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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 6
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Original Article

Sickle Cell Anemia and Major Organ Failure

Pages 573-598 | Received 02 Mar 1990, Accepted 07 Nov 1990, Published online: 07 Jul 2009

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (6)

Obi Peter Adigwe, Godspower Onavbavba & Solomon Oloche Onoja. (2022) Attitudes and practices of unmarried adults towards sickle cell disease: emergent factors from a cross sectional study in Nigeria’s capital. Hematology 27:1, pages 488-493.
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Adekunle D. Adekile, Sondus Al-Sherida, Rajaa Marouf, Nada Mustafa & Diana Thomas. (2019) The Sub-Phenotypes of Sickle Cell Disease in Kuwait. Hemoglobin 43:2, pages 83-87.
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Shereen A. Elshazly, Nihal M. Heiba & Waleed M. Abdelmageed. (2014) Plasma PTX3 levels in sickle cell disease patients, during vaso occlusion and acute chest syndrome (data from Saudi population). Hematology 19:1, pages 52-59.
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Kara-Marie H. Delaney, Karen C. Axelrod, Ashley Buscetta, Kathryn L. Hassell, Patricia E. Adams-Graves, Catherine Seamon, Gregory J. Kato & Caterina P. Minniti. (2013) Leg Ulcers in Sickle Cell Disease: Current Patterns and Practices. Hemoglobin 37:4, pages 325-332.
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Samir K. Ballas. (2011) Defining the Phenotypes of Sickle Cell Disease. Hemoglobin 35:5-6, pages 511-519.
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S. A. Noreldeen, C. Oppenheimer, C. Chapman & S. Pavord. (2008) Postpartum acute splenic sequestration in sickle cell disease. Journal of Obstetrics and Gynaecology 28:4, pages 440-441.
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Articles from other publishers (41)

