Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Annie Rosen-Heath"'
Autor:
Abrar Turki, Sylvia Stockler, Sandra Sirrs, Ramona Salvarinova, Gloria Ho, Jennifer Branov, Annie Rosen-Heath, Taryn Bosdet, Rajavel Elango
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100880- (2022)
Background: Glycogen storage disease type Ia (GSD Ia) is an autosomal recessive disorder caused by deficiency of glucose-6-phosphatase (G6Pase), resulting in fasting hypoglycemia. Dietary treatment with provision of uncooked cornstarch (UCCS) or a no
Externí odkaz:
https://doaj.org/article/920b0e4eec9349018abe02e4bad4c684
Autor:
Joseph Leung, Caroline Selvage, Taryn Bosdet, Jennifer Branov, Annie Rosen-Heath, Carole Bishop, Sandra Sirrs, Gabriella Horvath
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 15, Iss , Pp 100-105 (2018)
Introduction: Phenylketonuria (PKU) is an inborn error of metabolism associated with an increased risk of behavioural and mood disorders. There are currently no reliable markers for monitoring mood in PKU. The purpose of this study was to evaluate sa
Externí odkaz:
https://doaj.org/article/72cd37d8cfbd4dd68f11e4e7b3cde828
Autor:
Madeleine Ennis, Annie Rosen Heath, Jennifer Branov, Taryn Bosdet, Anna Lehman, Sandra Sirrs, Rajavel Elango
Background: Diet, with an emphasis on phenylalanine restriction, is recognized as an effective treatment for phenylketonuria (PKU). A similar approach is used in pregnant PKU patients to reduce teratogenic effects of elevated circulating phenylalanin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e165f1e0a97946c8bc0b72db1f8ca785
https://doi.org/10.21203/rs.3.rs-2609680/v1
https://doi.org/10.21203/rs.3.rs-2609680/v1