Philip M Farrell

Summary

Affiliation: University of Wisconsin
Country: USA

Publications

  1. doi request reprint The prevalence of cystic fibrosis in the European Union
    Philip M Farrell
    The School of Medicine and Public Health, University of Wisconsin Madison, 610 Walnut Street, 785 WARF, Madison, WI 53726 2397, United States
    J Cyst Fibros 7:450-3. 2008
  2. ncbi request reprint The meaning of "early" diagnosis in a new era of cystic fibrosis care
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, 610 Walnut St, Madison, WI 53726, USA
    Pediatrics 119:156-7. 2007
  3. pmc Is newborn screening for cystic fibrosis a basic human right?
    Philip M Farrell
    The School of Medicine and Public Health, University of Wisconsin Madison, 610 Walnut Street, 785 WARF, Madison, WI 53726 2397, USA
    J Cyst Fibros 7:262-5. 2008
  4. ncbi request reprint Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing
    Michael J Rock
    Department of Pediatrics and State Laboratory of Hygiene, University of Wisconsin, Madison, Wisconsin 53792, USA
    J Pediatr 147:S73-7. 2005
  5. ncbi request reprint Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: enough is enough!
    Philip M Farrell
    Department of Pediatrics, Biostatistics Medical Informatics, Radiology, Nutritional Sciences, and the State Laboratory of Hygiene, University of Wisconsin, Madison, WI 53706 1532, USA
    J Pediatr 147:S30-6. 2005
  6. ncbi request reprint Quality of life of children with cystic fibrosis
    Rebecca L Koscik
    Department of Biostatistics and Medical Informatics, Madison, WI 53792, USA
    J Pediatr 147:S64-8. 2005
  7. pmc Regional differences in the evolution of lung disease in children with cystic fibrosis
    Zhanhai Li
    Department of Pediatrics, University of Wisconsin Madison, Madison, Wisconsin 53792 9988, USA
    Pediatr Pulmonol 47:635-40. 2012
  8. ncbi request reprint Preventing early, prolonged vitamin E deficiency: an opportunity for better cognitive outcomes via early diagnosis through neonatal screening
    Rebecca L Koscik
    Department of Biostatistics Medical Informatics, Nutritional Sciences, and Pediatrics, University of Wisconsin, Madison, WI 53792, USA
    J Pediatr 147:S51-6. 2005
  9. pmc A decision-tree approach to cost comparison of newborn screening strategies for cystic fibrosis
    Janelle Wells
    Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA
    Pediatrics 129:e339-47. 2012
  10. ncbi request reprint Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis
    Zhanhai Li
    Department of Pediatrics, University of Wisconsin, Madison 53705 2221, USA
    JAMA 293:581-8. 2005

Collaborators

Detail Information

Publications64

  1. doi request reprint The prevalence of cystic fibrosis in the European Union
    Philip M Farrell
    The School of Medicine and Public Health, University of Wisconsin Madison, 610 Walnut Street, 785 WARF, Madison, WI 53726 2397, United States
    J Cyst Fibros 7:450-3. 2008
    ..737/10,000 in the 27 EU countries, which is similar to the value of 0.797 in the United States, and only one outlier, namely the Republic of Ireland at 2.98...
  2. ncbi request reprint The meaning of "early" diagnosis in a new era of cystic fibrosis care
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, 610 Walnut St, Madison, WI 53726, USA
    Pediatrics 119:156-7. 2007
  3. pmc Is newborn screening for cystic fibrosis a basic human right?
    Philip M Farrell
    The School of Medicine and Public Health, University of Wisconsin Madison, 610 Walnut Street, 785 WARF, Madison, WI 53726 2397, USA
    J Cyst Fibros 7:262-5. 2008
    ..However, if more harm than good is likely, or if regional "readiness" does not exist, newborn screening should be deferred...
  4. ncbi request reprint Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing
    Michael J Rock
    Department of Pediatrics and State Laboratory of Hygiene, University of Wisconsin, Madison, Wisconsin 53792, USA
    J Pediatr 147:S73-7. 2005
    ..To describe the development and follow-up confirmatory results of the routine cystic fibrosis (CF) newborn screening (NBS) program in Wisconsin...
  5. ncbi request reprint Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: enough is enough!
