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Books on the topic 'Fibrosis pulmonar'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Nakamura, Hiroyuki, and Kazutetsu Aoshiba, eds. Idiopathic Pulmonary Fibrosis. Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-55582-7.

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2

Meyer, Keith C., and Steven D. Nathan, eds. Idiopathic Pulmonary Fibrosis. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-99975-3.

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3

Meyer, Keith C., and Steven D. Nathan, eds. Idiopathic Pulmonary Fibrosis. Humana Press, 2014. http://dx.doi.org/10.1007/978-1-62703-682-5.

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4

Clinical profiles of diffuse interstitial pulmonary disease. Futura Pub. Co., 1990.

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5

Nathan, Steven D., A. Whitney Brown, and Christopher S. King. Guide to Clinical Management of Idiopathic Pulmonary Fibrosis. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-32794-5.

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6

Bauernfeind, Adolf, Melvin I. Marks, and Birgitta Strandvik, eds. Cystic Fibrosis Pulmonary Infections: Lessons from Around the World. Birkhäuser Basel, 1996. http://dx.doi.org/10.1007/978-3-0348-7359-8.

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7

Gifford, Glen Allan. A study of pulmonary lesions in experimental bovine pneumonic pasteurellosis. University of Saskatchewan, 1986.

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8

Lewin, Linda Orkin. Pseudomonas cepacia colonization in systic fibrosis: Mortality, predictors of poor outcome, and effect on pulmonary function. s.n.], 1987.

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9

Parker, James N., and Philip M. Parker. Pulmonary fibrosis: A medical dictionary, bibliography, and annotated research guide to Internet references. ICON Health Publications, 2004.

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10

Interstitial lung disease. 5th ed. People's Medical Pub. House, 2011.

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11

Tirkos, Sam. Investigation of S100A8 and S100A9 as potential genetic modifiers of the pulmonary phenotype in cystic fibrosis mice. National Library of Canada, 2003.

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12

Levy, Lance D. The effect of long-term nutritional rehabilitation on growth, body composition and pulmonary function in patients with cystic fibrosis and the effect of salbutamol on energy expenditure in patients with cystic fibrosis. National Library of Canada = Bibliothèque nationale du Canada, 1991.

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13

1949-, Phan Sem Hin, and Thrall Roger S. 1947-, eds. Pulmonary fibrosis. Marcel Dekker, 1995.

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14

Tzouvelekis, Argyrios, Oliver Eickelberg, Naftali Kaminski, Demosthenes Bouros, and Vassilis Aidinis, eds. Pulmonary Fibrosis. Frontiers Media SA, 2019. http://dx.doi.org/10.3389/978-2-88963-195-7.

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15

P, Lynch Joseph, ed. Idiopathic pulmonary fibrosis. Marcel Dekker, 2004.

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16

Swigris, Jeffrey, and Kevin K. Brown. Idiopathic Pulmonary Fibrosis. Elsevier - Health Sciences Division, 2018.

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17

Ross, Clare, and Athol Wells. Idiopathic pulmonary fibrosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199657742.003.0010.

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Interstitial lung diseases are a complex heterogeneous group which are challenging to diagnose and treat. The diagnosis of idiopathic pulmonary fibrosis, as opposed to connective tissue interstitial lung disease, is important, as treatments and prognoses are very different. This chapter focusses on a case where this diagnosis is challenging. The evidence for the treatment of idiopathic pulmonary fibrosis is reviewed, in light of recent trials and new recommendations.

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18

Costabel, Ulrich, Bruno Crestani, and Athol U. Wells, eds. Idiopathic Pulmonary Fibrosis. European Respiratory Society, 2016. http://dx.doi.org/10.1183/2312508x.erm7116.

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19

Idiopathic Pulmonary Fibrosis. Elsevier, 2019. http://dx.doi.org/10.1016/c2016-0-04562-x.

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20

Lynch, Joseph, ed. Idiopathic Pulmonary Fibrosis. CRC Press, 2003. http://dx.doi.org/10.1201/b14211.

