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Diagnostic Sweat Testing: The Cystic Fibrosis Foundation Guidelines

The Journal of pediatrics, 2007-07, Vol.151 (1), p.85-89

2007

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Genetic Modifiers of Lung Disease in Cystic Fibrosis

The New England journal of medicine, 2005-10, Vol.353 (14), p.1443-1453

2005

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Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

The Journal of clinical investigation, 2002-02, Vol.109 (3), p.317-325

2002

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Massive Hemoptysis in Cystic Fibrosis

Chest, 2005-08, Vol.128 (2), p.729-738

2005

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Classifying Severity of Cystic Fibrosis Lung Disease Using Longitudinal Pulmonary Function Data

American journal of respiratory and critical care medicine, 2006-10, Vol.174 (7), p.780-786

2006

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An Official American Thoracic Society Clinical Policy Statement : Palliative Care for Patients with Respiratory Diseases and Critical Illnesses

American journal of respiratory and critical care medicine, 2008-04, Vol.177 (8), p.912-927

2008

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Localization of Burkholderia cepacia complex bacteria in cystic fibrosis lungs and interactions with Pseudomonas aeruginosa in hypoxic mucus

Infection and immunity, 2014-11, Vol.82 (11), p.4729-4745

2014

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Outcomes of intensive care unit care in adults with cystic fibrosis

American journal of respiratory and critical care medicine, 2001-02, Vol.163 (2), p.335-338

2001

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Cystic fibrosis adult care: Consensus conference report

Chest, 2004-01, Vol.125 (1), p.1S-39S

2004

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Abnormal glutathione transport in cystic fibrosis airway epithelia

American journal of physiology. Lung cellular and molecular physiology, 1999-07, Vol.277 (1), p.113-L118

1999

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New concepts in palliative care in the intensive care unit

Revista Brasileira de terapia intensiva, 2017-04, Vol.29 (2), p.222-230

2017

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Role of Mutant CFTR in Hypersusceptibility of Cystic Fibrosis Patients to Lung Infections

Science (American Association for the Advancement of Science), 1996-01, Vol.271 (5245), p.64-67

1996

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Well-differentiated human airway epithelial cell cultures

Methods in molecular medicine, 2005, Vol.107, p.183

2005

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Submucosal glands are the predominant site of CFTR expression in the human bronchus

Nature genetics, 1992-11, Vol.2 (3), p.240-248

1992

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Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans

Nature (London), 1994-10, Vol.371 (6500), p.802-806

1994

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Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

The Journal of clinical investigation, 2002-02, Vol.109 (3), p.317-325

2002

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MUC5B and MUC7 Are Differentially Expressed in Mucous and Serous Cells of Submucosal Glands in Human Bronchial Airways

American journal of respiratory cell and molecular biology, 1998-07, Vol.19 (1), p.30-37

1998

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Effects of lung transplantation on inpatient end of life care in cystic fibrosis

Journal of cystic fibrosis, 2007-11, Vol.6 (6), p.396-402

2007

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Restoration of the cystic fibrosis transmembrane conductance regulator function by splicing modulation

EMBO reports, 2004-11, Vol.5 (11), p.1071-1077

2004

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Burkholderia gladioli : Five year experience in a cystic fibrosis and lung transplantation center

Journal of cystic fibrosis, 2007-07, Vol.6 (4), p.267-273

2007

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Factor viia for alveolar hemorrhage in microscopic polyangiitis

American journal of respiratory and critical care medicine, 2002-11, Vol.166 (9), p.1291-1292

2002

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Relationship of a Non-Cystic Fibrosis Transmembrane Conductance Regulator- Mediated Chloride Conductance to Organ-Level Disease in Cftr(-/-) Mice

Proceedings of the National Academy of Sciences - PNAS, 1994-01, Vol.91 (2), p.479-483

1994

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Bronchial artery embolization for the treatment of hemoptysis in patients with cystic fibrosis

American journal of respiratory and critical care medicine, 1998-06, Vol.157 (6), p.1951-1958

1998

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Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1-deleted adenoviruses

Nature genetics, 1993-05, Vol.4 (1), p.27-34

1993

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Progenitor cells of the adult human airway involved in submucosal gland development

Development (Cambridge), 1995-07, Vol.121 (7), p.2031-2046

1995

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Male
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Respiratory System
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Adult
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Cystic Fibrosis - Metabolism
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Adolescent
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Animals
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Bronchi - Metabolism
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Epithelial Cells
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Liver. Biliary Tract. Portal Circulation. Exocrine Pancreas
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Diagnostic Sweat Testing: The Cystic Fibrosis Foundation Guidelines

Genetic Modifiers of Lung Disease in Cystic Fibrosis

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

Massive Hemoptysis in Cystic Fibrosis

Classifying Severity of Cystic Fibrosis Lung Disease Using Longitudinal Pulmonary Function Data

An Official American Thoracic Society Clinical Policy Statement : Palliative Care for Patients with Respiratory Diseases and Critical Illnesses

Localization of Burkholderia cepacia complex bacteria in cystic fibrosis lungs and interactions with Pseudomonas aeruginosa in hypoxic mucus

Outcomes of intensive care unit care in adults with cystic fibrosis

Cystic fibrosis adult care: Consensus conference report

Abnormal glutathione transport in cystic fibrosis airway epithelia

New concepts in palliative care in the intensive care unit

Role of Mutant CFTR in Hypersusceptibility of Cystic Fibrosis Patients to Lung Infections

Well-differentiated human airway epithelial cell cultures

Submucosal glands are the predominant site of CFTR expression in the human bronchus

Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

MUC5B and MUC7 Are Differentially Expressed in Mucous and Serous Cells of Submucosal Glands in Human Bronchial Airways

Effects of lung transplantation on inpatient end of life care in cystic fibrosis

Restoration of the cystic fibrosis transmembrane conductance regulator function by splicing modulation

Burkholderia gladioli : Five year experience in a cystic fibrosis and lung transplantation center

Factor viia for alveolar hemorrhage in microscopic polyangiitis

Relationship of a Non-Cystic Fibrosis Transmembrane Conductance Regulator- Mediated Chloride Conductance to Organ-Level Disease in Cftr(-/-) Mice

Bronchial artery embolization for the treatment of hemoptysis in patients with cystic fibrosis

Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1-deleted adenoviruses

Progenitor cells of the adult human airway involved in submucosal gland development

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