Accedi

Bibliografie tematiche / Sickle cells diseases / Libri

Segui questo link per vedere altri tipi di pubblicazioni sul tema: Sickle cells diseases.

Libri sul tema "Sickle cells diseases"

Autore: Grafiati

Pubblicato: 12 aprile 2025

Cita una fonte nei formati APA, MLA, Chicago, Harvard e in molti altri stili

Scegli il tipo di fonte:

Vedi i top-50 libri per l'attività di ricerca sul tema "Sickle cells diseases".

Accanto a ogni fonte nell'elenco di riferimenti c'è un pulsante "Aggiungi alla bibliografia". Premilo e genereremo automaticamente la citazione bibliografica dell'opera scelta nello stile citazionale di cui hai bisogno: APA, MLA, Harvard, Chicago, Vancouver ecc.

Puoi anche scaricare il testo completo della pubblicazione scientifica nel formato .pdf e leggere online l'abstract (il sommario) dell'opera se è presente nei metadati.

Vedi i libri di molte aree scientifiche e compila una bibliografia corretta.

1

Alvin, Silverstein, Silverstein Virginia B e Nunn Laura Silverstein, a cura di. What you can do about sickle cell disease. New York, NY: Enslow Publishing, 2016.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

2

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

3

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

4

Serjeant, Graham R. Sickle cell disease. 2^a ed. Oxford: Oxford University Press, 1992.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

5

F, Whitten Charles, Bertles John F. 1925-, National Association for Sickle Cell Disease (U.S.) e New York Academy of Sciences., a cura di. Sickle cell disease. New York, N.Y: New York Academy of Sciences, 1989.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

6

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

7

Jones, Phill. Sickle cell disease. New York: Chelsea House, 2008.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

8

Samuel, Charache, e Johnson Cage S, a cura di. Sickle cell disease. Philadelphia: W.B. Saunders, 1996.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

9

McCormick, Marie, Henrietta Awo Osei-Anto e Rose Marie Martinez, a cura di. Addressing Sickle Cell Disease. Washington, D.C.: National Academies Press, 2020. http://dx.doi.org/10.17226/25632.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

10

Beshore, George. Sickle cell anemia. New York: F. Watts, 1994.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

11

P, Rodgers Griffin, a cura di. Sickle cell disease and thalassaemia. London: Baillière Tindall, 1998.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

12

author, Chilman-Blair Kim, e DeLoache Shawn author, a cura di. Medikidz explain sickle cell disease. London: Medikidz Ltd., 2013.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

13

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

14

National Heart, Lung, and Blood Institute. Division of Blood Diseases and Resources., a cura di. The Management of sickle cell disease. 4^a ed. Bethesda, MD: The Institute, 2002.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

15

National Heart, Lung, and Blood Institute. Division of Blood Diseases and Resources. The management of sickle cell disease. 4^a ed. Bethesda, MD: The Institute, 2002.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

16

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

17

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

18

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

19

N, Mankad Vipul, e Moore R. Blaine, a cura di. Sickle cell disease: Pathophysiology, diagnosis, and management. Westport, Conn: Praeger, 1992.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

20

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

21

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

22

Samuel, Charache, Lubin Bertram, Reid Clarice D, United States. Dept. of Health and Human Services., National Institutes of Health (U.S.) e United States. Public Health Service., a cura di. Management and therapy of sickle cell disease. 3^a ed. [Bethesda, Md.]: U. S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Heart, Lung, and Blood Institute, 1995.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

23

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

24

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

25

D, O'Malley Paul, a cura di. New developments in sickle cell disease research. New York: Nova Science Publishers, 2006.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

26

B, Jibril Harun, a cura di. Sickle cell disease: A guide for families. London: Collins, 1986.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

27

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

28

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

29

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

Testo completo

Abstract (sommario):

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, lung infections, end organ damage, and stroke. With improvements in the management and prevention of pain crises, infection, and other systemic involvement, these patients are living longer, thus increasing the potential for surgical needs. Whether it is for routine surgeries or surgeries that are due to the natural history of the disease; the pediatric anesthesiologist must be knowledgeable of the management of these patients in order to prevent morbidity and mortality.

