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Books on the topic 'Sickle cell disease (SCD)'

Author: Grafiati

Published: 4 June 2021

Last updated: 19 April 2025

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1

Peak, Lizabeth. Sickle cell disease. Lucent Books, 2008.

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2

Peak, Lizabeth. Sickle cell disease. Lucent Books, 2008.

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3

Serjeant, Graham R. Sickle cell disease. 2nd ed. Oxford University Press, 1992.

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4

F, Whitten Charles, Bertles John F. 1925-, National Association for Sickle Cell Disease (U.S.), and New York Academy of Sciences., eds. Sickle cell disease. New York Academy of Sciences, 1989.

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5

Eboh, Winifred Oluchukwu. Sickle cell disease. Birmingham Sickle Cell & Thalassaemia Centre, 1993.

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6

Jones, Phill. Sickle cell disease. Chelsea House, 2008.

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7

Samuel, Charache, and Johnson Cage S, eds. Sickle cell disease. W.B. Saunders, 1996.

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8

McCormick, Marie, Henrietta Awo Osei-Anto, and Rose Marie Martinez, eds. Addressing Sickle Cell Disease. National Academies Press, 2020. http://dx.doi.org/10.17226/25632.

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9

P, Rodgers Griffin, ed. Sickle cell disease and thalassaemia. Baillière Tindall, 1998.

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10

author, Chilman-Blair Kim, and DeLoache Shawn author, eds. Medikidz explain sickle cell disease. Medikidz Ltd., 2013.

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11

Meier, Emily Riehm, Allistair Abraham, and Ross M. Fasano, eds. Sickle Cell Disease and Hematopoietic Stem Cell Transplantation. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-62328-3.

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12

Howard, Jo, and Paul Telfer. Sickle Cell Disease in Clinical Practice. Springer London, 2015. http://dx.doi.org/10.1007/978-1-4471-2473-3.

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13

National Heart, Lung, and Blood Institute. Division of Blood Diseases and Resources., ed. The Management of sickle cell disease. 4th ed. The Institute, 2002.

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14

National Heart, Lung, and Blood Institute. Division of Blood Diseases and Resources. The management of sickle cell disease. 4th ed. The Institute, 2002.

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15

Midence, Kenny. Sickle cell disease: A psychosocial approach. Radcliffe Medical Press, 1994.

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16

1932-, Hurtig Anita Landau, and Viera Carol Therese 1952-, eds. Sickle cell disease: Psychological and psychosocial issues. University of Illinois Press, 1986.

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17

N, Mankad Vipul, and Moore R. Blaine, eds. Sickle cell disease: Pathophysiology, diagnosis, and management. Praeger, 1992.

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18

Ennis, Sylvia. The natural choice: Sickle cell disease/ thalassaemia. B.Jain Publishers, 1994.

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19

Anionwu, Elizabeth N. Sickle cell disease: A guide for families. Longman, 1991.

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20

Samuel, Charache, Lubin Bertram, Reid Clarice D, United States. Dept. of Health and Human Services., National Institutes of Health (U.S.), and United States. Public Health Service., eds. Management and therapy of sickle cell disease. 3rd ed. U. S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Heart, Lung, and Blood Institute, 1995.

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21

Inusa, Baba, Kanayo Nwankwo, Nkechikwu Azinge-Egbiri, and Bukola Bolarinwa. Sickle Cell Disease in Sub-Saharan Africa. Routledge, 2024. http://dx.doi.org/10.4324/9781003463931.

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22

Inusa, Baba, Kanayo Nwankwo, Nkechikwu Azinge-Egbiri, and Bukola Bolarinwa. Sickle Cell Disease in Sub-Saharan Africa. Routledge, 2024. http://dx.doi.org/10.4324/9781003467748.

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23

D, O'Malley Paul, ed. New developments in sickle cell disease research. Nova Science Publishers, 2006.

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24

B, Jibril Harun, ed. Sickle cell disease: A guide for families. Collins, 1986.

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25

Al-Jamʼa, Ali H. Management manual of sickel cell disease. Qatif Central Hospital], 1992.

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26

Rosse, Wendell F. Transfusion support for patients with sickle cell disease. AABB Press, 1998.

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27

Society, Sickle Cell, ed. Sickle cell disease: The need for improved services. 3rd ed. Sickle Cell Society, 1991.

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28

Alvin, Silverstein, Silverstein Virginia B, and Nunn Laura Silverstein, eds. What you can do about sickle cell disease. Enslow Publishing, 2016.

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29

H, Embury Stephen, ed. Sickle cell disease: Basic principles and clinical practice. Raven Press, 1994.

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30

9780197630846. Management of Sickle Cell Pain. Edited by Wally R. Smith and Thokozeni Lipato. Oxford University PressNew York, 2025. https://doi.org/10.1093/med/9780197630839.001.0001.

