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名词信息
中 文 名:
肝脂酶缺乏症
英 文 名:
hepatic lipase deficiency
中文又称:
中文曾称:
名词来源:
所属专业:
内分泌科
所属类别:
疾病诊断名词
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Pubmed相关的文献
hepatic lipase deficiency
相关文献:
Hepatic lipase deficiency.
Connelly PW, Hegele RA.
Crit Rev Clin Lab Sci. 1998 Dec;35(6):547-72. doi: 10.1080/10408369891234273.
PMID:9885775
[Familial hepatic lipase deficiency].
Matsuura F, Hirano K.
Nihon Rinsho. 2001 Mar;59 Suppl 3:94-7.
PMID:11347190
[Familial hepatic lipase deficiency].
Sasaki J.
Nihon Rinsho. 2007 Jul 28;65 Suppl 7:340-3.
PMID:17824054
Combined lipase deficiency (cld/cld) in mice affects differently post-translational processing of lipoprotein lipase, hepatic lipase and pancreatic lipase.
Scow RO, Schultz CJ, Park JW, Blanchette-Mackie EJ.
Chem Phys Lipids. 1998 Jun;93(1-2):149-55. doi: 10.1016/s0009-3084(98)00039-5.
PMID:9720257
Hepatic lipase deficiency produces glucose intolerance, inflammation and hepatic steatosis.
Andrés-Blasco I, Herrero-Cervera A, Vinué Á, Martínez-Hervás S, Piqueras L, Sanz MJ, Burks DJ, González-Navarro H.
J Endocrinol. 2015 Dec;227(3):179-91. doi: 10.1530/JOE-15-0219. Epub 2015 Sep 30.
PMID:26423094
Familial hepatic lipase deficiency.
Little JA, Connelly PW.
Adv Exp Med Biol. 1986;201:253-60. doi: 10.1007/978-1-4684-1262-8_22.
PMID:3799360
Compound heterozygosity for mutant hepatic lipase in familial hepatic lipase deficiency.
Hegele RA, Little JA, Connelly PW.
Biochem Biophys Res Commun. 1991 Aug 30;179(1):78-84. doi: 10.1016/0006-291x(91)91336-b.
PMID:1883393
A hepatic lipase gene mutation associated with heritable lipolytic deficiency.
Hegele RA, Vezina C, Moorjani S, Lupien PJ, Gagne C, Brun LD, Little JA, Connelly PW.
J Clin Endocrinol Metab. 1991 Mar;72(3):730-2. doi: 10.1210/jcem-72-3-730.
PMID:1671786
Plasma lipoproteins in familial hepatic lipase deficiency.
Connelly PW, Maguire GF, Lee M, Little JA.
Arteriosclerosis. 1990 Jan-Feb;10(1):40-8. doi: 10.1161/01.atv.10.1.40.
PMID:2297346
The rabbit as an animal model of hepatic lipase deficiency.
Clay MA, Hopkins GJ, Ehnholm CP, Barter PJ.
Biochim Biophys Acta. 1989 Apr 3;1002(2):173-81. doi: 10.1016/0005-2760(89)90284-1.
PMID:2930766
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