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Lung Transplantation in Cystic Fibrosis: Trends and Controversies
Joshua Blatter
,
Stuart Sweet
Institute of Clinical and Translational Sciences (ICTS)
Division of Allergy & Pulmonary Medicine
Research output
:
Contribution to journal
›
Review article
›
peer-review
7
Scopus citations
Overview
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Keyphrases
Antibody-mediated Rejection
25%
Chronic Lung Allograft Dysfunction
50%
Current Allocation
25%
Cystic Fibrosis
100%
Donor Selection
25%
End-stage Lung Disease
25%
Improved Diagnosis
25%
Long-term Survival
25%
Lung
25%
Lung Allocation
25%
Lung Transplantation
100%
Number of Patients
25%
Organ Shortage
25%
Organ Supply
25%
Pediatric
25%
Pediatric Donor
25%
Pediatric Lung Transplantation
75%
Pediatric Patients
25%
Pretransplant
25%
Recipient Selection
25%
Scarce Resources
25%
Survival Benefit
25%
Therapeutic Potential
25%
Transplant Program
25%
Medicine and Dentistry
Allograft
28%
Antibody Mediated Rejection
14%
Cystic Fibrosis
100%
Diagnosis
14%
Long Term Survival
14%
Lung
57%
Lung Transplantation
100%
Patient with Cystic Fibrosis
14%
Pediatrics
71%
Pediatrics Patient
14%
Silo-Filler's Disease
14%
Transplantation
42%