Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sumio Hyoudou"'
Autor:
Yasuyuki Ikeda, Atsuko Takagi, Yuusei Nakata, Yasuhiko Sera, Sumio Hyoudou, Kazuko Hamamoto, Yoshikazu Nishi, Akira Yamamoto
Publikováno v:
Journal of Lipid Research, Vol 42, Iss 7, Pp 1072-1081 (2001)
We systematically investigated the molecular defects causing a primary LPL deficiency in a Japanese male infant (patient DI) with fasting hyperchylomicronemia (type I hyperlipoproteinemia) and in his parents. Patient DI had neither LPL activity nor i
Externí odkaz:
https://doaj.org/article/613954a80ccf4faf8338a1f83d9564cd
Autor:
Norihisa Iida, Kazuteru Kouno, Satoshi Ueno, Rika Okano, Hajime Fujii, Sumio Hyoudou, Michiko Fujitaka, Tooru Komazawa, Hiroshi Nakahara, Masatoshi Doumen
Publikováno v:
Nihon Shoni Arerugi Gakkaishi. The Japanese Journal of Pediatric Allergy and Clinical Immunology. 17:190-194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e13a8cc537ccb8bc12aa4963be2ea97c
https://doi.org/10.3388/jspaci.17.190
https://doi.org/10.3388/jspaci.17.190
Autor:
Sumio Hyoudou, Yasuyuki Ikeda, Yuusei Nakata, Kazuko Hamamoto, Akira Yamamoto, Yoshikazu Nishi, Atsuko Takagi, Yasuhiko Sera
Publikováno v:
Journal of Lipid Research, Vol 42, Iss 7, Pp 1072-1081 (2001)
We systematically investigated the molecular defects causing a primary LPL deficiency in a Japanese male infant (patient DI) with fasting hyperchylomicronemia (type I hyperlipoproteinemia) and in his parents. Patient DI had neither LPL activity nor i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ee70a4e5fd448defa9c1fc7c734d885
http://www.sciencedirect.com/science/article/pii/S0022227520315960
http://www.sciencedirect.com/science/article/pii/S0022227520315960
Autor:
Yuusei Nakata, Yasuhiko Sera, Akira Yamamoto, Kazuko Hamamoto, Yasuyuki Ikeda, Sumio Hyoudou, Yoshikazu Nishi, Atsuko Takagi
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 316(1-2)
A case is presented of predisposing a patient's father with obligate heterozygous lipoprotein lipase (LPL) deficiency to mild hypertriglyceridemia in Japanese I-family members (n=8) with patient DI, who was a compound heterozygote for a novel missens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82085dd2b06ddaf7ed98efa6dbb9322a
https://pubmed.ncbi.nlm.nih.gov/11750290
https://pubmed.ncbi.nlm.nih.gov/11750290