Julie Makani
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Tanzanian medical researcher
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Philosophy
Julie Makani's Degrees
- Bachelors Medicine Muhimbili University of Health and Allied Sciences
Why Is Julie Makani Influential?
(Suggest an Edit or Addition)According to Wikipedia, Julie Makani is a Tanzanian medical researcher. From 2014 she is Wellcome Trust Research Fellow and Associate Professor in the Department of Haematology and Blood Transfusion at the Muhimbili University of Health and Allied Sciences . Also a visiting fellow and consultant to the Nuffield Department of Medicine, University of Oxford, she is based in Dar es Salaam, Tanzania. In 2011, she received the Royal Society Pfizer Award for her work with sickle cell disease.
Julie Makani's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genome-wide and fine-resolution association analysis of malaria in West Africa (2009) (394)
- Enabling the genomic revolution in Africa (2014) (327)
- Mortality in Sickle Cell Anemia in Africa: A Prospective Cohort Study in Tanzania (2011) (254)
- Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case–control study (2009) (228)
- A global network for investigating the genomic epidemiology of malaria (2008) (153)
- Sickle cell disease in Africa: burden and research priorities (2007) (153)
- Malaria in patients with sickle cell anemia: burden, risk factors, and outcome at the outpatient clinic and during hospitalization. (2010) (150)
- The Lancet NCDI Poverty Commission: bridging a gap in universal health coverage for the poorest billion (2020) (126)
- Admission diagnosis of cerebral malaria in adults in an endemic area of Tanzania: implications and clinical description. (2003) (123)
- Sickle Cell Disease: New Opportunities and Challenges in Africa (2013) (123)
- Valid Consent for Genomic Epidemiology in Developing Countries (2007) (110)
- High mortality from Plasmodium falciparum malaria in children living with sickle cell anemia on the coast of Kenya. (2010) (109)
- H3ABioNet, a sustainable pan-African bioinformatics network for human heredity and health in Africa (2016) (101)
- Contemporary aetiology, clinical characteristics and prognosis of adults with heart failure observed in a tertiary hospital in Tanzania: the prospective Tanzania Heart Failure (TaHeF) study (2014) (99)
- Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia. (2011) (99)
- Prevalence and factors associated with severe anaemia amongst under-five children hospitalized at Bugando Medical Centre, Mwanza, Tanzania (2015) (90)
- Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania (2014) (79)
- Human candidate gene polymorphisms and risk of severe malaria in children in Kilifi, Kenya: a case-control association study (2018) (73)
- Malaria as a cause of morbidity and mortality in children with homozygous sickle cell disease on the coast of Kenya. (2009) (72)
- An observational study of children with sickle cell disease in Kilifi, Kenya (2009) (57)
- Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania (2011) (55)
- Management of sickle cell disease in the community (2014) (54)
- Anemia at the Initiation of Tuberculosis Therapy Is Associated with Delayed Sputum Conversion among Pulmonary Tuberculosis Patients in Dar-es-Salaam, Tanzania (2014) (52)
- Addressing gaps in international blood availability and transfusion safety in low‐ and middle‐income countries: a NHLBI workshop (2018) (52)
- Haptoglobin, alpha‐thalassaemia and glucose‐6‐phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania (2014) (48)
- Sickle cell disease in Africa: an overview of the integrated approach to health, research, education and advocacy in Tanzania, 2004–2016 (2017) (47)
- Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality (2014) (47)
- Risk factors for high cerebral blood flow velocity and death in Kenyan children with Sickle Cell Anaemia: role of haemoglobin oxygen saturation and febrile illness (2009) (46)
- Clinical utility of HCV core antigen detection and quantification using serum samples and dried blood spots in people who inject drugs in Dar-es-Salaam, Tanzania (2017) (37)
- Alteration of lymphocyte phenotype and function in sickle cell anemia: Implications for vaccine responses (2016) (36)
