Search Results - "Farrell, PM"
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Longitudinal Development of Mucoid Pseudomonas aeruginosa Infection and Lung Disease Progression in Children With Cystic Fibrosis
Published in JAMA : the journal of the American Medical Association (02-02-2005)“…CONTEXT Although Pseudomonas aeruginosa is the most common virulent respiratory pathogen in cystic fibrosis (CF), the longitudinal development of P aeruginosa…”
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Respiratory Infections With Pseudomonas aeruginosa in Children With Cystic Fibrosis: Early Detection by Serology and Assessment of Risk Factors
Published in JAMA : the journal of the American Medical Association (12-06-2002)“…CONTEXT Patients with cystic fibrosis (CF) are susceptible to lower respiratory tract infections with Pseudomonas aeruginosa and typically acquire this…”
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Prenatal screening for cystic fibrosis: Where are we now?
Published in The Journal of pediatrics (01-12-2002)Get full text
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The prevalence of cystic fibrosis in the European Union
Published in Journal of cystic fibrosis (01-09-2008)“…Abstract This study combined a variety of methods to determine the prevalence of cystic fibrosis in the European Union. The results of literature reviews,…”
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Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report
Published in The Journal of pediatrics (01-08-2008)“…Newborn screening (NBS) for cystic fibrosis (CF) is increasingly being implemented and is soon likely to be in use throughout the United States, because early…”
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Cystic fibrosis: A worldwide analysis of CFTR mutations-correlation with incidence data and application to screening
Published in Human mutation (01-06-2002)“…Although there have been numerous reports from around the world of mutations in the gene of chromosome 7 known as CFTR (cystic fibrosis transmembrane…”
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ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals
Published in Journal of cystic fibrosis (01-05-2024)“…•Advantages and challenges of a dedicated patient registry for people with CFTR-RD.•The CFTR-RD risk for infants with a CRMS/CFSPID designation.•Peculiarities…”
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Refining the continuum of CFTR-associated disorders in the era of newborn screening
Published in Clinical genetics (01-05-2016)“…Clinical heterogeneity in cystic fibrosis (CF) often causes diagnostic uncertainty in infants without symptoms and in older patients with milder phenotypes. We…”
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Psychosocial Risk Associated With Newborn Screening for Cystic Fibrosis: Parents' Experience While Awaiting the Sweat-Test Appointment
Published in Pediatrics (Evanston) (01-06-2005)“…The psychosocial effects on parents of infants with abnormal results in cystic fibrosis (CF) newborn screening (NBS) that uses genetic testing remain unclear…”
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Assessing Personal Qualities in Medical School Admissions
Published in Academic medicine (01-03-2003)“…Analyzes the challenges to using academic measures (MCAT scores and GPAs) as thresholds for medical school admissions and, for applicants exceeding the…”
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Evidence on Improved Outcomes with Early Diagnosis of Cystic Fibrosis Through Neonatal Screening: Enough is Enough
Published in The Journal of pediatrics (01-09-2005)“…To generate and examine evidence in support of diagnosing cystic fibrosis (CF) early through newborn screening (NBS). Using a randomized controlled trial with…”
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Early Diagnosis of Cystic Fibrosis Through Neonatal Screening Prevents Severe Malnutrition and Improves Long-Term Growth
Published in Pediatrics (Evanston) (01-01-2001)“…Objective. Despite its relative frequency among autosomal recessive diseases and the availability of the sweat test, cystic fibrosis (CF) has been difficult to…”
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Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition
Published in Pediatric pulmonology (01-10-2001)“…Abstract only…”
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Association between Mucoid Pseudomonas Infection and Bronchiectasis in Children with Cystic Fibrosis
Published in Radiology (01-08-2009)“…To correlate the severity of bronchiectasis in children with cystic fibrosis with clinical and microbiologic variables in order to clarify risk factors for the…”
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The Survival Advantage of Patients with Cystic Fibrosis Diagnosed Through Neonatal Screening: Evidence from the United States Cystic Fibrosis Foundation Registry Data
Published in The Journal of pediatrics (01-09-2005)“…To determine the impact of age and condition at the time of diagnosis on survival of patients with cystic fibrosis (CF). By mode of diagnosis, 27,692 patients…”
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Association between Initial Disease Presentation, Lung Disease Outcomes, and Survival in Patients with Cystic Fibrosis
Published in American journal of epidemiology (15-03-2004)“…This US study was conducted to determine whether mode of diagnosis and initial disease presentation influence lung disease and survival in patients with cystic…”
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Newborn screening for cystic fibrosis: ensuring more good than harm
Published in The Journal of pediatrics (01-12-2003)Get full text
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Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing
Published in The Journal of pediatrics (01-09-2005)“…To describe the development and follow-up confirmatory results of the routine cystic fibrosis (CF) newborn screening (NBS) program in Wisconsin. CF NBS has…”
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Cognitive Function of Children With Cystic Fibrosis: Deleterious Effect of Early Malnutrition
Published in Pediatrics (Evanston) (01-06-2004)“…Patients who have cystic fibrosis (CF) and experience delayed diagnosis by traditional methods have greater nutritional insult compared with peers diagnosed…”
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Bronchopulmonary Disease in Children with Cystic Fibrosis after Early or Delayed Diagnosis
Published in American journal of respiratory and critical care medicine (01-11-2003)“…Although early diagnosis of cystic fibrosis (CF) can lead to nutritional benefits, there has been uncertainty about pulmonary outcomes. Using a randomized…”
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