نتائج البحث

Association between fetal hemoglobin, lactate dehydrogenase, and disease severity in patients with sickle cell disease at Bugando Medical Centre, Mwanza, Tanzania.

• Authors : Kahema, Samwel Edward^1,2 (AUTHOR) ; Mbulwa, Cosmas H.³ (AUTHOR); Bagenda, Charles Nkubi¹ (AUTHOR)

• Source: PLoS ONE. 7/15/2024, Vol. 19 Issue 7, p1-10. 10p.

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Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries.

• Authors : Munung, Nchangwi Syntia¹ (AUTHOR) ; Treadwell, Marsha² (AUTHOR); Kamga, Karen Kengne^1,3 (AUTHOR)

• Source: Quality of Life Research. Feb2024, Vol. 33 Issue 2, p423-432. 10p.

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Prevalence of Stroke in Individuals with Sickle Cell Disease Pre- and during Hydroxyurea Uses: A Descriptive Cross-Sectional Study in Tanzania.

• Authors : Moshi, Belinda Nestory¹ (AUTHOR); Philipo, Erick G.¹ (AUTHOR); Kileo, Nancy F.² (AUTHOR)

• Source: Advances in Hematology. 3/19/2024, Vol. 2024, p1-6. 6p.

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Presentation and challenges in management of COVID-19 in sickle cell disease: case report.

• Authors : Thaver, Sheliza Parvez¹ ; Dawood, Saliha Shafik¹; Walli, Nahida Zahir¹

• Source: Pan African Medical Journal. Sep-Dec2023, Vol. 46, p1-8. 8p.

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Potential of point of care tests for newborn screening for sickle cell disease: Evaluation of HemotypeSC™ and sickle SCAN® in Tanzania.

• Authors : Christopher, Heavenlight¹ ; Josephat, Emmanuel¹; Kaywanga, Frida¹

• Source: International Journal of Laboratory Hematology. Oct2022, Vol. 44 Issue 5, p959-965. 7p.

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Prevalence and predictors of iron deficiency anaemia among children with sickle cell disease in Dodoma, Tanzania: a cross-sectional study.

• Authors : Bossy AO; Department of Pediatrics and Child Health, School of Medicine and Dentistry, University of Dodoma, Dodoma, Tanzania.; Department of Pediatrics and Child Health, Morogoro Regional Referral Hospital, Morogoro, Tanzania.

Subjects: Anemia, Iron-Deficiency*/Anemia, Iron-Deficiency*/Anemia, Iron-Deficiency*/diagnosis ; Anemia, Iron-Deficiency*/Anemia, Iron-Deficiency*/Anemia, Iron-Deficiency*/epidemiology ; Anemia, Sickle Cell*/Anemia, Sickle Cell*/Anemia, Sickle Cell*/complications

• Source: BMC public health [BMC Public Health] 2024 Apr 12; Vol. 24 (1), pp. 1026. Date of Electronic Publication: 2024 Apr 12.Publisher: BioMed Central Country of Publication: England NLM ID: 100968562 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2458

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Using DNA testing for the precise, definite, and low-cost diagnosis of sickle cell disease and other Haemoglobinopathies: findings from Tanzania.

• Authors : Christopher, Heavenlight¹ (AUTHOR) ; Burns, Adam² (AUTHOR); Josephat, Emmanuel¹ (AUTHOR)

• Source: BMC Genomics. 12/16/2021, Vol. 22 Issue 1, p1-9. 9p.

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Utilization of Pneumococcal Vaccine and Penicillin Prophylaxis in Sickle Cell Disease in Three African Countries: Assessment among Healthcare Providers in SickleInAfrica.

• Authors : Brown, Biobele J.¹ (AUTHOR); Madu, Anazoeze² (AUTHOR); Sangeda, Raphael Z.³ (AUTHOR)

• Source: Hemoglobin. May2021, Vol. 45 Issue 3, p163-170. 8p.

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Surveillance for sickle cell disease, United Republic of Tanzania.

• Authors : Ambrose, Emmanuela E.¹; Smart, Luke R.² ; Charles, Mwesige³

• Source: Bulletin of the World Health Organization. Dec2020, Vol. 98 Issue 12, p859-868. 10p.

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Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania.

• Authors : Nkya, Siana^1,2 (AUTHOR) ; Mwita, Liberata² (AUTHOR); Mgaya, Josephine² (AUTHOR)

• Source: BMC Medical Genetics. 6/5/2020, Vol. 21 Issue 1, p1-12. 12p.

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