    Philip M Farrell
    Department of Pediatrics, Biostatistics Medical Informatics, Radiology, Nutritional Sciences, and the State Laboratory of Hygiene, University of Wisconsin, Madison, WI 53706 1532, USA
    J Pediatr 147:S30-6. 2005
    ..To generate and examine evidence in support of diagnosing cystic fibrosis (CF) early through newborn screening (NBS)...
  6. ncbi request reprint Quality of life of children with cystic fibrosis
    Rebecca L Koscik
    Department of Biostatistics and Medical Informatics, Madison, WI 53792, USA
    J Pediatr 147:S64-8. 2005
    ....
  7. pmc Regional differences in the evolution of lung disease in children with cystic fibrosis
    Zhanhai Li
    Department of Pediatrics, University of Wisconsin Madison, Madison, Wisconsin 53792 9988, USA
    Pediatr Pulmonol 47:635-40. 2012
    ..A variety of potential explanations such as aspiration episodes may be clinically relevant and provide insights regarding therapies...
  8. ncbi request reprint Preventing early, prolonged vitamin E deficiency: an opportunity for better cognitive outcomes via early diagnosis through neonatal screening
    Rebecca L Koscik
    Department of Biostatistics Medical Informatics, Nutritional Sciences, and Pediatrics, University of Wisconsin, Madison, WI 53792, USA
    J Pediatr 147:S51-6. 2005
    ..To evaluate whether early diagnosis of cystic fibrosis (CF) through newborn screening (NBS) and early vitamin E status are associated with cognitive function...
  9. pmc A decision-tree approach to cost comparison of newborn screening strategies for cystic fibrosis
    Janelle Wells
    Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA
    Pediatrics 129:e339-47. 2012
    ..We therefore investigated the costs and consequences or specific outcomes of the 2 most commonly used methods...
  10. ncbi request reprint Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis
    Zhanhai Li
    Department of Pediatrics, University of Wisconsin, Madison 53705 2221, USA
    JAMA 293:581-8. 2005
    ....
  11. ncbi request reprint Newborn screening for cystic fibrosis: parents' preferences regarding counseling at the time of infants' sweat test
    Audrey Tluczek
    School of Nursing, University of Wisconsin Madison, 600 Highland Ave, Madison, Wisconsin 53792, USA
    J Genet Couns 15:277-91. 2006
    ..Counseling that matched parents preferences reduced parents' distress while mismatched counseling tended to increase parents' worry about their infant...
  12. ncbi request reprint Bronchopulmonary disease in children with cystic fibrosis after early or delayed diagnosis
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin Medical School, Madison, WI 53706 1532, USA
    Am J Respir Crit Care Med 168:1100-8. 2003
    ..Although CF neonatal screening provides a potential opportunity for better pulmonary outcomes, it appears that respiratory infections and pancreatic status are the dominant factors in pulmonary prognosis...
  13. pmc Relationships among health-related quality of life, pulmonary health, and newborn screening for cystic fibrosis
    Audrey Tluczek
    School of Nursing, University of Wisconsin, Madison, WI 53792, USA
    Chest 140:170-7. 2011
    ..The objective of this study was to examine relationships between pulmonary health and health-related quality of life (HRQOL) in patients with cystic fibrosis (CF) evaluated longitudinally in the Wisconsin Newborn Screening Project...
  14. ncbi request reprint Cystic fibrosis mutations and genotype-pulmonary phenotype analysis
    Andrew T Braun
    Department of Pediatrics and Biostatistics Medical Informatics, University of Wisconsin, Madison, WI 53705 2221, USA
    J Cyst Fibros 5:33-41. 2006
    ..Although there are more than 1000 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, most of them are uncommon and only limited information exists regarding genotype-pulmonary phenotype relationships...
  15. ncbi request reprint The survival advantage of patients with cystic fibrosis diagnosed through neonatal screening: evidence from the United States Cystic Fibrosis Foundation registry data
    HuiChuan J Lai
    Department of Nutritional Sciences, University of Wisconsin Madison, WI 53706 1562, USA
    J Pediatr 147:S57-63. 2005
    ..To determine the impact of age and condition at the time of diagnosis on survival of patients with cystic fibrosis (CF)...
