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Books on the topic 'Anemia management'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Provenzano, Robert, Edgar V. Lerma, and Lynda Szczech, eds. Management of Anemia. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7360-6.

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2

Okpala, Iheanyi E. Practical management of haemoglobinopathies. Blackwell Pub., 2004.

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3

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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4

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

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5

United States. Agency for Health Care Policy and Research, ed. Sickle cell disease: Comprehensive screening and management in newborns and infants. U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1993.

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6

United States. Sickle Cell Disease Guideline Panel. Sickle cell disease: Screening, diagnosis, management, and counseling in newborns and infants. Agency for Health Care Policy and Research, Public Health Service, US Department of Health and Human Services, 1993.

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7

United States. Agency for Health Care Policy and Research., ed. Sickle Cell disease: Screening, diagnosis, management, and counseling in newborns and infants. U.S. Dept. of Health and Human Services, Agency for Health Care Policy and Research, 1993.

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8

McCorkle, Ruth. Anemia and fatigue in cancer patients: Nursing care management : a nursing symposium, April 1997, Philadelphia, PA. Associates in Medical Marketing Co., 1998.

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9

O, Earl Robert, Woteki Catherine E, Calloway Doris Howes, Institute of Medicine (U.S.). Committee on the Prevention, Detection, and Management of Iron Deficiency Anemia among U.S. Children and Women of Childbearing Age., and Institute of Medicine (U.S.). Food and Nutrition Board., eds. Iron deficiency anemia: Recommended guidelines for the prevention, detection, and management among U.S. children and women of childbearing age. National Academy Press, 1993.

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10

Oni, L. Care and management of women with sickle cell disease in maternity care settings. Brent Sickle Cell & Thalassaemia Centre, 2002.

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11

D, Chang B., and Canada. Dept. of Fisheries and Oceans. Biological Station (St. Andrews, N.B.), eds. Water circulation and management of infectious salmon anemia in the salmon aquaculture industry in Passamaquoddy Bay, southwestern New Brunswick. Fisheries and Oceans Canada, 2006.

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12

Alonge, Temitope Oluwagbenga. Arrest the first leg of the quartet: Bone infarction or bone infection? : an inaugural lecture delivered at the University of Ibadan on Thursday, 27 September, 2018. Ibadan University Press Publishing House, University of Ibadan, 2018.

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13

H, Page F., and Canada. Dept. of Fisheries and Oceans., eds. Water circulation and management of infectious salmon anemia in the salmon aquaculture industry of southern Grand Manan Island, Bay of Fundy. Fisheries and Oceans Canada, 2005.

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14

D, Chang B., and Canada. Dept. of Fisheries and Oceans. Biological Station (St. Andrews, N.B.), eds. Water circulation and management of infectious salmon anemia in the salmon aquaculture industry of Cobscook Bay, Maine and adjacent southwestern New Brunswick. Fisheries and Oceans Canada, 2005.

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15

D, Chang B., and Canada. Dept. of Fisheries and Oceans. Biological Station (St. Andrews, N.B.), eds. Water circulation and management of infectious salmon anemia in the salmon aquaculture industry of Letete Passage, Back Bay, Bliss Harbour, and Lime Kiln Bay in southwestern New Brunswick. Fisheries and Oceans Canada, 2005.

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16

Renee, Shirley. The stranger within me. Hilton Pub., 2011.

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17

Frey, Kathrine, Deborah Tolich, Kelly McCoy, Rita K. Schwab, and Shylah Quast. Preoperative Anemia Management. American Association of Blood Banks, 2019.

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18

White, Camille. Anemia : Effective Guide on Anemia Treatment and Management: Freedom from Anemia. Independently Published, 2021.

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19

Berliner, Nancy, Edward J. Benz, and Fred J. Schiffman. Anemia: Pathophysiology, Diagnosis and Management. Cambridge University Press, 2017.

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20

Okpala, Iheanyi. Practical Management of Haemoglobinopathies. Wiley & Sons, Incorporated, John, 2008.

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21

Okpala, Iheanyi. Practical Management of Haemoglobinopathies. Wiley & Sons, Incorporated, John, 2008.

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22

Pratt, Martha. Causes, Symptoms and Management of Anemia. American Medical Publishers, 2021.

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23

Guidelines for the management of anemia. MUMS Guideline Clearinghouse, 2004.

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24

Hallman, Alice. Anemia: Prevalence, Risk Factors and Management Strategies. Nova Science Publishers, Incorporated, 2014.

