| P50 | author | Paola Sebastiani | Q7132103 |
| | Martin H Steinberg | Q37380250 |
| | Hazem A. Ghabbour | Q42152782 |
| | David H K Chui | Q66829380 |
| P2093 | author name string | Abdulrahman Alsultan | |
| | Waleed H Albuali | |
| | Amein K Al-Ali | |
| | Mohammed K Alabdulaali | |
| | Paula J Griffin | |
| | Ahmed M Alsuliman | |
| P2860 | cites work | Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia | Q27026479 |
| | Hypersplenism in homozygous sickle-cell disease in Saudi Arabia | Q33411080 |
| | Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin | Q34053823 |
| | Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype | Q34610322 |
| | Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway | Q35191429 |
| | Sickle beta 0 thalassemia in Eastern Saudi Arabia | Q35203514 |
| | A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia | Q74144407 |
| | Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)) | Q74167056 |
| | Splenic function in children with sickle cell disease: two different patterns in Saudi Arabia | Q93623919 |
| | Benign sickle-cell anaemia | Q93730107 |
| | Genetic modifiers of sickle cell disease | Q36035471 |
| | Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations | Q36333394 |
| | Indications and complications of splenectomy for children with sickle cell disease | Q36652431 |
| | DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease | Q36800496 |
| | Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemia | Q37021584 |
| | Ten-year review of hospital admissions among children with sickle cell disease in Kuwait | Q37236829 |
| | Sickle cell disease subphenotypes in patients from Southwestern Province of Saudi Arabia | Q37983011 |
| | Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients | Q38471171 |
| | Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene. | Q39745092 |
| | Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects | Q40108760 |
| | Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease | Q40441624 |
| | Sickle cell disease as a cause of osteonecrosis of the femoral head | Q44105081 |
| | A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype | Q44362006 |
| | Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans | Q46327662 |
| | Silent brain infarcts in adult Kuwaiti sickle cell disease patients | Q48246104 |
| | Silent brain infarcts are rare in Kuwaiti children with sickle cell disease and high Hb F. | Q48553801 |
| | Limitations of Hb F as a phenotypic modifier in sickle cell disease: study of Kuwaiti Arab patients | Q48840343 |
| | Patterns of mortality in adult sickle cell disease in the Al-Hasa region of Saudi Arabia | Q50075197 |
| | Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patients. | Q50692954 |
| | Splenectomy in patients with sickle-cell disease. | Q51001209 |
| | The prevalence of sickle cell disease in Saudi children and adolescents. A community-based survey. | Q51677474 |
| | Two different forms of homozygous sickle cell disease occur in Saudi Arabia | Q53857113 |
| | Distribution of Sickle-cell Hæmoglobin in Saudi Arabia | Q59020396 |
| | Acute chest syndrome in adult sickle cell disease in eastern Saudi Arabia. | Q64891128 |
| | Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia | Q67447872 |
| | Pain in sickle cell disease. Rates and risk factors | Q67691472 |
| | Priapism associated with the sickle cell hemoglobinopathies: prevalence, natural history and sequelae | Q68175066 |
| | Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia | Q68273357 |
| | Leg Ulceration in Sickle Cell Anemia | Q69744791 |
| | Infections and sickle cell disease in Eastern Saudi Arabian children | Q69946178 |
| | Cholelithiasis in patients with major sickle hemoglobinopathies | Q71253874 |
| | The acute chest syndrome in sickle cell disease: incidence and risk factors. The Cooperative Study of Sickle Cell Disease | Q71632332 |
| | Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease | Q71654523 |
| | Splenic function in Saudi children with sickle cell disease | Q72379159 |
| | Splenic function in sickle cell disease in the Eastern Province of Saudi Arabia | Q72730698 |
| | Splenic function in sickle cell anemia patients in Qatif, Saudi Arabia | Q73341711 |
| | Avascular necrosis of the hip in children with sickle cell disease and high Hb F: magnetic resonance imaging findings and influence of alpha-thalassemia trait | Q73843461 |
| | Avascular necrosis of the femoral head in adult Kuwaiti sickle cell disease patients | Q73944784 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | India | Q668 |
| | Saudi Arabia | Q851 |
| | phenotype | Q104053 |
| | sickle-cell disease | Q185034 |
| P304 | page(s) | 597-604 | |
| P577 | publication date | 2013-11-13 | |
| P1433 | published in | British Journal of Haematology | Q4970200 |
| P1476 | title | Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign | |
| P478 | volume | 164 | |