M. Corey

M. Corey, P. Durie, K. Gaskin, 2006, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Increased vitamin A and E levels in adult cystic fibrosis patients after lung transplantation.

M. Corey, E. Tullis, P. Durie, 2005, Transplantation.

Infant feeding practices and ulcerative colitis in childhood.

M. Corey, A. Griffiths, S. Koletzko, 1991, BMJ.

Role of infant feeding practices in development of Crohn's disease in childhood.

M. Corey, A. Griffiths, S. Koletzko, 1989, BMJ.

Supplementary enteral nutrition maintains remission in paediatric Crohn's disease.

M. Corey, A. Griffiths, P. Pencharz, 1996, Gut.

Diabetes mellitus in patients with cystic fibrosis: effect on survival.

M. Corey, H. Levison, G. Canny, 1990, Pediatrics.

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.

Effect of cimetidine and sodium bicarbonate on pancreatic replacement therapy in cystic fibrosis.

M. Corey, P. Durie, G. Forstner, 1980, Gut.

Bias in CFTR screening panels

M. Corey, J. Rommens, G. Cutting, 2015, Genetics in Medicine.

Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis

P. Paré, M. Corey, J. Zieleński, 2011, Pediatric pulmonology.

Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis

M. Corey, J. Rommens, G. Cutting, 2019, American journal of respiratory and critical care medicine.

Hypoalbuminemia at initial examination in patients with cystic fibrosis.

M. Corey, H. Levison, D. Stringer, 1989, The Journal of pediatrics.

Amiloride‐insensitive nasal potential difference varies with the menstrual cycle in cystic fibrosis

M. Corey, H. O'brodovich, D. E. Tullis, 2007, Pediatric pulmonology.

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

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

Realities of expectorated sputum collection in the pediatric cystic fibrosis clinic.

M. Corey, S. Dell, D. Radhakrishnan, 2007, Archives of pediatrics & adolescent medicine.

Growth Assessment in Infants and Toddlers Using Three Different Reference Charts

M. Corey, D. O’Connor, Kelly L. Sherwood, 2005, Journal of pediatric gastroenterology and nutrition.

Correlating CFTR Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis

M. Corey, J. Rommens, G. Cutting, 2019 .

Further insights into early acquisition of Pseudomonas aeruginosa

M. Corey, L. Saiman, Mary Corey, 1998, Pediatric pulmonology.

Risk factors for Pseudomonas aeruginosa colonization in cystic fibrosis patients.

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

Serum immunoreactive pancreatic lipase and cationic trypsinogen for the assessment of exocrine pancreatic function in older patients with cystic fibrosis.

M. Corey, F. Dati, G. Cleghorn, 1986, Pediatrics.

Determinants of mortality from cystic fibrosis in Canada, 1970-1989.

M. Corey, V. Farewell, M Corey, 1996, American journal of epidemiology.

Interactions with Home and Health Environments Discourage Physical Activity: Reports from Children with Complex Congenital Heart Disease and Their Parents

M. Corey, B. McCrindle, P. Longmuir, 2021, International journal of environmental research and public health.

European Cystic Fibrosis Society Standards of Care: Quality Management in cystic fibrosis.

Laura Viviani, Mary Corey, M. Corey, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Prediction of mortality in patients with cystic fibrosis.

M. Corey, H. Levison, E. Kerem, 1992, The New England journal of medicine.

Allergic bronchopulmonary aspergillosis in cystic fibrosis: a secretory immune response to a colonizing organism.

M. Corey, H. Levison, B. Zimmerman, 1988, Annals of allergy.

Genetic modifiers of lung disease in cystic fibrosis.

Michael R Knowles, Fei Zou, Fred A Wright, 2005, The New England journal of medicine.

