Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.
about
BP1, a homeodomain-containing isoform of DLX4, represses the beta-globin geneHaemoglobin F modulation in childhood sickle cell diseaseFetal hemoglobin during infancy and in sickle cell adultsPyridyl derivatives of benzaldehyde as potential antisickling agents.Management of sickle cell disease: recent advances and controversies.Hypersplenism in homozygous sickle-cell disease in Saudi Arabia.Evaluation of haematological findings in 50 Bahraini patients with sickle cell disease and in some of their parentsButyrate increases the efficiency of translation of gamma-globin mRNA.Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.Management of cerebral vasculopathy in children with sickle cell anaemia.National trends in hospitalizations for sickle cell disease in the United States following the FDA approval of hydroxyurea, 1998-2008.Hydroxyurea for sickle cell disease.Foetal haemoglobin and disease severity in sickle cell anaemia patients in Kampala, UgandaSustained induction of fetal hemoglobin by pulse butyrate therapy in sickle cell disease.Pharmacologic induction of fetal hemoglobin synthesis: cellular and molecular mechanisms.Fetal hemoglobin in sickle cell anemiaSickle cell disease in Saudi Arabs in early childhood.BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.Sickle beta 0 thalassemia in Eastern Saudi Arabia.Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives.Health related quality of life among adolescents with sickle cell disease in Saudi ArabiaFetal haemoglobin and early manifestations of homozygous sickle cell diseaseSickle cell disease: old discoveries, new concepts, and future promise.Pharmacological induction of fetal hemoglobin synthesis using histone deacetylase inhibitors.DNA hypo-methylating agents and sickle cell disease.Regulation of human fetal hemoglobin: new players, new complexities.Frequency distribution of sickle cell anemia, sickle cell trait and sickle/beta-thalassemia among anemic patients in Saudi Arabia.5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons.Modification of globin gene expression by RNA targeting strategies.The genomics of new drugs in sickle cell disease.Current concerns in haematology. 1. Is the painful crisis of sickle cell disease a "steal" syndrome?Correction of murine sickle cell disease using gamma-globin lentiviral vectors to mediate high-level expression of fetal hemoglobin.Variation in serum electrolytes and enzyme concentrations in patients with sickle cell disease.Leg ulcers in sickle cell disease: current patterns and practices.Sickle cell cholangiopathy: an endoscopic retrograde cholangiopancreatography evaluation.Evaluation of safety and pharmacokinetics of sodium 2,2 dimethylbutyrate, a novel short chain fatty acid derivative, in a phase 1, double-blind, placebo-controlled, single-dose, and repeat-dose studies in healthy volunteers.A phase 1/2 trial of HQK-1001, an oral fetal globin inducer, in sickle cell diseaseA case series of cholecystectomy in Jamaican sickle cell disease patients - The need for a new strategyDelivery of nucleic acid therapeutics by genetically engineered hematopoietic stem cells.Splenic complications of sickle cell anemia and the role of splenectomy.
P2860
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P2860
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh
1978年學術文章
@zh-hant
name
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.
@en
type
label
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.
@en
prefLabel
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.
@en
P2093
P356
P1476
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.
@en
P2093
P356
10.7326/0003-4819-88-1-1
P407
P577
1978-01-01T00:00:00Z