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25

Berliner, Nancy, Fred J. Schiffman, and Benz, Jr., Edward J., Jr. Anemia South Asia Edition: Pathophysiology, Diagnosis, and Management. University of Cambridge ESOL Examinations, 2018.

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26

Lerma, Edgar V., Robert Provenzano, and Lynda Szczech. Management of Anemia: A Comprehensive Guide for Clinicians. Springer, 2017.

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27

Jr, Robert T. Means. Anemia in the Young and Old: Diagnosis and Management. Springer, 2018.

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28

Anemia Paperback with Online Resource: Pathophysiology, Diagnosis, and Management. Cambridge University Press, 2018.

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29

Lewis, Marilyn E. Sickle Cell Disease: Genetics, Management and Prognosis. Nova Science Publishers, Incorporated, 2015.

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30

Management and Therapy of Sickle Cell Disease. United States Government Printing, 1989.

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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

US GOVERNMENT. Sickle Cell Disease No. 6: Comprehensive Screening and Management in Newborns and Infants, Quick Reference Guide for Clinicians (Clinical Practice Guideline). U.S. Government Printing Office, 1993.

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33

Zacharowski, Kai, Hans Gombotz, and Donat Rudolf Spahn. Patient Blood Management. Thieme Verlag, George, 2015.

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34

Avram, Morrell M. Management of Comorbidities in Kidney Disease in the 21st Century: Anemia, Bone Disease, Malnutrition, and Inflammation. Wiley & Sons, Incorporated, John, 2008.

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35

Avram, M. M. Management of Comorbidities in Kidney Disease in the 21st Century: Anemia, Bone Disease, Malnutrition and Inflammation. Blackwell Publishing Limited, 2003.

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36

(Editor), Robert Earl, and Catherine E. Woteki (Editor), eds. Iron Deficiency Anemia: Recommended Guidelines for the Prevention, Detection, and Management Among U.S. Children and Women of Childbearing Age. National Academies Press, 1994.

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37

Iron Deficiency Anemia: Recommended Guidelines for the Prevention, Detection, and Management among U. S. Children and Women of Childbearing Age. National Academies Press, 1994.

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38

Young, Raymond. Infection in the Patient with Sickle Cell Anemia. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199976805.003.0060.

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This chapter provides a brief overview of the clinical manifestations of and management strategies for infectious complications in the immunocompromised sickle cell disease patient. The chapter discusses infections in various organ systems, including the respiratory tract, central nervous system, bone, hematopoietic cell lineage, and blood-borne infections. Differentiating infections from noninfectious processes that often have similar presentations in the sickle cell patient may at times be difficult, and clinicians managing sickle cell patients should be keenly aware of this fact. This chapt

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39

Forget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2010.

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40

Bricker, Leanne, Julian N. Robinson, and Baskaran Thilaganathan, eds. Management of Multiple Pregnancies. Cambridge University Press, 2022. http://dx.doi.org/10.1017/9781108915038.

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Multiple pregnancies are associated with higher risks for both mother and babies. Women with multiple pregnancies have an increased risk of miscarriage, anemia, hypertensive disorders, haemorrhage, and postnatal illness. These pregnancies are more likely to need an operative delivery, and maternal mortality is generally 2.5 times that of singleton births. Fetuses are at increased risk for anatomic and genetic anomalies, growth abnormalities, prematurity, and several physiological problems related to monochorionicity. This book provides a much needed, up-to-date guide to the management of multi

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41

Anemia Cookbook and Diet Plan: The Complete Guidebook on the Causes, Symptom, Diagnosis, Treatment and Management. Independently Published, 2022.

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42

(Foreword), H. Franklin Bunn, Martin H. Steinberg (Editor), Bernard G. Forget (Editor), Douglas R. Higgs (Editor), and Ronald L. Nagel (Editor), eds. Disorders of Hemoglobin: Genetics, Pathophysiology and Clinical Management. Cambridge University Press, 2001.

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43

Forget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009.

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44

Forget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009.

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45

Forget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009.

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46

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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47

D, Daniels Ross Ph. CBD Oil for Sickle Cell Amenia: Comprehensive Guide on Using Cbd Oil for Effective Management of Sickle Cell Anemia. Independently Published, 2019.

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48

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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49

Water circulation and management of infectious salmon anemia in the salmon aquaculture industry of eastern Grand Manan Island, Bay of Fundy. Fisheries and Oceans Canada, 2006.

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50

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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