Results 311 to 320 of about 935,642 (332)
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The Cystic Fibrosis Foundation
, 2017Scientific): No more than 250 words (up to 2,000 characters max, including spaces) Hypothesis and Specific Aims. State concisely and realistically the intent of the proposed research and the hypothesis to be tested.
Ben Birkman
semanticscholar +1 more source
Primary Care: Clinics in Office Practice, 1977
Cystic fibrosis has been regarded as a disease of infants. Yet, with improved management, a high percentage of patients how survive into young adulthood. In addition, mild cases may not be detected until long after infance. The older patient often has minimal symptoms, and the majority are socially active and productive.
openaire +2 more sources
Cystic fibrosis has been regarded as a disease of infants. Yet, with improved management, a high percentage of patients how survive into young adulthood. In addition, mild cases may not be detected until long after infance. The older patient often has minimal symptoms, and the majority are socially active and productive.
openaire +2 more sources
Annals of the American Thoracic Society, 2016
RATIONALE The Cystic Fibrosis Foundation Patient Registry (CFFPR) is an ongoing patient registry study that collects longitudinal demographic, clinical, and treatment information about persons with cystic fibrosis (CF) in the United States.
Emily A. Knapp +8 more
semanticscholar +1 more source
RATIONALE The Cystic Fibrosis Foundation Patient Registry (CFFPR) is an ongoing patient registry study that collects longitudinal demographic, clinical, and treatment information about persons with cystic fibrosis (CF) in the United States.
Emily A. Knapp +8 more
semanticscholar +1 more source
Pseudomonas aeruginosa adaptation and evolution in patients with cystic fibrosis
Nature Reviews Microbiology, 2020E. Rossi +7 more
semanticscholar +1 more source
Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR
Yearbook of Pulmonary Disease, 2016S. Willsie
semanticscholar +1 more source