Nephropathy of Familial Lecithin-Cholesterol Acyltransferase Deficiency: Report of a Case
- 1 January 1986
- journal article
- case report
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 7 (1) , 41-46
- https://doi.org/10.1016/s0272-6386(86)80055-5
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
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- Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: Evidence for functionally defective enzyme in homozygotes and obligate heterozygotesHuman Genetics, 1982
- Familial Lecithin:Cholesterol Acyltransferase DeficiencyActa Medica Scandinavica, 1981
- Familial Lecithin: Cholesterol Acyltransferase Deficiency Complicated with Unconjugated Hyperbilirubinemia and Peripheral NeuropathyActa Medica Scandinavica, 1978
- Renal Failure in Familial Lecithin-Cholesterol Acyltransferase DeficiencyNephron, 1977
- PRIMARY L.C.A.T.-DEFICIENCY DISEASEThe Lancet, 1975
- Possible association between an abnormal low density lipoprotein and nephropathy in lecithin: CHolesterol acyltransferase deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- Familial Lecithin: Cholesterol Acyltransferase Deficiency: Ultrastructural Studies on Lipid Deposition and Tissue ReactionsScandinavian Journal of Clinical and Laboratory Investigation, 1974
- Familial Lecithin: Cholesterol Acyltransferase Deficiency: Report of a Third Norwegian Family with Two Afflicted MembersScandinavian Journal of Clinical and Laboratory Investigation, 1974
- Lipoproteins in LCAT-deficiencyHuman Genetics, 1972