  16. pmc Pulmonary outcome differences in U.S. and French cystic fibrosis cohorts diagnosed through newborn screening
    Aimee C Walsh
    School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin, USA
    J Cyst Fibros 9:44-50. 2010
    ....
  17. pmc Growth and pulmonary outcomes during the first 2 y of life of breastfed and formula-fed infants diagnosed with cystic fibrosis through the Wisconsin Routine Newborn Screening Program
    Sarah A Jadin
    Department of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin, Madison, WI 53706, USA
    Am J Clin Nutr 93:1038-47. 2011
    ..The optimal feeding (breast milk, formula, or a combination) for infants with cystic fibrosis (CF) is unknown. Recommendations from the CF Foundation are based on limited data...
  18. ncbi request reprint Longitudinal pulmonary status of cystic fibrosis children with meconium ileus
    Zhanhai Li
    Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, USA
    Pediatr Pulmonol 38:277-84. 2004
    ..In conclusion, MI children have worse lung function and more obstructive lung disease than those without MI. Such abnormalities are accompanied by reduced lung volume. MI is a distinct CF phenotype with more severe pulmonary dysfunction...
  19. pmc The sensitivity of lung disease surrogates in detecting chest CT abnormalities in children with cystic fibrosis
    Don B Sanders
    Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA
    Pediatr Pulmonol 47:567-73. 2012
    ..Quantitative chest radiography scores are useful in detecting mild lung disease, but whether they are sensitive to the presence of CT scan abnormalities has not been evaluated...
  20. pmc Comparing age of cystic fibrosis diagnosis and treatment initiation after newborn screening with two common strategies
    Don B Sanders
    Department of Pediatrics, University of Wisconsin, Madison, WI, United States
    J Cyst Fibros 11:150-3. 2012
    ..Newborn screening (NBS) for CF has become widespread, although there are multiple strategies. Little is known about outcomes such as age of diagnosis after different NBS methods...
  21. ncbi request reprint Assessing the cost of cystic fibrosis diagnosis and treatment
    Marjorie A Rosenberg
    University of Wisconsin, Madison, Wisconsin 53705 2221, USA
    J Pediatr 147:S101-5. 2005
    ..To extend previous evaluations of costs of cystic fibrosis (CF) diagnosis and examine key issues in assessing the CF cost of care...
  22. pmc Association between mucoid Pseudomonas infection and bronchiectasis in children with cystic fibrosis
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin, Madison, Wis, USA
    Radiology 252:534-43. 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 development of irreversible lung disease...
  23. doi request reprint Factors accounting for a missed diagnosis of cystic fibrosis after newborn screening
    Michael J Rock
    School of Medicine and Public Health, University of Wisconsin Madison, Madison, Wisconsin 53792, USA
    Pediatr Pulmonol 46:1166-74. 2011
    ....
  24. ncbi request reprint Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment
    Audrey Tluczek
    Department of Psychiatry, University of Wisconsin, 6001 Research Park Blvd, Madison, WI 53719 1179, USA
    Pediatrics 115:1692-703. 2005
    ..The psychosocial effects on parents of infants with abnormal results in cystic fibrosis (CF) newborn screening (NBS) that uses genetic testing remain unclear...
  25. pmc Chest computed tomography scores of severity are associated with future lung disease progression in children with cystic fibrosis
    Don B Sanders
    Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA
    Am J Respir Crit Care Med 184:816-21. 2011
    ..Chest computed tomography (CT) scans have been shown to be more sensitive to changes in lung disease than spirometry and may provide a means for predicting future lung disease progression...
  26. pmc Optimal DNA tier for the IRT/DNA algorithm determined by CFTR mutation results over 14 years of newborn screening
    Mei W Baker
    School of Medicine and Public Health, Newborn Screening Laboratory, Wisconsin State Laboratory of Hygiene, University of Wisconsin Madison, Madison, WI 53706, USA
    J Cyst Fibros 10:278-81. 2011
    ..There has been great variation and uncertainty about how many and what CFTR mutations to include in cystic fibrosis (CF) newborn screening algorithms, and very little research on this topic using large populations of newborns...
  27. pmc Health-related quality of life in children and adolescents with cystic fibrosis: convergent validity with parent-reports and objective measures of pulmonary health
    Audrey Tluczek
    University of Wisconsin School of Nursing, Madison, WI, USA
    J Dev Behav Pediatr 34:252-61. 2013
    ..This study examined the convergent validity of health-related quality of life (HRQOL) reported by patients with cystic fibrosis compared with their parents' reports and objective pulmonary measures across 3 time points...