- Complications of sickle cell anaemia in children in Northwestern Tanzania (2016) (34)
- Newborn screening for sickle cell disease: an innovative pilot program to improve child survival in Dar es Salaam, Tanzania. (2019) (30)
- g(HbF): a genetic model of fetal hemoglobin in sickle cell disease. (2018) (30)
- A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania (2018) (29)
- High birth prevalence of sickle cell disease in Northwestern Tanzania (2018) (28)
- Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania (2015) (25)
- Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2 (2014) (25)
- Prevalence and prognostic implications of anaemia and iron deficiency in Tanzanian patients with heart failure (2014) (23)
- Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer (2015) (23)
- Genetic variants at HbF‐modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania (2014) (22)
- Sickle cell disease in Africa: an urgent need for longitudinal cohort studies (2019) (20)
- Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia (2013) (19)
- Negative Epistasis between Sickle and Foetal Haemoglobin Suggests a Reduction in Protection against Malaria (2015) (19)
- Turf wars: exploring splenomegaly in sickle cell disease in malaria‐endemic regions (2017) (18)
- Hydroxyurea - An Essential Medicine for Sickle Cell Disease in Africa. (2019) (18)
- Global arginine bioavailability in Tanzanian sickle cell anaemia patients at steady‐state: a nested case control study of deaths versus survivors (2011) (18)
- Ready-to-use food supplement, with or without arginine and citrulline, with daily chloroquine in Tanzanian children with sickle-cell disease: a double-blind, random order crossover trial (2018) (18)
- Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening (2016) (17)
- Peripheral vascular response to inspiratory breath hold in paediatric homozygous sickle cell disease (2012) (17)
- A robust mass spectrometry method for rapid profiling of erythrocyte ghost membrane proteomes (2018) (16)
- End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settings. (2019) (16)
- Strengthening medical education in haematology and blood transfusion: postgraduate programmes in Tanzania (2017) (14)
- Making hydroxyurea affordable for sickle cell disease in Tanzania is essential (HASTE): How to meet major health needs at a reasonable cost (2020) (14)
- Hematology in Africa. (2016) (13)
- Tanzania's position on the COVID-19 pandemic (2021) (12)
- Establishing a Multi-Country Sickle Cell Disease Registry in Africa: Ethical Considerations (2019) (12)
- Red Blood Cell Alloimmunization in Sickle Cell Disease Patients in Tanzania. (2014) (12)
- Cerebral Infarcts and Vasculopathy in Tanzanian Children With Sickle Cell Anemia. (2019) (12)
- Analysis of the indications for routine lumbar puncture and results of cerebrospinal fluid examination in children admitted to the paediatric wards of two hospitals in East Africa. (2006) (11)
- High prevalence of individuals with low concentration of fetal hemoglobin in F‐cells in sickle cell anemia in Tanzania (2016) (11)
- Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania (2017) (11)
- Sickle cell disease and H3Africa: enhancing genomic research on cardiovascular diseases in African patients (2015) (11)
- SickleInAfrica. (2020) (11)
- Sickle cell disease: tipping the balance of genomic research to catalyse discoveries in Africa (2017) (10)
- Perspectives from NHLBI Global Health Think Tank Meeting for Late Stage (T4) Translation Research. (2017) (10)
- Sickle cell anemia: iron availability and nocturnal oximetry. (2012) (10)
- A common molecular signature of patients with sickle cell disease revealed by microarray meta-analysis and a genome-wide association study (2018) (9)
- Treating Rare Diseases in Africa: The Drugs Exist but the Need Is Unmet (2022) (9)
- Heart failure in Tanzania and Sweden: Comparative characterization and prognosis in the Tanzania Heart Failure (TaHeF) study and the Swedish Heart Failure Registry (SwedeHF). (2016) (9)
- White Matter Integrity in Tanzanian Children With Sickle Cell Anemia (2020) (9)
- Burden of disease among the world’s poorest billion people: An expert-informed secondary analysis of Global Burden of Disease estimates (2021) (8)
