Zobrazeno 1 - 3
of 3
pro vyhledávání: '"C. Bieneck Haglind"'
Autor:
Jan Gustafsson, Anna Nordenström, M. Halldin Stenlid, S. Ask, U. von Döbeln, C. Bieneck Haglind
Publikováno v:
Journal of Inherited Metabolic Disease. 38:315-322
Children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) have a defect in the degradation of long-chain fatty acids and are at risk of hypoketotic hypoglycemia and insufficient energy production as well as accumulation of toxic fat
Autor:
Anna Strandqvist, C. Bieneck Haglind, Rolf Zetterström, U. von Döbeln, M. Halldin Stenlid, Anna Nordenström, Antal Nemeth
Publikováno v:
JIMD Reports ISBN: 9783662528464
Reports on cognitive outcomes in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) are scarce. We present results from neuropsychological assessments of eight patients diagnosed with LCHADD prior to newborn screening with regard to clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::265966aee23dd2157bde57632972dc96
https://europepmc.org/articles/PMC5059195/
https://europepmc.org/articles/PMC5059195/
Autor:
M. Halldin Stenlid, C. Bieneck Haglind, S. Ask, J. Alm, A. Nemeth, Uv. Döbeln, Anna Nordenström
Publikováno v:
JIMD Reports ISBN: 9783642334320
Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is an inborn error of fatty acid metabolism that affects the degradation of long chain fatty acids and causes insufficient energy production and accumulation of toxic intermediates. The tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3793aa2efc5b0bd38f28af0fdc88878
https://europepmc.org/articles/PMC3565647/
https://europepmc.org/articles/PMC3565647/