Gli stili APA, Harvard, Vancouver, ISO e altri

30

Sickle Cell Disease (Diseases and Disorders). Lucent Books, 2007.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

31

Vescia, Monique, e Virginia Silverstein. What You Can Do about Sickle Cell Disease. Enslow Publishing, LLC, 2015.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

32

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

Testo completo

Abstract (sommario):

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.

Gli stili APA, Harvard, Vancouver, ISO e altri

33

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

34

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

35

Franklin, Andrew. Sickle Cell Disease. A cura di Matthew D. McEvoy e Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0084.

Testo completo

Abstract (sommario):

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 of surgical treatment. Both acute painful episodes and acute chest syndrome result from vaso-occlusive crises, and early stabilization of these emergencies is crucial to ensuring a positive patient outcome. The singular perioperative objective for the care of sickle cell disease patients is both simple and daunting: to achieve physiologic homeostasis in patients with preexisting multiorgan dysfunction undergoing a series of physiologic insults during and after surgery.

Gli stili APA, Harvard, Vancouver, ISO e altri

36

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

Testo completo

Abstract (sommario):

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 urine output, providing supplemental oxygen, and limiting surgical and anesthesia times to reduce pulmonary complications constitute the best management for patients with sickle cell disease.

Gli stili APA, Harvard, Vancouver, ISO e altri

37

Anionwu, Elizabeth, e H. Jibril. Sickle Cell Disease. 2^a ed. Longman, 1992.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

38

Sickle cell disease. 2^a ed. Oxford: Oxford University Press, 1992.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

39

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

40

Sickle cell disease. Oxford: Oxford University Press, 1985.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

41

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

42

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

43

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

44

Batchelor, Tracy, Joshua P. Klein, Andrés José María Ferreri e Lisa M. DeAngelis, a cura di. Oxford Textbook of Neurohaematology. Oxford University PressOxford, 2024. http://dx.doi.org/10.1093/med/9780198884903.001.0001.

Testo completo

Abstract (sommario):

Abstract The Oxford Textbook of Neurohaematology is the first dedicated source of knowledge on the diverse neurological conditions associated with malignant and classical haematological diseases. The book is divided into three sections. In the first section, neurological conditions associated with malignant haematological diseases are covered. This section begins with chapters on primary haematological malignancies of the nervous system, including primary central nervous system lymphomas, vitreoretinal lymphoma, and other rare primary malignancies such as Hodgkin disease and lymphoproliferative disorders. Next, a chapter on histiocytic tumours of the central nervous system presents the neurological conditions associated with the Langerhans and non-Langerhans histiocytoses. This is followed by chapters covering the neurological complications of systemic myeloid and lymphoid malignancies. The second section of the book covers neurological complications of treatments used in the management of haematological malignancies such as chemotherapy, radiation, and immunotherapy, including chimeric antigen receptor T cells. The third and final section of the book features chapters on neurological complications associated with classical haematological diseases, including disorders of red blood cells (e.g. sickle cell anaemia), disorders of platelets and coagulation (e.g. immune thrombocytopenia), and disorders of white blood cells (e.g. hyperviscosity syndrome).

Gli stili APA, Harvard, Vancouver, ISO e altri

45

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

Testo completo

Abstract (sommario):

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 this time to see if risk of stroke and other neurologic complications can be reduced (ClinicalTrials.gov identifiers: NCT01425307, NCT01389024, NCT00152113).

Gli stili APA, Harvard, Vancouver, ISO e altri

46

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

47

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

48

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

49

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

50

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

Offriamo sconti su tutti i piani premium per gli autori le cui opere sono incluse in raccolte letterarie tematiche. Contattaci per ottenere un codice promozionale unico!