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Idiopathic Pulmonary Fibrosis : A Comprehensive Clinical Guide / edited by Keith C. Meyer, Steven D. Nathan.

Contributor(s): Meyer, Keith C, editor literario | Nathan, Steven D, editor literario | SpringerLink (Online service)
Material type: materialTypeLabelE-bookSeries: Respiratory Medicine; 99Publisher: Totowa, NJ : Humana Press Imprint: Humana Press, 2014Description: 1 recurso en línea (XV, 451 p.) : 87 ilustraciones, 56 ilustraciones en color.ISBN: 9781627036825.Subject: Aparato respiratorio -- EnfermedadesDDC classification: 616.2 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
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. Â{uE000}
Summary: 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.šch chapterÂ{u0A6E}cludes 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 chapterÂ{u086C}so provides a summary of ongoing research and identifies the needs for future research in the field.Â{u0264}iopathic 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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Holdings
Item type Current library Collection Call number Copy number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC776.F5 I356 2014 EB (Browse shelf(Opens below)) .i11560642 Acceso electrónico eBOOK .i11560642
Total holds: 0

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. Â{uE000}

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.šch chapterÂ{u0A6E}cludes 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 chapterÂ{u086C}so provides a summary of ongoing research and identifies the needs for future research in the field.Â{u0264}iopathic 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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