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Готові списки джерел за темами / Organic disease management / Книги

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Organic disease management.

Книги з теми "Organic disease management"

Автор: Grafiati

Опубліковано: 7 червня 2025

Оновлено: 2 серпня 2025

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Ознайомтеся з топ-50 книг для дослідження на тему "Organic disease management".

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1

Alan, Caldwell Brian, and New York State Agricultural Experiment Station., eds. Resource guide for organic insect and disease management. New York State Agricultural Experiment Station, 2005.

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2

Meghvansi, Mukesh K., and Ajit Varma, eds. Organic Amendments and Soil Suppressiveness in Plant Disease Management. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23075-7.

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3

Finckh, Maria R., Ariena H. C. van Bruggen, and Lucius Tamm. Plant diseases and their management in organic agriculture. The American Phytopathological Society, 2015.

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4

MacNee, William. Clinical management of chronic obstructive pulmonary disease. Professional Communications, 2005.

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5

Edwards, Linda. Organic tree fruit management. Certified Organic Associations of British Columbia, 1998.

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6

Edwards, Linda. Organic tree fruit management. Certified Organic Associations of British Columbia, 1998.

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7

H, Sleisenger Marvin, and Fordtran John S, eds. Gastrointestinal disease: Pathophysiology, diagnosis, management. 4th ed. W.B. Saunders, 1989.

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8

David, Abramson G., and Martin Dan C, eds. Endoscopic management of gynecologic disease. Lippincott-Raven, 1996.

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9

Karram, Mickey M. Surgical management of pelvic organ prolapse. Elsevier/Saunders, 2013.

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10

D, Varner Dickson, and Pratt Paul W, eds. Diseases and management of breeding stallions. American Veterinary Publications, 1991.

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11

Joshi, S. K. Management of urinary diseases: An Ayurvedic approach. Satyam Pub. House, 2009.

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12

M, Potts Jeannette, ed. Genitourinary pain and inflammation: Diagnosis and management. Humana Press, 2008.

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13

1951-, Mohsenifar Zab, and Hoo Guy W. Soo, eds. Practical pulmonary and critical care medicine management. Taylor & Francis, 2006.

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14

Crowell, Michael D., and Michael P. Jones. Contemporary diagnosis and management of functional digestive disorders. Handbooks in Health Care Co., 2009.

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15

R, Wyllie, Hyams Jeffrey S, and Kay Marsha, eds. Pediatric gastrointestinal and liver disease: Pathophysiology, diagnosis, management. 3rd ed. Saunders Elsevier, 2006.

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16

G, Skinner Donald, and Lieskovsky Gary, eds. Diagnosis and management of genitourinary cancer. Saunders, 1988.

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17

Darke, P. G. G. The Henston guide to the management of coughing in dogs. Henston, 1996.

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18

1930-, Schofield P. F., and Lupton E. W. 1946-, eds. The Causation and clinical management of pelvic radiation disease. Springer-Verlag, 1989.

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19

Varma, Ajit, and Mukesh K. Meghvansi. Organic Amendments and Soil Suppressiveness in Plant Disease Management. Springer, 2015.

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20

Varma, Ajit, and Mukesh K. Meghvansi. Organic Amendments and Soil Suppressiveness in Plant Disease Management. Springer International Publishing AG, 2015.

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21

Varma, Ajit, and Mukesh K. Meghvansi. Organic Amendments and Soil Suppressiveness in Plant Disease Management. Springer, 2016.

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22

Pest And Disease Management For Organic Farmers Growers And Smallholders A Complete Guide. Crowood Press (UK), 2010.

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23

Fine, Perry G., and Matthew Kestenbaum. Clinical Processes and Symptom Management. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190456900.003.0003.

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This chapter describes what to do when a patient experiences severe anxiety and uncontrolled agitation that negatively affect care and the caregiving environment. Agitation and severe anxiety (panic) represent some of the few true emergency conditions in a hospice setting, so early recognition and prevention are critical. The discussion covers causes in depth, including psychosocial/spiritual and biomedical causes. The chapter details a tactical approach to evaluating and managing severe anxiety and agitation. An example of this is assessing if the patient has an organic brain syndrome due to

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24

Hardacker, Doris M. Cushing’s Disease. Edited by Matthew D. McEvoy and Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0029.

