A case of familial lecithin-cholesterol: Acyltransferase deficiency on hemodialysis: For over 20 years

Clinical Nephrology

Volumn 76, Issue 6, 2011, Pages 492-498

  Tsuchiya, Y ^a   Ubara, Y ^a   Hiramatsu, R ^a   Suwabe, T ^a   Hoshino, J ^a   Sumida, K ^a   Hasegawa, E ^a   Yamanouchi, M ^a   Hayami, N ^a   Marui, Y ^a   Sawa, N ^a   Hara, S ^a   Takaichi, K ^a   Oohashi, K ^a  

^a TORANOMON HOSPITAL   (Japan)

Author keywords

Autosomal recessive disease; LCAT deficiency; Renal failure

Indexed keywords

BILIRUBIN; CHOLESTEROL; CREATININE; FRESH FROZEN PLASMA; GLYCINE; TICLOPIDINE;

ADULT; ARTICLE; BILIRUBIN BLOOD LEVEL; CASE REPORT; CELL INFILTRATION; CELL VACUOLE; CHOLESTEROL BLOOD LEVEL; CODON; CONJUNCTIVA; CONSANGUINEOUS MARRIAGE; CORNEA OPACITY; CREATININE BLOOD LEVEL; ECHOGRAPHY; EDEMA; ELECTRON MICROSCOPY; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; FEMALE; FOAM CELL; GENETIC ANALYSIS; GENETIC CODE; GLOMERULUS BASEMENT MEMBRANE; HEMATURIA; HEMODIALYSIS; HEMOLYTIC ANEMIA; HEPATOSPLENOMEGALY; HUMAN; IMMUNOFLUORESCENCE; JAPANESE; JAUNDICE; KIDNEY BIOPSY; LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY; LIPID STORAGE; MALE; MICROSCOPY; PROTEINURIA; XANTHOMA;

ADULT; BIOPSY; HUMANS; KIDNEY; LECITHIN ACYLTRANSFERASE DEFICIENCY; LIPIDS; MALE; RENAL DIALYSIS; TIME FACTORS;

EID: 84855425769     PISSN: 03010430     EISSN: None     Source Type: Journal    
DOI: 10.5414/CN107007     Document Type: Article

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