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Books on the topic 'SS sickle cell disease'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 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

Alan, Sacerdote, ed. Hope and destiny: The patient's and parent's guide to sickle cell disease and sickle cell trait. Hilton Pub. Co., 2006.

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31

Lance, Eboni I., and Andrew W. Zimmerman. Sickle Cell Anemia. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0079.

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Sickle cell disease is a genetic hematological disorder involving red blood cells that become deformed when stressed. Patients with homozygous hemoglobin SS disease often have multiple systemic and neurologic complications, particularly stroke. Intellectual disability is commonly seen in the population, in patients with and without a history of stroke, attributed to different underlying mechanisms of brain injury. Autism is rare and not described in sickle cell disease in the literature to date. Many treatments (chronic transfusion therapy, hydroxyurea, bone marrow transplant) are in trials at

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32

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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33

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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34

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

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35

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

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36

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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37

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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38

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

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39

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

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40

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

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41

Sickle cell disease. Oxford University Press, 1985.

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42

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

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43

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

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44

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

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45

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

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46

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

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47

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

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48

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

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49

GLADWIN. Sickle Cell Disease (ie). McGraw-Hill Education, 2021.

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50

Understanding Sickle Cell Disease. University Press of Mississippi, 2009.

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