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Books on the topic 'Red blood cell separation'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Bjorn, Neu, and Meiselman Herbert J, eds. Red blood cell aggregation. CRC Press, 2012.

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2

Magnani, Mauro, and Antonio De Flora, eds. Red Blood Cell Aging. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-5985-2.

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3

Schonewille, Henk. Red blood cell alloimmunization after blood transfusion. Leiden University Press, 2008.

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4

Hemoglobin-based red cell substitutes. Johns Hopkins University Press, 1992.

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5

Klein, Lori. Perioperative red cell transfusion: January 1985 through May 1988 : 803 citations. U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Library of Medicine, Reference Section, 1988.

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6

Edwards-Moulds, JoAnn. Standards for molecular testing for red cell, platelet, and neutrophil antigens. AABB, 2008.

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7

1930-, Brewer George J., ed. The red cell: Seventh Ann Arbor Conference : proceedings of the Seventh International Conference on Red Cell Metabolism and Function, held in Ann Arbor, Michigan, October 25-27, 1988. A.R. Liss, 1989.

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8

International, Meeting on Anion Transport Protein of the Red Blood Cell Membrane as well as Kidney and Diverse Cells (1989 Fukuoka-shi Japan). Anion transport protein of the red blood cell membrane: Proceedings of the International Meeting on Anion Transport Protein of the Red Blood Cell Membrane as well as Kidney and Diverse Cells, Fukuoka, 1-3 May 1989. Elsevier, 1989.

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9

Madden, John Eugene. Evaluation of the polyethylene glycol anti globulin test for detection of red blood cell antibodies and incorporation into microtitre plate technology. The Author], 1994.

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10

Mauro, Magnani, and De Flora Antonio, eds. Red blood cell aging. Plenum Press, 1991.

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11

Rudolph, Alan. Red Blood Cell Substitutes. CRC, 1997.

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12

Baskurt, Oguz, Björn Neu, and Herbert J. Meiselman. Red Blood Cell Aggregation. CRC Press, 2011. http://dx.doi.org/10.1201/b11221.

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13

1934-, Shohet Stephen B., and Mohandas Narla, eds. Red cell membranes. Churchill Livingstone, 1988.

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14

Reid, Marion E. Red Cell Transfusion. Humana, 2012.

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15

Cell Membrane: The Red Blood Cell as a Model. Wiley-VCH, 2003.

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16

Yawata, Yoshihito. Cell Membrane: The Red Blood Cell As a Model. Wiley & Sons, Incorporated, John, 2006.

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17

Yawata, Yoshihito. Cell Membrane: The Red Blood Cell As a Model. Wiley & Sons, Limited, John, 2004.

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18

M, Zborowski, and Chalmers J. J, eds. Magnetic cell separation. Elsevier, 2008.

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19

George, Garratty, and American Association of Blood Banks. Meeting, eds. Red cell antigens and antibodies. American Association of Blood Banks, 1986.

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20

1949-, Agre Peter, and Parker John C. 1935-, eds. Red blood cell membranes: Structure, function, clinical implications. Dekker, 1989.

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21

Oxford, Rex J. Dynamics and control of a centrifugal blood cell separator. 1987.

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22

Red Cell Transfusion: A Practical Guide. Humana Press, 2011.

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23

E, Reid Marion, and Nance Sandra J, eds. Red cell transfusion: A practical guide. Humana Press, 1998.

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24

1954-, Rudolph Alan S., Rabinovici Reuven, and Feuerstein Giora Z. 1946-, eds. Red blood cell substitutes: Basic principles and clinical applications. M. Dekker, 1998.

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25

Tsuyoshi, Ohnishi S., and Ohnishi Tomoko, eds. Membrane abnormalities in sickle cell disease and in other red blood cell disorders. CRC Press, 1994.

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26

Provan, Drew, Trevor Baglin, Inderjeet Dokal, and Johannes de Vos. Red cell disorders. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199683307.003.0002.

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The peripheral blood film in anaemias - Anaemia in renal disease - Anaemia in endocrine disease - Anaemia in joint disease - Anaemia in gastrointestinal disease - Anaemia in liver disease - Iron (Fe) deficiency anaemia - Vitamin B12 deficiency - Folate deficiency - Other causes of megaloblastic anaemia - Anaemia in other deficiency states - Haemolytic syndromes - Genetic control of haemoglobin production - Sickling disorders - HbS—sickle-modifying therapies - Sickle cell trait (HbAS) - Other sickling disorders - Other haemoglobinopathies - Unstable haemoglobins - Thalassaemias - α thalassaemia

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27

Provan, Drew, Trevor Baglin, Inderjeet Dokal, Johannes de Vos, Banu Kaya, and Angela Theodoulou. Red cell disorders. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199683307.003.0002_update_001.

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The peripheral blood film in anaemias - Anaemia in renal disease - Anaemia in endocrine disease - Anaemia in joint disease - Anaemia in gastrointestinal disease - Anaemia in liver disease - Iron (Fe) deficiency anaemia - Vitamin B12 deficiency - Folate deficiency - Other causes of megaloblastic anaemia - Anaemia in other deficiency states - Haemolytic syndromes - Genetic control of haemoglobin production - Sickling disorders - HbS—sickle-modifying therapies - Sickle cell trait (HbAS) - Other sickling disorders - Other haemoglobinopathies - Unstable haemoglobins - Thalassaemias - α‎ thalassaemi

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28

(Editor), Marion E. Reid, and Sandra J. Nance (Editor), eds. Red Cell Transfusion: A Practical Guide (Contemporary Hematology). Humana Press, 1998.

