CLINICAL, BIOCHEMICAL, AND GENETIC FEATURES IN FAMILIAL DISORDERS OF HIGH-DENSITY LIPOPROTEIN DEFICIENCY

被引：149
|
作者：
SCHAEFER, EJ [1 ]
机构：
[1] NEW ENGLAND MED CTR,DIV ENDOCRINOL,BOSTON,MA 02111
来源：
ARTERIOSCLEROSIS | 1984年 / 4卷 / 04期
关键词：
D O I：
10.1161/01.ATV.4.4.303
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：303 / 322
页数：20
相关论文
共 50 条
  • [1] The clinical relevance and management of high-density lipoprotein deficiency
    Zlaket-Matta, G
    Vela, BS
    Brinton, EA
    [J]. ENDOCRINOLOGIST, 2001, 11 (01): : 16 - 25
  • [2] OCULAR MANIFESTATIONS OF FAMILIAL HIGH-DENSITY LIPOPROTEIN DEFICIENCY (TANGIER DISEASE)
    CHU, FC
    KUWABARA, T
    COGAN, DG
    SCHAEFER, EJ
    BREWER, HB
    [J]. ARCHIVES OF OPHTHALMOLOGY, 1979, 97 (10) : 1926 - 1928
  • [3] CORONARY HEART-DISEASE PREVALENCE AND OTHER CLINICAL-FEATURES IN FAMILIAL HIGH-DENSITY LIPOPROTEIN DEFICIENCY (TANGIER DISEASE)
    SCHAEFER, EJ
    ZECH, LA
    SCHWARTZ, DE
    BREWER, HB
    [J]. ANNALS OF INTERNAL MEDICINE, 1980, 93 (02) : 261 - 266
  • [4] CORNEAL OPACIFICATION AND FAMILIAL DISORDERS AFFECTING PLASMA HIGH-DENSITY LIPOPROTEIN
    WINDER, AF
    BORYSIEWICZ, LK
    [J]. BIRTH DEFECTS-ORIGINAL ARTICLE SERIES, 1982, 18 (06) : 433 - 440
  • [5] Disorders of high-density lipoprotein biogenesis
    Krimbou, Larbi
    Ruel, Isabelle
    Dastani, Zari
    Alrasadi, Khalid
    Hassan, Houssein Hajj
    Iatan, Iulia
    Marcil, Michel
    Genest, Jacques
    [J]. ANNALS OF MEDICINE, 2008, 40 : 39 - 47
  • [6] Genetic and Clinical Heterogeneity of Marked High Density Lipoprotein Deficiency
    Polisecki, Eliana
    Geller, Andrew S.
    Sacco, Taylor
    Diffenderfer, Margaret R.
    Asztalos, Bela F.
    Karathanasis, Sotirios K.
    Hegele, Robert A.
    Schaefer, Ernst J.
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2017, 37
  • [7] Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
    Angela Brooks-Wilson
    Michel Marcil
    Susanne M. Clee
    Lin-Hua Zhang
    Kirsten Roomp
    Marjel van Dam
    Lu Yu
    Carl Brewer
    Jennifer A. Collins
    Henri O.F. Molhuizen
    Odell Loubser
    B.F. Francis Ouelette
    Keith Fichter
    Katherine J.D. Ashbourne-Excoffon
    Christoph W. Sensen
    Stephen Scherer
    Stephanie Mott
    Maxime Denis
    Duane Martindale
    Jiri Frohlich
    Kenneth Morgan
    Ben Koop
    Simon Pimstone
    John J.P. Kastelein
    Jacques Genest
    Michael R. Hayden
    [J]. Nature Genetics, 1999, 22 : 336 - 345
  • [8] Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
    Brooks-Wilson, A
    Marcil, M
    Clee, SM
    Zhang, LH
    Roomp, K
    van Dam, M
    Yu, L
    Brewer, C
    Collins, JA
    Molhuizen, HOF
    Loubser, O
    Ouelette, BFF
    Fichter, K
    Ashbourne-Excoffon, KJD
    Sensen, CW
    Scherer, S
    Mott, S
    Denis, M
    Martindale, D
    Frohlich, J
    Morgan, K
    Koop, B
    Pimstone, S
    Kastelein, JJP
    Genest, J
    Hayden, MR
    [J]. NATURE GENETICS, 1999, 22 (04) : 336 - 345
  • [9] CHOLESTERYL ESTER TRANSFER ACTIVITY IN PLASMA OF PATIENTS WITH FAMILIAL HIGH-DENSITY LIPOPROTEIN DEFICIENCY
    SPARKS, DL
    FROHLICH, J
    PRITCHARD, PH
    [J]. CLINICAL CHEMISTRY, 1988, 34 (09) : 1812 - 1815
  • [10] Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency
    Hayden, MR
    Clee, SM
    Brooks-Wilson, A
    Genest, J
    Attie, A
    Kastelein, JJP
    [J]. CURRENT OPINION IN LIPIDOLOGY, 2000, 11 (02) : 117 - 122
12345