Michael J Rock

Summary

Affiliation: University of Wisconsin
Country: USA

Publications

  1. ncbi 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
  2. ncbi 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
  3. ncbi Newborn screening for cystic fibrosis
    Michael J Rock
    Division of Pediatric Pulmonology, University of Wisconsin Hospital and Clinics, 600 Highland Avenue, Room K4 946, Madison, WI 53792, USA
    Clin Chest Med 28:297-305. 2007
  4. ncbi 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
  5. ncbi 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
  6. ncbi 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
  7. ncbi 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
  8. ncbi 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
  9. ncbi 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
  10. ncbi 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

Collaborators

Detail Information

Publications22

  1. ncbi 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...
  2. ncbi 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
    ....
  3. ncbi Newborn screening for cystic fibrosis
    Michael J Rock
    Division of Pediatric Pulmonology, University of Wisconsin Hospital and Clinics, 600 Highland Avenue, Room K4 946, Madison, WI 53792, USA
    Clin Chest Med 28:297-305. 2007
    ..Studies have demonstrated benefits of newborn screening in the areas of nutrition, cognitive function, pulmonary function, and survival...
  4. ncbi 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)...
  5. ncbi 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...
  6. ncbi 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...
  7. ncbi 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
    ....
  8. ncbi 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...
  9. ncbi 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
    ..Antibody titers, cough scores, and chest radiographs are early signs of nonmucoid P aeruginosa and especially mucoid P aeruginosa stages...
  10. ncbi 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...
  11. ncbi 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...
  12. ncbi 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...
  13. ncbi 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
    ....
  14. ncbi 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...
  15. ncbi 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...
  16. ncbi 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...
  17. ncbi 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...
  18. ncbi 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...
  19. ncbi 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...
  20. ncbi 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...
  21. ncbi 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 longitudinal monitoring of P aeruginosa antibody titers, in concert with WCXR score, should facilitate diagnosis and treatment of P aeruginosa pulmonary infections in young children with CF...
  22. ncbi 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