7 Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults

8 Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices

9 Case Report: Kryptonite—A Rare Case of Left-Sided Bilothorax in a Sickle Cell Patient

10 Relationship between antibiotic resistance and sickle cell anemia: preliminary evidence from a pediatric carriage study in Ghana

11 Prevalence and Patterns of Sickle Cell Disease among Children Attending Tertiary and Non-Tertiary Health Care Institutions in a South Eastern State, Nigeria: A 10 year Survey

12 Integrated psychology support and comprehensive cognitive evaluation improves access to special education services for children with sickle cell disease

13 The epidemiology of sickle cell disease in children recruited in infancy in Kilifi, Kenya: a prospective cohort study.

14 Frequency of Inflammasome Nlrp1/Nlrp3 Gene Receptor Polimorphisms And The Interleukins IL-1ß/IL-18 Gene Polymorphisms And Their Association With Severity Score In Sickle Cell Disease Patients.

15 Erythrocyte and plasma oxidative stress appears to be compensated in patients with sickle cell disease during a period of relative health, despite the presence of known oxidative agents.

16 Sickle cell disease: Clinical presentation and management of a global health challenge.

17 Generation of three control iPS cell lines for sickle cell disease studies by reprogramming erythroblasts from individuals without hemoglobinopathies.

18 Generation of integration-free iPS cell lines from three sickle cell disease patients from the state of Bahia, Brazil

19 Implementation of an educational intervention to optimize self-management and transition readiness in young adults with sickle cell disease

20 Simultaneous polymerization and adhesion under hypoxia in sickle cell disease.

21 Surfactant protein D as a marker for pulmonary complications in pediatric patients with sickle cell disease: Relation to lung function tests

22 Dysfunction of the auditory system in sickle cell anemia: a systematic review with meta-analysis.

23 Erratum: Faster lactate transport across red blood cell membrane in sickle cell trait carriers (Journal of Applied Physiology (February 2006) 100 (427-432))

24 Improvement in processing speed following haploidentical bone marrow transplant with posttransplant cytoxan in children and adolescents with sickle cell disease.

25 Alteration of humoral, cellular and cytokine immune response to inactivated influenza vaccine in patients with Sickle Cell Disease.

26 "Waiting for a miracle": Spirituality/Religiosity in coping with sickle cell disease.

27 Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM).

28 Dysregulated NO/PDE5 signaling in the sickle cell mouse lower urinary tract: Reversal by oral nitrate therapy.

29 Social and Psychological Factors Associated With Health Care Transition for Young Adults Living With Sickle Cell Disease.

30 An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective.

31 Prevention of Morbidity in Sickle Cell Disease (POMS2a)—overnight auto-adjusting continuous positive airway pressure compared with nocturnal oxygen therapy: a randomised crossover pilot study examining patient preference and safety in adults and children

32 Significant Quantitative Differences in Orexin Neuronal Activation After Pain Assessments in an Animal Model of Sickle Cell Disease

33 Corrigendum to “Polymorphisms in genes that affect the variation of lipid levels in a Brazilian pediatric population with sickle cell disease: rs662799 APOA5 and rs964184 ZPR1” (Blood Cells, Molecules and Diseases (2020) 80, (S1079979619302487), (10.1016/j.bcmd.2019.102376))

34 Phase 2 trial of montelukast for prevention of pain in sickle cell disease.

35 comprehensive healthcare for individuals with sickle cell disease: a constant challenge

36 newborn screening for sickle cell disease: technical and legal aspects of a german pilot study with 38,220 participants

37 an &ldquo;acquired&rdquo; hemoglobin j variant in a sickle cell disease patient

38 perception of primary care doctors and nurses about care provided to sickle cell disease patients

39 mri-based cerebrovascular reactivity using transfer function analysis reveals temporal group differences between patients with sickle cell disease and healthy controls

40 sickle cell disease: management options and challenges in developing countries

41 pattern of ast and alt changes in relation to hemolysis in sickle cell disease

42 acute headache and sickle cell disease

43 complicações hepáticas na doença falciforme hepatic complications in sickle cell disease

44 doença falciforme e qualidade de vida: um estudo da percepção subjetiva dos pacientes da fundação hemominas, minas gerais, brasil sickle cell disease and quality of life: a study on the subjective perception of patients from the fundação hemominas, minas gerais, brazil

45 an unexpected full neurological recovery after cardiac arrest in a sickle cell anemia patient with bilateral cervical carotid artery disease

46 innate-like t cells in children with sickle cell disease.

