Claude C Roy

Summary

Affiliation: University of Montreal
Country: Canada

Publications

  1. ncbi request reprint Short-chain fatty acids: ready for prime time?
    Claude C Roy
    Ste Justine Hospital, 3175 Ste Catherine Road, Montreal, Quebec H3T 1C5, Canada
    Nutr Clin Pract 21:351-66. 2006
  2. pmc Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers
    Noel Peretti
    Department of Nutrition, CHU Sainte Justine Research Center, Universite de Montreal, 3175, Ste Catherine Road, Montreal, Quebec, H3T 1C5, Canada
    Orphanet J Rare Dis 5:24. 2010
  3. ncbi request reprint [Teasing out the various factors associated with the digestive and absorptive phases of intestinal transport]
    Emile Levy
    Centre de Recherche, CHU Sainte Justine, 3175, Chemin de la Cote Sainte Catherine, Montreal, Quebec, H3T 1C5 Canada
    Med Sci (Paris) 23:1014-9. 2007
  4. ncbi request reprint [Brief history of the Ste-Justine Hospital Research Centre]
    Emile Levy
    Centre de Recherche, CHU Sainte Justine 3175, Cote Sainte Catherine, Montreal Quebec H3T 1C5, Canada
    Med Sci (Paris) 23:901-3. 2007
  5. ncbi request reprint New lipids in enteral feeding
    Claude C Roy
    Departments of Pediatrics and Nutrition, University of Montreal, Hospital Sainte Justine, 3175 Ste Catherine Road, Montreal, Quebec, Canada H3T 1C5
    Curr Opin Clin Nutr Metab Care 7:117-22. 2004
  6. doi request reprint Chylomicron retention disease: a long term study of two cohorts
    Noel Peretti
    Department of Nutrition, CHU Sainte Justine, Universite de Montreal, GI Nutrition Unit, 3175 Ste Catherine Road, Montreal, Que, Canada
    Mol Genet Metab 97:136-42. 2009
  7. ncbi request reprint Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein
    Mathilde Charcosset
    UF Lipides Dyslipidémies, Laboratoire de Biochimie, CBE, 59 Boulevard Pinel, Bron Cedex, France
    Mol Genet Metab 93:74-84. 2008
  8. ncbi request reprint Abnormal intracellular lipid processing contributes to fat malabsorption in cystic fibrosis patients
    Noel Peretti
    Departments of Nutrition, CHU Ste Justine, Universite de Montreal, Quebec, Canada
    Am J Physiol Gastrointest Liver Physiol 290:G609-15. 2006
  9. ncbi request reprint Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
    Bethan Jones
    Genomic and Molecular Medicine Group, MRC Clinical Sciences Centre, Imperial College, London, England, UK
    Nat Genet 34:29-31. 2003
  10. ncbi request reprint Effect of an organized lipid matrix on lipid absorption and clinical outcomes in patients with cystic fibrosis
    Guy Lepage
    Department of Pediatrics, Hopital Ste Justine, Universite de Montreal, Quebec, Canada
    J Pediatr 141:178-85. 2002

Collaborators

  • E Levy
  • C L Kien
  • Noel Peretti
  • Mathilde Charcosset
  • Agnes Sassolas
  • Colette Deslandres
  • Alain Lachaux
  • Sylvie Labarge
  • Pierre Brochu
  • Ernest Seidman
  • Eric Drouin
  • Bethan Jones
  • Guy Lepage
  • Justine Castagnetti
  • Lise Bouthillier
  • Laurence Pugnet-Chardon
  • Philippe Moulin
  • Raymonde Bouvier
  • Marie Claude Vohl
  • Andrée Rasquin
  • Marie Elizabeth Samson-Bouma
  • Daniel Sinnett
  • Georges Casimir
  • Aldo Quattrone
  • Recaredo Infante
  • Sandhia Naik
  • Arjen R Mensenkamp
  • Grazia Annesi
  • Mats Rudling
  • Emma L Jones
  • Bo Angelin
  • Sophie Eichenbaum-Voline
  • Rossitza P Naoumova
  • Urban Myrdal
  • Hetal N Patel
  • Carol C Shoulders
  • James Scott
  • Paul S Freemont
  • Nigel Meadows
  • Suhail A Islam
  • Stephanie A Bonney
  • David W Yesair
  • Denis Bérubé
  • Sylvain Chemtob
  • Josée Champagne
  • Nancy Ronco
  • Nathalie Bureau

