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Institution

Montreal Children's Hospital

HealthcareMontreal, Quebec, Canada
About: Montreal Children's Hospital is a healthcare organization based out in Montreal, Quebec, Canada. It is known for research contribution in the topics: Population & Poison control. The organization has 3842 authors who have published 4816 publications receiving 200198 citations.
Topics: Population, Poison control, Gene, Medicine, Kidney


Papers
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Journal ArticleDOI
TL;DR: Congenital and infantile neoplasia of the kidney is shown to be mostly comprised of several more or less distinct clinical and pathological entities: congenital mesoblastic nephroma of infancy, the well-differentiated epithelial nephroblastomata, and nephrogenic blastema.

59 citations

Journal ArticleDOI
TL;DR: The identification of response perseveration and underlying processes has implications for developmental theories of physical aggression; they may help discriminate those children who show early physical aggression and who will remain aggressive from those who will only show occasional physical aggression during later childhood.
Abstract: BACKGROUND: It was unclear whether response perseveration and underlying processes, often related to antisocial externalizing disorders, were also related to histories of physical aggression. METHOD: Boys of age 13 years were selected on the basis of childhood histories of physical aggression: stable, unstable, and non-aggressive. Performance on a Card Playing Task provided a perseveration index. RESULTS: Physical aggression, regardless of history, predicted perseveration in adolescence. However, qualitative differences revealed that Neuroticism increased the risk for perseveration only in the unstable aggressive group relative to the other groups. Perseveration in the stable aggressive group maybe related to a more fundamental information-processing deficit. CONCLUSION: The identification of these processes has implications for developmental theories of physical aggression; they may help discriminate those children who show early physical aggression and who will remain aggressive from those who will only show occasional physical aggression during later childhood. Language: en

59 citations

Journal ArticleDOI
TL;DR: Infants with CDH defects requiring a patch repair and those requiring advanced physiologic support, especially extracorporeal life support, are likely to develop severe GER necessitating fundoplication, likely to shorten hospital stay and minimize patient morbidity.

59 citations

Journal ArticleDOI
TL;DR: Whey protein isolates may provide anti-inflammatory benefits to cystic fibrosis, which could be mediated via peptides, as proteolytic digests of WPI enhance intracellular glutathione (GSH) concentrations.
Abstract: Whey protein isolates (WPI) may provide anti-inflammatory benefits to cystic fibrosis (CF), which could be mediated via peptides, as proteolytic digests of WPI enhance intracellular glutathione (GSH) concentrations. The objectives of this study were to investigate whether high hydrostatic pressure can (i) improve the in vitro digestibility of WPI; and (ii) generate low molecular weight (< 1 kDa) peptides from WPI hydrolysates that exert GSH-enhancing and anti-inflammatory properties in wild type and mutant CF transmembrane conductance regulator (CFTR) tracheal epithelial cells. Hydrostatic pressure processing enhanced the in vitro digestibility of WPI to proteolytic enzymes resulting in altered peptide profiles as assessed by CZE and GC-MS. The exposure of mutant CFTR cells to low molecular weight (< 1 kDa) peptides isolated from WPI hydrolysates exposed to pressure processing (pressurized WPI hydrolysates, pWPH), showed increased intracellular levels of reduced GSH and total GSH relative to treatment with peptides obtained from native WPI hydrolysates (nWPH). A tendency for decreased interleukin-8 secretion was associated with the pWPH and nWPH treatments in mutant CFTR cells, which was not observed in wild type cells. Hydrostatic pressure processing of whey proteins appears to enhance their impact on cellular GSH status in cells with the mutant CFTR condition.

59 citations


Authors

Showing all 3844 results

NameH-indexPapersCitations
Paul M. Matthews14061788802
Joost J. Oppenheim13045459601
Michael Camilleri125108458867
James M. Swanson11741547131
Rhian M. Touyz11462043738
Ian Roberts11271451933
William D. Foulkes10868245013
Stephen P. Hinshaw10633037336
Michael S. Kramer10456843803
Liam Smeeth10475353433
Eric Fombonne10033644447
Douglas L. Arnold10062437040
Erwin W. Gelfand9967536059
Frederick Andermann9036525638
Robert W. Platt8863831918
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20232
202214
2021169
2020134
2019120
2018125