C. B. Webb, S. G. Yates, R. Sarode & J. Kim. (2023) Plasma exchange—A useful adjunct therapy to red cell exchange in patients with sickle cell disease and multiorgan dysfunction. Transfusion 63:7, pages 1384-1390.
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Alexander Dick, Gabrielle Schwartzman & Amor Khachemoune. (2022) Cutaneous manifestations of sickle cell disease: an updated review. Archives of Dermatological Research 315:4, pages 729-734.
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Adnan Bibic, Tea Sordia, Erik Henningsson, Linda Knutsson, Freddy Ståhlberg & Ronnie Wirestam. (2021) Effects of red blood cells with reduced deformability on cerebral blood flow and vascular water transport: measurements in rats using time-resolved pulsed arterial spin labelling at 9.4 T. European Radiology Experimental 5:1.
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Ravi Vats, Silvia Liu, Junjie Zhu, Dhanunjay Mukhi, Egemen Tutuncuoglu, Nayra Cardenes, Sucha Singh, Tomasz Brzoska, Karis Kosar, Mikhil Bamne, Jude Jonassaint, Adeola Adebayo Michael, Simon C. Watkins, Cheryl Hillery, Xiaochao Ma, Kari Nejak‐Bowen, Mauricio Rojas, Mark T. Gladwin, Gregory J. Kato, Sadeesh Ramakrishnan, Prithu Sundd, Satdarshan Pal Monga & Tirthadipa Pradhan‐Sundd. (2020) Impaired Bile Secretion Promotes Hepatobiliary Injury in Sickle Cell Disease. Hepatology 72:6, pages 2165-2181.
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Rasaki Aliu, Jalo Iliya, Oladeji R Quadri, Olayinka R Ibrahim & Ezra Daniel. (2020) Haematological Profile of Children With Sickle Cell Anaemia in Steady State. Cureus.
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Samina Hirani, Supriya Gupta, Diana Veillon, Shajadi Patan, Samip Master & Richard Mansour. (2020) The Curious Case of Hemoglobin DC Disease Masquerading as Sickle Cell Anemia. Hematology Reports 12:1, pages 8519.
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Akram Mohammed, Pradeep S B Podila, Robert L Davis, Kenneth I Ataga, Jane S Hankins & Rishikesan Kamaleswaran. (2020) Using Machine Learning to Predict Early Onset Acute Organ Failure in Critically Ill Intensive Care Unit Patients With Sickle Cell Disease: Retrospective Study. Journal of Medical Internet Research 22:5, pages e14693.
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Rasaki Aliu, Jalo Iliya, PatienceNgozi Obiagwu & Adamu Sani. (2020) Relationship between microalbuminuria and glomerular filtration rate in children with sickle cell anemia in steady state. Sahel Medical Journal 23:3, pages 147.
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Adedokun Oluwafemi Ojelabi, Afolabi Elijah Bamgboye & Jonathan Ling. (2019) Preference-based measure of health-related quality of life and its determinants in sickle cell disease in Nigeria. PLOS ONE 14:11, pages e0223043.
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Shruti Chaturvedi, Djamila Labib Ghafuri, Natalie Jordan, Adetola Kassim, Mark Rodeghier & Michael R. DeBaun. (2018) Clustering of end-organ disease and earlier mortality in adults with sickle cell disease: A retrospective-prospective cohort study. American Journal of Hematology 93:9, pages 1153-1160.
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Graham R. Serjeant & Elliott Vichinsky. (2018) Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors. Blood Cells, Molecules, and Diseases 70, pages 66-77.
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Courtney D. Fitzhugh, Matthew M. Hsieh, Tiffani TaylorWynona ColesKatherine RoskomDelon WilsonElizabeth Wright, Neal Jeffries, Christopher J. Gamper, Jonathan Powell, Leo Luznik & John F. Tisdale. (2017) Cyclophosphamide improves engraftment in patients with SCD and severe organ damage who undergo haploidentical PBSCT. Blood Advances 1:11, pages 652-661.
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Yesim Oztas & Ahmet Yalcinkaya. (2017) Oxidative alterations in sickle cell disease: Possible involvement in disease pathogenesis. World Journal of Hematology 6:3, pages 55.
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N. Galadanci, B. J. Wudil, T. M. Balogun, G. O. Ogunrinde, A. Akinsulie, F. Hasan-Hanga, A. S. Mohammed, M. O. Kehinde, J. A. Olaniyi, I. N. Diaku-Akinwumi, B. J. Brown, S. Adeleke, O. E. Nnodu, I. Emodi, S. Ahmed, A. O. Osegbue, N. Akinola, H. I. O. Opara, S. A. Adegoke, J. Aneke & A. D. Adekile. (2013) Current sickle cell disease management practices in Nigeria. International Health 6:1, pages 23-28.
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J. N. Oko-Ose, V. Iyawe, E. Egbagbe & M. Ebomoyi. (2012) Lung Function Tests in Sickle-Cell Patients in Benin City. ISRN Pulmonology 2012, pages 1-5.
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Ersi Voskaridou, Dimitrios Christoulas & Evangelos Terpos. (2012) Sickle-cell disease and the heart: review of the current literature. British Journal of Haematology 157:6, pages 664-673.
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Samir K. Ballas. 2011. Pain Management. Pain Management 243 248 .
Bolanle O. P. Musa, Geoffrey C. Onyemelukwe, Joseph O. Hambolu, Aisha I. Mamman & Albarka H. Isa. (2010) Pattern of Serum Cytokine Expression and T-Cell Subsets in Sickle Cell Disease Patients in Vaso-Occlusive Crisis. Clinical and Vaccine Immunology 17:4, pages 602-608.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSamir K. Ballas & James R. Eckman. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 497 524 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 435 436 .
