Professor, Medicine, Boston University School of Medicine
Hematology
Dr. Martin H. Steinberg, MD
|
|
Give Review
Martin H. Steinberg practices Hematology. He went to Tufts University School of Medicine. Tufts University School of Medicine is ranked 49/52 in Research/PrimaryCare. He received awards:"Elected Member". Martin H. Steinberg, MD is a published doctor and has 78 publications published. The lastest was: 'BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.' Martin Steinberg accepts Medicare payments and is registered with Medicare.gov.
Publications
- BCL11A enhancer haplotypes and fetal hemoglobin in Sickle cell anemia.
- The genetics of hemoglobin A2 regulation in Sickle cell anemia.
- Reply: Practice Guideline for Pulmonary Hypertension in Sickle Cell: Direct Evidence Needed before Universal Adoption.
- Quantitative Magnetic Resonance Imaging Analysis of the Lacrimal Gland in Sickle Cell Disease.
- Fetal hemoglobin in Sickle cell anemia: a glass half full?
- Genetic modulation of HbF in Brazilians with HbSC disease and Sickle cell anemia.
- The aryl hydrocarbon receptor directs hematopoietic progenitor Cell expansion and differentiation.
- Fetal hemoglobin in Sickle cell anemia: Genetic studies of the Arab-Indian haplotype.
- Genetic determinants of haemolysis in Sickle cell anaemia.
- Quantitative MRI analysis of salivary glands in Sickle cell disease.
- qMRI relaxometry of mandibular bone marrow: A monomodal distribution in Sickle cell disease.
- Quantitative MRI analysis of craniofacial bone marrow in patients with Sickle cell disease.
- Genetic modifiers of Sickle cell disease.
- Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.
- Fetal hemoglobin in Sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.
- Is HbA(2) level a reliable diagnostic measurement for ?-thalassemia trait in people with iron deficiency?
- Erratum to: unexpectedly low pulse oximetry measurements associated with variant hemoglobins: a systematic review.
- Senicapoc trial results support the existence of different sub-phenotypes of Sickle cell disease with possible drug-induced phenotypic shifts.
- Ancestry of African Americans with Sickle cell disease.
- A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.
- Fetal hemoglobin in Sickle cell anemia.
- Fetal hemoglobin in Sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans.
- G6PD deficiency and stroke in the CSSCD.
- Severe Sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1.
- Genetic Signatures of Exceptional Longevity in Humans.
- Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: a systematic review.
- Leg ulcers in Sickle cell disease.
- Pulmonary hypertension and NO in Sickle cell.
- Fetal hemoglobin in Sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
- Genetic modifiers of the severity of Sickle cell anemia identified through a genome-wide association study.
- Vasculopathy in Sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions.
- Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
- Genome-wide association studies and the genetic dissection of complex traits.
- Effect of sodium butyrate on lung vascular TNFSF15 (TL1A) expression: differential expression patterns in pulmonary artery and microvascular endothelial Cells.
- Hemoglobin SE Disease in Maine, and severe thalassemia in New Hampshire.
- BCL11A represses HBG transcription in K562 Cells.
- RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans.
- Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
- BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
- A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.
- Pulmonary arterial hypertension and left-sided heart disease in Sickle cell disease: clinical characteristics and association with soluble adhesion molecule expression.
- SNPing away at Sickle cell pathophysiology.
- Variation and heritability of Hb F and F-Cells among beta-thalassemia heterozygotes in Hong Kong.
- Sickle cell bone disease: response to vitamin D and calcium.
- Fetal hemoglobin in Sickle cell anemia: Bayesian modeling of genetic associations.
- Chronic hyper-hemolysis in Sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain.
- Clinical trials in Sickle cell disease: adopting the combination chemotherapy paradigm.
- Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in Sickle cell disease.
- A network model to predict the risk of death in Sickle cell disease.
- Hemoglobin SE Disease: a concise review.
- Pneumococcus and Sickle cell disease: the beginning of the end?
- Estimated glomerular filtration rate in Sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B.
- Two new alpha-thalassemia frameshift mutations.
- Lacrimal gland enlargement in Sickle cell disease.
- Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in Sickle cell anemia.
- Abnormal pulmonary function in adults with Sickle cell anemia.
- Modifier genes and Sickle cell anemia.
- Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
- Screening and counseling for thalassemia.
- Hemolysis-associated priapism in Sickle cell disease.
- Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with Sickle cell osteonecrosis.
- Patients with thalassemia in the United States.
- Differential gene expression in pulmonary artery endothelial cells exposed to Sickle cell plasma.
- Genetic dissection and prognostic modeling of overt stroke in Sickle cell anemia.
- Sickle cell vaso-occlusive crisis induces the release of circulating serum heat shock protein-70.
- Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background.
- A novel Sickle hemoglobin: hemoglobin S-south end.
- Hb Hope [beta136(H14)Gly-->Asp (GGT-->GAT)]: interactions with Hb S [beta6(A3)Glu-->Val (GAG-->GTG)], other variant hemoglobins and thalassemia.
- Sickle cell anemia is associated with reduced nitric oxide bioactivity in peripheral conduit and resistance vessels.
- Bone marrow transplantation in Sickle cell disease: indications and successes.
- Effect of hydroxyurea on mortality and morbidity in adult Sickle cell anemia: risks and benefits up to 9 years of treatment.
- Therapies to increase fetal hemoglobin in Sickle cell disease.
- Concordant fetal hemoglobin response to hydroxyurea in siblings with Sickle cell disease.
- Pathophysiological-based approaches to treatment of Sickle cell disease.
- Hydroxyurea treatment for Sickle cell disease.
- New Views of Sickle Cell Disease Pathophysiology and Treatment.
- Evaluation of an ensemble of genetic models for prediction of a quantitative trait.
Schools
Tufts University
Bellevue Hospital Center
New Eng Med Center Hosps
Conditions Treated
- Sickle Cell Disease
- Venous Embolism and Thrombosis
Doctors Specialties
- Hematology
Accepted Insurances
Awards
- Elected Member
Education
-
Tufts Medical Center -
NYU School of Medicine -
Tufts University School of Medicine
Hospital
-
Boston Medical Center
Helpful Reviews
Similar Doctors
|
|
Dr. Hanno R. Hock, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Adrienne Gropper, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Mary L. Peters, MD |
|
|
Dr. Ruben D. Carrasco, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Benjamin L. Ebert, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Janet L. Abrahm, MD |
|
|
Dr. Elisabeth M. Battinelli, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Karen K. Ballen, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. David W. Allen, MD |