Idiopathic Pulmonary Fibrosis A Comprehensive Clinical Guide /

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 upda...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Άλλοι συγγραφείς: Meyer, Keith C. (Επιμελητής έκδοσης), Nathan, Steven D. (Επιμελητής έκδοσης)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Totowa, NJ : Humana Press : Imprint: Humana Press, 2014.
Σειρά:Respiratory Medicine ; 9
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
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245 1 0 |a Idiopathic Pulmonary Fibrosis  |h [electronic resource] :  |b A Comprehensive Clinical Guide /  |c edited by Keith C. Meyer, Steven D. Nathan. 
264 1 |a Totowa, NJ :  |b Humana Press :  |b Imprint: Humana Press,  |c 2014. 
300 |a XV, 451 p. 87 illus., 56 illus. in color.  |b online resource. 
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490 1 |a Respiratory Medicine ;  |v 9 
505 0 |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.  . 
520 |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. 
650 0 |a Medicine. 
650 0 |a Internal medicine. 
650 0 |a Respiratory organs  |x Diseases. 
650 0 |a Primary care (Medicine). 
650 1 4 |a Medicine & Public Health. 
650 2 4 |a Pneumology/Respiratory System. 
650 2 4 |a Internal Medicine. 
650 2 4 |a Primary Care Medicine. 
700 1 |a Meyer, Keith C.  |e editor. 
700 1 |a Nathan, Steven D.  |e editor. 
710 2 |a SpringerLink (Online service) 
773 0 |t Springer eBooks 
776 0 8 |i Printed edition:  |z 9781627036818 
830 0 |a Respiratory Medicine ;  |v 9 
856 4 0 |u http://dx.doi.org/10.1007/978-1-62703-682-5  |z Full Text via HEAL-Link 
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950 |a Medicine (Springer-11650)