Pages that link to "Q93730107"
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The following pages link to Benign sickle-cell anaemia (Q93730107):
Displaying 50 items.
- Sickle cell disease in Middle East Arab countries (Q24615860) (← links)
- Genomic approaches to identifying targets for treating β hemoglobinopathies (Q26799214) (← links)
- Structure of human foetal deoxyhaemoglobin (Q27733441) (← links)
- Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies (Q30249259) (← links)
- Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin (Q33587548) (← links)
- A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. (Q33595430) (← links)
- Sickle cell disease in Sicily. (Q33667649) (← links)
- Substitution of the human beta-spectrin promoter for the human agamma-globin promoter prevents silencing of a linked human beta-globin gene in transgenic mice (Q33781540) (← links)
- Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign. (Q33888761) (← links)
- Recent developments in foetal haemoglobin research (Q34056437) (← links)
- Hereditary persistence of fetal haemoglobin (Q34064704) (← links)
- Sustained induction of fetal hemoglobin by pulse butyrate therapy in sickle cell disease (Q34723434) (← links)
- Short-chain fatty acid derivatives induce fetal globin expression and erythropoiesis in vivo (Q34723868) (← links)
- Fetal hemoglobin in sickle cell anemia (Q35114500) (← links)
- Sickle cell disease in Saudi Arabs in early childhood (Q35114962) (← links)
- Sickle cell haemoglobinopathies in England (Q35115241) (← links)
- BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. (Q35124793) (← links)
- Heterogeneity of sickle-cell anemia based on a profile of hematological variables (Q35203570) (← links)
- Genetic epidemiology of the beta s gene (Q35757615) (← links)
- Sickle Cell Disease: Reappraisal of the Role of Foetal Haemoglobin Levels in the Frequency of Vaso-Occlusive Crisis (Q35996840) (← links)
- The switch from fetal to adult hemoglobin (Q36488272) (← links)
- Hydroxyurea as Treatment for Sickle Cell Anemia (Q36670392) (← links)
- 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. (Q37524864) (← links)
- A phase 1/2 trial of HQK-1001, an oral fetal globin inducer, in sickle cell disease (Q37524888) (← links)
- Advances in the understanding of haemoglobin switching (Q37702418) (← links)
- A phased SNP-based classification of sickle cell anemia HBB haplotypes (Q38628569) (← links)
- Modification of the Acid Elution Technique for Quantitation of Fetal Hemoglobin in Individual Erythrocytes (Q39449252) (← links)
- Fetal hemoglobin in sickle cell anemia: The Arab-Indian haplotype and new therapeutic agents (Q39453785) (← links)
- Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid (Q39467477) (← links)
- Heterogeneity of sickle cell anaemia in Arabs: review of cases with various amounts of fetal haemoglobin (Q39588226) (← links)
- Genetic studies in Saudi Arabia: Red cell enzyme, haemoglobin and serum protein polymorphisms (Q39663947) (← links)
- Sickle cell anemia as a syndrome: A review of diagnostic features (Q39805216) (← links)
- The potential molecular mechanism of thalassemias and related disorders (Q39949559) (← links)
- Clinical implications of recent advances in hemoglobin disorders. (Q40098326) (← links)
- Hematological and Clinical Features of Sickle Cell Diseases: a Review (Q40098666) (← links)
- The Synthesis and Chemical Heterogeneity of Human Fetal Hemoglobin: Overview and present concepts (Q40098676) (← links)
- Pharmacological modification of hemoglobin F expression in sickle cell anemia: An update on hydroxyurea studies (Q40485105) (← links)
- Butyrate-induced reactivation of the fetal globin genes: A molecular treatment for theβ-hemoglobinophaties (Q40485112) (← links)
- Fetal erythropoiesis and the diagnosis and treatment of hemoglobin disorders in the fetus and child (Q41504802) (← links)
- Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia (Q41959356) (← links)
- Regulation of fetal hemoglobin synthesis in sickle cell anemia (Q42135390) (← links)
- The effect of maternal partial exchange transfusion on the infants of patients with sickle cell anemia (Q44224321) (← links)
- The demonstration of asymmetric hemoglobin hybrids by polyacrylamide electrophoresis (Q44326851) (← links)
- Long survival in sickle-cell disease (Q45162884) (← links)
- Splenectomy and acute splenic sequestration crises in sickle cell disease (Q45236826) (← links)
- Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin (Q46222871) (← links)
- Pregnancy in sickle-cell anemia in a Caucasian group (Q46331998) (← links)
- Ocular manifestations of sickle cell anaemia in Arab children (Q46818940) (← links)
- Splenic abscess and sickle cell disease (Q50130786) (← links)
- Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach. (Q52204062) (← links)