Jon I. Scheinman. 2009. Pediatric Nephrology. Pediatric Nephrology 1181 1197 .
Nitin Patel, Caryn S. Gonsalves, Punam Malik & Vijay K. Kalra. (2008) Placenta growth factor augments endothelin-1 and endothelin-B receptor expression via hypoxia-inducible factor-1α. Blood 112:3, pages 856-865.
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Samir K. Ballas. (2007) Current Issues in Sickle Cell Pain and Its Management. Hematology 2007:1, pages 97-105.
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Karl P. Sylvester, Richard A. Patey, Peter Milligan, Gerrard F. Rafferty, Simon Broughton, David Rees, Swee Lay Thein & Anne Greenough. (2006) Impact of acute chest syndrome on lung function of children with sickle cell disease. The Journal of Pediatrics 149:1, pages 17-22.
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Betty S. Pace & Sima Zein. (2006) Understanding mechanisms of γ‐globin gene regulation to develop strategies for pharmacological fetal hemoglobin induction. Developmental Dynamics 235:7, pages 1727-1737.
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Babatunde O. Onadeko, Rajaa Marouf, Abdelmoneim M. Omar, Zeinat Hijazi, Mousa Khadadah, Mohammed Qurtom, Bert D. Collier, Abdelhamid H. Elgazzar & Adekunle D. Adekile. (2006) Technetium 99m-diethylene triamine penta-acetic acid aerosol clearance in the evaluation of pulmonary involvement in sickle cell disease. European Journal of Haematology 76:2, pages 147-152.
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Darleen R. Powars, Linda S. Chan, Alan Hiti, Emily Ramicone & Cage Johnson. (2005) Outcome of Sickle Cell Anemia. Medicine 84:6, pages 363-376.
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Sam O. Wanko & Marilyn J. Telen. (2005) Transfusion Management in Sickle Cell Disease. Hematology/Oncology Clinics of North America 19:5, pages 803-826.
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Suresh K. SelvarajRanjit K. GiriNatalya PerelmanCage JohnsonPunam MalikVijay K. Kalra. (2003) Mechanism of monocyte activation and expression of proinflammatory cytochemokines by placenta growth factor. Blood 102:4, pages 1515-1524.
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A K Siddiqui & S Ahmed. (2003) Pulmonary manifestations of sickle cell disease. Postgraduate Medical Journal 79:933, pages 384-390.
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Darleen R. Powars, Alan Hiti, Emily Ramicone, Cage Johnson & Linda Chan. (2002) Outcome in hemoglobin SC disease: A four‐decade observational study of clinical, hematologic, and genetic factors. American Journal of Hematology 70:3, pages 206-215.
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Alexandra Dorn-Beineke & Thomas Frietsch. (2002) Sickle Cell Disease – Pathophysiology, Clinical and Diagnostic Implications. Clinical Chemistry and Laboratory Medicine 40:11.
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Samir K. Ballas. (2002) Sickle Cell Anaemia. Drugs 62:8, pages 1143-1172.
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C. Le Turdu-Chicot, L. Foucan, M. Étienne-Julan, Y. Leborgne-Samuel, R. Fanhan & C. Berchel. (2000) Analyse des hospitalisations chez les patients drépanocytaires adultes en Guadeloupe. La Revue de Médecine Interne 21:1, pages 24-29.
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Akinlolu O. Ojo, Timothy C. Govaerts, Robert L. Schmouder, Alan B. Leichtman, Sean F. Leavey, Robert A. Wolfe, Philip J. Held, Friedrich K. Port & Lawrence Y. Agodoa. (1999) RENAL TRANSPLANTATION IN END-STAGE SICKLE CELL NEPHROPATHY1,2. Transplantation 67:2, pages 291-295.
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W. Clauss, B. Gloebel, P. Dawson, J. E. Scherberich, R. Dickerhoff, H. Katayama, K. A. Wandl-Vergesslich & H. Imhof. 1999. Contrast Media in Practice. Contrast Media in Practice 96 117 .
Samir K. Ballas. (1998) 7 Sickle cell disease: clinical management. Baillière's Clinical Haematology 11:1, pages 185-214.
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Samir K. Ballas & Narla Mohandas. (1996) PATHOPHYSIOLOGY OF VASO-OCCLUSION. Hematology/Oncology Clinics of North America 10:6, pages 1221-1239.
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Archil Shartava, Paul Miranda, Kenya N. Williams, Arvind Shah, Carlos A. Monteiro & Steven R. Goodman. (1998) High density sickle cell erythrocyte core membrane skeletons demonstrate slow temperature dependent dissociation. American Journal of Hematology 51:3, pages 214-219.
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J. Randolph Sharpsteen, Darleen Powars, Cage Johnson, Zora R. Rogers, W. Donald Williams & Ralph J. Posch. (1993) Multisystem damage associated with tricorporal priapism in sickle cell disease. The American Journal of Medicine 94:3, pages 289-295.
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Darleen R. Powars. (1991) ß s -Gene-Cluster Haplotypes in Sickle Cell Anemia: Clinical and Hematologic Features. Hematology/Oncology Clinics of North America 5:3, pages 475-493.
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