000 03943nam a22004935i 4500
001 978-1-62703-682-5
003 DE-He213
005 20140220082506.0
007 cr nn 008mamaa
008 131015s2014 xxu| s |||| 0|eng d
020 _a9781627036825
_9978-1-62703-682-5
024 7 _a10.1007/978-1-62703-682-5
_2doi
050 4 _aRC705-779
072 7 _aMJL
_2bicssc
072 7 _aMED079000
_2bisacsh
082 0 4 _a616.2
_223
100 1 _aMeyer, Keith C.
_eeditor.
245 1 0 _aIdiopathic Pulmonary Fibrosis
_h[electronic resource] :
_bA Comprehensive Clinical Guide /
_cedited by Keith C. Meyer, Steven D. Nathan.
264 1 _aTotowa, NJ :
_bHumana Press :
_bImprint: Humana Press,
_c2014.
300 _aXV, 451 p. 87 illus., 56 illus. in color.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
490 1 _aRespiratory Medicine ;
_v9
505 0 _aChapter 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 _aIdiopathic 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 _aMedicine.
650 0 _aInternal medicine.
650 0 _aPneumology.
650 0 _aEmergency medicine.
650 1 4 _aMedicine & Public Health.
650 2 4 _aPneumology/Respiratory System.
650 2 4 _aInternal Medicine.
650 2 4 _aPrimary Care Medicine.
700 1 _aNathan, Steven D.
_eeditor.
710 2 _aSpringerLink (Online service)
773 0 _tSpringer eBooks
776 0 8 _iPrinted edition:
_z9781627036818
830 0 _aRespiratory Medicine ;
_v9
856 4 0 _uhttp://dx.doi.org/10.1007/978-1-62703-682-5
912 _aZDB-2-SME
999 _c92425
_d92425