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Literature DB >> 9394340

Recurrence of lecithin cholesterol acyltransferase deficiency after kidney transplantation.

V Panescu¹, Y Grignon, D Hestin, G Rostoker, L Frimat, E Renoult, J Gamberoni, G Grignon, M Kessler.

Abstract

Entities: Disease

Mesh：

Year: 1997 PMID： 9394340 DOI： 10.1093/ndt/12.11.2430

Source DB: PubMed Journal: Nephrol Dial Transplant ISSN： 0931-0509 Impact factor: 5.992

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11 in total

1. Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.

Authors: Robert D Shamburek; Rebecca Bakker-Arkema; Bruce J Auerbach; Brian R Krause; Reynold Homan; Marcelo J Amar; Lita A Freeman; Alan T Remaley
Journal: J Clin Lipidol Date: 2015-12-23 Impact factor: 4.766

2. Nephrotic syndrome caused by immune-mediated acquired LCAT deficiency.

Authors: Satoshi Takahashi; Keiju Hiromura; Mayuko Tsukida; Yuko Ohishi; Hiroko Hamatani; Noriyuki Sakurai; Toru Sakairi; Hidekazu Ikeuchi; Yoriaki Kaneko; Akito Maeshima; Takashi Kuroiwa; Hideaki Yokoo; Takeo Aoki; Michio Nagata; Yoshihisa Nojima
Journal: J Am Soc Nephrol Date: 2013-04-25 Impact factor: 10.121

3. Effect of recombinant human lecithin cholesterol acyltransferase infusion on lipoprotein metabolism in mice.

Authors: Xavier Rousset; Boris Vaisman; Bruce Auerbach; Brian R Krause; Reyn Homan; John Stonik; Gyorgy Csako; Robert Shamburek; Alan T Remaley
Journal: J Pharmacol Exp Ther Date: 2010-07-06 Impact factor: 4.030

Review 4. Approach to the patient with extremely low HDL-cholesterol.

Authors: Daniel J Rader; Emil M deGoma
Journal: J Clin Endocrinol Metab Date: 2012-10 Impact factor: 5.958

5. Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.

Authors: I Castro-Ferreira; Rute Carmo; Sérgio Estrela Silva; Otília Corrêa; Susana Fernandes; Susana Sampaio; Rodrigues-Pereira Pedro; Augusta Praça; João Paulo Oliveira
Journal: JIMD Rep Date: 2017-10-06

Recurrence of lecithin cholesterol acyltransferase deficiency after kidney transplantation.

1. Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.

2. Nephrotic syndrome caused by immune-mediated acquired LCAT deficiency.

3. Effect of recombinant human lecithin cholesterol acyltransferase infusion on lipoprotein metabolism in mice.

Review 4. Approach to the patient with extremely low HDL-cholesterol.

5. Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.

Review 6. Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease.

7. Familial lecithin-cholesterol acyltransferase (LCAT) deficiency; a differential of proteinuria.

8. An unusual presentation of LCAT deficiency as nephrotic syndrome with normal serum HDL-C level.

Review 9. Combined liver-kidney transplantation for rare diseases.

10. LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.