- Stroke in sickle cell disease in Africa: case report. (2005) (8)
- Rationale and design of mDOT-HuA study: a randomized trial to assess the effect of mobile-directly observed therapy on adherence to hydroxyurea in adults with sickle cell anemia in Tanzania (2016) (8)
- The role of haematopoietic stem cell transplantation for sickle cell disease in the era of targeted disease-modifying therapies and gene editing. (2020) (7)
- Possible Risk Factors for Severe Anemia in Hospitalized Sickle Cell Patients at Muhimbili National Hospital, Tanzania: Protocol for a Cross-Sectional Study (2018) (7)
- P1481: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES (2021) (7)
- Curative options for sickle cell disease in Africa: Approach in Tanzania. (2020) (7)
- Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum (2020) (7)
- Audit of clinical-laboratory practices in haematology and blood transfusion at Muhimbili National Hospital in Tanzania. (2012) (7)
- Rates and risk factors of hypertension in adolescents and adults with sickle cell anaemia in Tanzania: 10 years’ experience (2017) (7)
- Artemisinin Therapy for Malaria in Hemoglobinopathies: A Systematic Review (2018) (7)
- Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana (2022) (7)
- F cell numbers are associated with an X‐linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease (2020) (6)
- Decreased Hepcidin Levels Are Associated with Low Steady-state Hemoglobin in Children With Sickle Cell Disease in Tanzania (2018) (6)
- Exploring the Role of Shared Decision Making in the Consent Process for Pediatric Genomics Research in Cameroon, Tanzania, and Ghana (2019) (6)
- Immunoglobulin G responses against falciparum malaria specific antigens are higher in children with homozygous sickle cell trait than those with normal hemoglobin (2019) (6)
- Newborn screening for hemoglobinopathies at Muhimbili National Hospital, Dar es Salaam – Tanzania (2015) (6)
- Barriers and Facilitators of Use of Hydroxyurea among Children with Sickle Cell Disease: Experiences of Stakeholders in Tanzania (2021) (6)
- Nocturnal haemoglobin oxygen saturation variability is associated with vitamin C deficiency in Tanzanian children with sickle cell anaemia (2011) (6)
- Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania (2020) (5)
- Haematopoietic stem cell transplantation in Tanzania (2020) (5)
- Using DNA testing for the precise, definite, and low-cost diagnosis of sickle cell disease and other Haemoglobinopathies: findings from Tanzania (2021) (5)
- The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania (2018) (5)
- Moyamoya Disease, a Rare Cause of Recurrent Strokes in an African Sickle Cell Child: Does hydroxyurea have a Role in this Context? (2012) (5)
- The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications (2020) (5)
- Relationships between sickle cell trait, malaria, and educational outcomes in Tanzania (2017) (5)
- The Sickle Cell Disease Ontology: enabling universal sickle cell-based knowledge representation (2019) (5)
- A pilot study of a non-invasive oral nitrate stable isotopic method suggests that arginine and citrulline supplementation increases whole-body NO production in Tanzanian children with sickle cell disease (2018) (4)
- Nocturnal haemoglobin oxygen desaturation in urban and rural East African paediatric cohorts with and without sickle cell anaemia: a cross-sectional study (2015) (4)
- Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia (2014) (4)
- Limited Exchange Transfusion Can Be Very Beneficial in Sickle Cell Anemia with Acute Chest Syndrome: A Case Report from Tanzania (2018) (4)
- Neuroimaging in patients with sickle cell anemia: capacity building in Africa. (2018) (4)
- A qualitative study on aspects of consent for genomic research in communities with low literacy (2020) (4)
- Effect of age, cerebral infarcts, vasculopathy and haemoglobin on cognitive function, in Tanzanian children with sickle cell anaemia. (2022) (3)
- Mortality in sickle cell anaemia in Africa: rates and risk factors from a prospective cohort study in Tanzania (2011) (3)
- Enablers and barriers to newborn screening for sickle cell disease in Africa: results from a qualitative study involving programmes in six countries (2022) (3)