  28. pmc Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report
    Philip M Farrell
    Department of Pediatrics and Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA
    J Pediatr 153:S4-S14. 2008
    ..Their recommendations, presented herein, involve a combination of clinical presentation, laboratory testing, and genetics to confirm a diagnosis of CF...
  29. doi request reprint Clarification of laboratory and clinical variables that influence cystic fibrosis newborn screening with initial analysis of immunoreactive trypsinogen
    Molly Kloosterboer
    Departments of Population Health Sciences, University of Wisconsin, Madison, WI 53726 2397, USA
    Pediatrics 123:e338-46. 2009
    ..Our objectives included clarification of various factors that influence immunoreactive trypsinogen concentrations and resolution of long-standing questions about variations in immunoreactive trypsinogen levels among newborns...
  30. ncbi request reprint Applying CFTR molecular genetics to facilitate the diagnosis of cystic fibrosis through screening
    Joseph L Bobadilla
    Department of Pediatrics, University of Wisconsin, USA
    Adv Pediatr 49:131-90. 2002
  31. ncbi request reprint Association between initial disease presentation, lung disease outcomes, and survival in patients with cystic fibrosis
    HuiChuan J Lai
    Department of Nutritional Sciences, University of Wisconsin College of Agriculture and Life Sciences, 1415 Linden Drive, Madison, WI 53706 1562, USA
    Am J Epidemiol 159:537-46. 2004
    ..aeruginosa acquisition compared with patients with presumably "mild" genotypes (class IV or V mutations in one or both alleles)...
  32. pmc Proteomic identification of OprL as a seromarker for initial diagnosis of Pseudomonas aeruginosa infection of patients with cystic fibrosis
    Aparna R Rao
    Department of Pediatrics, Medical College of Wisconsin, Milwaukee, 5322 0509, USA
    J Clin Microbiol 47:2483-8. 2009
    ..aeruginosa infections during initial infections. Detection of serum reactivity to OprL, along with proteins of the TTSS, and in conjunction with microbiology may diagnose initial P. aeruginosa infections in patients with CF...
  33. ncbi request reprint Prenatal screening for cystic fibrosis: where are we now?
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin Madison, USA
    J Pediatr 141:758-63. 2002
  34. pmc Nutritional status is associated with health-related quality of life in children with cystic fibrosis aged 9-19 years
    Suzanne M Shoff
    University of Wisconsin College of Agriculture and Life Sciences, Department of Nutritional Sciences, 1415 Linden Drive, Madison, WI 53706, USA University of Wisconsin School of Nursing, K6 346 Clinical Sciences Center, 600 Highland Ave, Madison, WI 53792, USA University of Wisconsin School of Medicine and Public Health, Department of Pediatrics, K4 922 Clinical Sciences Center, 600 Highland Ave, Madison, WI 53792, USA University of Wisconsin School of Medicine and Public Health, Departments of Pediatrics and Population Health Sciences, WARF Building, Room 756, 610 Walnut St, Madison, WI 53726, USA
    J Cyst Fibros 12:746-53. 2013
    ..The impact of improved nutritional status on health-related quality of life (HRQOL) is unknown for children with cystic fibrosis (CF)...
  35. pmc Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis
    HuiChuan J Lai
    Departments of Nutritional Sciences, University of Wisconsin, Madison, WI 53706, USA
    Pediatrics 123:714-22. 2009
    ..The present study examined the impact of this early weight recovery on subsequent growth pattern and pulmonary status at 6 years of age...
  36. doi request reprint Enhanced methods for assessment of the trace element composition of Iron Age bone
    Martin M Shafer
    State Laboratory of Hygiene, University of Wisconsin Madison, 2601 Agriculture Drive, Madison, WI 53707 7996, United States
    Sci Total Environ 401:144-61. 2008
    ..Large variations in bone core concentrations between the 80 Iron Age specimens examined were observed for all the primary trace elements and in many of the supporting elements, even after correction for major contaminant components...
  37. pmc Multiplexed genetic analysis using an expanded genetic alphabet
    Scott C Johnson
    Eragen Biosciences, Inc, Madison, WI 53717, USA
    Clin Chem 50:2019-27. 2004
    ..We describe the development and technical evaluation of a multiplex platform that may foster increased newborn genetic screening...
