CEO, Vanguard Therapeutics, Inc.
Hematology
Dr. Stephen H. Embury, MD
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Stephen Embury practices Hematology. He researched medicine at Northwestern University Feinberg School of Medicine. Northwestern University Feinberg School of Medicine is ranked 19/29 in Research/PrimaryCare. Stephen H. Embury, MD is a published doctor as well. He has 79 publications published. The latest was: Viral burden and disease progression in HIV-1-infected patients with sickle cell anemia.
Publications
- Cellular Adhesion and the Endothelium: P-Selectin.
- Age-Dependent Changes in the Membrane Surface Area: Sickle Red Blood Cell Volume May Account for Differential Clinical Effects of Coinherited ? Thalassemia on Sickle C...
- Can pain studies influence regulatory policy?
- Sickle cell anemia pathophysiology: back to the data.
- Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis.
- The contribution of endothelial cell P-selectin to the microvascular flow of mouse sickle erythrocytes in vivo.
- The not-so-simple process of sickle cell vasoocclusion.
- Heparin inhibits the flow adhesion of sickle red blood cells to P-selectin.
- Using a microcomputer for intravenous drug protocols.
- Levels of alpha-fetoprotein in amniotic fluids of mice (curly-tail) with neural tube defects.
- Neural tube defects in curly-tail mice. II. Effect of maternal administration of vitamin A.
- Neural tube defects in curly-tail mice. I. Incidence, expression and similarity to the human condition.
- Nurses involvement in political action. How to be involved politically.
- Nurses involvement in political action.
- Decreased ribosomal RNA content and in vitro RNA synthesis in purified bone marrow erythroblasts of patients with idiopathic ineffective erythropoiesis and DiGuglielmo...
- Idiopathic thrombocytopenic purpura with high-titer, speckled pattern antinuclear antibodies: possible marker for systemic lupus erythematosus.
- The diagnosis of iron deficiency anemia in sickle cell disease.
- Cerebrovascular accidents in sickle cell disease: rates and risk factors.
- The Haitian connection.
- Viral burden and disease progression in HIV-1-infected patients with sickle cell anemia.
- Alpha Thalassemia is associated with decreased risk of abnormal transcranial Doppler ultrasonography in children with sickle cell anemia.
- Mycoplasma disease and acute chest syndrome in sickle cell disease.
- Hematologic improvement following splenectomy for hemoglobin-H disease.
- A simple laboratory alternative to irreversibly sickled cell (ISC) counts.
- Molecular mechanisms in alpha thalassemia: racial differences in alpha-globin gene organization.
- Triplicated alpha-globin loci in humans.
- Anemia and hemoglobinopathies in Southeast Asian refugee children.
- Effects of oxygen inhalation on endogenous erythropoietin kinetics, erythropoiesis, and properties of blood cells in sickle-cell anemia.
- Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes.
- Clomiphene-responsive hypogonadism in sickle cell anemia.
- Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster.
- Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia.
- Rheumatic carditis: in vitro responses of peripheral blood leukocytes to heart and streptococcal antigens.
- Monovalent cation changes in sickle erythrocytes: a direct reflection of alpha-globin gene number.
- The leftward deletion alpha-thal-2 haplotype in a black subject with hemoglobin SS.
- The interaction of coexistent alpha-thalassemia and sickle cell anemia: a model for the clinical and cellular results of diminished polymerization?
- Visualization of oriented hemoglobin S in individual erythrocytes by differential extinction of polarized light.
- Remission maintenance therapy in acute myelogenous leukemia.
- The frequent occurrence of alpha thalassemia in blacks.
- Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis.
- Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene.
- The role of fluctuating populations of blood cells in the acute painful episodes of sickle cell disease.
- Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.
- Hematologic malignancy in sickle cell disease: report of four cases and review of the literature.
- The effect of speed of deoxygenation on the percentage of aligned hemoglobin in sickle cells. Application of differential polarization microscopy.
- Advances in the prenatal diagnosis of sickle cell anemia.
- Preservation of sickle cell blood-flow patterns during MR imaging: an in vivo study.
- The interaction of alpha-thalassemia with sickle cell anemia.
- The incidence of painful crisis in homozygous sickle cell disease: correlation with red cell deformability.
- Oxygen-induced marrow red cell hypoplasia leading to transfusion in sickle painful crisis.
- The different types of alpha-thalassemia-2: genetic aspects.
- Reduced transglutaminase-catalyzed cross-linking of exogenous amines to membrane proteins in sickle erythrocytes.
- Selective enzymatic amplification of alpha 2-globin DNA for detection of the hemoglobin Constant Spring mutation.
- Two BglII RFLPs of the human alpha-globin gene cluster in the American sickle cell population.
- Alpha thalassemia. A modifier of sickle cell disease.
- Human embryonic zeta-globin chains in fetal and newborn blood.
- The clinical pathophysiology of sickle cell disease.
- Detection of the hemoglobin E mutation using the color complementation assay: application to complex genotyping.
- Sickle cell disease as a cause of osteonecrosis of the femoral head.
- Hemoglobin constant spring in Bangkok: molecular screening by selective enzymatic amplification of the alpha 2-globin gene.
- Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation.
- alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
- Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
- Advances in molecular diagnosis of inherited hemoglobin disorders.
- Revised transthyretin Ile 122 allele frequency in African-Americans.
- New treatments of sickle cell disease.
- Advances in the prenatal and molecular diagnosis of the hemoglobinopathies and thalassemias.
- Osteonecrosis of the humeral head in sickle cell disease.
- Chronic pulmonary disorders in sickle cell disease: findings at thin-section CT.
- Reverse dot-blot detection of Thai beta-thalassaemia mutations.
- Reverse dot-blot detection of the African-American beta-thalassemia mutations.
- Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
- Enhanced adherence of sickle erythrocytes to thrombin-treated endothelial cells involves interendothelial cell gap formation.
- Risk of altitude exposure in sickle cell disease.
- P-selectin mediates the adhesion of sickle erythrocytes to the endothelium.
- In vivo blood flow abnormalities in the transgenic knockout sickle cell mouse.
- Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia.
- L-glutamine therapy reduces endothelial adhesion of sickle red blood cells to human umbilical vein endothelial cells.
Schools
Northwestern Center Feinberg School of Medicine
Doctors Specialties
- Hematology
Accepted Insurances
Education
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Stanford University -
Northwestern University Feinberg School of Medicine