INHERITED DISORDERS OF COMPLEMENT

被引:27
作者
GUENTHER, LC [1 ]
机构
[1] UNIV MICHIGAN,DEPT DERMATOL,ANN ARBOR,MI 48109
关键词
D O I
10.1016/S0190-9622(83)70195-7
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:815 / 839
页数:25
相关论文
共 272 条
[1]  
ABRAMOWICZ M, 1981, MED LETT DRUGS THER, V23, P83
[2]  
ABRAMSON N, 1971, J IMMUNOL, V107, P19
[3]  
AGNELLO V, 1978, J IMMUNOL, V120, P1761
[4]  
AGNELLO V, 1972, J IMMUNOL, V108, P837
[5]  
AGNELLO V, 1978, MEDICINE, V57, P1
[6]  
Agnello V, 1975, Birth Defects Orig Artic Ser, V11, P312
[7]   LINKAGE OF HL-A AND GBG [J].
ALLEN, FH .
VOX SANGUINIS, 1974, 27 (04) :382-384
[8]  
ALPER CA, 1972, LANCET, V2, P1179
[9]   STUDIES IN-VIVO AND IN-VITRO ON AN ABNORMALITY IN METABOLISM OF C3 IN A PATIENT WITH INCREASED SUSCEPTIBILITY TO INFECTION [J].
ALPER, CA ;
ABRAMSON, N ;
JOHNSTON, RB ;
JANDL, JH ;
ROSEN, FS ;
WATSON, L .
JOURNAL OF CLINICAL INVESTIGATION, 1970, 49 (11) :1975-&
[10]   INACTIVATOR OF THIRD COMPONENT OF COMPLEMENT AS AN INHIBITOR IN PROPERDIN PATHWAY [J].
ALPER, CA ;
ROSEN, FS ;
LACHMANN, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (10) :2910-&