  38. ncbi request reprint Cystic fibrosis newborn screening: shifting the key question from "should we screen?" to "how should we screen?"
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin Medical School, Madison, WI 53706, USA
    Pediatrics 113:1811-2. 2004
  39. ncbi request reprint Delayed diagnosis of US females with cystic fibrosis
    Hui Chuan Lai
    Department of Pediatrics, University of Wisconsin School of Medicine, Madison, WI 53792 9988, USA
    Am J Epidemiol 156:165-73. 2002
    ..A delay in diagnosis of females with cystic fibrosis was discovered, suggesting either differential recognition of respiratory symptoms or a gender bias...
  40. doi request reprint Associations between academic achievement and psychosocial variables in adolescents with cystic fibrosis
    Adam J Grieve
    School of Medicine and Public Health, University of Wisconsin, Madison, USA
    J Sch Health 81:713-20. 2011
    ..This cross-sectional, correlational study examined the potential effects of CF on students' psychosocial and academic development...
  41. pmc Opportunities for quality improvement in cystic fibrosis newborn screening
    Molly K Groose
    Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, 53726, USA
    J Cyst Fibros 9:284-7. 2010
    ..Using Process Failure Modes and Effects Analysis (PFMEA), we adapted this method to determine if it could be applied to discover and rank high priority QI opportunities...
  42. ncbi request reprint Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis
    Philip M Farrell
    Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, USA
    Pediatr Pulmonol 36:230-40. 2003
    ..Our results also suggest that bronchiectasis and other radiographic evidence of chronic infection are apparent prior to airways obstruction in young CF patients...
  43. ncbi request reprint A fruitful and gratifying collaboration
    Philip M Farrell
    University of Wisconsin Medical School, Madison, USA
    WMJ 102:89-90. 2003
  44. ncbi request reprint Using the power of genetics, genomics and molecular biology to fight cancer
    Philip M Farrell
    University of Wisconsin Medical School, Madison, USA
    WMJ 102:51-2. 2003
  45. ncbi request reprint Analysis of the costs of diagnosing cystic fibrosis with a newborn screening program
    Don S Lee
    University of Wisconsin, Madison, Wisconsin, USA
    J Pediatr 142:617-23. 2003
    ..To compare the cost of diagnosing cystic fibrosis (CF) through a newborn screening program with the traditional method and to estimate the cost of CF diagnosis if a national newborn screening program is implemented...
  46. ncbi request reprint Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening
    Joseph L Bobadilla
    Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, USA
    Hum Mutat 19:575-606. 2002
    ....
  47. ncbi request reprint Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: early detection by serology and assessment of risk factors
    Susan E H West
    Department of Pathobiological Sciences and School of Veterinary Medicine, University of Wisconsin, 1300 University Ave, Madison, WI 53706, USA
    JAMA 287:2958-67. 2002
    ..The ability to diagnose CF by genetic testing at birth makes it possible to determine the temporal sequence of events that result in P aeruginosa-associated pulmonary infections...
  48. ncbi request reprint Matriculating student perceptions of changes to the admissions interview process at the University of Wisconsin Medical School: a prospective, controlled comparison
    Mark A Albanese
    Office of Medical Education Research and Development, University of Wisconsin Medical School, Madison, Wis, USA
    WMJ 102:30-3. 2003
    ..The purpose of this study was to assess whether changes in the admissions interview process improved matriculating students' perceptions of the quality of the admissions interview process...
  49. ncbi request reprint Welcoming incremental, measurable change
    Philip M Farrell
    University of Wisconsin Medical School, Madison, USA
    WMJ 103:67-8. 2004
  50. ncbi request reprint Mission aligned management and allocation: a successfully implemented model of mission-based budgeting
    Gordon T Ridley
    Administration and finance, University of Wisconsin Medical School, Madison, Wisconsin 52706 1532, USA
    Acad Med 77:124-9. 2002
    ..Finally, they discuss outcomes tracked during two years of full implementation to assess the success of the new MAMA budget process...
