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

2 Methodological quality of clinical practice guidelines for genetic testing in children: A systematic assessment using the appraisal of guidelines for research and evaluation II instrument.

3 An mHealth Framework to Improve Birth Outcomes in Benue State, Nigeria: A Study Protocol

4 A Patient-Held Smartcard With a Unique Identifier and an mHealth Platform to Improve the Availability of Prenatal Test Results in Rural Nigeria: Demonstration Study

5 management of total cancer pain: a case of young adult

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

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

8 acute headache and sickle cell disease

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

10 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

11 prevalence of sickle cell trait in the southern suburbs of beirut, lebanon

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

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

14 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.

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

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

17 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

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

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

20 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.

21 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.

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

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

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

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

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

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

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

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

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

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

32 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

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

34 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))

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

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

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

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

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

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

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

42 massive splenic infarction leading to sickle cell disease

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

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

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

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

47 the ccr5Δ32 polymorphism in brazilian patients with sickle cell disease

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

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

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

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

52 assessment of the in vivo genotoxicity of new lead compounds to treat sickle cell disease

53 iron metabolism in thalassemia and sickle cell disease

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

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

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

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

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

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