Otolaryngological and Rhinomanometric Findings in Cystic Fibrosis

M. Corey, H. Levison, P. Cole, 1991 .

Survival estimates in cystic fibrosis: Snapshots of a moving target

M. Corey, 1996, Pediatric pulmonology.

Fecal clearance of α1-antitrypsin: A reliable measure of enteric protein loss in children

M. Corey, J. Hamilton, R. Hill, 1981 .

CFTR gene variant for patients with congenital absence of vas deferens.

M. Corey, L. Tsui, J. Zieleński, 1995, American journal of human genetics.

The risk of cancer among patients with cystic fibrosis. Cystic Fibrosis and Cancer Study Group.

M. Corey, J. Neglia, P. Maisonneuve, 1995, The New England journal of medicine.

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.

M. Corey, J. Zieleński, H. Levison, 1995, The Journal of pediatrics.

Pseudomonas cepacia infection in cystic fibrosis: an emerging problem.

M. Corey, H. Levison, C. Prober, 1984, The Journal of pediatrics.

Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas.

M. Corey, P. Durie, K. Gaskin, 1988, Gastroenterology.

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

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

A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotype.

M. Corey, B. Kerem, M. Nissim-Rafinia, 1997, Pediatrics.

Long-term docosahexaenoic acid therapy in a congenic murine model of cystic fibrosis.

M. Corey, C. Ackerley, R. Yantiss, 2007, American journal of physiology. Gastrointestinal and liver physiology.

Reference percentiles of FEV1 for the Canadian cystic fibrosis population: comparisons across time and countries

M. Corey, L. Strug, A. Stephenson, 2018, Thorax.

A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis Genetic modifier studies

M. Corey, J. Zieleński, M. Drumm, 2011, Pediatric pulmonology.

Primary sclerosing cholangitis in 32 children: Clinical, laboratory, and radiographic features, with survival analysis

M. Corey, A. Griffiths, L. Blendis, 1995, Hepatology.

Growing Older with Cystic Fibrosis: Psychologic Adjustment of Patients More Than 16 Years Old

M. Corey, H. Levison, J. Robertson, 1984, Psychosomatic medicine.

High-dose ibuprofen in cystic fibrosis: Canadian safety and effectiveness trial.

M. Corey, D. Manson, L. Lands, 2007, The Journal of pediatrics.

Exclusion of linkage of Shwachman-Diamond syndrome to chromosome regions 6q and 12q implicated by a de novo translocation.

M. Corey, J. Rommens, M. Masuno, 1999, American journal of medical genetics.

Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption.

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

Pseudomonas species contamination of cystic fibrosis patients' home inhalation equipment.

M. Corey, H. Levison, R. Bannatyne, 1987, Jornal de Pediatria.

An evaluation of incentive spirometry in the management of pulmonary complications after cardiac surgery in a pediatric population

M. Corey, H. Levison, J. Edmonds, 1982, Critical care medicine.

Immunoassay of serum conjugates of cholic acid in cystic fibrosis.

M. Corey, J. Sondheimer, G. Davidson, 1980, Journal of clinical pathology.

The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis

M. Corey, L. Tsui, J. Zieleński, 2005, Human Genetics.

Home-Based Rehabilitation Enhances Daily Physical Activity and Motor Skill in Children Who Have Undergone the Fontan Procedure

M. Corey, B. McCrindle, G. Faulkner, 2013, Pediatric Cardiology.

Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome.

M. Corey, J. Rommens, P. Durie, 2002, The Journal of pediatrics.

The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants

M. Corey, L. Tsui, J. Zieleński, 2005, Archives of Disease in Childhood.

Fecal clearance of alpha 1-antitrypsin: a reliable measure of enteric protein loss in children.

M. Corey, J. Hamilton, D. Gilday, 1981, Jornal de Pediatria.

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

M. Corey, X. Estivill, L. Tsui, 1999, Nature Genetics.

Pattern of growth of very low birth weight preterm infants, assessed using the WHO Growth Standards, is associated with neurodevelopment.

M. Corey, E. Asztalos, D. O’Connor, 2011, Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme.

Thallium myocardial perfusion scans for the assessment of right ventricular hypertrophy in patients with cystic fibrosis. A comparison with other noninvasive techniques.