- Prioritizing Health-Sector Interventions for Noncommunicable Diseases and Injuries in Low- and Lower-Middle Income Countries: National NCDI Poverty Commissions (2021) (3)
- Sickle cell disease, malaria and dengue fever: a case of triple jeopardy (2019) (3)
- A Case of a Child with Chronic Myeloid Leukemia Presenting with Vision and Hearing Loss (2016) (3)
- Prevalence of Hemoglobin-S and Baseline Level of Knowledge on Sickle Cell Disease Among Pregnant Women Attending Antenatal Clinics in Dar-Es-Salaam, Tanzania (2022) (3)
- Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania (2020) (3)
- Finding a cure for sickle cell disease (2019) (2)
- Patterns and patient factors associated with loss to follow-up in the Muhimbili sickle cell cohort, Tanzania (2020) (2)
- From Mendel to a Mendelian disorder: towards a cure for sickle cell disease (2022) (2)
- Clinical epidemiology of individuals with Sickle cell anemia using Hydroxyurea at Muhimbili National Hospital, Dar Es Salaam, Tanzania (2020) (2)
- Blood diseases in Africa: Redressing unjust disparities is an urgent unmet need (2022) (2)
- Barriers and Facilitators of Availability of Hydroxyurea for Sickle Cell Disease in Tanzania; A Qualitative Study of Pharmaceutical Manufacturers, Importers, and Regulators (2022) (2)
- Sickle cell anaemia in East Africa: Preliminary results from a cohort study. (2006) (2)
- Of mice and men: From hematopoiesis in mouse models to curative gene therapy for sickle cell disease (2022) (2)
- Endothelial Function In Tanzanian Children With Sickle Cell Disease: Baseline Results From The Vascular Function Intervention Trial (VFIT) (2013) (2)
- Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania (2019) (2)
- Perspectives on Building Sustainable Newborn Screening Programs for Sickle Cell Disease: Experience from Tanzania (2021) (2)
- Sickle cell disease in Africa: an overview of the integrated approach to health, research, education and advocacy in Tanzania, 20042016 (2018) (1)
- From a Lancet Commission to the NCDI Poverty Network: reaching the poorest billion through integration science (2021) (1)
- Developing Research Education Groups in African Cancer Centers: The Experience in Tanzania (2021) (1)
- Skills Capacity Building For Health Care Services and Research Through the Sickle Pan African Research Consortium (2022) (1)
- A Baseline Evaluation of Bioinformatics Capacity in Tanzania Reveals Areas for Training (2021) (1)
- The Effects of Sickle Cell Disease on the Quality of Life: A Focus on the Untold Experiences of Parents in Tanzania (2022) (1)
- High prevalence of chronic hepatitis C in injecting drug users in Tanzania, East Africa: a neglected burden of disease (2017) (1)
- Erythema multiforme in a young adult following COVID-19 infection and vaccination in Tanzania (2022) (1)
- Nasopharyngeal Carriage and Antibiogram of Pneumococcal and Other Bacterial Pathogens from Children with Sickle Cell Disease in Tanzania (2022) (1)
- Analysis of the indications and results of cerebrospinal fluid examination in children admitted to the paediatric wards of two hospitals in east Africa (2010) (1)
- Oxygen Saturation in Primary Teeth of Individuals With Sickle Cell Disease and Sickle Cell Trait (2022) (1)
- Baseline Evaluation of Bioinformatics Capacity in Tanzania (2020) (1)
- Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica (2021) (1)
- Ready-to-Use Supplementary Food Supplements Improve Endothelial Function, Hemoglobin and Growth in Tanzanian Children with Sickle Cell Anaemia: The Vascular Function Intervention Study (V-FIT), a Random Order Crossover Trial (2014) (1)
- Sickle Cell Disease in Africa and the Arabian Peninsula: Current Management and Challenges (2016) (1)
- A Massive Extradural Hematoma in Sickle Cell Disease and the Importance of Rapid Neuroimaging (2019) (1)
- Molecular genetics research in sub-Saharan Africa: how can the international community help? (2014) (1)
- Inauguration of the Tanzania Society of Human Genetics: Biomedical Research in Tanzania with Emphasis on Human Genetics and Genomics. (2020) (1)
- “Black Lives Matter and Black Research Matters”: the African Society of Human Genetics’ call to halt racism in science (2022) (1)