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Cushing’s syndrome is caused by adrenocorticotropic hormone (ACTH)-secreting or cortisol-secreting tumors. In most cases, the hypercortisolism is caused by an ACTH-secreting tumor of the pituitary. An excess of circulating cortisol adversely affects all major organ systems, including the cardiovascular system and therefore produces a wide range of clinical features. Perioperative morbidity and mortality will largely be determined by the magnitude of cardiac dysfunction encountered. Successful perioperative management depends on a thorough preoperative assessment of affected organs, comprehensi

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25

Baba, S., and Y. Ono. Interventional Management of Urological Diseases. Baba S Ono Y, 2010.

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26

Sleisenger and Fordtran. Gastrointestinal Disease: Pathophysiology,diagnosis,management. Elsevier, 1988.

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27

Sleisenger and Fordtran. Gastrointestinal Disease: Pathophysiology,diagnosis,management. Elsevier, 1988.

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28

Gastrointestinal disease: Pathophysiology, diagnosis, management. 4th ed. Saunders, 1989.

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29

van Aerts, René M. M., Tom J. G. Gevers, and Joost P. H. Drenth. Management of cystic liver disease. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0311_update_001.

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In a subset of autosomal dominant polycystic kidney disease patients, hepatic cysts dominate the clinical picture. These patients may develop polycystic liver disease, and enlargement of the liver leads to compression of adjacent abdominal and thoracic organs. The main risk factors for growth of liver cysts are female sex, exogenous oestrogen use, multiple pregnancies, and severity of renal disease. Treatment is only indicated in those with symptoms, and choice of treatment depends on total liver volume, size, and location of the liver cysts. Current radiological and surgical therapies include

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30

Chronic Care for Neglected Infectious Diseases: Leprosy/Hansen's Disease, Lymphatic Filariasis, Trachoma, and Chagas Disease. Pan American Health Organization, 2021. http://dx.doi.org/10.37774/9789275122501.

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In 2016, PAHO's Directing Council, through Resolution CD55.R9, approved the “Plan of Action for Elimination of Neglected Infectious Diseases (NID) and Post-Elimination Actions, 2016-2022.” This Resolution urges Member States to implement a set of interventions to reduce the burden of disease by NID in the Americas by 2022, including “…support promotion of treatment, rehabilitation, and related support services through an approach focused on integrated morbidity management and disability prevention for individuals and families afflicted by those neglected infectious diseases that cause disabili

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31

Nakada, Stephen Y., and Margaret S. Pearle. Urolithiasis: Medical and Surgical Management of Stone Disease. Taylor & Francis Group, 2009.

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32

Al-Mamari, Said Abdallah, and Salim Said Al-Busaidy. Urological Cancer Management. Springer, 2015.

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33

Al-Mamari, Said Abdallah, and Salim Said Al-Busaidy. Urological Cancer Management. Springer International Publishing AG, 2016.

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34

Al-Mamari, Said Abdallah, and Salim Said Al-Busaidy. Urological Cancer Management. Springer, 2015.

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35

Goonewardene, Sanchia S., Peter Pietrzak, and David Albala. Basic Urological Management. Springer, 2018.

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36

Neyrinck, Arne P., Patrick Ferdinande, Dirk Van Raemdonck, and Marc Van de Velde. Donor organ management. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199687039.003.0034.

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Organ transplantation is the standard treatment modality for end-stage organ disease in selected cases. Two types of potential organ donors can be identified: the brain-dead ‘heart-beating donors’, referred to as DBD (donation after brain death), and the warm ischaemic ‘non-heart-beating donors’, referred to as DCD (donation after circulatory death). Brain death induces several physiological changes in the DBD donor. An autonomic storm is characterized by massive catecholamine release, followed by autonomic depletion during a vasoplegic phase. This is associated with several hormonal changes (

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37

Hoo, Guy W. Soo, and Zab Mosenifar. Practical Pulmonary and Critical Care Medicine: Disease Management. Taylor & Francis Group, 2006.