M. Corey, C. Newth, I. Mitchell, 1981, The American review of respiratory disease.

Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2

Fred A. Wright, Fei Zou, Clayton W. Commander, 2011, Nature Genetics.

Factors influencing postoperative recurrence of Crohn's disease in childhood.

M. Corey, A. Griffiths, D. Wesson, 1991, Gut.

Supplementary enterai nutrition maintains remission in paediatric Crohn's disease

M. Corey, A. Griffiths, P. Pencharz, 1996 .

Assessing activity of pediatric Crohn's disease: which index to use?

M. Corey, A. Griffiths, A. Otley, 1999, Gastroenterology.

Sputum bacteriology in patients with cystic fibrosis in a Toronto hospital during 1970-1981.

M. Corey, H. Levison, C. Prober, 1984, The Journal of infectious diseases.

Complex two-gene modulation of lung disease severity in children with cystic fibrosis.

M. Corey, L. Tsui, J. Zieleński, 2008, The Journal of clinical investigation.

Five- to seven-year course of pulmonary function in cystic fibrosis.

M. Corey, H. Levison, D. Crozier, 1976, The American review of respiratory disease.

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results

M. Corey, L. Tsui, J. Zieleński, 2009, Human Genetics.

Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variants.

M. Corey, J. Rommens, M. Lewis, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis.

M. Corey, J. Zieleński, S. Freedman, 2011, Gastroenterology.

Prevalence of vertebral fractures in adults with cystic fibrosis and their relationship to bone mineral density.

M. Corey, S. Jamal, T. Dowdell, 2006, Chest.

Genetic modifiers of liver disease in cystic fibrosis.

M. Corey, J. Zieleński, M. Drumm, 2009, JAMA.

Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials.

M. Corey, L. Tsui, J. Zieleński, 2006, American journal of respiratory and critical care medicine.

Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood.

M. Corey, J. Zieleński, D. E. Tullis, 2004, Chest.

Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis.

M. Corey, L. Tsui, J. Zieleński, 2002, Gastroenterology.

Decline of Exocrine Pancreatic Function in Cystic Fibrosis Patients with Pancreatic Sufficiency

M. Corey, R. Couper, D. Moore, 1992, Pediatric Research.

A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto.

M. Corey, H. Levison, F. J. Mclaughlin, 1988, Journal of clinical epidemiology.

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.

Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection

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

Alpha 1-antitrypsin deficiency alleles in cystic fibrosis lung disease.

M. Corey, J. Zieleński, A. Freitag, 2003, American journal of respiratory cell and molecular biology.

Socioeconomic status and risk of hospitalization among individuals with cystic fibrosis in Ontario, Canada

M. Corey, P. Austin, J. Hux, 2011, Pediatric pulmonology.

Iatrogenic hyperuricemia in children with cystic fibrosis.

M. Corey, G. Davidson, G. Forstner, 1978, The Journal of pediatrics.

Effects of nutritional status on exercise performance in advanced cystic fibrosis.

A. Coates, M. Corey, H. Levison, 1986, Chest.

Nocturnal home oxygen in the treatment of hypoxemic cystic fibrosis patients.

A. Coates, M. Corey, H. Levison, 1989, The Journal of pediatrics.

Determination of maximal voluntary ventilation in children with cystic fibrosis

A. Coates, M. Corey, H. Selvadurai, 2003, Pediatric pulmonology.

Role of conventional physiotherapy in cystic fibrosis.

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

Evidence for a Primary Defect of Pancreatic HCO3− Secretion in Cystic Fibrosis

M. Corey, P. Durie, K. Gaskin, 1982, Pediatric Research.

Children After Fontan have Strength and Body Composition Similar to Healthy Peers and Can Successfully Participate in Daily Moderate-to-Vigorous Physical Activity

M. Corey, B. McCrindle, G. Faulkner, 2015, Pediatric Cardiology.

One-stage design is empirically more powerful than two-stage design for family-based genome-wide association studies

Lucia Mirea, Shelley B Bull, Rori V Rohlfs, 2007, BMC proceedings.

