Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sorcha A. Collins"'
Autor:
Sorcha A. Collins, Sharon Edmunds, Gwen Healey Akearok, J. Robert Thompson, Anders C. Erickson, Elske Hildes-Ripstein, Amber Miners, Martin Somerville, David M. Goldfarb, Cheryl Rockman-Greenberg, Laura Arbour
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Objective: Infectious illness, including lower respiratory tract infection (LRTI), is a leading cause of childhood morbidity and infant mortality in Inuit children in Nunavut Canada. The carnitine palmitoyltransferase 1A (CPT1A) p.P479L variant is co
Externí odkaz:
https://doaj.org/article/f75e9481d76c43b19b31dcc174ede376
Autor:
Martin J. Somerville, Laura Arbour, Gwen Healey Akearok, Anders C. Erickson, Amber Miners, David M. Goldfarb, Sorcha A. Collins, Sharon Edmunds, J. Robert Thompson, Elske Hildes-Ripstein, Cheryl Rockman-Greenberg
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Objective: Infectious illness, including lower respiratory tract infection (LRTI), is a leading cause of childhood morbidity and infant mortality in Inuit children in Nunavut Canada. The carnitine palmitoyltransferase 1A (CPT1A) p.P479L variant is co
Autor:
Sorcha A, Collins, Sharon, Edmunds, Gwen Healey, Akearok, J Robert, Thompson, Anders C, Erickson, Elske, Hildes-Ripstein, Amber, Miners, Martin, Somerville, David M, Goldfarb, Cheryl, Rockman-Greenberg, Laura, Arbour
Publikováno v:
Frontiers in Pediatrics
Objective: Infectious illness, including lower respiratory tract infection (LRTI), is a leading cause of childhood morbidity and infant mortality in Inuit children in Nunavut Canada. The carnitine palmitoyltransferase 1A (CPT1A) p.P479L variant is co
Publikováno v:
Paediatrics & Child Health. 24:e111-e115
BACKGROUND: The hepatic carnitine palmitoyltransferase I (CPT1A) p.P479L variant is common in Aboriginal populations across coastal British Columbia, Alaska, the Canadian North, and Greenland. While the high frequency of this variant suggests positiv
Autor:
Cheryl Rockman-Greenberg, Laura Arbour, James Robert Thompson, Sorcha A. Collins, Sharon Edmunds, Gertrude Elizabeth Hildes-Ripstein, Amber Miners
Publikováno v:
Paediatr Child Health
IntroductionNeonatal hypoglycemia (NH) in the first days of life can largely be prevented by recognizing those at risk and managing accordingly. The CPT1A P479L variant is prevalent in northern Indigenous populations and is a possible risk factor for
Autor:
Laura Arbour, Sarah McIntosh, Sorcha A. Collins, Isaac Sobol, Hilary Vallance, Cheryl R. Greenberg, Robert Thompson, Graham Sinclair, Geraldine Osborne, Brendan Hanley, Fiona Bamforth, Andre Corriveau, Maria Santos
Publikováno v:
Molecular Genetics and Metabolism. 101:200-204
Carnitine palmitoyltransferase 1A (CPT1A), encoded by the gene CPT1A, is the hepatic isoform of CPT1 and is a major regulatory point in long-chain fatty acid oxidation. CPT1A deficiency confers risk for hypoketotic hypoglycaemia, hepatic encephalopat
Autor:
Laura Arbour, Padma Surmala, Cheryl R. Greenberg, Sharon Edmunds-Potvin, Sorcha A. Collins, Laakkuluk Williamson Bathory, Geraldine Osborne
Publikováno v:
BMC Pediatrics, Vol 12, Iss 1, p 190 (2012)
BMC Pediatrics
BMC Pediatrics
Background The northern territory Nunavut has Canada’s largest jurisdictional land mass with 33,322 inhabitants, of which 85% self-identify as Inuit. Nunavut has rates of infant mortality, postneonatal mortality and hospitalisation of infants for r