferoxamine chelation therapy.
- Erythrocytic calmodulin correlates with red cell age.
- Tests for pernicious anemia: the "Schilling test".
- Mcleod syndrome (hemolysis, acanthocytosis, and increased serum creatine kinase): potential confusion with polymyositis.
- Hemochromatosis: genetic or alcohol-induced?
- Tests for pernicious anemia: serum intrinsic factor blocking antibody.
- "Improved" vitamin B12 assays: a report on two commercial kits.
- Tests for pernicious anemia: serum vitamin B12 assay.
- Ferritin.
- Is measurement of erythrocyte Na+ influx useful for ascertainment of essential hypertension?
- Transferrin assay and total iron-binding capacity.
- Measurement of glycosylated hemoglobin by affinity chromatography.
- HemoQuant test for occult blood: the Sherlock Holmes test?
- Radiation absorbed doses from iron-52, iron-55, and iron-59 used to study ferrokinetics.
- Proton nuclear magnetic resonance studies of hemoglobin Malmö: implications of mutations at homologous positions of the alpha and beta chains.
- The amino acid substitution in Hb Olmsted: beta141 (H19) leucine yields arginine.
- Cobalt excretion test as index of iron absorption and diagnostic test for iron deficiency.
- In memoriam: Winifred M. Ashby 1879-1975.
- Hemoccult detection of fecal occult blood quantitated by radioassay.
- Routine erythrocyte measurements in diagnosis of iron-deficiency anemia and thalassemia minor.
- Hemoccult stool tests: false-negative results due to storage of specimens.
- Methemoglobinemia induced by a topical anesthetic spray (cetacaine).
- Hemoglobin E trait reexamined: a cause of microcytosis and erythrocytosis.
- Chronic iron overload: new chelators and new strategies.
- Deferoxamine-chelatable iron in hemochromatosis and other disorders of iron overload.
- Pseudospirochetes, a cause of erroneous diagnoses of leptospirosis.
- Red-cell-membrane polypeptide aggregates in glucose-6-phosphate dehydrogenase mutants with chronic hemolytic disease. A clue to the mechanism of hemolysis.
- Restoration of hemoglobin function in stored EDTA blood. Application in identification of hemoglobin variants with abnormal oxygen affinity.
- Lead neuropathy. 1) Morphometry, nerve conduction, and choline acetyltransferase transport: new finding of endoneurial edema associated with segmental demyelination.
- Intra-abdominal, angiofollicular lymph node hyperplasia (plasma-cell variant) with an antierythropoietic factor.
- Comparison of hemoglobins Wood (alpha 2 beta 2 97 leu) and Malmö (alpha 2 beta 2 97 gln). Diagnostic value of citrate agar electrophoresis.
- Evidence for multiple origins of the beta E-globin gene in Southeast Asia.
- Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.
- Hemoglobin E in Europeans: further evidence for multiple origins of the beta E-globin gene.
- The syndrome of gastric argyrophil carcinoid tumors and nonantral gastric atrophy.
- Deficiency of glucose-6-phosphate dehydrogenase.
- Copper-induced hemolysis.
- The identification of metabolic errors associated with hemolytic anemia.
- Three families with unstable hemoglobinopathies (Köln, Olmsted and Santa Ana) causing hemolytic anemia with inclusion bodies and pigmenturia.
- Hepatic failure with acanthocytosis: association with hemolytic anemia and deficiency of erythrocyte glutathione peroxidase.
- Glucose-6-phosphate dehydrogenase deficiency in the Philippines: report of a new variant--G6PD Panay.
- A tetrazolium-linked cytochemical method for estimation of glucose-6-phosphate dehydrogenase activity in individual erythrocytes: applications in the study of heterozy...
- Emergency semiquantitative estimation of plasma iron concentration. Diagnosis of acute iron poisoning.
- Is the peripheral blood film reliable for the diagnosis of iron deficiency anemia?
- The kinetics of urinary excretion of 51Cr from labeled erythrocytes in hemolytic anemia and the anemia of blood loss.
- Iron, arthritis, and anemia.
- Iron deficiency: still a diagnostic challenge.
