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Items where Subject is "WH Hemic and Lymphatic Systems > Hematologic Diseases. Immunologic Factors. Blood Banks > WH 170 Hemolytic anemia (e.g., Sickle cell anemia)"

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Number of items at this level: 24.


Adegoke, Adetoro and Kongnyuy, Eugene J (2015) 'Iron supplementation for sickle cell disease during pregnancy'. Cochrane Database of Systematic Reviews, CD009492.

Adepoju, A A, Akere, A, Ogun, G O, Ogunbosi, B O, Asinobi, A O, Bello, O, Orimadegun, A E, Allen, Stephen ORCID: and Akinyinka, O O (2021) 'Co-existing sickle cell anaemia and inflammatory bowel disease: case report and review of the literature'. Paediatrics and international child health, pp. 1-7. (In Press)

Al-Saqladi, A. W., Delpisheh, Ali, Bin-Gadeem, H. and Brabin, Bernard (2007) 'Clinical profile of sickle cell disease in Yemeni children'. Annals of Tropical Paediatrics, Vol 27, Issue 4, pp. 253-259.

Al-Saqladi, A.-W. M., Bin-Gadeem, H. A. and Brabin, Bernard (2012) 'Utility of plasma transferrin receptor, ferritin and inflammatory markers in children with sickle cell disease'. Paediatrics and International Child Health, Vol 32, Issue 1, pp. 27-34.

Al-Saqladi, Abdul-Wahab M., Brabin, Bernard, Bin-Gadeem, Hassan A and Kanhai, Warsha A (2010) 'Beta-Globin Gene Cluster Haplotypes in Yemeni Children with Sickle Cell Disease'. Acta Haematologica, Vol 123, Issue 3, pp. 182-185.

Ateba, Francois Freddy, Doumbia, Seydou, terKuile, Feiko ORCID:, Terlouw, Anja ORCID:, Lefebvre, Genevieve, Kariuki, Simon and Small, Dylan (2021) 'The effect of malaria on stunting: an instrumental variables approach'. Transactions of the Royal Society of Tropical Medicine and Hygiene, Vol 115, Issue 9, pp. 1094-1098.


Bates, Imelda ORCID: (2009) 'Haemoglobinopathies and red cell enzymopathies. Chapter 56' in: Gill, Geoff and Beeching, Nick, (eds) Lecture Notes: Tropical Medicine, 6th ed., Chichester, Wiley-Blackwell, pp. 333-337.

Boateng, Lilian, Schonewille, Henk, Ligthart, Peter C., Javadi, Ahmad, Veldhuisen, Barbera, Osei-Akoto, Alex, Dei-Adomakoh, Yvonne, Bates, Imelda ORCID: and Van der Schoot, C. Ellen (2021) 'One third of alloantibodies in patients with sickle cell disease transfused with African blood are missed by the standard red blood cell test panel'. Haematologica, Vol 106, Issue 8, pp. 2274-2276.

Boateng, Lilian, Campbell, Andrew D, Davenport, Robertson D, Osei-Akoto, Alex, Hugan, Sheri, Asamoah, Akwasi and Schonewille, Henk (2019) 'Red blood cell alloimmunization and minor red blood cell antigen phenotypes in transfused Ghanaian patients with sickle cell disease.'. Transfusion, Vol 59, Issue 6, pp. 2016-2022.

Boateng, Lilian Antwi, Ngoma, Alain M., Bates, Imelda ORCID: and Schonewille, Henk (2019) 'Red Blood Cell Alloimmunization in Transfused Patients with Sickle Cell Disease in Sub-Saharan Africa; a Systematic Review and Meta-Analysis'. Transfusion Medicine Reviews, Vol 33, Issue 3, pp. 162-169.

Boonyuen, Usa, Songdej, Duantida, Tanyaratsrisakul, Sasipa, Phuanukoonnon, Suparat, Chamchoy, Kamonwan, Praoparotai, Aun, Pakparnich, Phonchanan, Sudsumrit, Sirapapha, Edwards, Thomas, Williams, Christopher, Byrne, Rachel, Adams, Emily ORCID: and Imwong, Mallika (2021) 'Glucose-6-phosphate dehydrogenase mutations in malaria endemic area of Thailand by multiplexed high‐resolution melting curve analysis'. Malaria Journal, Vol 20, p. 194.


Cook, J., Jefferis, O., Matchere, P., Mbale, E. and Rylance, Jamie ORCID: (2013) 'Sickle-cell disease in Malawian children is associated with restrictive spirometry: a cross-sectional survey'. International Journal of Tuberculosis and Lung Disease, Vol 17, Issue 9, pp. 1235-1238.