- Dataset and supplementary materials for baseline evaluation of bioinformatics capacity in Tanzania in 2018 (2021) (1)
- Systemic Nitric Oxide (NO) Production is Increased in Children with Sickle Cell Disease (SCD) Receiving Fortified Supplementary Food (2015) (1)
- Healthcare Workers’ Knowledge and Resource Availability for Care of Sickle Cell Disease in Dar es Salaam, Tanzania (2022) (1)
- P117: THE INTERNATIONAL HAEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HAEMOGLOBINOPATHIES (2022) (0)
- Gender effect on production and enrichment of F cell numbers in Sickle Cell Disease patients in Tanzania. (2023) (0)
- Cerebral Infarcts and Cerebrovascular Disease in Neurologically Intact Tanzanian Children with Sickle Cell Anaemia (2018) (0)
- Potential of point of care tests for newborn screening for sickle cell disease: Evaluation of HemotypeSC™ and sickle SCAN® in Tanzania (2022) (0)
- Building research capacity for sickle cell disease in Africa: Lessons and challenges from establishing a birth cohort in Tanzania (2022) (0)
- The efficacy of maternal health education and maternal screening on knowledge and the uptake of infant screening for sickle cell disease in Dar-Es-Salaam, Tanzania; a quasi experimental study (2023) (0)
- Relationship between skin microvascular reactivity, cerebral blood flow and hypoxaemia in children with sickle cell disease (2010) (0)
- Cognitive Function Of Nigerian Children With Sickle Cell Disease (2013) (0)
- Amino Acids in Tanzanian Children with Sickle Cell Disease: Baseline results of the Vascular Function Intervention Trial (V‐FIT) (2015) (0)
- 5612560 A MONITORING AND EVALUATION FRAMEWORK AND ASSOCIATED TOOLS FOR THE SICKLEINAFRICA CONSORTIUM (2023) (0)
- Development of the sickle Pan-African research consortium registry in Tanzania: opportunity to harness data science for sickle cell disease (2023) (0)
- Clinical and laboratory features of homozygous sickle cell patients in Tanzania; Malaria, infections and cerebral blood flow velocity (2005) (0)
- Hematological and Biochemical Reference Ranges for Population With Sickle Cell Disease at Steady-State in Tanzania (2021) (0)
- Improved biorepository to support sickle cell disease genomics and clinical research: A practical approach to link patient data and biospecimens from Muhimbili Sickle Cell Program, Tanzania (2023) (0)
- Pairing parents and offspring's HemoTypeSC Test to validate results and confirm sickle cell pedigree: a case study in Kisangani, the Democratic Republic of the Congo (2022) (0)
- Transcranial doppler in sickle cell disease in Africa (2007) (0)
- A qualitative study on consenting approaches for genomic research in communities with low literacy (2019) (0)
- Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania (2020) (0)
- Neurological events and abnormalities in SCD cohort in Tanzania (2011) (0)
- The association between delayed sputum conversion and anemia among Tuberculosis patients (N = 1245)*. (2014) (0)
- Haematology in sub-Saharan Africa: advances and opportunities in health care, education, and research. (2021) (0)
- Dataset for: Hepcidin in Tanzanian children with sickle cell disease (2018) (0)
- Africa must participate in finding a gene therapy cure for sickle-cell disease (2022) (0)
- Clinical Study Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia (2013) (0)
- Using DNA testing for the precise, definite, and low-cost diagnosis of sickle cell disease and other Haemoglobinopathies: findings from Tanzania (2021) (0)
- The effect of sickle cell genotype on the pharmacokinetic properties of artemether-lumefantrine in Tanzanian children (2022) (0)
- Promoting access of hydroxyurea to sickle cell disease individuals: Time to make it an essential medicine (2022) (0)
- Abstract 13893: Sickle Cell Disease Alters Myocardial Deformation Mechanics: A Study of Cardiac Strain and Strain Rate in East African Children (2011) (0)
- Rationale, design and protocol of a cross-sectional study on pregnancy-related cardiovascular diseases in Tanzania (PRECARDT): burden, characterisation and prognostic significance at delivery (2021) (0)
- Continuous Cultures of Plasmodium Falciparum Established in Tanzania from Patients with Acute Malaria (2021) (0)
- Splenomegaly in Adolescents and Adults with Sickle Cell Anemia in Tanzania Is Associated with Less Severe Disease (2017) (0)
