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Molecular Basis of Pulmonary Disease

Overview of attention for book
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 19: Scleroderma Lung Disease
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Readers on

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1 Mendeley
Summary
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Chapter title
Scleroderma Lung Disease
Chapter number 19
Book title
Molecular Basis of Pulmonary Disease
Published by
Humana Press, January 2010
DOI 10.1007/978-1-59745-384-4_19
Book ISBNs
978-1-58829-963-5, 978-1-59745-384-4
Authors

Brent W. Kinder, Kinder, Brent W.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 1 Mendeley reader of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 1 100%
Readers by discipline Count As %
Unknown 1 100%

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