Dekker, Louise H., Fijnvandraat, Karin, Brabin, Bernard and van Hensbroek, Michael Boele (2012) 'Micronutrients and sickle cell disease, effects on growth, infection and vaso-occlusive crisis: A systematic review'. Pediatric Blood and Cancer, Vol 59, Issue 2, pp. 211-215.


Effective Health Care Research Consortium (2008) Do drugs that aim to reduce the dehydration of red blood cells prevent crises in people with sickle cell disease? Evidence update - Summary of a Cochrane Review. Liverpool, Effective Health Care Research Consortium, Liverpool School of Tropical Medicine.

Effective Health Care Research Consortium (2011) In children with sickle cell disease, does penicillin prevent pneumococcal infection? Evidence update - Summary of a Cochrane Review. Liverpool, Effective Health Care Research Consortium, Liverpool School of Tropical Medicine.


Ladu, Adama, Aiyenigba, Abiola, Adekile, Adekunle and Bates, Imelda ORCID: (2021) 'The spectrum of splenic complications in patients with sickle cell disease in Africa: a systematic review'. British Journal of Haematology, Vol 193, Issue 1, pp. 26-42.


Mehta, Vikita, Kirubarajan, Abirami, Sabouhanian, Amir, Jayawardena, Sanasi M, Chandrakumaran, Priya, Thangavelu, Nila, Cader, Refai, Mettananda, Sachith, Bandara, Dayananda, Khan, Shawn, Weatherall, David J, Allen, Angie, Premawardhena, Anuja P and Olivieri, Nancy F (2022) 'Leg Ulcers: A Report in Patients with Hemoglobin E Beta Thalassemia and Review of the Literature in Severe Beta Thalassemia'. Acta haematologica, Vol 45, Issue 3, pp. 334-343.


Patel, J. C., Mwapasa, V., Kalilani, L., terKuile, Feiko ORCID:, Khairallah, Carole, Thwai, K. L., Meshnick, S. R. and Taylor, S. M. (2016) 'Absence of Association Between Sickle Trait Hemoglobin and Placental Malaria Outcomes'. American Journal of Tropical Medicine and Hygiene, Vol 94, Issue 5, pp. 1002-1007.

Perera, Shiromi, Allen, Angela, Silva, Ishari, Hapugoda, Menaka, Wickramarathne, M Nirmali, Wijesiriwardena, Indira, Allen, Stephen ORCID:, Rees, David, Efremov, Dimitar G, Fisher, Christopher A, Weatherall, David J and Premawardhena, Anuja (2019) 'Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka.'. Scientific Reports, Vol 9, Issue 1, e10116.

Perera, Shiromi, Allen, Angie, Rees, David C and Premawardhena, Anuja (2021) 'Pitfalls in the Diagnosis of β-Thalassemia Intermedia'. Hemoglobin, Vol 45, Issue 4, pp. 265-268.

Premawardhena, Anuja P, Ediriweera, Dileepa Senajith, Sabouhanian, Amir, Allen, Angie, Rees, David, de Silva, Shanthimala, Perera, Windsor, Katugaha, Nimal, Arambepola, Mahinda, Yamashita, Robert C, Mettananda, Sachith, Jiffry, Nilam, Mehta, Vikita, Cader, Refai, Bandara, Dayananda, St Pierre, Timothy, Muraca, Giulia, Fisher, Christopher, Kirubarajan, Abirami, Khan, Shawn, Allen, Stephen ORCID:, Lamabadusuriya, Sanath P, Weatherall, David J and Olivieri, Nancy F (2022) 'Survival and complications in patients with haemoglobin E thalassaemia in Sri Lanka: a prospective, longitudinal cohort study'. Lancet Global Health, Vol 10, Issue 1, e134-e141.


Rowe, Sam and Alcheikh, Ahmad (2020) 'Harm or Benefit of High-Dose Vitamin C in Adult Patients With Sepsis and Glucose-6-Phosphate Dehydrogenase Deficiency?'. Critical Care Medicine, Vol 48, Issue 12, e1356-e1356.


Terlouw, Anja ORCID:, Desai, M. R., Wannemuehler, K. A., Kariuki, S. K., Pfeiffer, C. M., Kager, P. A., Shi, Y. P. and terKuile, Feiko ORCID: (2004) 'Relation between the response to iron supplementation and sickle cell hemoglobin phenotype in preschool children in western Kenya'. American Journal of Clinical Nutrition, Vol 79, Issue 3, pp. 466-472.

Thachil, Jecko and Bates, Imelda ORCID: (2014) 'Haemoglobinopathies and red cell enzymopathies' in: Tropical medicine : lecture notes, 7th ed., Chichester, Wiley, pp. 321-325.

This list was generated on Tue Aug 16 02:50:53 2022 BST.