- A robust mass spectrometry method for rapid profiling of erythrocyte ghost membrane proteomes (2018) (0)
- Anaemia and iron deficiency in heart failure: epidemiological gaps, diagnostic challenges and therapeutic barriers in sub-Saharan Africa (2017) (0)
- The contribution of social and family networks in supporting care of children with sickle cell disease in Tanzania (2022) (0)
- Arginine to ornithine ratios in Tanzanian sickle cell anaemia patients at steady-state: a nested case control of deaths versus survivors (2011) (0)
- Adherence patterns among patients receiving healthcare services in the Muhimbili Sickle Cell Cohort, Tanzania (2020) (0)
- The role of malaria infection in morbidity and mortality in sickle cell disease in east africa: Preliminary evidence from a cohort study [MIM-JM-1200] (2005) (0)
- Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica (2023) (0)
- Immunoglobulin G responses against falciparum malaria specific antigens are higher in children with homozygous sickle cell trait than those with normal hemoglobin (2019) (0)
- Defining the clinical spectrum of sickle cell disease in Tanzania : a clinico-epidemiological study (2011) (0)
- Proteomics Pathways of Sickle Cell Anemia (P2SCA): A Comprehensive Analysis By Liquid Chromatography Mass Spectrometry of Erythrocyte Membrane Proteins Characterized from the Muhimbili Sickle Cell Programme, Tanzania (2018) (0)
- Health education for sickle cell disease: Strategies to support families and health care workers in Tanzania (2014) (0)
- Ready-to-use food supplement +/- arginine & citrulline with daily chloroquine in Tanzanian children with sickle cell disease: a double blind random order cross-over trial (2018) (0)
- Evaluation of Newborns Screening Laboratory Tests for Sickle Cell Disease and Other Haemoglobinopathies in Tanzania (2019) (0)
- A qualitative study on aspects of consent for genomic research in communities with low literacy (2020) (0)
- Data migration of consistent Sickle Cell Disease clinical-database at Muhimbili National Hospital in Tanzania (2015) (0)
- High-performance liquid chromatography local reference ranges of hemoglobin fractions (HbA, HbA2, and HbF) in detection of hemoglobinopathies in western Kenya (2022) (0)
- The Importance of Culturally Relevant Breast Clinic Navigation in Improving Breast Cancer Care in Africa. (2022) (0)
- Brain volume in Tanzanian children with sickle cell anaemia: A neuroimaging study (2022) (0)
- Outcomes of Hydroxyurea Accessed via Various Means and Barriers Affecting Its Usage Among Children with Sickle Cell Anaemia in North-Western Tanzania (2023) (0)
- Increased memory phenotypes of CD4+ and CD8+ T cells in children with sickle cell anaemia in Tanzania (2017) (0)
- Increased memory phenotypes of CD4+ and CD8+ T cells in children with sickle cell anaemia in Tanzania (2017) (0)
- with sickle cell anemia on the coast of Kenya malaria in children living Plasmodium falciparum High mortality from (2013) (0)
- Perspectives on building sustainable newborn screening programs for sickle cell disease: Experiences from Tanzania (2020) (0)
- High incidence of malaria in patients with sickle cell disease (2022) (0)
- Annual audit of haematology tests performed at a laboratory of a tertiary teaching hospital in Dar es salaam Tanzania (2019) (0)
- Spectrum of cerebral blood flow velocities measured by transcranial Doppler ultrasonography in children with sickle cell disease in Africa (2005) (0)
- Infrastructure for bioinformatics applications in Tanzania: Lessons from the Sickle Cell Programme (2023) (0)
- P108: ASSESSMENT OF HEALTHCARE WORKERS’ KNOWLEDGE AND RESOURCE AVAILABILITY FOR CARE OF SICKLE CELL DISEASE AT HEALTH FACILITIES IN DAR ES SALAAM, TANZANIA (2022) (0)
- Communicating sickle cell trait results after newborn screening: Approaches and implications to families (2022) (0)
- Iron status and nocturnal oximetry in paediatric sickle cell anaemia patients (2011) (0)
- sickle cell anemia Genetics of fetal hemoglobin in Tanzanian and British patients with (2011) (0)
- Effects of Hydroxyurea Treatment on Haemolysis in Patients with Sickle Cell Disease at Muhimbili National Hospital, Tanzania (2021) (0)
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