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020			_a9783319999753
024	7		_a10.1007/978-3-319-99975-3 _2doi
040			_bspa _cES-MaUEC _dES-MaUEC
050		4	_aRC776 .F5 _b2019 EB
245	0	0	_aIdiopathic Pulmonary Fibrosis : _bA Comprehensive Clinical Guide _cedited by Keith C. Meyer, Steven D. Nathan
250			_a2nd ed. 2019.
264		1	_aCham _bSpringer International Publishing : _bImprint: Humana Press _c2019
300			_a1 recurso en línea (XVII, 475 páginas 79 ilustraciones, 50 ilustraciones a color)
336			_2rdacontent _aTexto _btxt
337			_2rdamedia _aelectrónico _bc
338			_2rdacarrier _arecurso electrónico _bcr
347			_atext file _bPDF
490	1		_aRespiratory Medicine, _x2197-7372
490	0		_aMedicine (Springer-11650)
505	0		_aClassification and Nomenclature of Interstitial Lung Disease -- Epidemiology and Natural History of IPF -- Histopathology of IPF and Related Disorders -- Imaging of IPF -- Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis -- The Role of Immunity and Inflammation in IPF Pathogenesis -- Mechanisms of Fibrosis in IPF -- The Genetics of Pulmonary Fibrosis -- Genomics and Epigenetics of Pulmonary Fibrosis -- Biomarkers and IPF -- Clinical Phenotypes and Co-morbidities in IPF -- The Keys to Making a Confident Diagnosis of IPF -- Pharmacologic Treatment of IPF -- Mimics of IPF -- Gastroesophageal Reflux and IPF -- The Role of Pulmonary Rehabilitation and Oxygen Therapy -- Acute Exacerbations of IPF -- Lung Transplantation for IPF -- Clinical Trials in IFP: What are the Best Endpoints? -- Future Directions for IPF Research.
520	3		_aThis book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management. Since the first edition, many new developments have occurred in the understanding and management of this serious disease, revising our understanding of how it presents, manifests, and reacts to certain treatments. This second edition is fully updated with six new chapters by our team of international, expert authors. New topics include: classification of interstitial lung disease, pulmonary function tests in IPF, biomarkers, clinical phenotypes, mimics, and a discussion of clinical trials. Each chapter additionally includes a brief summary of ongoing research and potential future directions. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide, Second Edition is an invaluable resource for clinicians who desire a deeper understanding of IPF in order to better help their patients.
988			_aSpringer_Medicine_2019
650		7	_aFibrosis pulmonar _9469329 _2embne
700	1		_aMeyer, Keith C. _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt _988396
700	1		_aNathan, Steven D. _eeditor literario _4edt _4http://id.loc.gov/vocabulary/relators/edt _988397
776	0	8	_iPrinted edition: _z9783319999746
776	0	8	_iPrinted edition: _z9783319999760
830		0	_aRespiratory Medicine, _x2197-7372
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-319-99975-3 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942			_2lcc _cLE
998			_dz _feng _ggw _h0 _b07/2019 _eu _zSI