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Keyword Connections - sickle cell disease Keywords

Connection Type	Connection
Journals	Medicine journal of clinical medicine Cureus the journal of clinical endocrinology and metabolism blood reviews
Research Groups	No Research Group Connected
Bibliographies	[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] An Educational Study Promoting the Delivery of Transcranial Doppler Ultrasound Screening in Paediatric Sickle Cell Disease: A European Multi-Centre Perspective. [33] 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 [34] Significant Quantitative Differences in Orexin Neuronal Activation After Pain Assessments in an Animal Model of Sickle Cell Disease [35] 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)) [36] Phase 2 trial of montelukast for prevention of pain in sickle cell disease. [37] comprehensive healthcare for individuals with sickle cell disease: a constant challenge [38] newborn screening for sickle cell disease: technical and legal aspects of a german pilot study with 38,220 participants [39] an &ldquo;acquired&rdquo; hemoglobin j variant in a sickle cell disease patient [40] perception of primary care doctors and nurses about care provided to sickle cell disease patients [41] mri-based cerebrovascular reactivity using transfer function analysis reveals temporal group differences between patients with sickle cell disease and healthy controls [42] sickle cell disease: management options and challenges in developing countries [43] pattern of ast and alt changes in relation to hemolysis in sickle cell disease [44] acute headache and sickle cell disease [45] complicações hepáticas na doença falciforme hepatic complications in sickle cell disease [46] 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 [47] innate-like t cells in children with sickle cell disease. [48] massive splenic infarction leading to sickle cell disease [49] electrocardiographic study in adult homozygous sickle cell disease patients in lagos, nigeria [50] brazilian guidelines for transcranial doppler in children and adolescents with sickle cell disease [51] the association of cd81 polymorphisms with alloimmunization in sickle cell disease [52] hematopoietic stem cell transplantation in sickle cell disease: patient selection and special considerations [53] the ccr5Δ32 polymorphism in brazilian patients with sickle cell disease [54] sobrecarga e quelação de ferro na anemia falciforme iron overload and iron chelation in sickle cell disease [55] pulmonic valve repair in a patient with isolated pulmonic valve endocarditis and sickle cell disease [56] crise de seqüestro esplênico na doença falciforme splenic sequestration crisis in sickle cell disease [57] endothelial nitric oxide synthase (enos) gene polymorphism is associated with age onset of menarche in sickle cell disease females of india [58] assessment of the in vivo genotoxicity of new lead compounds to treat sickle cell disease [59] iron metabolism in thalassemia and sickle cell disease [60] dexmedetomidine as sedative and analgesic in a patient of sickle cell disease for total hip replacement [61] secondhand smoke is an important modifiable risk factor in sickle cell disease: a review of the current literature and areas for future research [62] stroke in patients with sickle cell disease: clinical and neurological aspects acidente cerebrovascular em pacientes com anemia falciforme: aspectos clínicos e neurológicos [63] percutaneous vertebroplasty for osteoporotic vertebral fracture in a patient with sickle cell disease [64] Undernutrition: a major but potentially preventable cause of poor outcomes in children living with sickle cell disease in Africa [65] Association of sickle cell disease with anthropometric indices among under-five children: evidence from 2018 Nigeria Demographic and Health Survey [66] 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.