Search Results - "Steinberg, M.H."
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BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia
Published in Blood cells, molecules, & diseases (01-03-2015)“…: Fetal hemoglobin (HbF) levels in sickle cell anemia patients vary. We genotyped polymorphisms in the erythroid-specific enhancer of BCL11A to see if they…”
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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea
Published in The pharmacogenomics journal (01-12-2007)“…The increase in fetal hemoglobin (HbF) in response to hydroxyurea (HU) varies among patients with sickle cell anemia. Twenty-nine candidate genes within loci…”
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Quantitative MRI analysis of craniofacial bone marrow in patients with sickle cell disease
Published in American journal of neuroradiology : AJNR (01-03-2013)“…Assessment of bone marrow is most commonly performed qualitatively in the spine or other large long bones. The craniofacial bones are less ideal for bone…”
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Clinical and Radiologic Findings of Inner Ear Involvement in Sickle Cell Disease
Published in American journal of neuroradiology : AJNR (01-12-2011)“…SCD has been reported to involve the inner ear and result in LH and LO. Our purpose was to examine the prevalence of inner ear involvement and to assess the…”
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BCL11A Enhancer Haplotypes and Fetal Hemoglobin in Sickle Cell Anemia: Enhancers and HbF
Published in Blood cells, molecules, & diseases (30-01-2015)Get full text
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Low-density lipoprotein susceptibility to oxidation and cytotoxicity to endothelium in sickle cell anemia
Published in The Journal of laboratory and clinical medicine (01-06-1999)“…Patients with sickle-cell anemia exhibit pro-oxidative metabolic perturbations. We hypothesize that because of chronic oxidative stress, plasma low-density…”
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A Mutation in a GATA-1 Binding Site 5′ to the Gγ-Globin Gene (nt -567, T>G) May Be Associated with Increased Levels of Fetal Hemoglobin
Published in Blood (16-11-2004)“…The identification of single nucleotide polymorphisms (SNPs) associated with increased fetal hemoglobin (Hb F) levels in adults provide important insights to…”
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Genetic modulation of sickle cell anemia
Published in Proceedings of the Society for Experimental Biology and Medicine (01-05-1995)“…Sickle cell anemia, a common disorder associated with reduced life span of the red blood cell and vasoocclusive events, is caused by a mutation in the…”
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Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia
Published in The American journal of the medical sciences (01-05-1999)“…A beta-thalassemia intermedia phenotype can be caused by multiple genotypes. We studied a family where the mother was hematologically normal and both father…”
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AIDS and South Africa - towards a comprehensive strategy - Part I. The world-wide experience
Published in South African medical journal (16-04-1988)“…In this, the first of a three-part series of articles in which we propose steps towards a comprehensive strategy for the control of HIV infection, we consider…”
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beta-thalassemia-? Selected pseudogenes
Published in Medical hypotheses (01-12-1982)“…The synthesis of delta-globin is directed by a gene whose inherent characteristics permit only limited expression, a gene resembling in some respects that of…”
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AIDS and South Africa - towards a comprehensive strategy - Part II. Screening and control
Published in South African medical journal (16-04-1988)“…In this, the second of a three-part series of articles in which we propose steps towards a comprehensive strategy for the control of HIV infection, we consider…”
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AIDS and South Africa - towards a comprehensive strategy - Part III. The role of education
Published in South African medical journal (16-04-1988)“…In this, the third of a three-part series of articles in which we emphasise the urgent need for and propose steps towards a comprehensive strategy for the…”
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