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.

Genetic determination of exocrine pancreatic function in cystic fibrosis.

M. Corey, L. Tsui, J. Rommens, 1992, American journal of human genetics.

Pregnancy and Cystic Fibrosis

M. Corey, H. Levison, G. Canny, 1991, Obstetrics and gynecology.

Pregnancy in cystic fibrosis: a better prognosis in patients with pancreatic function?

M. Corey, H. Levison, C. Newth, 1981, American journal of obstetrics and gynecology.

Passive Smoking and Lung Funrtion in Cystic Fibrosis

M. Corey, H. Levison, T. Kovesi, 1993 .

Family adaptation and psychosocial adjustment to cystic fibrosis in the preschool child.

M. Corey, H. Levison, E. Arndt, 1985, Social science & medicine.

Confidence intervals for candidate gene effects and environmental factors in population‐based association studies of families

M. Corey, S. Bull, G. Darlington, 2007, Annals of human genetics.

Behavioral adjustment of latency age children with cystic fibrosis.

M. Corey, H. Levison, J. Robertson, 1987, Psychosomatic medicine.

The cystic fibrosis gene and resting energy expenditure.

M. Corey, H. Levison, L. Tsui, 1991, The Journal of pediatrics.

False positivity of Legionella serology in patients with cystic fibrosis.

M. Corey, E. Wang, C. Prober, 1987, The Pediatric infectious disease journal.

Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus.

M. Corey, L. Tsui, T. Dörk, 1992, American journal of human genetics.

Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout mice

M. Corey, L. Tsui, C. McKerlie, 2002, Mammalian Genome.

Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas

M. Corey, L. Tsui, J. Zieleński, 2003, Gut.

The Flutter Device versus the PEP Mask in the Treatment of Adults with Cystic Fibrosis

M. Corey, D. Brooks, E. Tullis, 2005 .

Comparison of growth status of patients with cystic fibrosis between the United States and Canada.

M. Kosorok, M. Corey, P. Farrell, 1999, The American journal of clinical nutrition.

DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis.

M. Corey, L. Tsui, J. Rommens, 1989, American journal of human genetics.

Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

M. Corey, L. Tsui, J. Zieleński, 1995, Human mutation.

Energy expenditure of patients with cystic fibrosis.

M. Corey, N. Vaisman, P. Pencharz, 1987, The Journal of pediatrics.

Defining the modifiers of CF pathophysiology

Nguyen, M. Corey, L. Tsui, 1998 .

Evaluation of the ambulatory and home care record: Agreement between self-reports and administrative data

M. Corey, P. Coyte, E. Tullis, 2006, International Journal of Technology Assessment in Health Care.

Wheezing in infants with cystic fibrosis: clinical course, pulmonary function, and survival analysis.

M. Corey, H. Levison, E. Kerem, 1992, Pediatrics.

Factors associated with the physical activity level of children who have the Fontan procedure.

M. Corey, B. McCrindle, G. Faulkner, 2011, American heart journal.

A comparison of inhaled fluticasone and oral prednisone for children with severe acute asthma.

M. Corey, J. Reisman, S. Schuh, 2000, The New England journal of medicine.

Glucose intolerance in children with cystic fibrosis.

M. Corey, L. Tsui, J. Zieleński, 2003, The Journal of pediatrics.

Economic Burden of Ambulatory and Home-Based Care for Adults with Cystic Fibrosis

M. Corey, P. Coyte, E. Tullis, 2006, Treatments in respiratory medicine.

Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?

M. Corey, J. Zieleński, K. Jarvi, 2013, Thorax.

LINICAL — LIVER , PANCREAS , AND BILIARY RACT ype of CFTR Mutation Determines Risk of Pancreatitis in Patients With ystic Fibrosis

M. Corey, J. Zieleński, S. Freedman, 2010 .

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.

