M. Corey

发表

Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis.

M. Corey, H. Levison, M. Knowles, 1997, The Journal of pediatrics.

Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements.

M. Corey, L. Tsui, J. Zieleński, 1998, The Journal of pediatrics.

Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa.

M. Corey, H. Levison, E. Kerem, 1990, The Journal of pediatrics.

Antibiotic prophylaxis in cystic fibrosis: inhaled cephaloridine as an adjunct to oral cloxacillin.

M. Corey, H. Levison, H Levison, 1982, The Journal of pediatrics.

Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection

M. Corey, J. Zieleński, R. Dorfman, 2011, Genes and Immunity.

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar.

M. Corey, J. Rommens, L. Heitlinger, 1999, The Journal of pediatrics.

Dietary intakes of young children with cystic fibrosis: is there a difference?

M. Corey, H. Levison, L. Bentur, 1996, Journal of pediatric gastroenterology and nutrition.

Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis.

M. Corey, P. Pencharz, P. Durie, 1985, The Journal of pediatrics.

Symposium Session Summaries: Sessions 13.4 to 18.4

J. Zieleński, P. Durie, L. Ellis, 1998 .

Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis.

A. Coates, M. Corey, L. Lands, 2005, The Journal of pediatrics.

A randomized controlled trial of a 3-year home exercise program in cystic fibrosis.

M. Corey, G. Canny, J. Reisman, 2000, The Journal of pediatrics.

Role of conventional physiotherapy in cystic fibrosis.

M. Corey, H. Levison, J. Reisman, 1988, The Journal of pediatrics.

Treatment of vitamin K deficiency in cystic fibrosis: Effectiveness of a daily fat-soluble vitamin combination.

M. Corey, P. Pencharz, E. Tullis, 2001, The Journal of pediatrics.

Immunolocalisation of Burkholderia cepacia in the lungs of cystic fibrosis patients.

M. Corey, C. Ackerley, A. Humar, 2001, Journal of medical microbiology.

Do common in silico tools predict the clinical consequences of amino‐acid substitutions in the CFTR gene?

J. Zieleński, L. Tsui, R. Dorfman, 2010, Clinical genetics.

Risk factors for Pseudomonas aeruginosa colonization in cystic fibrosis patients.

M. Corey, H. Levison, E. Kerem, 1990, The Pediatric infectious disease journal.

Prognostic Factors Associated with Patient Survival During Nutritional Rehabilitation in Malnourished Children and Adolescents with Cystic Fibrosis

M. Corey, P. Pencharz, P. Durie, 1986, Journal of pediatric gastroenterology and nutrition.

Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis.

M. Corey, R. Couper, D. Moore, 1995, The Journal of pediatrics.

Do infants with cystic fibrosis need a protein hydrolysate formula? A prospective, randomized, comparative study.

M. Corey, P. Pencharz, P. Durie, 1998, The Journal of pediatrics.