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21

Lynch, Joseph P., ed. Idiopathic Pulmonary Fibrosis. CRC Press, 2003. http://dx.doi.org/10.3109/9780203913444.

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22

Simpson, John, and Ann Millar. Advances in Pulmonary Fibrosis. Informa Healthcare, 2004.

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23

Idiopathic Pulmonary Fibrosis [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.87624.

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24

Tamotsu, Takishima, ed. Basic and clinical aspects of pulmonary fibrosis. CRC Press, 1994.

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25

P, Phipps Richard, ed. Pulmonary fibroblast heterogeneity. CRC Press, 1992.

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26

Jarvi, Eric J. Biochemical changes associated with BCNU-induced pulmonary toxicity. 1985.

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27

Bright-Thomas, Rowland J., and Andrew M. Jones. Cystic fibrosis. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0132.

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Cystic fibrosis is the most common lethal autosomal recessive disorder in Caucasians. There is no known survival advantage of the heterozygote carrier state. Chronic progressive pulmonary infection and bronchiectasis are the major causes of morbidity and mortality. The disease affects all ductal systems where the basic defect is manifest, including the pancreas, gastrointestinal tract, sinuses, hepatobiliary system, and male reproductive system, and has significant effects on nutrition and growth.

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28

Meyer, Keith C., and Steven D. Nathan. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide. Humana, 2016.

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29

Meyer, Keith C., and Steven D. Nathan. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide. Humana Press, 2013.

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30

Jolly, Elaine, Andrew Fry, and Afzal Chaudhry, eds. Respiratory medicine. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199230457.003.0018.

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Chapter 18 covers the basic science and clinical topics relating to respiratory medicine which trainees are required to learn as part of their basic training and demonstrate in the MRCP. The chapter starts with an introduction to the respiratory system, before covering respiratory defence and physiology, respiratory investigations, respiratory failure, pneumonia, tuberculosis, cystic fibrosis, bronchiectasis, pleural effusion, chronic obstructive pulmonary Disease, adult respiratory distress syndrome, asthma , fungal lung diseases, pulmonary embolism , lung cancer, pulmonary fibrosis, extrinsi

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31

Chronicling Idiopathic Pulmonary Fibrosis: A Collection of Personal Stories. Michigan Publishing, 2016.

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32

Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide. Humana, 2018.

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33

Nakamura, Hiroyuki, and Kazutetsu Aoshiba. Idiopathic Pulmonary Fibrosis: Advances in Diagnostic Tools and Disease Management. Springer, 2016.

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34

Nakamura, Hiroyuki, and Kazutetsu Aoshiba. Idiopathic Pulmonary Fibrosis: Advances in Diagnostic Tools and Disease Management. Ingramcontent, 2015.

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35

Nakamura, Hiroyuki, and Kazutetsu Aoshiba. Idiopathic Pulmonary Fibrosis: Advances in Diagnostic Tools and Disease Management. Springer, 2015.

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36

III, Joseph P. Lynch. Idiopathic Pulmonary Fibrosis (Lung Biology in Health and Disease). Informa Healthcare, 2003.

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37

Snell, Jamey, and Thomas J. Mancuso. Cystic Fibrosis. 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/9780190685157.003.0023.

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Cystic fibrosis (CF) is an inherited, autosomal recessive, multisystem disease. Dysfunction of the cystic fibrosis transmembrane conductance regulator protein (CFTR) in epithelial cells is the primary defect in CF. Defects in CFTR are the cause for lung disease, exocrine pancreatic insufficiency and failure, male infertility, and liver disease. CF can present with a variety of respiratory and gastrointestinal signs, including meconium ileus in the newborn period, hypernatremic dehydration, pulmonary insufficiency, nasal polyps, and insulin-dependent diabetes mellitus. As affected children grow

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38

Parker, James N. The Official Patient's Sourcebook on Idiopathic Pulmonary Fibrosis. Icon Health Publications, 2002.

