PRIMARY LCAT-DEFICIENCY DISEASE

被引:0
|
作者
BRON, AJ
LLOYD, JK
FOSBROOKE, AS
WINDER, AF
TRIPATHI, RC
机构
[1] NUFFIELD LAB OPHTHALMOL,WALTON ST,OXFORD,ENGLAND
[2] INST CHILD HLTH,LONDON,ENGLAND
[3] INST OPHTHALMOL,LONDON,ENGLAND
来源
LANCET | 1975年 / 1卷 / 7912期
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:928 / 929
页数:2
相关论文
共 50 条
  • [31] ERYTHROCYTE ALTERATIONS IN PRASEODYMIUM-INDUCED LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) DEFICIENCY IN THE RAT - COMPARISON WITH FAMILIAL LCAT DEFICIENCY IN MAN
    GODIN, DV
    FROHLICH, J
    RESEARCH COMMUNICATIONS IN CHEMICAL PATHOLOGY AND PHARMACOLOGY, 1981, 31 (03): : 555 - 566
  • [32] FAMILIAL LCAT DEFICIENCY AND CARDIOVASCULAR DISEASE: THE GAME IS NOT OVER. A CASE OF DRAMATIC MULTIVESSEL ATHEROSCLEROSIS
    Bigazzi, F.
    Dal Pino, B.
    Pavanello, C.
    Sbrana, F.
    Aquaro, G. D.
    Napoli, V.
    Palmieri, C.
    Barison, A.
    Calabresi, L.
    Sampietro, T.
    ATHEROSCLEROSIS, 2020, 315 : E155 - E155
  • [33] MOLECULAR DEFECT IN FAMILIAL LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) DEFICIENCY - A SINGLE NUCLEOTIDE INSERTION IN LCAT GENE CAUSES A COMPLETE DEFICIENT TYPE OF THE DISEASE
    BUJO, H
    KUSUNOKI, J
    OGASAWARA, M
    YAMAMOTO, T
    OHTA, Y
    SHIMADA, T
    SAITO, Y
    YOSHIDA, S
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (03) : 933 - 940
  • [34] CORNEAL OPACITY IN LCAT DISEASE
    COGAN, DG
    KRUTH, HS
    DATILIS, MB
    MARTIN, N
    CORNEA, 1992, 11 (06) : 595 - 599
  • [35] 2 NOVEL POINT MUTATIONS IN THE LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE RESULTING IN LCAT DEFICIENCY - LCAT (G(873) DELETION) AND LCAT (GLY(344)-]SER)
    MORIYAMA, K
    SASAKI, J
    ARAKAWA, F
    TAKAMI, N
    MAEDA, E
    MATSUNAGA, A
    TAKADA, Y
    MIDORIKAWA, K
    YANASE, T
    YOSHINO, G
    MARCOVINA, SM
    ALBERS, JJ
    ARAKAWA, K
    JOURNAL OF LIPID RESEARCH, 1995, 36 (11) : 2329 - 2343
  • [36] 2 DIFFERENT ALLELIC MUTATIONS IN THE LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE RESULTING IN CLASSIC LCAT DEFICIENCY - LCAT (TYR(83)-]STOP) AND LCAT (TYR(156)-]ASN)
    KLEIN, HG
    LOHSE, P
    DUVERGER, N
    ALBERS, JJ
    RADER, DJ
    ZECH, LA
    SANTAMARINAFOJO, S
    BREWER, HB
    JOURNAL OF LIPID RESEARCH, 1993, 34 (01) : 49 - 58
  • [37] FAMILIAL LECITHIN: CHOLESTEROL ACYLTRANSFERASE (LCAT) DEFICIENCY AS A CAUSE OF CHRONIC KIDNEY DISEASE - A CASE REPORT
    Obeidat, Motaz
    Obeidat, Marya
    Al-Shboul, Mohammad
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2023, 38 : I232 - I233
  • [38] Progression of chronic kidney disease in familial LCAT deficiency: a follow-up of the Italian cohort
    Pavanello, Chiara
    Ossoli, Alice
    Arca, Marcello
    D'Erasmo, Laura
    Boscutti, Giuliano
    Gesualdo, Loreto
    Lucchi, Tiziano
    Sampietro, Tiziana
    Veglia, Fabrizio
    Calabresi, Laura
    JOURNAL OF LIPID RESEARCH, 2020, 61 (12) : 1784 - 1788
  • [39] LECITHIN-CHOLESTEROL ACYLTRANSFERASE DEFICIENCY - INVITRO EXPRESSION OF GENE DEFECTS ASSOCIATED WITH CLASSIC LCAT DEFICIENCY AND FISH EYE DISEASE
    KLEIN, HG
    DUVERGER, N
    ALBERS, JJ
    BREWER, HB
    SANTAMARINAFOJO, S
    CIRCULATION, 1992, 86 (04) : 420 - 420
  • [40] Mutations in LCAT gene causing familial LUXI deficiency, fish eye disease and co-dominant familial HDL deficiency
    Bertolini, S
    Calabresi, L
    Pisciotta, L
    Balboni, M
    Arca, M
    Cantafora, A
    Franceschini, G
    Calandra, S
    ATHEROSCLEROSIS SUPPLEMENTS, 2004, 5 (01) : 80 - 80