SELECTIVE COMPLETE CLQ DEFICIENCY - REPORT OF 2 NEW CASES

被引：16

作者：

BERKEL, AI

LOOS, M

SANAL, O

ERSOY, F

YEGIN, O

机构：

[1] UNIV MAINZ,INST MED MIKROBIOL,D-6500 MAINZ,FED REP GER

[2] HACETTEPE UNIV,HACETTEPE CHILDRENS HOSP,INST CHILD HLTH,IMMUNOL LAB,ANKARA,TURKEY

来源：

关键词：

D O I：

10.1016/0165-2478(81)90017-1

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

引用

页码：263 / 267

页数：5

共 21 条

[1] AGNELLO V, 1978, MEDICINE, V57, P1
[2] BAKKALOGLU A, 1977, LANCET, V2, P430
[3] Berkel A, 1977, TURKISH J PEDIATR, V19, P101
[4] BERKEL AI, 1979, CLIN EXP IMMUNOL, V38, P52
[5] CHAPUIS RM, 1980, 5TH EUR COMPL WORKSH
[6] COLTEN HR, 1969, J IMMUNOL, V103, P862
[7] C1R DEFICIENCY - INBORN ERROR ASSOCIATED WITH CUTANEOUS AND RENAL-DISEASE
DAY, NK
DEBRACCO, M
MANCADO, B
WINDHORST, D
STROUD, R
GOOD, RA
GEIGER, H
[J]. JOURNAL OF CLINICAL INVESTIGATION, 1972, 51 (05) : 1102 - +
[8] HAUPTMANN G, 1974, NOUV PRESSE MED, V3, P881
[9] GENETIC DEFECTS OF COMPLEMENT IN MAN
LACHMANN, PJ
ROSEN, FS
[J]. SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 1978, 1 (04): : 339 - 353
[10] LEYVACOBIAN F, 1980, 4TH INT C IMM PAR