  51. ncbi request reprint Cognitive function of children with cystic fibrosis: deleterious effect of early malnutrition
    Rebecca L Koscik
    Department of Biostatistics Medical Informatics, University of Wisconsin, Madison 53706 1532, USA
    Pediatrics 113:1549-58. 2004
    ..The objective of this study was to evaluate cognitive function in children with CF and the influence of both early diagnosis through neonatal screening and the potential effect of early malnutrition...
  52. ncbi request reprint Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms
    Claude Ferec
    INSERM, U613 Génétique Moléculaire et Génétique Epidémiologique, Brest, France
    Eur J Hum Genet 14:567-76. 2006
    ....
  53. ncbi request reprint Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis
    Scott D Grosse
    National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Atlanta, GA 30333, USA
    J Pediatr 149:362-6. 2006
    ..To estimate the population impact of child mortality as a result of cystic fibrosis (CF) potentially preventable by newborn screening...
  54. ncbi request reprint Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report
    Anne Marie Comeau
    New England Newborn Screening Program and Department of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts, USA
    Pediatrics 119:e495-518. 2007
    ....
  55. ncbi request reprint Enhancing men's urologic health
    Philip M Farrell
    University of Wisconsin Medical School, USA
    WMJ 101:46-7. 2002
  56. ncbi request reprint Celebrating the importance of medical history
    Philip M Farrell
    University of Wisconsin Medical School, USA
    WMJ 103:76. 2004
  57. ncbi request reprint Excellent progress has been made but significant challenges remain
    Philip M Farrell
    University of Wisconsin Medical School, USA
    WMJ 103:91-2. 2004
  58. ncbi request reprint New research, perspectives required to understand impact of gender on health
    Philip M Farrell
    University of Wisconsin Medical School, USA
    WMJ 102:57-8. 2003
  59. ncbi request reprint Plan to address physician shortage requires proper support
    Philip M Farrell
    University of Wisconsin Medical School, USA
    WMJ 104:73-4. 2005
  60. ncbi request reprint Reproducibility of a scoring system for computed tomography scanning in cystic fibrosis
    Alan S Brody
    Department of Radiology, Cincinnati Children s Hospital, Cincinnati, OH 45229 3039, USA
    J Thorac Imaging 21:14-21. 2006
    ..The scoring system used to convert the CT image to numeric data is an essential determinant of the performance of CT scanning...
  61. ncbi request reprint Children with cystic fibrosis produce an immune response against exoenzyme S, a type III cytotoxin of Pseudomonas aeruginosa
    Bruce Banwart
    J Infect Dis 185:269-70. 2002
  62. ncbi request reprint Using science to improve health care delivery and patient care
    Philip M Farrell
    University of Wisconsin Medical School, UW Madison, USA
    WMJ 103:87-8. 2004
  63. ncbi request reprint Newborn screening for cystic fibrosis: ensuring more good than harm
    Michael H Farrell
    Departments of Pediatrics and Internal Medicine, Yale University Medical School, New Haven, Connecticut, USA
    J Pediatr 143:707-12. 2003
  64. ncbi request reprint Much more research needed on injury prevention
    Philip M Farrell
    WMJ 104:55-6. 2005

Research Grants27

  1. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip Farrell; Fiscal Year: 2000
    ..The state that this project will generate that important information. ..
  2. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip Farrell; Fiscal Year: 2005
    ..We will also clarify the risks of screening and delineate for the first time the costs of diagnosis and treatment of CF throughout childhood as well as the cost-effectiveness of screening. ..
  3. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip Farrell; Fiscal Year: 2007
    ..This project has the potential to impact healthcare quite significantly by promoting molecular genetics screening of all newborn infants. ..
  4. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip Farrell; Fiscal Year: 2009
    ..This project has the potential to impact healthcare quite significantly by promoting molecular genetics screening of all newborn infants. ..
  5. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip M Farrell; Fiscal Year: 2010
    ..This project has the potential to impact healthcare quite significantly by promoting molecular genetics screening of all newborn infants. ..
  6. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip Farrell; Fiscal Year: 1993
    ....
  7. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip Farrell; Fiscal Year: 1990
    ....
  8. PULMONARY BENEFITS OF CYSTIC FIBROSIS NEONATAL SCREENING
    Philip M Farrell; Fiscal Year: 2010
    ..This project has the potential to impact healthcare quite significantly by promoting molecular genetics screening of all newborn infants. ..