Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Caroline T. Carreras"'
Autor:
Kate Hoyt, Christopher Lumpkin, Laurie M. Brown, Sara D. Siegel, Margaret A. Chen, David A. Weinstein, Michelle M. Corrado, Rixt M. van der Ende, Terry G J Derks, Catherine E. Correia, Theresa B. Flanagan, Caroline T. Carreras
Publikováno v:
Journal of Inherited Metabolic Disease, 38(3), 489-493. SPRINGER
INTRODUCTION: Ketone formation is a normal response when hypoglycemia occurs. Since the majority of children with recurrent hypoglycemia cannot be diagnosed with a known endocrine or metabolic disorder on a critical sample, ketotic hypoglycemia has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::026b7ab872d7aea008c83b008709508f
https://doi.org/10.1007/s10545-014-9744-1
https://doi.org/10.1007/s10545-014-9744-1
Publikováno v:
The Journal of Pediatrics. 159:442-446
Glycogen storage disease type I (GSD I) is an autosomal recessive inborn error of metabolism caused by defects in the glucose-6-phosphatase complex. Deficient activity of the glucose-6-phosphatase-α (G6Pase) catalytic unit characterizes glycogen sto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f97ebf6fc0ffcdb36785440dda3f74
https://doi.org/10.1016/j.jpeds.2011.02.031
https://doi.org/10.1016/j.jpeds.2011.02.031
Autor:
Brown, Laurie, Corrado, Michelle, Ende, Rixt, Derks, Terry, Chen, Margaret, Siegel, Sara, Hoyt, Kate, Correia, Catherine, Lumpkin, Christopher, Flanagan, Theresa, Carreras, Caroline, Weinstein, David
Publikováno v:
Journal of Inherited Metabolic Disease; May2015, Vol. 38 Issue 3, p489-493, 5p