Professor, Laboratory Medicine and Pathology, Mayo Medical School
Pathology
Dr. James D. Hoyer, MD
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James D. Hoyer practices Pathology. He went to The Ohio State University College of Medicine. James Hoyer is also published. He has 56 publications published. The lastest publication: "A Novel -Globin Chain Hemoglobin Variant, Hb Allentown [137(H15)ValTrp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Interm...' James Hoyer is registered with Medicare and accepts Medicare payments.
Publications
- A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Interm...
- Long-term complete clinical and hematological responses of the TEMPI syndrome after autologous stem Cell transplantation.
- Bone marrow findings of the newly described TEMPI syndrome: when erythrocytosis and plasma Cell dyscrasia coexist.
- Hb Manukau [β67(E11)Val → Gly; HBB: c.203T>G]: The Role of Genetic Testing in the Diagnosis of Idiopathic Hemolytic Anemia.
- Hb Memphis [HBA2: c.70G>C (or HBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C).
- Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: A New Low Oxygen Affinity β Chain Variant.
- Temporal sequence of major biochemical events during Blood Bank storage of packed red blood Cells.
- An assessment of the usefulness of immunohistochemical stains in the diagnosis of hairy cell Leukemia.
- Isolated del(5q) in Myeloid malignancies: clinicopathologic and molecular features in 143 consecutive patients.
- Bone marrow histopathology in POEMS syndrome: a distinctive combination of plasma cell, lymphoid and Myeloid findings in 87 patients.
- Hemoglobin Raleigh results in factitiously low hemoglobin A1c when evaluated via immunoassay analyzer.
- Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
- Bone marrow morphologic features in polycythemia vera with JAK2 exon 12 mutations.
- Hemoglobin lansing: a novel hemoglobin variant causing falsely decreased oxygen saturation by pulse oximetry.
- Changes in Band 3 oligomeric state precede Cell membrane phospholipid loss during blood bank storage of red blood Cells.
- Percentage of smudge cells on routine blood smear predicts survival in chronic lymphocytic Leukemia.
- Spontaneous mutation of hemoglobin Lufkin in a white boy.
- Relative red blood Cell enzyme levels as a clue to the diagnosis of pyruvate kinase deficiency.
- Hemolytic Anemia following attempted suicide.
- Myelodysplastic syndromes associated with interstitial deletion of chromosome 5q: clinicopathologic correlations and new insights from the pre-lenalidomide era.
- Predictive value of blood and bone marrow flow cytometry in B-cell Lymphoma classification: comparative analysis of flow cytometry and tissue biopsy in 252 patients.
- Isolated trisomy 15: a clonal chromosome abnormality in bone marrow with doubtful hematologic significance.
- CD33 detection by immunohistochemistry in paraffin-embedded tissues: a new antibody shows exCellent specificity and sensitivity for Cells of myelomonocytic lineage.
- Hb Jeddah [alpha68(E17)Asn-->His (alpha1)]: a newly recognized alpha chain variant, seen in combination with Hb S [beta6(A3)Glu-->Val], and found in three separate fam...
- Five variants of the beta-globin gene without clinical or hematological effects: Hb Maryland [beta 47(CD6)Asp-->His], Hb Kent [beta 37(C3)Trp-->Cys], Hb Visayan ...
- Using smudge cells on routine blood smears to predict clinical outcome in chronic lymphocytic Leukemia: a universally available prognostic test.
- Hemoglobin Bassett produces low pulse oximeter and co-oximeter readings.
- Clinical manifestations of hemoglobin Chico at high altitude.
- Neonatal hyperbilirubinemia in African American males: the importance of glucose-6-phosphate dehydrogenase deficiency.
- Hemoglobin Loves Park [beta68 (E12) Leu-->Phe]: report of five cases including one originating from a de novo mutation.
- Quintuple alpha-globin gene: a novel allele in a Sudanese man.
- The JAK2 V617F mutation is absent in patients with erythrocytosis due to high oxygen affinity hemoglobin variants.
- Homozygous hemoglobin Abruzzo in a North American child.
- Identification of hemoglobin variants by HPLC.
- "Myelodysplasia," myeloneuropathy, and copper deficiency.
- The detection and diagnosis of hemoglobin A2' by high-performance liquid chromatography.
- Diffuse large B-cell Lymphoma with distinctive patterns of splenic and bone marrow involvement: clinicopathologic features of two cases.
- A young girl with hemolytic Anemia and elevated hemoglobin F.
- Methemoglobinemia in children with Acute lymphoblastic leukemia (ALL) receiving dapsone for pneumocystis carinii pneumonia (PCP) prophylaxis: a correlation with cytoch...
- Two unstable beta chain variants associated with beta-thalassemia: Hb Miami [beta116(G18)his-->Pro], and Hb Hershey [beta70(E14)Ala-->Gly], and a second unstable...
- Hyperbilirubinemia among African American, glucose-6-phosphate dehydrogenase-deficient neonates.
- DNA sequence of Hb Iowa.
- 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...
- Hb Rampa [alpha 95(G2)pro-->Ser (alpha 2)] in a family of European ancestry: DNA analysis confirms the CCG-->TCG mutation at codon 95 of the alpha 2-globin gene; clini...
- Genomic abnormalities in monoclonal gammopathy of undetermined significance.
- 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...
- Myeloma and the t(11;14)(q13;q32); evidence for a biologically defined unique subset of patients.
- 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--&...
- Effects of hemoglobin C and S traits on eight glycohemoglobin methods.
- Cardiac amyloidosis presenting with elevations of cardiac troponin I and angina pectoris.
- β-Thalassemia Major Resulting from Compound Heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a Novel β(0)-Thalassemia Frameshift Mutation: HBB: ...
- Hb Grand Junction (HBB: c.348_349delinsG; p.His117IlefsX42): a new hyperunstable hemoglobin variant.
Schools
Ohio State University College Of Medicine and Public Health
St Marys Hospital Med Center
University Of Wi Hospital and Cli
Conditions Treated
- Acute Leukemia
- Anemia
- Chronic Myeloid Leukemia (CML)
- Coagulation Disorders (incl. Hemophilia)
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Doctors Specialties
- Hematology
- Hematopathology
- Pathology
Accepted Insurances
Education
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University of Wisconsin -
The Ohio State University College of Medicine
Hospital
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Mayo Clinic - Rochester, Minnesota
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1285610204 |
| Last Name Of The Provider | HOYER |
| First Name Of The Provider | JAMES |
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