Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ingrid Wiig"'
Autor:
Kaare R. Norum, Alan T. Remaley, Helena E. Miettinen, Erik H. Strøm, Bruno E.P. Balbo, Carlos A.T.L. Sampaio, Ingrid Wiig, Jan Albert Kuivenhoven, Laura Calabresi, John J. Tesmer, Mingyue Zhou, Dominic S. Ng, Bjørn Skeie, Sotirios K. Karathanasis, Kelly A. Manthei, Kjetil Retterstøl
Publikováno v:
Journal of Lipid Research, Vol 61, Iss 8, Pp 1142-1149 (2020)
LCAT converts free cholesterol to cholesteryl esters in the process of reverse cholesterol transport. Familial LCAT deficiency (FLD) is a genetic disease that was first described by Kaare R. Norum and Egil Gjone in 1967. This report is a summary from
Externí odkaz:
https://doaj.org/article/1eb59149604d406ab618b04f2a2cf3f0
Publikováno v:
Scandinavian Journal of Disability Research, Vol 17, Iss 4, Pp 321-334 (2014)
Today most adults with phenylketonuria (PKU) have followed a protein restricted diet from early infancy. This makes their disorder an invisible impairment which becomes visible only when food is served. When adhering to medical advice in public, adul
Externí odkaz:
https://doaj.org/article/8c9947a8ffab4fe8aace36a49b6527ee
Autor:
Erik H. Strøm, Alan T. Remaley, Mingyue Zhou, Dominic S. Ng, Helena E. Miettinen, Ingrid Wiig, Jan Albert Kuivenhoven, John J.G. Tesmer, Carlos A.T.L. Sampaio, Kjetil Retterstøl, Laura Calabresi, Kelly A. Manthei, Bjørn Skeie, Bruno Eduardo Pedroso Balbo, Kaare R. Norum, Sotirios K. Karathanasis
Publikováno v:
Journal of Lipid Research, 61(8), 1142-1149. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Journal of Lipid Research, Vol 61, Iss 8, Pp 1142-1149 (2020)
Journal of Lipid Research
Journal of Lipid Research, Vol 61, Iss 8, Pp 1142-1149 (2020)
Journal of Lipid Research
LCAT converts free cholesterol to cholesteryl esters in the process of reverse cholesterol transport. Familial LCAT deficiency (FLD) is a genetic disease that was first described by Kaare R. Norum and Egil Gjone in 1967. This report is a summary from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1777729792af43281ba3ed6bd138094
https://research.rug.nl/en/publications/fd824db0-b663-4e08-b6e4-9e86a4ab06c1
https://research.rug.nl/en/publications/fd824db0-b663-4e08-b6e4-9e86a4ab06c1
Publikováno v:
Scandinavian Journal of Disability Research. 17:321-334
Today most adults with phenylketonuria (PKU) have followed a protein restricted diet from early infancy. This makes their disorder an invisible impairment which becomes visible only when food is served. When adhering to medical advice in public, adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07325f15edfa362f867fb7b767718f96
https://doi.org/10.1080/15017419.2014.941003
https://doi.org/10.1080/15017419.2014.941003
Publikováno v:
JIMD Reports ISBN: 9783642324413
The main treatment for phenylketonuria (PKU) is a low phenylalanine (Phe) diet, phenylalanine-free protein substitute and low-protein special foods. This study describes dietary composition and nutritional status in late-diagnosed adult patients adhe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c175f78f2403d82d94b2dfe6f451ce3
https://pubmed.ncbi.nlm.nih.gov/23430504
https://pubmed.ncbi.nlm.nih.gov/23430504