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Items: 20

1.

Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.

Shoji K, Morita H, Ishigaki Y, Rivard CJ, Takayasu M, Nakayama K, Nakayama T, Inoue Y, Ayaki M, Yoshimura A.

Clin Nephrol. 2011 Oct;76(4):323-8. Review.

PMID:
21955868
2.

[LCAT deficiency: a nephrological diagnosis].

Boscutti G, Calabresi L, Pizzolitto S, Boer E, Bosco M, Mattei PL, Martone M, Milutinovic N, Berbecar D, Beltram E, Franceschini G.

G Ital Nefrol. 2011 Jul-Aug;28(4):369-82. Review. Italian.

PMID:
21809306
3.
4.

[Molecular defects in familial LCAT deficiency].

Bujo H, Saito Y.

Nihon Rinsho. 1993 Feb;51(2):482-7. Review. Japanese.

PMID:
8464161
5.

[Familial LCAT deficiency].

Kinoshita M.

Nihon Rinsho. 1994 Dec;52(12):3210-5. Review. Japanese.

PMID:
7853712
6.

[LCAT (lecithin:cholesterol acyltransferase)].

Kinoshita M, Teramoto T.

Rinsho Byori. 2001 Nov;Suppl 116:125-30. Review. Japanese.

PMID:
11797372
7.

A review on lecithin:cholesterol acyltransferase deficiency.

Saeedi R, Li M, Frohlich J.

Clin Biochem. 2015 May;48(7-8):472-5. doi: 10.1016/j.clinbiochem.2014.08.014. Epub 2014 Aug 27. Review.

PMID:
25172171
8.

Characteristic kidney pathology, gene abnormality and treatments in LCAT deficiency.

Hirashio S, Ueno T, Naito T, Masaki T.

Clin Exp Nephrol. 2014 Apr;18(2):189-93. doi: 10.1007/s10157-013-0895-4. Epub 2013 Oct 31. Review.

PMID:
24174160
9.

Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature.

Roshan B, Ganda OP, Desilva R, Ganim RB, Ward E, Haessler SD, Polisecki EY, Asztalos BF, Schaefer EJ.

J Clin Lipidol. 2011 Nov-Dec;5(6):493-9. doi: 10.1016/j.jacl.2011.07.002. Epub 2011 Aug 23. Review.

10.

[Familial LCAT deficiency].

Idzior-Waluś B.

Przegl Lek. 2001;58(10):919-23. Review. Polish.

PMID:
11957819
11.

[Lecithin-cholesterol acyltransferase deficiency and fish eye disease].

Gotoda T.

Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):100-3. Review. Japanese. No abstract available.

PMID:
9645018
12.

Familial lecithin: cholesterol acyltransferase (LCAT) deficiency. An updated review Spring 1988.

Gjone E.

Ophthalmic Paediatr Genet. 1988 Nov;9(3):167-9. Review.

PMID:
3068599
13.

[Clinical features of lecithin-cholesterol acyltransferase deficiency].

Hrycek A, Cieślik P, Trzeciak HI.

Przegl Lek. 1994;51(12):516-9. Review. Polish.

PMID:
7746888
14.

Familial LCAT deficiency and fish-eye disease.

McIntyre N.

J Inherit Metab Dis. 1988;11 Suppl 1:45-56. Review.

PMID:
3141686
15.

The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes.

Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J.

J Lipid Res. 1997 Feb;38(2):191-205. Review.

16.

Two novel molecular defects in the LCAT gene are associated with fish eye disease.

Kuivenhoven JA, Stalenhoef AF, Hill JS, Demacker PN, Errami A, Kastelein JJ, Pritchard PH.

Arterioscler Thromb Vasc Biol. 1996 Feb;16(2):294-303. Review.

17.

Very low levels of HDL cholesterol and atherosclerosis, a variable relationship--a review of LCAT deficiency.

Savel J, Lafitte M, Pucheu Y, Pradeau V, Tabarin A, Couffinhal T.

Vasc Health Risk Manag. 2012;8:357-61. doi: 10.2147/VHRM.S29985. Epub 2012 Jun 5. Review.

18.

Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.

Calabresi L, Simonelli S, Gomaraschi M, Franceschini G.

Atherosclerosis. 2012 Jun;222(2):299-306. doi: 10.1016/j.atherosclerosis.2011.11.034. Epub 2011 Nov 28. Review.

PMID:
22189200
19.

Lecithin: cholesterol acyl transferase (LCAT).

Frohlich J, McLeod R, Hon K.

Clin Biochem. 1982 Dec;15(6):269-78. Review.

PMID:
6762928
20.

Gene-manipulated Adipocytes for the Treatment of Various Intractable Diseases.

Kuroda M, Bujo H, Aso M, Saito Y, Yokote K.

Yakugaku Zasshi. 2016;136(5):705-9. doi: 10.1248/yakushi.15-00262-4. Review. Japanese.

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