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29

(Editor), Antonio De Flora, and Mauro Magnani (Editor), eds. Red Blood Cell Aging (Advances in Experimental Medicine and Biology). Springer, 1992.

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30

Monoclonal antibodies against human red blood cell and related antigens. Arnette, 1988.

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31

Greenburg, A. Gerson, and Hae Won Kim. Hemoglobin-Based Oxygen Carriers as Red Cell Substitutes and Oxygen Therapeutics. Springer, 2013.

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32

Greenburg, A. Gerson, and Hae Won Kim. Hemoglobin-Based Oxygen Carriers as Red Cell Substitutes and Oxygen Therapeutics. Springer, 2013.

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33

Lim, Brian. Modeling ultrasound imaging of red blood cell aggregation in shear flow. 1999.

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34

Research opportunities in loss of red blood cell mass in space flight. Life Sciences Research Office, Federation of American Societies for Experimental Biology, 1985.

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35

1952-, Sweeney Joseph, and Heaton Andrew, eds. Clinical benefits of leukodepleted blood products. R.G. Landes, 1995.

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36

1949-, Agre Peter, and Cartron Jean Pierre, eds. Protein blood group antigens of the human red cell: Structure, function, and clinical significance. Johns Hopkins University Press, 1992.

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37

Nakai, Harumi. Factors influencing plasma and red blood cell free and total choline in the premature infant. 1985.

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38

Red Blood Cell Carriers: A Method for Disseminating Chemicals Via the Circulatory System (Current Studies in Hematology and Blood Transfusion). S. Karger AG (Switzerland), 1985.

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39

Bogdanova, Anna, and Lars Kaestner, eds. Red Blood Cells at the Mount of Truth: Highlights of the 22nd Meeting of the European Red Cell Research Society. Frontiers Media SA, 2021. http://dx.doi.org/10.3389/978-2-88966-351-4.

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40

1943-, Simpson Joe Leigh, Elias Sherman, and New York Academy of Sciences., eds. Fetal cells in maternal blood: Prospects for noninvasive prenatal diagnosis. New York Academy of Sciences, 1994.

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41

Protein Blood Group Antigens of the Human Red Cell: Structure, Function, and Clinical Significance (The Johns Hopkins Series in Hematology/Oncology). The Johns Hopkins University Press, 1992.

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42

Albert, Tyler J., and Erik R. Swenson. The blood cells and blood count. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0265.

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Blood is a dynamic fluid consisting of cellular and plasma components undergoing constant regeneration and recycling. Like most physiological systems, the concentrations of these components are tightly regulated within narrow limits under normal conditions. In the critically-ill population, however, haematological abnormalities frequently occur and are largely due to non-haematological single- or multiple-organ pathology. Haematopoiesis originates from the pluripotent stem cell, which undergoes replication, proliferation, and differentiation, giving rise to cells of the erythroid, myeloid, and

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43

Martinson, Kerry Elizabeth. Changes in plasma pyridoxal 5'-phosphate and red blood cell pyridoxal 5'-phosphate concentration during an oral glucose tolerance test in persons with diabetes mellitus. 1994.

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44

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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45

Hahn, Sinuhe. Fetal Cells and Fetal DNA in Maternal Blood: New Developments for a New Millennium. Edited by Sinuhe Hahn. Karger, 2001.

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46

Telford, Richard. Blood products and fluid therapy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198719410.003.0039.

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This chapter discusses the anaesthetic uses of blood products and other fluids. It begins with a discussion of blood products (red cells, platelets, fresh frozen plasma, and so on). It goes on to describe blood conservation techniques such as cell salvage. Massive transfusion is discussed with its protocol. The problems posed by Jehovah’s Witnesses who refuse blood products are explored. The chapter concludes with a discussion of fluid and electrolyte therapy.

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47

Telford, Richard. Blood products and fluid therapy. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198719410.003.0039_update_001.

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This chapter discusses the anaesthetic uses of blood products and other fluids. It begins with a discussion of blood products (red cells, platelets, fresh frozen plasma, and so on). It goes on to describe blood conservation techniques such as cell salvage. Massive transfusion is discussed with its protocol. The problems posed by Jehovah’s Witnesses who refuse blood products are explored. The chapter concludes with a discussion of fluid and electrolyte therapy.

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48

Bonnie Fagan, Melinda. Individuality, Organisms, and Cell Differentiation. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190636814.003.0006.

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This chapter builds on earlier arguments concerning the individuality of stem cells. The author has argued in previous work that stem cells are not biological individuals in the same way as specialized cells of multicellular organisms (e.g., neurons, red blood cells, muscle cells) but that some stem cells (cultured pluripotent stem cells) can be considered biological individuals by analogy with multicellular organisms. More precisely, the author claims that cultured pluripotent stem cells can be considered model organisms for studying early mammalian development. An important objection to this

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49

Qu, Lirong, and Darrell J. Triulzi. Blood product therapy in the ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0267.

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Transfusions are among the most common medical procedures in the intensive care unit. Several randomized controlled trials (RCT) indicate that restrictive red cell transfusion practice using a haemoglobin of <7g/dL is safe in critically-ill patients. Although similar RCT are not available for plasma or platelet transfusion guidelines, a large body of observational studies suggest that plasma transfusion for an invasive procedure has not been shown to be of benefit in patients with INR <2.0. Similarly, in thrombocytopenic patients, the target platelet count for bleeding or for an invasive

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50

National Center for Health Statistics (U. S.). Serum and Red Blood Cell Folate and Serum Vitamin B12 of Persons 4 Years and Older: United States, 1988-1994 (Vital and Health Statistics. Series 11, Data from the National Health Survey, No. 243). Dept of Health and Hum L and Prevention Natio, 1998.

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