Field testing of the 2006 World Health Organization growth charts from birth to 2 years: assessment of hospital undernutrition and overnutrition rates and the usefulness of BMI.

M. Corey, D. O’Connor, D. Secker, 2008, JPEN. Journal of parenteral and enteral nutrition.

Higher risk of hospitalization among females with cystic fibrosis.

M. Corey, P. Austin, J. Hux, 2011, Journal of Cystic Fibrosis.

Recursive partitioning models for linkage in COGA data

M. Corey, C. Greenwood, S. Bull, 2005, BMC Genetics.

Use of the Pediatric Risk of Mortality score to predict nosocomial infection in a pediatric intensive care unit

M. Corey, D. Bohn, E. Ford-Jones, 1991, Critical care medicine.

Abstract 2208: Factors Associated with the Objectively Measured Activity Levels for Children after the Fontan Procedure

M. Corey, B. McCrindle, J. Russell, 2007 .

Exocrine Pancreatic Alterations in Long-Lived Surviving Cystic Fibrosis Mice

M. Corey, P. Durie, W. Ip, 1996, Pediatric Research.

Psychologic adjustment of the family with a member who has cystic fibrosis.

M. Corey, H. Levison, H. MacMillan, 1986, Pediatrics.

An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years.

Warren J Warwick, Mary Corey, M. Corey, 2008, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The General Approach to Cystic Fibrosis Pulmonary Infection in Canada

M. Corey, N. MacDonald, R. Morrison, 1996 .

The genetics of cross-sectional and longitudinal body mass index

M. Corey, L. Strug, Lei Sun, 2003, BMC Genetics.

Coagulase-negative staphylococci as true pathogens in newborn infants: a cohort study.

M. Corey, D. Low, H. Kirpalani, 1987, The Pediatric infectious disease journal.

Does the Macroduct collection system reliably define sweat chloride concentration in subjects with intermediate results?

M. Corey, K. Adeli, E. Tullis, 2009, Clinical biochemistry.

LONG-TERM MICROVASCULAR, BUT NOT MACROVASCULAR, DIABETIC COMPLICATIONS ARE COMMON IN CYSTIC FIBROSIS RELATED DIABETES MELLITUS

M. Corey, P. Pencharz, E. Tullis, 1998, Pediatric Research.

Perspectives in cystic fibrosis.

M. Corey, H. Levison, P. Francis, 1979, The Proceedings of the Institute of Medicine of Chicago.

Mapping of genetic factors influencing the weight of cystic fibrosis knockout mice

M. Corey, L. Tsui, C. Haston, 2002, Mammalian Genome.

The HIV information project for transfusion recipients a decade after transfusion.

M. Corey, B. McCrindle, T. Murphy, 1995, Archives of pediatrics & adolescent medicine.

Perspectives in cystic fibrosis.

M. Corey, H. Levison, P. Francis, 1979, Pediatric clinics of North America.

Diversity of reproductive tract abnormalities in men with cystic fibrosis.

M. Corey, K. Jarvi, E. Tullis, 1996, JAMA.

Factors influencing postoperative recurrence of Crohn's disease in childhood.

M. Corey, B. Shandling, Philip M. Sherman, 1991, Gut.

Cytomegalovirus infections in Toronto child-care centers: a prospective study of viral excretion in children and seroconversion among day-care providers.

M. Corey, I. Kitai, M. Petric, 1996, The Pediatric infectious disease journal.

Symposium Session Summaries: Sessions 8.4 to 13.3

Nguyen, M. Corey, L. Tsui, 1998 .

Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?

M. Corey, J. Zieleński, K. Jarvi, 2013, Thorax.

TLR5 as an Anti-Inflammatory Target and Modifier Gene in Cystic Fibrosis

M. Corey, J. Zieleński, R. Dorfman, 2010, The Journal of Immunology.