- Familial erythrocytosis due to electrophoretically undetectable hemoglobin with impaired oxygen dissociation (hemoglobin Malmö, alpha 2 beta 2 97 gln).
- Diagnostic tests for iron deficiency.
- Microwave warming of bank blood.
- Urinary excretion of 51 Cr from labeled erythrocytes. An index of erythrocyte survival.
- Sickledex tests with unstable hemoglobin disorders.
- Scintigraphic visualization of abdominal lymph nodes with 99m Tc-pertechnetate-labeled sulfur colloid.
- Hemoglobin Malmö Beta-97 (FG-4) histidine--glutamine: a cause of polycythemia.
- Introduction to discussion of Heinz body anemias--unstable hemoglobinopathies.
- Postsplenectomy erythrocytosis in hemoglobin Köln disease.
- Iron kinetics in man: new studies with mouse hemoglobin.
- Intravascular coagulation and arterial disease.
- Prolonged remissions in acute myelocytic leukemia in adults.
- Copper sulfate-induced hemolytic anemia. Inhibition of glucose-6-phosphate dehydrogenase and other possible etiologic mechanisms.
- Hematologic genetic disorders among Southeast Asian refugees.
- Assay for thyroid stimulating immunoglobulin.
- Hereditary red cell disorders in Southeast Asian refugees and the effect on the prevalence of thalassemia disorders in the United States.
- Hemochromatosis: the neglected diagnosis.
- Identification of the binding domain for NADP+ of human glucose-6-phosphate dehydrogenase by sequence analysis of mutants.
- Two families with hemoglobin Sogn, beta(A11)14 Leu----Arg, in Minnesota and Indiana: hematologic, functional, and biosynthetic features.
- Cost containment, quality assurance, and physician microscopy of cerebrospinal fluid with normal cell counts. Analysis of 1,677 consecutive specimens.
- Beta-globin chain hemoglobin polymorphism and hemoglobin stability in black rhinoceroses (Diceros bicornis).
- Hb Johnstown [beta 109 (G11) Val----Leu]: a new electrophoretically silent variant that causes erythrocytosis.
- Clinical and histologic features of iron-related bone disease in dialysis patients.
- Hereditary sideroblastic anemia.
- Laboratory testing for iron status.
- Hemoglobin Columbia Missouri or alpha 2[88 (F9) Ala----Val]beta 2: a new high-oxygen-affinity hemoglobin that causes erythrocytosis.
- Methods for measuring plasma hemoglobin in micromolar concentration compared.
- Afferent reflex factors in veriloid-induced hypotension.
- Hereditary red blood cell disorders in middle eastern patients.
- Molecular characterization of a case of atransferrinemia.
- Normal ranges for packed cell volume and hemoglobin concentration in adults: relevance to ''apparent polycythemia''.
- Prevalence and clinical significance of HFE gene mutations in patients with iron overload.
Schools
University of Mi Med Sch
Doctors Specialties
- Hematology
- Hematopathology
Accepted Insurances
Education
-
Memorial Sloan-Kettering Cancer Center -
Scripps Clinic -
University of Utah -
University of Michigan Medical School
Hospital
-
Mayo Clinic - Rochester, Minnesota
Helpful Reviews
Similar Doctors
|
|
Dr. Gita Thanarajasingam, MD
 This Doctor is OpenDoctor Recommended.
|
|
Dr. Ahmed K. Abou Hussein, MD |
|
|
Dr. Francis K. Buadi, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Thomas M. Habermann, MD
This Doctor is OpenDoctor Recommended.
 This doctor has more publications
|
|
|
Dr. Glenn S. Harman, MD |
|
|
Dr. Tamana Walia, MD |
|
|
Dr. Svetomir N. Markovic, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Steven I. Robinson, MD |
|
|
Dr. Arleigh B. Robertson McCurdy, MD |
|
Dr. David P. Steensma, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Ryan E. Wilcox, MD |
|
|
Dr. Jessemy D. Neiger, MD |
|
|
Dr. Dong Chen, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Brian J. Davis, MD |
|
|
Dr. Howard C. Hoagland, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Fernando J. Quevedo |
|
|
Dr. Ryan A. Wilcox, MD |