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39

Cystic Fibrosis Pulmonary Infections: Lessons from Around the World. Birkhäuser, 2012.

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40

A, Bauernfeind, Marks Melvin I, and Strandvik B, eds. Cystic fibrosis pulmonary infections: Lessons from around the world. Birkhauser Verlag, 1996.

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41

Robertson, Lorenzo. Cystic and Idiopathic Pulmonary Fibrosis: Risk Factors, Management and Long-Term Health Outcomes. Nova Science Publishers, Incorporated, 2016.

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42

1946-, Lama Moisés Selman, and Barrios Roberto 1946-, eds. Interstitial pulmonary diseases: Selected topics. CRC Press, 1991.

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43

Carton, James. Lung pathology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198759584.003.0005.

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This chapter discusses lung pathology and covers respiratory malformations, respiratory failure, acute respiratory distress syndrome (ARDS), bronchiectasis, cystic fibrosis, pulmonary thromboembolism, pulmonary hypertension, asthma, chronic obstructive pulmonary disease (COPD), bacterial pneumonia, idiopathic pulmonary fibrosis (IPF), hypersensitivity pneumonitis, lung carcinoma, pleural effusion, pneumothorax, and malignant mesothelioma.

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44

Hill, Uta, Jane Ashbrook, and Charles Haworth. Metabolic and musculoskeletal effects of cystic fibrosis. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780198702948.003.0009.

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This chapter provides a comprehensive update on the prevention, recognition, and treatment of low bone mineral density in people with CF. As life expectancy improves, the extra-pulmonary complications of CF are becoming increasingly important to quality of life. Up to 25 per cent of CF patients have reduced bone mineral density in adulthood, leading to the development of fragility fractures which cause pain, thereby interfering with airway clearance and predisposing to pulmonary infection. Osteoporosis can be a relative contraindication for lung transplantation. Other important musculoskeletal

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45

Interstitial Pneumonia of Unknown Etiology. Univ of Tokyo Press, 1990.

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46

I, Schwarz Marvin, and King Talmadge E, eds. Interstitial lung disease. 2nd ed. Mosby-Year Book, 1993.

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47

Cystic Fibrosis Pulmonary Infections: Lessons from Around the World (Respiratory Pharmacology and Pharmacotherapy). Birkhauser, 1996.

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48

(Editor), Adolf Bauernfeind, Melvin I. Marks (Editor), and Brigitta Strandvik (Editor), eds. Cystic Fibrosis Pulmonary Infections: Lessons from Around the World (Respiratory Pharmacology and Pharmacotherapy). Birkhauser, 2004.

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49

Launois, Sandrine H., and Patrick Lévy. Pulmonary disorders and sleep. Edited by Sudhansu Chokroverty, Luigi Ferini-Strambi, and Christopher Kennard. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199682003.003.0041.

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Sleep disorders and pulmonary diseases are closely associated, a fact clearly underestimated in routine patient care, despite evidence that these disorders interact to impact on quality of life as well as on morbidity and mortality. The prevalence of chronic insomnia, sleep-related breathing disorders, and restless leg syndrome is high in patients with chronic pulmonary disorders such as asthma, chronic obstructive pulmonary disease, cystic fibrosis, interstitial lung disease, chest wall and neuromuscular disorders, and chronic respiratory failure. This association may be fortuitous and reflec

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50

Horsley, Alex, Steve Cunningham, and J. Alastair Innes, eds. Cystic Fibrosis (Oxford Respiratory Medicine Library). Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780198702948.001.0001.

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Cystic Fibrosis (CF) is a multi-system disorder, requiring not just respiratory expertise but also management of nutrition, diabetes, musculoskeletal and psychosocial issues. This online resource is a concise companion for all health care professionals who manage patients with CF, and it covers all aspects of care, including both paediatric and adult-specific issues, and summarizes up-to-date literature in a concise and focussed style. There is an emphasis on the practical aspects of management with separate chapters covering the effects of CF in the lung, the microbiology of pulmonary CF, and

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