Jointly provided by the Johns Hopkins University School of Medicine and the Institute for Johns Hopkins Nursing.
Volume 10 supported by educational grants from Chiesi USA, Inc. and Vertex Pharmaceuticals Incorporated.
Expert insight and analysis providing information directly relevant to cystic fibrosis care, through topic-focused newsletters summarizing the peer-reviewed literature and accompanying podcasts to illustrate how to apply that information in the clinic.
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Authors:
Katie McDonald, PhD
Megan Gabel, MD
Amanda Leonard, MPH, RD, LD, CDE
Alexandra Wilson, MS, RDN, CDE
Authors:
Katie McDonald, PhD
Megan Gabel, MD
Amanda Leonard, MPH, RD, LD, CDE
Alexandra Wilson, MS, RDN, CDE
Expired
Author:
Edward McKone, MD
Expired
Author:
Edward McKone, MD
Expired
Author:
D.B. Sanders, MD, MS
Expired
Author:
D.B. Sanders, MD, MS
Expired
Author:
Jennifer Taylor-Cousar, MD, MSCS
Expired
Authors:
Jennifer Taylor-Cousar, MD, MSCS
Kamyron Jordan, MD
To read past issues, click button below.
Issue 12: CFTR Modulators: Clinical Insights
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Issue 11: Emerging Disease-Modifying Therapies in Cystic Fibrosis
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Issue 10: Screening and Diagnosis of CFRD
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Issue 9: Cystic Fibrosis-Related Diabetes: Screening and Diagnosis
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Issue 8: New Directions in CFTR Modification
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Issue 7: Genotype-Phenotype Correlation and Individualizing Therapy
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Issue 6: Nutritional Management for Individuals with CF: Practical Applications
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Issue 5: New Guidelines in Nutritional Management for Patients with CF
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Issue 4: Adherence – What You Should be Telling Your Patients
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Issue 3: Chronic Respiratory Therapies in Cystic Fibrosis: Addressing Adherence
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Issue 2: Weighing the Options in Managing Exacerbations
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Issue 1: CF Pulmonary Exacerbations: Known Unknowns?
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Issue 12: Future Landscape of CFTR Modulators
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Issue 11: CFTR Modulation: Today and Tomorrow
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Issue 10: Pseudomonas Eradication and Outcomes: Key Questions
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Issue 9: Pseudomonas aeruginosa Eradication and Outcomes: Key Questions
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Issue 8: Nutritional Issues in Cystic Fibrosis
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Issue 7: Nutritional Issues in Cystic Fibrosis
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Issue 6: Trends in Inhaled Antibiotic Therapy
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Issue 5: Trends in Inhaled Antibiotic Therapy
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Issue 4: Pulmonary Exacerbations and the Microbiology of the CF Lung
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Issue 3: Understanding the Microbiology of the CF Lung
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Issue 2: The Current State of CFTR Modification
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Issue 1: The Current State of CFTR Modifier Therapy
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Issue 14: Agents for the management of Pseudomonas aeruginosa infection
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Issue 13: Antipseudomonal agents for the management of P. aeruginosa infection
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Issue 12: Benefits of CFTR Modification Beyond FEV1 Improvement
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Issue 11: Benefits of CFTR Modification Beyond FEV1 Improvement
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Issue 10: The Effects of CFTR-modifying Therapies
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Issue 9: The Effects of CFTR-modifying Therapies
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Issue 8: Optimizing Nutrition in People with Cystic Fibrosis
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Issue 7: Optimizing Nutrition in People with Cystic Fibrosis
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Issue 6: Improving Digestive Capabilities in Nutritionally Compromised Patients with CF
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Issue 5: Improving Digestive Capabilities in Nutritionally Compromised Patients with CF
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Issue 4: P. aeruginosa eradication and reinfection
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Issue 3: P. aeruginosa eradication and reinfection
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Issue 2: Pulmonary exacerbations: diagnoses, and therapeutic regimens
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Issue 1: Pulmonary exacerbations: diagnoses, and therapeutic regimens
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Issue 12: Featured Cases: What Does CFTR Tell Us About Lung Disease?
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Issue 11: What Does CFTR Tell Us About Lung Disease?
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Issue 10: Featured Cases: Behavioral treatment to improve dietary adherence and weight gain in children with cystic fibrosis
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Issue 9: Behavioral Treatment to Improve Dietary Adherence and Weight Gain in Children with Cystic Fibrosis
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Issue 8: Featured Cases: New Therapies in Cystic Fibrosis Directed Toward the Basic Defect
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Issue 7: New Therapies in Cystic Fibrosis Directed Toward the Basic Defect
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Issue 6: Featured Cases: Modifiers of CF Lung Disease
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Issue 5: P. aeruginosa Eradication
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Issue 4: Featured Cases: Strategies for the Improvement of Nutrition Outcomes
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Issue 3: Strategies for the Improvement of Nutrition Outcomes
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Issue 2: Featured Cases: Adherence to Chronic Inhaled Therapies
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Issue 1: Adherence to Chronic Inhaled Therapies
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Issue 12: Featured Cases: Emerging Pathogens in Cystic Fibrosis
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Issue 11: Emerging Pathogens in Cystic Fibrosis
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Issue 10: Featured Cases: Interventions to Improve Nutrition in Patients with CF
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Issue 9: Interventions to Improve Nutrition in Patients With Cystic Fibrosis
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Issue 8: Featured Cases: The Role of Exercise and Physical Activity in Optimizing Outcomes Among Patients with CF
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Issue 7: The Role of Exercise and Physical Activity in Optimizing Outcomes Among Patients With Cystic Fibrosis
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Issue 6: Featured Cases: Modifiers of CF Lung Disease
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Issue 5: Modifiers of Cystic Fibrosis Disease
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Issue 4: Featured Cases: Pulmonary Exacerbation Therapies
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Issue 3: Pulmonary Exacerbation Therapies
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Issue 2: Special Edition: Highlights of the 34th European Cystic Fibrosis Conference
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Issue 1: Special Edition: Highlights of the 34th European Cystic Fibrosis Conference
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Issue 12: Featured Cases: New Inhalation Therapies
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Issue 11: New Inhalation Therapies
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Issue 10: Featured Cases: State-of-the-Art Treatment for CF Lung Disease
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Issue 9: Guidelines: State-of-the-Art Treatment for CF Lung Disease
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Issue 8: Featured Cases: Vitamin D and Bone Health
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Issue 7: Vitamin D and Bone Health
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Issue 6: Featured Cases: Nutritional Challenges and Complications in Patients with Cystic Fibrosis
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Issue 5: Newborn Encephalopathy
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Issue 4: Featured Cases: Allergic Bronchopulmonary Aspergillosis (ABPA)
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Issue 3: Allergic Bronchopulmonary Aspergillosis (ABPA)
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Issue 2: Featured Cases: Cystic Fibrosis–Related Diabetes
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Issue 1: Cystic Fibrosis–Related Diabetes
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Issue 6: Optimizing Nutritional Status in Cystic Fibrosis
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Issue 5: Measurement of Early Lung Disease in Children With Cystic Fibrosis
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Issue 4: Emerging Pathogens in Cystic Fibrosis
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Issue 3: How to Interpret Genetic Tests for Cystic Fibrosis
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Issue 2: Issues in Lung Transplantation for Cystic Fibrosis
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Issue 1: Issues Related to Newborn Screening
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