Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide: Respiratory Medicine
Editat de Keith C. Meyer, Steven D. Nathanen Limba Engleză Hardback – 15 oct 2013
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Specificații
ISBN-13: 9781627036818
ISBN-10: 1627036814
Pagini: 468
Dimensiuni: 155 x 235 x 27 mm
Greutate: 1.02 kg
Ediția:2014
Editura: Humana Press Inc.
Colecția Humana Press
Seria Respiratory Medicine
Locul publicării:Totowa, NJ, United States
ISBN-10: 1627036814
Pagini: 468
Dimensiuni: 155 x 235 x 27 mm
Greutate: 1.02 kg
Ediția:2014
Editura: Humana Press Inc.
Colecția Humana Press
Seria Respiratory Medicine
Locul publicării:Totowa, NJ, United States
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Public țintă
Professional/practitionerCuprins
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.
Textul de pe ultima copertă
Idiopathic
Pulmonary
Fibrosis:
A
Comprehensive
Clinical
Guidedelivers
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
Guideis
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.
Caracteristici
Provides
current
knowledge
regarding
diagnosis
and
management
Each chapter contains a summary and key points
Written by an international group of expert authors
Each chapter contains a summary and key points
Written by an international group of expert authors
Recenzii
“This is likely one of the most comprehensive and complete books on idiopathic pulmonary fibrosis currently available, and it should be extremely useful to pulmonologists and researchers who are interested in the pathogenesis, diagnosis, and treatment of this fatal disease.” (Santosh Dhungana, Doody's Book Reviews, April 26, 2019)
Notă biografică
Keith C. Meyer, MD is a professor of pulmonary and critical care medicine at the University of Wisconsin School of Medicine and Public Health. He is volume editor of three successful Springer books: Idiopathic Pulmonary Fibrosis, Gastroesophageal Reflux and the Lung, and Bronchiolitis Obliterans Syndrome in Lung Transplantation.
Steven D. Nathan, MD is professor of medicine at Virginia Commonwealth University Inova Campus and director of the Lung Transplant and Advanced Lung Disease programs. He is also volume editor of Idiopathic Pulmonary Fibrosis and the upcoming Guide to Clinical Management of Idiopathic Pulmonary Fibrosis (with Springer Healthcare)
Steven D. Nathan, MD is professor of medicine at Virginia Commonwealth University Inova Campus and director of the Lung Transplant and Advanced Lung Disease programs. He is also volume editor of Idiopathic Pulmonary Fibrosis and the upcoming Guide to Clinical Management of Idiopathic Pulmonary Fibrosis (with Springer Healthcare)