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EBSCO_ocn953695085 |
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20231017213018.0 |
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160520s2016 nyua ob 001 0 eng |
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|a 2020678497
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|a DLC
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|a 957127332
|a 987429367
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|a 9781634855488
|q (ebook)
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|a 1634855485
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|a 616.3/72
|2 23
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|a UAMI
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245 |
0 |
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|a Cystic and idiopathic pulmonary fibrosis :
|b risk factors, management and long-term health outcomes /
|c Lorenzo Robertson, editor.
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264 |
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1 |
|b New York :
|b Nova Biomedical,
|c [2016]
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|a 1 online resource
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336 |
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
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490 |
1 |
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|a Pulmonary and respiratory diseases and disorders
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|a Includes bibliographical references and index.
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505 |
0 |
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|a CYSTIC AND IDIOPATHIC PULMONARY FIBROSIS RISK FACTORS, MANAGEMENT AND LONG-TERM HEALTH OUTCOMES ; CYSTIC AND IDIOPATHIC PULMONARY FIBROSIS RISK FACTORS, MANAGEMENT AND LONG-TERM HEALTH OUTCOMES ; CONTENTS ; PREFACE; Chapter 1 CLINICAL MANIFESTATIONS OF CYSTIC FIBROSIS AND THEIR MANAGEMENT ; Abstract; List of Abbreviations; Introduction; Epidemiology; Molecular Biology; CFTR Gene; CFTR Biosynthesis; Structure of CFTR; Overview of CFTR Function; Pathophysiology; Types of Mutations; Class I Mutations; Class II Mutations; Class III Mutations; Class IV Mutations; Class V Mutations
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505 |
8 |
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|a Class VI MutationsEffect of CFTR Dysfunction on Various Tissues; Sweat Glands; Lung and Small Airways; Paranasal Sinuses; Pancreas; Intestines; Liver and Gallbladder; Reproductive Tract; Bones; Other Organ Systems; Management; Clinical Features; Differential Diagnosis; Overview of Treatment; Treatment of Pulmonary Disease; Treatment of Gastrointestinal Disease; Treatment of Endocrine Abnormalities; Other Aspects of Treatment; Novel Treatment Strategies; Outcome Measures; Pulmonary Function Testing; Imaging-Based Measures; Sputum Biomarkers; Blood-Based Biomarkers; Potential Difference
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505 |
8 |
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|a Sweat Chloride TestPrognosis and Risk Factors; Conclusion; Conflict of Interests; References; Biographical Sketch; Chapter 2 LIVER DISEASE IN CYSTIC FIBROSIS: PREVALENCE, RISK FACTORS, AND OUTCOMES ; Abstract; Introduction; Objective; Methods; Screening for Liver Disease; Physical Examination; Liver Biochemistry Studies; Echographic Examination; Hepatobiliary Scintigraphy; Analysis of Clinical and CFTR Genotype Data; Statistic Analysis; Results; Discussion; Conclusion; References; Chapter 3 LUNG TRANSPLANTATION FOR CYSTIC FIBROSIS ; Abstract; Introduction
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505 |
8 |
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|a Selection of Patients for Lung TransplantationCriteria for Referral; Contraindications; Pre-Transplant Evaluation; Listing for Transplantation; Preparation for Transplantation; Surgical Issues and Technical Considerations; Post-Transplant Management; Peri-Operative Management and Complications; Delayed Onset and Chronic Complications; Post-Transplant Surveillance; Outcomes; Conclusion; References; Chapter 4 NEW CYSTIC FIBROSIS THERAPY ; Abstract; Introduction; Evolution of CF Therapy; Nutritional Management; Clinical Trials of Ivacaftor in Patients with the Gly551Asp CFTR Mutation
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505 |
8 |
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|a Clinical Trials of Ivacaftor in Patients with CFTR Mutation Other Than G551DTargeted Therapies for Patients with Phe508del CFTR Mutation; Targeted Therapies for Patients with Class I Mutation; Gene Therapy; Conclusion; References; Biographical Sketch; Chapter 5 DISTINCT PATTERNS OF PULMONARY INJURY AND FIBROSIS INDUCED BY INTRATRACHEAL AND SUBCUTANEOUS BLEOMYCIN IN THE MOUSE: RELEVANCE FOR DISTINCT FORMS OF HUMAN LUNG FIBROSIS ; Abstract; List of Abbreviations; Introduction; Results
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590 |
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|a eBooks on EBSCOhost
|b EBSCO eBook Subscription Academic Collection - Worldwide
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650 |
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0 |
|a Cystic fibrosis.
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650 |
|
0 |
|a Pulmonary fibrosis.
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650 |
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2 |
|a Cystic Fibrosis
|x therapy
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650 |
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2 |
|a Cystic Fibrosis
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650 |
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2 |
|a Pulmonary Fibrosis
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650 |
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6 |
|a Mucoviscidose.
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650 |
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|a Fibrose pulmonaire.
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650 |
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|a HEALTH & FITNESS
|x Diseases
|x General.
|2 bisacsh
|
650 |
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7 |
|a MEDICAL
|x Clinical Medicine.
|2 bisacsh
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650 |
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7 |
|a MEDICAL
|x Diseases.
|2 bisacsh
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650 |
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|a MEDICAL
|x Evidence-Based Medicine.
|2 bisacsh
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650 |
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7 |
|a MEDICAL
|x Internal Medicine.
|2 bisacsh
|
650 |
|
7 |
|a Pulmonary fibrosis.
|2 fast
|0 (OCoLC)fst01083828
|
650 |
|
7 |
|a Cystic fibrosis.
|2 fast
|0 (OCoLC)fst00886186
|
700 |
1 |
|
|a Robertson, Lorenzo,
|e editor.
|
776 |
0 |
8 |
|i Print version:
|t Cystic and idiopathic pulmonary fibrosis.
|d New York : [2016]
|z 9781634855082
|w (DLC) 2016942393
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830 |
|
0 |
|a Pulmonary and respiratory diseases and disorders series.
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856 |
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|z Texto completo
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|a ProQuest Ebook Central
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|a EBSCOhost
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