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Abstract While sickle cell disease (SCD) is uncommon in Europe and North America, SCD patients presenting for pain account for an outsized and prominent proportion of all acute care utilization in these countries. Managing SCD pain requires one treatment paradigm for the hallmark, disruptive, infrequent vaso-occlusive crisis (VOC). But it also requires a different treatment paradigm for the under-recognized but sometimes daily chronic pain of SCD. Both paradigms require a biopsychosocial framework and an infrastructure that is lacking in most hospitals. Because providers don’t understand the c

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31

Reid, Clarice D. Management And Therapy Of Sickle Cell Disease. 3rd ed. Edited by Clarice D. Reid. DIANE PUBLISHING COMPANY, 1997.

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32

Haymann, Jean-Philippe, and Francois Lionnet. The patient with sickle cell anaemia. Edited by Giuseppe Remuzzi. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0167.

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In sickle cell anaemia (SCA) a single mutation in the haemoglobin beta-globin gene is responsible for a pleomorphic phenotype leading to acute and chronic life-threatening complications. Healthcare management programmes, patient and family education, infection prophylaxis (especially in childhood), and long-term treatment for some patients (such as hydroxyurea) have significantly improved survival, giving rise to some new long-term issues.Sickle cell-associated nephropathy (SCAN) leads in some cases to chronic renal failure with a significant impact on survival. SCAN is characterized by an inc

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33

Glasper, Edward Alan, Gillian McEwing, and Jim Richardson, eds. Haematology and immunity problems. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780198569572.003.0017.

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The blood 564Immune protection in children 566Anaemia 568Sickle cell disease (SCD) 570Management of sickle cell disease 572Haemophilia 574Henoch-Schnölein purpura 576Idiopathic thrombocytopenic purpura (ITP) 578Thalassaemia 580Thrombocytopenia 582HIV infection 584Primary deficiencies of the innate immune system in children ...

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34

Szabova, Alexandra, and Kenneth R. Goldschneider. Sickle Cell Disease. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0040.

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0.2% of African-Americans have sickle cell anemia while, with 8% to 10% have sickle cell trait. This chapter provides an overiew of the etiology, pathophysiology, and treatment of sickle cell anemia as they affect anesthetic management—before, during, and after surgery.

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35

Ng, Ann, and Erin S. Williams. Sickle Cell Disease. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0033.

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Sickle cell anemia (sickle cell disease) is a common hemoglobinopathy with anywhere from 90,000 to 100,000 Americans affected. This chronic condition has a predominance in populations of African descent, occurring in approximately 1 out of 365 African American births, compared to 1 out of 16,300 Hispanic births. The sickle cell trait can be detected in 1 of 13 African American births. One of the most common complications associated with sickle cell anemia, vaso-occlusive crises by sickled cells, results in severe pain. Other issues associated with this condition include acute chest syndrome, l

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36

Serjeant, Graham R. Sickle Cell Disease. Oxford University Press, USA, 1988.

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37

Anionwu, Elizabeth, and H. Jibril. Sickle Cell Disease. Longman, 1986.

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38

Franklin, Andrew. Sickle Cell Disease. Edited by Matthew D. McEvoy and Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0084.

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Sickle cell disease, a hemoglobinopathy that affects multiple organ systems, is a complex disease entity that presents unique challenges during the perioperative period. The hallmark of sickle cell disease, vaso-occlusion, results from sickling of erythrocytes containing hemoglobin of abnormal conformation due to genetically mutated beta globin genes. The perioperative clinician must properly care for acute sickle cell crises including acute painful episodes and acute chest syndrome, and safely care for the sickle cell patient through the preoperative, intraoperative, and postoperative phases

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39

Ferrari, Lynne R. Sickle Cell Disease. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0051.

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Sickle cell anemia is a disease that combines molecular biology, clinical features, biochemistry, pathology, natural selection, population genetics, gene expression, and genomics and is the world’s most common life-threatening monogenic disorder. Clinical features include anemia; painful crisis especially in fingers, chest, and long bones; hemolysis; splenic infarction resulting in functional asplenia; and microinfarction leading to neurologic and renal impairment. The maintenance of adequate body temperature with active warming devices and warmed intravenous fluids, monitoring hydration and u

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40

Anionwu, Elizabeth, and H. Jibril. Sickle Cell Disease. 2nd ed. Longman, 1992.

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41

Sickle cell disease. 2nd ed. Oxford University Press, 1992.

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42

Erhabor, Osaro. Sickle Cell Disease. IntechOpen, 2022.

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43

Sickle cell disease. Oxford University Press, 1985.

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44

Gladwin, Mark T., Gregory J. Kato, and Enrico M. Novelli. Sickle Cell Disease. McGraw-Hill Education, 2021.

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45

Alebiosu, Christopher Olutayo. Sickle Cell Disease. Cambridge Scholars Publishing, 2020.

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46

Midence, Kenny. Sickle Cell Disease. Scovill-Paterson, 1994.

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47

LaPierre, Yvette. Handling Sickle Cell Disease. ABDO Publishing Company, 2021.

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48

Sickle Cell Disease Patient. Tettah-A'Domeno Co, 1998.

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49

Bloom, Miriam. Understanding Sickle Cell Disease. University Press of Mississippi, 1995.

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50

Lapierre, Yvette. Handling Sickle Cell Disease. Essential Library, 2021.

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