國立高雄大學圖資館 |

語系: 繁體中文

說明(常見問題)

圖資館首頁

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Idiopathic pulmonary fibrosisa compr...

Meyer, Keith C.

Idiopathic pulmonary fibrosisa comprehensive clinical guide /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Idiopathic pulmonary fibrosisedited by Keith C. Meyer, Steven D. Nathan.
其他題名:	a comprehensive clinical guide /
其他作者:	Meyer, Keith C.
出版者:	Cham :Springer International Publishing :2019.
面頁冊數:	xvii, 475 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
標題:	Pulmonary fibrosis.
電子資源:	https://doi.org/10.1007/978-3-319-99975-3
ISBN:	9783319999753$q(electronic bk.)

Idiopathic pulmonary fibrosisa comprehensive clinical guide /
Idiopathic pulmonary fibrosisa comprehensive clinical guide /[electronic resource] :edited by Keith C. Meyer, Steven D. Nathan. - 7nd ed. - Cham :Springer International Publishing :2019. - xvii, 475 p. :ill., digital ;24 cm. - Respiratory medicine,2197-7372. - Respiratory medicine..

Classification 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.

This 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.

ISBN: 9783319999753$q(electronic bk.)

Standard No.: 10.1007/978-3-319-99975-3doiSubjects--Topical Terms:

676426
Pulmonary fibrosis.

LC Class. No.: RC776.F5 / I356 2019

Dewey Class. No.: 616.24

Idiopathic pulmonary fibrosisa comprehensive clinical guide /
LDR:02874nmm a2200349 a 4500 001 555872
003 DE-He213
005 20190715100646.0
006 m d
007 cr nn 008maaau
008 191121s2019 gw s 0 eng d
020 $a 9783319999753$q(electronic bk.)
020 $a 9783319999746$q(paper)
024 7 $a 10.1007/978-3-319-99975-3 $2 doi
035 $a 978-3-319-99975-3
040 $a GP $c GP
041 0 $a eng
050 4 $a RC776.F5 $b I356 2019
072 7 $a MJL $2 bicssc
072 7 $a MED079000 $2 bisacsh
072 7 $a MJL $2 thema
082 0 4 $a 616.24 $2 23
090 $a RC776.F5 $b I19 2019
245 0 0 $a Idiopathic pulmonary fibrosis $h [electronic resource] : $b a comprehensive clinical guide / $c edited by Keith C. Meyer, Steven D. Nathan.
250 $a 7nd ed.
260 $a Cham : $b Springer International Publishing : $b Imprint: Humana Press, $c 2019.
300 $a xvii, 475 p. : $b ill., digital ; $c 24 cm.
490 1 $a Respiratory medicine, $x 2197-7372
505 0 $a Classification 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 $a This 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.
650 0 $a Pulmonary fibrosis. $3 676426
650 1 4 $a Pneumology/Respiratory System. $3 274253
650 2 4 $a Primary Care Medicine. $3 275823
700 1 $a Meyer, Keith C. $3 676424
700 1 $a Nathan, Steven D. $3 676425
710 2 $a SpringerLink (Online service) $3 273601
773 0 $t Springer eBooks
830 0 $a Respiratory medicine. $3 558279
856 4 0 $u https://doi.org/10.1007/978-3-319-99975-3
950 $a Medicine (Springer-11650)