Modeling Steatohepatitis in Humans with Pluripotent Stem Cell-Derived Organoids.
Ouchi R, Togo S, Kimura M, Shinozawa T, Koido M, Koike H, Thompson W, Karns RA, Mayhew CN, McGrath PS, McCauley HA, Zhang RR, Lewis K, Hakozaki S, Ferguson A, Saiki N, Yoneyama Y, Takeuchi I, Mabuchi Y, Akazawa C, Yoshikawa HY, Wells JM, Takebe T.
Cell Metab. 2019 Aug 6;30(2):374-384.e6. doi: 10.1016/j.cmet.2019.05.007. Epub 2019 May 30.
Recent insights into lysosomal acid lipase deficiency.
Korbelius M, Kuentzel KB, Bradić I, Vujić N, Kratky D.
Trends Mol Med. 2023 Jun;29(6):425-438. doi: 10.1016/j.molmed.2023.03.001. Epub 2023 Apr 5.
Sebelipase alfa.
[No authors listed]
2016 Mar 10. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012–.
Rare diseases presenting with hemophagocytic lymphohistiocytosis.
Kanegane H, Noguchi A, Yamada Y, Yasumi T.
Pediatr Int. 2023 Jan-Dec;65(1):e15516. doi: 10.1111/ped.15516.
Familial xanthomatosis.
TAYLOR RE.
J Am Med Womens Assoc. 1955 Mar;10(3):82-3.
Primary histiocytic dermatoses.
Ringel E, Moschella S.
Arch Dermatol. 1985 Dec;121(12):1531-41.
Hyperlipidaemia in children.
Lloyd JK.
Br Heart J. 1975 Feb;37(2):105-14. doi: 10.1136/hrt.37.2.105.
[Osgood-Schlatter disease].
Weiler R, Ingram M, Wolman R.
Praxis (Bern 1994). 2011 Nov 2;100(22):1369-70. doi: 10.1024/1661-8157/a000715.
Primary familial xanthomatosis with adrenal involvement (Wolman's disease). Report of a further case with nervous system involvement and pathogenetic considerations.
Kahana D, Berant M, Wolman M.
Pediatrics. 1968 Jul;42(1):70-6.
"Mutation-negative" familial hypercholesterolemia-When negative is positive.
Shapiro MD.
J Clin Lipidol. 2017 Mar-Apr;11(2):325-327. doi: 10.1016/j.jacl.2017.01.015. Epub 2017 Feb 6.
