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|a 9781627036825
|9 978-1-62703-682-5
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|a 10.1007/978-1-62703-682-5
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|a 616.2
|2 23
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|a Idiopathic Pulmonary Fibrosis
|h [electronic resource] :
|b A Comprehensive Clinical Guide /
|c edited by Keith C. Meyer, Steven D. Nathan.
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|a 1st ed. 2014.
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|a Totowa, NJ :
|b Humana Press :
|b Imprint: Humana,
|c 2014.
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|a XV, 451 p. 87 illus., 56 illus. in color.
|b online resource.
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
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|a text file
|b PDF
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|a Respiratory Medicine,
|x 2197-7380
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|a Chapter 1: Idiopathic Pulmonary Fibrosis: A Historical Perspective -- Chapter 2: Idiopathic Pulmonary Fibrosis: The Epidemiology and Natural History of Disease -- Chapter 3: Histopathology of IPF and Related Disorders -- Chapter 4: Imaging of Idiopathic Pulmonary Fibrosis -- Chapter 5: The Keys to Making a Confident Diagnosis of IPF -- Chapter 6: Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis -- Chapter 7: The Role of Adaptive Immunity in Idiopathic Pulmonary Fibrosis: Hiding in Plain Sight -- Chapter 8: Mechanisms of Fibrosis in IPF -- Chapter 9: The Emerging Genetics of Interstitial Lung Disease -- Chapter 10: Idiopathic Pulmonary Fibrosis Phenotypes -- Chapter 11: Idiopathic Interstitial Pneumonia and Connective Tissue Disease-Associated Interstitial Lung Disease: Similarities and Differences -- Chapter 12: Aging and IPF: What Is the Link? -- Chapter 13: Gastroesophageal Reflux and IPF -- Chapter 14: Pharmacological Treatment of Idiopathic Pulmonary Fibrosis -- Chapter 15: Recognizing and Treating Comorbidities of IPF -- Chapter 16: The Role of Pulmonary Rehabilitation and Supplemental Oxygen Therapy in the Treatment of Patients with Idiopathic Pulmonary Fibrosis -- Chapter 17: Acute Exacerbation of Idiopathic Pulmonary Fibrosis -- Chapter 18: Lung Transplantation for Idiopathic Pulmonary Fibrosis -- Chapter 19: Evolving Genomics of Pulmonary Fibrosis -- Chapter 20: Idiopathic Pulmonary Fibrosis Clinical Trials: Evolving Concepts -- Chapter 21: Future Directions in Basic and Clinical Science. .
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|a Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide delivers a concise review of our current understanding of disease pathogenesis and provides current evidence in the medical literature regarding its diagnosis and management. Each chapter includes key points and a summary aiming to update clinicians about various issues concerning the diagnosis and management of IPF. In addition to outlining the current state of knowledge, each chapter also provides a summary of ongoing research and identifies the needs for future research in the field. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide is an important new text that provides its readers with a better understanding of the pathobiology and natural history of IPF as it continues to evolve.
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650 |
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|a Respiratory organs-Diseases.
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|a Internal medicine.
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|a Primary care (Medicine).
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|a Pneumology.
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|a Internal Medicine.
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|a Primary Care Medicine.
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700 |
1 |
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|a Meyer, Keith C.
|e editor.
|4 edt
|4 http://id.loc.gov/vocabulary/relators/edt
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700 |
1 |
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|a Nathan, Steven D.
|e editor.
|4 edt
|4 http://id.loc.gov/vocabulary/relators/edt
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710 |
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|a SpringerLink (Online service)
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773 |
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|t Springer Nature eBook
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776 |
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|i Printed edition:
|z 9781627036832
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776 |
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|i Printed edition:
|z 9781627036818
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776 |
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8 |
|i Printed edition:
|z 9781493960224
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830 |
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|a Respiratory Medicine,
|x 2197-7380
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856 |
4 |
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|u https://doi.uam.elogim.com/10.1007/978-1-62703-682-5
|z Texto Completo
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912 |
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|a ZDB-2-SME
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912 |
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|a ZDB-2-SXM
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|a Medicine (SpringerNature-11650)
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950 |
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|a Medicine (R0) (SpringerNature-43714)
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