Detail Information

Publications10

  1. ncbi request reprint Short-chain fatty acids: ready for prime time?
    Claude C Roy
    Ste Justine Hospital, 3175 Ste Catherine Road, Montreal, Quebec H3T 1C5, Canada
    Nutr Clin Pract 21:351-66. 2006
    ..The future lies with the design of studies to further explore basic mechanisms, and gene expression in particular, but emphasis should be placed on human intervention trials...
  2. pmc Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers
    Noel Peretti
    Department of Nutrition, CHU Sainte Justine Research Center, Universite de Montreal, 3175, Ste Catherine Road, Montreal, Quebec, H3T 1C5, Canada
    Orphanet J Rare Dis 5:24. 2010
    ..The clinical guidelines proposed will helpfully lead to an earlier diagnosis and the prevention of complications...
  3. ncbi request reprint [Teasing out the various factors associated with the digestive and absorptive phases of intestinal transport]
    Emile Levy
    Centre de Recherche, CHU Sainte Justine, 3175, Chemin de la Cote Sainte Catherine, Montreal, Quebec, H3T 1C5 Canada
    Med Sci (Paris) 23:1014-9. 2007
    ....
  4. ncbi request reprint [Brief history of the Ste-Justine Hospital Research Centre]
    Emile Levy
    Centre de Recherche, CHU Sainte Justine 3175, Cote Sainte Catherine, Montreal Quebec H3T 1C5, Canada
    Med Sci (Paris) 23:901-3. 2007
  5. ncbi request reprint New lipids in enteral feeding
    Claude C Roy
    Departments of Pediatrics and Nutrition, University of Montreal, Hospital Sainte Justine, 3175 Ste Catherine Road, Montreal, Quebec, Canada H3T 1C5
    Curr Opin Clin Nutr Metab Care 7:117-22. 2004
    ..Lipid sources for enteral nutrition continue to be an exciting area of investigation. It is timely to review recent developments which have largely contributed to thrust enteral feeding into a new era...
  6. doi request reprint Chylomicron retention disease: a long term study of two cohorts
    Noel Peretti
    Department of Nutrition, CHU Sainte Justine, Universite de Montreal, GI Nutrition Unit, 3175 Ste Catherine Road, Montreal, Que, Canada
    Mol Genet Metab 97:136-42. 2009
    ..This study provides new insights on the phenotypic expression of CRD over time and emphasizes the need to screen the lipid profile of infants with chronic diarrhea and failure to thrive...
  7. ncbi request reprint Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein
    Mathilde Charcosset
    UF Lipides Dyslipidémies, Laboratoire de Biochimie, CBE, 59 Boulevard Pinel, Bron Cedex, France
    Mol Genet Metab 93:74-84. 2008
    ..A determination of the specific mutation in Anderson disease or CMRD is required to ensure diagnosis and allow prompt therapeutic intervention in these children...
  8. ncbi request reprint Abnormal intracellular lipid processing contributes to fat malabsorption in cystic fibrosis patients
    Noel Peretti
    Departments of Nutrition, CHU Ste Justine, Universite de Montreal, Quebec, Canada
    Am J Physiol Gastrointest Liver Physiol 290:G609-15. 2006
    ..Together, these results suggest that CF malabsorption may also be caused by defects in mucosal mechanisms leading to abnormal lipoprotein delivery into the blood circulation...
  9. ncbi request reprint Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
    Bethan Jones
    Genomic and Molecular Medicine Group, MRC Clinical Sciences Centre, Imperial College, London, England, UK
    Nat Genet 34:29-31. 2003
    ..Our data suggest that chylomicrons, which vastly exceed the size of typical COPII vesicles, are selectively recruited by the COPII machinery for transport through the secretory pathways of the cell...
  10. ncbi request reprint Effect of an organized lipid matrix on lipid absorption and clinical outcomes in patients with cystic fibrosis
    Guy Lepage
    Department of Pediatrics, Hopital Ste Justine, Universite de Montreal, Quebec, Canada
    J Pediatr 141:178-85. 2002
    ..To compare the absorption of a lysophosphatidylcholine, monoglyceride, and fatty acid matrix (organized lipid matrix, OLM) with that of a triacylglycerol (TG)-based fat meal in patients with cystic fibrosis (CF)...