Search Results - "Farrell, PM"

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    Longitudinal Development of Mucoid Pseudomonas aeruginosa Infection and Lung Disease Progression in Children With Cystic Fibrosis by Li, Zhanhai, Kosorok, Michael R, Farrell, Philip M, Laxova, Anita, West, Susan E. H, Green, Christopher G, Collins, Jannette, Rock, Michael J, Splaingard, Mark L

    “…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 by West, Susan E. H, Zeng, Lan, Lee, Bee Leng, Kosorok, Michael R, Laxova, Anita, Rock, Michael J, Splaingard, Mark J, Farrell, Philip M

    “…CONTEXT Patients with cystic fibrosis (CF) are susceptible to lower respiratory tract infections with Pseudomonas aeruginosa and typically acquire this…”
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    The prevalence of cystic fibrosis in the European Union by Farrell, Philip M

    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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    Cystic fibrosis: A worldwide analysis of CFTR mutations-correlation with incidence data and application to screening by Bobadilla, Joseph L., Macek Jr, Milan, Fine, Jason P., Farrell, Philip M.

    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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    Refining the continuum of CFTR-associated disorders in the era of newborn screening by Levy, H., Nugent, M., Schneck, K., Stachiw-Hietpas, D., Laxova, A., Lakser, O., Rock, M., Dahmer, M.K., Biller, J., Nasr, S.Z., Baker, M., McColley, S.A., Simpson, P., Farrell, P.M.

    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 by Tluczek, Audrey, Koscik, Rebecca L, Farrell, Philip M, Rock, Michael J

    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 by Albanese, Mark A, Snow, Mikel H, Skochelak, Susan E, Huggett, Kathryn N, Farrell, Philip M

    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 by Farrell, Philip M., Lai, HuiChuan J., Li, Zhanhai, Kosorok, Michael R., Laxova, Anita, Green, Christopher G., Collins, Jannette, Hoffman, Gary, Laessig, Ronald, Rock, Michael J., Splaingard, Mark L.

    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 by Farrell, Philip M, Kosorok, Michael R, Rock, Michael J, Laxova, Anita, Zeng, Lan, Lai, Hui-Chuan, Hoffman, Gary, Laessig, Ronald H, Splaingard, Mark L, Wisconsin Cystic Fibrosis Neonatal Screening Study Group

    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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    Association between Mucoid Pseudomonas Infection and Bronchiectasis in Children with Cystic Fibrosis by FARRELL, Philip M, COLLINS, Jannette, BRODERICK, Lynn S, ROCK, Michael J, ZHANHAI LI, KOSOROK, Michael R, LAXOVA, Anita, GERSHAN, William M, BRODY, Alan S

    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 by Lai, HuiChuan J., Cheng, Yu, Farrell, Philip M.

    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 by Lai, HuiChuan J., Cheng, Yu, Cho, Hyungjun, Kosorok, Michael R., Farrell, Philip M.

    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 in Wisconsin: nine-year experience with routine trypsinogen/DNA testing by Rock, Michael J., Hoffman, Gary, Laessig, Ronald H., Kopish, Greg J., Litsheim, Thomas J., Farrell, Philip M.

    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 by Koscik, Rebecca L, Farrell, Philip M, Kosorok, Michael R, Zaremba, Kathleen M, Laxova, Anita, Lai, Hui-Chuan, Douglas, Jeff A, Rock, Michael J, Splaingard, Mark L

    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 by Farrell, Philip M, Li, Zhanhai, Kosorok, Michael R, Laxova, Anita, Green, Christopher G, Collins, Jannette, Lai, Hui-Chuan, Rock, Michael J, Splaingard, Mark L

    “…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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