Literature DB >> 29535099

LCAT deficiency as a cause of proteinuria and corneal opacification.

Enrique Morales1, Montserrat Morales2, Marina Alonso3, Beatriz Sarmiento4.   

Abstract

Entities:  

Keywords:  chronic renal failure; genetic screening / counselling; proteinuria; visual pathway

Mesh：

Substances：

Year:  2018        PMID： 29535099      PMCID： PMC5878272          DOI： 10.1136/bcr-2017-224129

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


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  3 in total

1.  Stability of lipids on peritoneal dialysis in a patient with familial LCAT deficiency.

Authors:  Catherine L Weber; Jiri Frohlich; Jian Wang; Robert A Hegele; Clifford Chan-Yan
Journal:  Nephrol Dial Transplant       Date:  2007-04-23       Impact factor: 5.992

2.  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

Review 3.  Very low levels of HDL cholesterol and atherosclerosis, a variable relationship--a review of LCAT deficiency.

Authors:  Julia Savel; Marianne Lafitte; Yann Pucheu; Vincent Pradeau; Antoine Tabarin; Thierry Couffinhal
Journal:  Vasc Health Risk Manag       Date:  2012-06-05
  3 in total
  1 in total

Review 1.  A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency.

Authors:  Cecilia Vitali; Archna Bajaj; Christina Nguyen; Jill Schnall; Jinbo Chen; Kostas Stylianou; Daniel J Rader; Marina Cuchel
Journal:  J Lipid Res       Date:  2022-01-20       Impact factor: 5.922
  1 in total

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