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Molecular Basis of Pulmonary Disease

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Cover of 'Molecular Basis of Pulmonary Disease'

Table of Contents

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    Book Overview
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    Chapter 1 A Clinical Approach to Rare Lung Diseases
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    Chapter 2 Clinical Trials for Rare Lung Diseases
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    Chapter 3 Idiopathic and Familial Pulmonary Arterial Hypertension
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    Chapter 4 Lymphangioleiomyomatosis
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    Chapter 5 Autoimmune Pulmonary Alveolar Proteinosis
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    Chapter 6 Mutations in Surfactant Protein C and Interstitial Lung Disease
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    Chapter 7 Hereditary Haemorrhagic Telangiectasia
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    Chapter 8 Hermansky–Pudlak Syndrome
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    Chapter 9 Alpha-1 Antitrypsin Deficiency
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    Chapter 10 The Marfan Syndrome
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    Chapter 11 Surfactant Deficiency Disorders: SP-B and ABCA3
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    Chapter 12 Pulmonary Capillary Hemangiomatosis
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    Chapter 13 Anti-glomerular Basement Disease: Goodpasture’s Syndrome
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    Chapter 14 Primary Ciliary Dyskinesia
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    Chapter 15 Pulmonary Alveolar Microlithiasis
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    Chapter 16 Cystic Fibrosis
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    Chapter 17 Pulmonary Langerhans’ Cell Histiocytosis – Advances in the Understanding of a True Dendritic Cell Lung Disease
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    Chapter 18 Sarcoidosis
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    Chapter 19 Scleroderma Lung Disease
Attention for Chapter 9: Alpha-1 Antitrypsin Deficiency
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Chapter title
Alpha-1 Antitrypsin Deficiency
Chapter number 9
Book title
Molecular Basis of Pulmonary Disease
Published by
Humana Press, January 2010
DOI 10.1007/978-1-59745-384-4_9
Book ISBNs
978-1-58829-963-5, 978-1-59745-384-4
Authors

Charlie Strange, Sabina Janciauskiene, Strange, Charlie, Janciauskiene, Sabina

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