CFTR Modulators: Clinical Insights

Volume 7, Issue 12.

In this podcast Dr. John P. Clancy reviews CFTR modulators, and discusses insights presented at the 2017 NACFC.

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New Directions in CFTR Modification

Volume 7, Issue 8.

In this podcast Dr. George Solomon discusses new directions in CFTR modification in the context of case studies.

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Nutritional Management for Individuals with CF: Practical Applications

Volume 7, Issue 6.

Our guest author is Amanda Leonard, MPH, RD, CDE, from the Johns Hopkins Children’s Hospital in Baltimore, MD.

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Adherence – What You Should be Telling Your Patients

Volume 7, Issue 4.

Our guest author is Gregory Sawicki, MD, MPH from Boston Children’s Hospital, and Harvard Medical School in Boston, MA.

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Weighing the Options in Managing Exacerbations

Volume 7, Issue 2.

Our guest authors are Mark T. Jennings, MD, MHS and Rebecca Dezube, MD from the Johns Hopkins University School of Medicine in Baltimore, MD.

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Future Landscape of CFTR Modulators

Volume 6, Issue 12.

Claire Wainwright, FRACP, MD and Tonia Douglas, MD cover the important topic of the Future Landscape of CFTR Modulators in the format of case-study scenarios for the clinical practice.

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Pseudomonas aeruginosa Eradication and Outcomes: Key Questions

Volume 6, Issue 10.

Christopher Oermann, MD covers the important topic of the Pseudomonas Eradication in the format of case-study scenarios for the clinical practice.

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Nutritional Issues in Cystic Fibrosis

Volume 6, Issue 8.

Dr. Deepak Agrawal, MD covers the important topic of Nutritional Issues in Cystic Fibrosis in the format of case-study scenarios for the clinical practice.

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Trends in Inhaled Antibiotic Therapy

Volume 6, Issue 6.

Daniel Heintz, MD and Karen McCoy, MD cover the important topic of Trends in Inhaled Antibiotic Therapy in the format of case-study scenarios for the clinical practice.

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Agents for the management of Pseudomonas aeruginosa infection

Volume 5, Issue 14.

In this issue we are joined by Dr. Shawn Aaron of University of Ottawa in Ontario, Canada. Dr. Aaron will discuss infection in patients with optimal therapy of chronic Pseudomonas aeruginosa cystic fibrosis, describe the pathophysiology of pulmonary exacerbations associated with Pseudomonas infection in patients with cystic fibrosis, and evaluate the optimal choice of antibiotics to treat Pseudomonas-associated pulmonary exacerbations in patients with cystic fibrosis.