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38

Mohsenifar, Zab, and Guy W. Soo Hoo. Practical Pulmonary and Critical Care Medicine: Disease Management. Taylor & Francis Group, 2006.

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39

Hoo, Guy W. Soo, and Zab Mosenifar. Practical Pulmonary and Critical Care Medicine: Disease Management. Taylor & Francis Group, 2006.

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40

Chronic Pelvic Pain: Evaluation and Management. Springer, 1997.

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41

Olive, David L., and Richard E. Blackwell. Chronic Pelvic Pain: Evaluation and Management. Springer London, Limited, 2012.

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42

Schreiber, Karen, Eliza Chakravarty, and Monika Østensen, eds. Practical management of the pregnant patient with rheumatic disease. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198845096.001.0001.

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Specialists from different medical specialties need to gain familiarity with reproductive health issues in women with chronic rheumatic diseases of childbearing age. Health care providers must have easy access to summary recommendations for management of pregnancy, antenatal care, and care in the postpartum period. This book is intended as a quick-access guide of the most up-to-date understanding of the interplay between pregnancy and rheumatic diseases and principles of management before, during, and after pregnancy assisting in decision-making regarding treatment of women with autoimmune dis

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43

Scullion, Jane, and Steve Holmes. Respiratory Management in Primary Care. Taylor & Francis Group, 2023.

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44

Denton, Christopher P., and Pia Moinzadeh. Systemic sclerosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0121.

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The term 'scleroderma' describes a group of conditions in which the development of thickened, fibrotic skin is a cardinal feature. This includes localized forms of scleroderma (e.g. morphoea) and also systemic forms of the disease that are more correctly termed systemic sclerosis. Systemic sclerosis (SSc) is a multiorgan, autoimmune disease that has a high clinical burden and mortality, due to affecting the skin as well as internal organs. As with other related diseases there is a female predominance and marked clinical diversity. The pathogenesis of SSc is not fully elucidated; it includes en

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45

Rahman, Shamima, and Mirian C. H. Janssen. Disorders of Mitochondrial Energy Metabolism. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0007.

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Mitochondrial disease can be diagnosed at every age, and the clinical presentation is very heterogeneous. In rare cases only a single organ is affected, but multisystem involvement may develop with progression of the disease. Organ systems relying most on aerobic metabolism are preferentially affected, including the central nervous system, peripheral nerves, eye, skeletal and cardiac muscle, and endocrine organs. These disorders can be classified according to whether the causative mutations affect mitochondrial DNA or nuclear DNA. Since specific treatment options are still limited, the managem

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46

Felberg, Mary A. Mitochondrial Disease and Anesthesia. 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/9780190678333.003.0042.

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Mitochondrial disease is a genetically, biochemically, and clinically heterogeneous group of disorders that arise from defects in cellular oxidative phosphorylation, most commonly within the electron transport chain. All mitochondrial diseases involve disruption in energy production; clinical symptoms usually manifest in tissues with high energy demands although all organs may be affected. The extent of disease depends not only on the mitochondrial defect but on the numbers of dysfunctional mitochondria present in each tissue. Despite in vitro evidence that almost every anesthetic agent studie

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47

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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48

Liang, Yafen, and Andrew Shaw. Severe Valvular Disease. Edited by Matthew D. McEvoy and Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0008.

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The pathophysiology of valvular diseases follows the fundamental principles of fluid and pressure dynamics. Alteration in any of the major components that determine forward flow can translate into a change in stroke volume, which in turn results in a change in cardiac output. The goal of managing severe valvular disease in the perioperative period is to maintain the forward flow required for end organ perfusion and minimize regurgitation. Accordingly, this chapter discusses the major principles involved in the pathophysiology of valve disease, as well as the perioperative assessment of disease

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49

Kamat, Madhav H., and R. P. Jindal. Management of Urologic Problems in General Practice. Jaypee Brothers Medical Publishers, 2018.

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50

Schoenberg, Mark P., Seth P. Lerner, and Cora N. Sternberg. Bladder Cancer: Diagnosis and Clinical Management. Wiley & Sons, Incorporated, John, 2015.

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