Literature DB >> 8224938

Ophthalmological findings in three patients with cholesterol acyltransferase deficiency syndrome before and after kidney transplantation.

A Langmann1, G Langmann, C Faschinger, J Horina.   

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Year:  1993        PMID: 8224938     DOI: 10.1007/bf00936527

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


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  7 in total

1.  Corneal and fundus changes in familial LCAT-deficiency.

Authors:  I Borven; K Egge; E Gjone
Journal:  Acta Ophthalmol (Copenh)       Date:  1974

2.  Ocular manifestations in familial lecithin: cholesterol acyltransferase deficiency.

Authors:  I Hörven
Journal:  Scand J Clin Lab Invest Suppl       Date:  1974

3.  Familial serum cholesterol ester deficiency. Clinical study of a patient with a new syndrome.

Authors:  E Gjone; K R Norum
Journal:  Acta Med Scand       Date:  1968 Jan-Feb

4.  Lecithin:cholesterol acyl transferase deficiency presenting as visual impairment, with hypocholesterolaemia and normal renal function.

Authors:  A F Winder; A J Bron
Journal:  Scand J Clin Lab Invest Suppl       Date:  1978

5.  Lecithin cholesterol acyl transferase deficiency. Light and electron microscopic finding from two corneas.

Authors:  W Bethell; C McCulloch; M Ghosh
Journal:  Can J Ophthalmol       Date:  1975-10       Impact factor: 1.882

6.  [Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature].

Authors:  E G Weidle; W Lisch
Journal:  Klin Monbl Augenheilkd       Date:  1987-03       Impact factor: 0.700

7.  Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea.

Authors:  A F Winder; A Garner; G A Sheraidah; P Barry
Journal:  J Lipid Res       Date:  1985-03       Impact factor: 5.922

  7 in total

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