大葉大學圖書館 |

Idiopathic pulmonary fibrosis[electronic resource] :advances in diagnostic tools and disease management /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
杜威分類號:	616.24
書名/作者:	Idiopathic pulmonary fibrosis : advances in diagnostic tools and disease management // edited by Hiroyuki Nakamura, Kazutetsu Aoshiba.
其他作者:	Nakamura, Hiroyuki.
出版者:	Tokyo : : Springer Japan :, 2016.
面頁冊數:	x, 259 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Pulmonary fibrosis.
標題:	Medicine & Public Health.
標題:	Pneumology/Respiratory System.
標題:	Cytokines and Growth Factors.
ISBN:	9784431555827
ISBN:	9784431555810
摘要、提要註:	From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF) A subtype of Idiopathic Interstitial Pneumonias (IIP), IPF is one of the most elusive and intractable respiratory disease to date and its triggering factors remain unclear. However, new developments such as serum markers that are highly specific to IPF (i.e. KL-6, SP-A, and SP-D), the establishment of systematic diagnostic imaging (HRCT) and accumulated reports of treatment using an antifibrotic agent (pirfenidone) are slowly improving our understanding of the disease. Edited by an established authority in the field and written by experts, this book will be valuable to not only to beginning learners but also to physicians, instructors and researchers whose work involves IIPs. With each chapter exploring critical questions, with unresolved issues and future prospects, the book offers a valuable resource for understanding issues such as the newly proposed entity of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema: CPFE) and the mechanism of how so many IP sufferers develop lung cancer.
電子資源:	http://dx.doi.org/10.1007/978-4-431-55582-7

Idiopathic pulmonary fibrosis[electronic resource] :advances in diagnostic tools and disease management /
Idiopathic pulmonary fibrosisadvances in diagnostic tools and disease management /[electronic resource] :edited by Hiroyuki Nakamura, Kazutetsu Aoshiba. - Tokyo :Springer Japan :2016. - x, 259 p. :ill., digital ;24 cm.

From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF) A subtype of Idiopathic Interstitial Pneumonias (IIP), IPF is one of the most elusive and intractable respiratory disease to date and its triggering factors remain unclear. However, new developments such as serum markers that are highly specific to IPF (i.e. KL-6, SP-A, and SP-D), the establishment of systematic diagnostic imaging (HRCT) and accumulated reports of treatment using an antifibrotic agent (pirfenidone) are slowly improving our understanding of the disease. Edited by an established authority in the field and written by experts, this book will be valuable to not only to beginning learners but also to physicians, instructors and researchers whose work involves IIPs. With each chapter exploring critical questions, with unresolved issues and future prospects, the book offers a valuable resource for understanding issues such as the newly proposed entity of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema: CPFE) and the mechanism of how so many IP sufferers develop lung cancer.

ISBN: 9784431555827

Standard No.: 10.1007/978-4-431-55582-7doiSubjects--Topical Terms:

612405
Pulmonary fibrosis.

LC Class. No.: RC776.F5

Dewey Class. No.: 616.24

Idiopathic pulmonary fibrosis[electronic resource] :advances in diagnostic tools and disease management /
LDR:02168nam a2200301 a 4500 001 455232
003 DE-He213
005 20160727151452.0
006 m d
007 cr nn 008maaau
008 161227s2016 ja s 0 eng d
020 $a 9784431555827 $q (electronic bk.)
020 $a 9784431555810 $q (paper)
024 7 $a 10.1007/978-4-431-55582-7 $2 doi
035 $a 978-4-431-55582-7
040 $a GP $c GP
041 0 $a eng
050 4 $a RC776.F5
072 7 $a MJL $2 bicssc
072 7 $a MED079000 $2 bisacsh
082 0 4 $a 616.24 $2 23
090 $a RC776.F5 $b I19 2016
245 0 0 $a Idiopathic pulmonary fibrosis $h [electronic resource] : $b advances in diagnostic tools and disease management / $c edited by Hiroyuki Nakamura, Kazutetsu Aoshiba.
260 $a Tokyo : $b Springer Japan : $b Imprint: Springer, $c 2016.
300 $a x, 259 p. : $b ill., digital ; $c 24 cm.
520 $a From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF) A subtype of Idiopathic Interstitial Pneumonias (IIP), IPF is one of the most elusive and intractable respiratory disease to date and its triggering factors remain unclear. However, new developments such as serum markers that are highly specific to IPF (i.e. KL-6, SP-A, and SP-D), the establishment of systematic diagnostic imaging (HRCT) and accumulated reports of treatment using an antifibrotic agent (pirfenidone) are slowly improving our understanding of the disease. Edited by an established authority in the field and written by experts, this book will be valuable to not only to beginning learners but also to physicians, instructors and researchers whose work involves IIPs. With each chapter exploring critical questions, with unresolved issues and future prospects, the book offers a valuable resource for understanding issues such as the newly proposed entity of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema: CPFE) and the mechanism of how so many IP sufferers develop lung cancer.
650 0 $a Pulmonary fibrosis. $3 612405
650 1 4 $a Medicine & Public Health. $3 463493
650 2 4 $a Pneumology/Respiratory System. $3 464971
650 2 4 $a Cytokines and Growth Factors. $3 465271
700 1 $a Nakamura, Hiroyuki. $3 653414
700 1 $a Aoshiba, Kazutetsu. $3 653415
710 2 $a SpringerLink (Online service) $3 463450
773 0 $t Springer eBooks
856 4 0 $u http://dx.doi.org/10.1007/978-4-431-55582-7
950 $a Medicine (Springer-11650)