Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Neema Chokshi"'
Publikováno v:
Journal of Clinical Lipidology. 8:287-295
Context Type I hyperlipoproteinemia (T1HLP) is a rare, autosomal recessive disorder characterized by extreme hypertriglyceridemia that fails to respond to lipid-lowering agents, predisposing to frequent attacks of acute pancreatitis. Mutations in lip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2618f9f59d30e033d777c3df3808bf
https://doi.org/10.1016/j.jacl.2014.02.006
https://doi.org/10.1016/j.jacl.2014.02.006
Autor:
Clayton K. Trimmer, David Leonard, Wanpen Vongpatanasin, Bart Dolmatch, Shellie C. Josephs, Shawna D. Nesbitt, Richard J. Auchus, Ronald G. Victor, Frank H. Wians, Fiemu E. Nwariaku, Jorge E. Lopera, Sarita Singeetham, Shelby A. Holt, Neema Chokshi, Donald W. Chandler
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 92:2648-2651
In primary aldosteronism, elevated serum 18-hydroxycorticosterone (18OHB) suggests aldosterone-producing adenoma (APA) rather than bilateral, idiopathic hyperaldosteronism (IHA), but little is known about the relative production of 18OHB and aldoster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2592df7e4c8d7c42c26ec5884a6c92
https://doi.org/10.1210/jc.2006-2631
https://doi.org/10.1210/jc.2006-2631