47 can csf spectrophotometry for “xanthochromia” be used to detect leaking subarachnoid aneurysms in patients with sickle cell anemia with negative mri or ct angiogram despite hyperbilirubinemia?

48 massive splenic infarction leading to sickle cell disease

49 amelioration of sickle cell pain after parathyroidectomy in two patients with concurrent hyperparathyroidism: an interesting finding

50 impact of iron overload on interleukin-10 levels, biochemical parameters and oxidative stress in patients with sickle cell anemia

51 brodie’s abscess in a patient presenting with sickle cell vasoocclusive crisis

52 unclassified renal cell carcinoma with medullary phenotype versus renal medullary carcinoma: lessons from diagnosis in an italian man found to harbor sickle cell trait

53 intravitreal ranibizumab for stage iv proliferative sickle cell retinopathy: a first case report

54 electrocardiographic study in adult homozygous sickle cell disease patients in lagos, nigeria

55 self-care practice in people with sickle cell anemia

56 brazilian guidelines for transcranial doppler in children and adolescents with sickle cell disease

57 craniofacial bone abnormalities and malocclusion in individuals with sickle cell anemia: a critical review of the literature

58 musculoskeletal manifestations of sickle cell anaemia: a pictorial review

59 the association of cd81 polymorphisms with alloimmunization in sickle cell disease

60 limited exchange transfusion can be very beneficial in sickle cell anemia with acute chest syndrome: a case report from tanzania

61 presence of atypical beta globin (hbb) gene cluster haplotypes in sickle cell anemia patients of india

62 hematopoietic stem cell transplantation in sickle cell disease: patient selection and special considerations

63 the ccr5Δ32 polymorphism in brazilian patients with sickle cell disease

64 sobrecarga e quelação de ferro na anemia falciforme iron overload and iron chelation in sickle cell disease

65 pulmonic valve repair in a patient with isolated pulmonic valve endocarditis and sickle cell disease

66 crise de seqüestro esplênico na doença falciforme splenic sequestration crisis in sickle cell disease

67 sickle cell anemia patients in use of hydroxyurea: association between polymorphisms in genes encoding metabolizing drug enzymes and laboratory parameters

68 endothelial nitric oxide synthase (enos) gene polymorphism is associated with age onset of menarche in sickle cell disease females of india

69 iron metabolism in thalassemia and sickle cell disease

70 multiple bone and joint disease in a sickle cell anaemia patient: a case report

71 dexmedetomidine as sedative and analgesic in a patient of sickle cell disease for total hip replacement

72 bilateral pulmonary embolism after a short-haul flight in a man with multiple risk factors including sickle cell trait

73 secondhand smoke is an important modifiable risk factor in sickle cell disease: a review of the current literature and areas for future research

74 función esplénica en la anemia drepanocítica splenic function in sickle cell anemia

75 stroke in patients with sickle cell disease: clinical and neurological aspects acidente cerebrovascular em pacientes com anemia falciforme: aspectos clínicos e neurológicos

76 delayed hemolytic transfusion reaction presenting as a painful crisis in a patient with sickle cell anemia

77 sickle cell trait: not as benign as once thought

78 circulating microparticles, protein c, free protein s and endothelial vascular markers in children with sickle cell anaemia

79 percutaneous vertebroplasty for osteoporotic vertebral fracture in a patient with sickle cell disease

80 procalcitonin as a biomarker of bacterial infection in sickle cell vaso-occlusive crisis.

81 qualidade de sono e função pulmonar em adolescentes portadores de anemia falciforme clinicamente estáveis quality of sleep and pulmonary function in clinically stable adolescents with sickle cell anemia

82 Undernutrition: a major but potentially preventable cause of poor outcomes in children living with sickle cell disease in Africa

83 Association of sickle cell disease with anthropometric indices among under-five children: evidence from 2018 Nigeria Demographic and Health Survey

84 Elastographic evaluation of the effect of sickle cell anemia on testicles: a prospective study.

85 Correlation of Transfusion Dependence and Its Associated Sequelae to Hematological and Biochemical Parameters in Patients With Sickle Cell Disease and Beta Thalassemia Major in Khobar: A Retrospective Study.

86 Blood count changes in malaria patients according to blood groups (ABO/Rh) and sickle cell trait

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