-
13
-
-
0016370329
-
Systemic lupus erythematosus in the community: incidence, prevalence, outcome, and first symptoms; the high prevalence in black women.
-
(1974)
Arch Intern Med
, vol.134
, pp. 1027-1035
-
-
Fessel, WJ1
-
21
-
-
0018868978
-
Hydralazine induced systemic lupus erythematosus: influence of HLA‐DR and sex on susceptibility.
-
(1980)
Lancet
, vol.1
, pp. 1107-1109
-
-
Batchelor, JR1
Welch, KI2
Tinoco, RM3
Dollery, CT4
Hughes, GR5
Bernstein, R6
Ryan, P7
Naish, PF8
Aber, GM9
Bing, RF10
Russell, GI11
-
23
-
-
0019944157
-
Interrelationships of HLA–DR, MB, and MT phenotypes, autoantibody expression, and clinical features in systemic lupus erythematosus.
-
(1982)
Arthritis Rheum
, vol.25
, pp. 1031-1040
-
-
Ahearn, JM1
Provost, TT2
Dorsch, CA3
Stevens, MB4
Bias, WB5
Arnett, FC6
-
31
-
-
0022603870
-
Inherited complement component abnormalities.
-
(1986)
Annu Rev Med
, vol.37
, pp. 333-346
-
-
Schur, PH1
-
38
-
-
0024273145
-
Complete C4B deficiency cardiolipin antibodies in black Americans with systemic lupus erythematosus.
-
(1988)
J Rheumatol
, vol.15
, pp. 1855-1858
-
-
Wilson, WA1
Perez, MC2
-
43
-
-
0020436689
-
The 1982 revised criteria for the classification of systemic lupus erythematosus.
-
(1982)
Arthritis Rheum
, vol.25
, pp. 1272-1277
-
-
Tan, EM1
Cohen, AS2
Fries, JF3
Masi, AT4
McShane, DJ5
Rothfield, NF6
Schaller, JG7
Talal, N8
Winchester, RJ9
-
44
-
-
0003309689
-
Clinical features of systemic lupus erythematosus
-
Third edition., Edited by, WN. Kelley, ED. Harris Jr, S. Ruddy, CB. Sledge, Philadelphia, WB Saunders
-
(1989)
Textbook of Rheumatology.
-
-
Schur, PH1
-
48
-
-
84996075177
-
Histocompatibilit
-
Bodmer WF, Batchelor JR, Bodmer JG, Festenstein H, Morris PJ, editors:, Copenhagen, Munksgaard
-
(1978)
Testing 1977.
-
-
-
52
-
-
0017130867
-
Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.
-
(1976)
J Exp Med
, vol.144
, pp. 1111-1115
-
-
Alper, CA1
-
56
-
-
0022539141
-
Polymorphism of the human complement C4 and steroid 21‐hydroxylase genes: restriction fragment length polymorphisms revealing structural deletion, homoduplications, and size variants.
-
(1986)
J Clin Invest
, vol.78
, pp. 650-657
-
-
Schneider, PM1
Carroll, MC2
Alper, CA3
Rittner, C4
White‐head, AS5
Yunis, EJ6
Colten, HR7
-
57
-
-
0001658169
-
Population analysis on the basis of deduced haplotypes from random families
-
Edited by, ED. Albert, MP. Baur, WR. Mayr, New York, Springer Verlag
-
(1984)
Histocompatibility Testing 1984.
-
-
Baur, MP1
Neugebauer, M2
Deppe, H3
Sigmund, M4
Luton, T5
Mayr, WR6
Albert, ED7
-
60
-
-
0020666820
-
Extended MHC haplotypes in 21‐hydroxylase‐deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients.
-
(1983)
Lancet
, vol.1
, pp. 152-156
-
-
Fleischnick, E1
Awdeh, ZL2
Raum, D3
Granados, J4
Alosco, SM5
Crigler, JF6
Gerald, PS7
Giles, CM8
Yunis, EJ9
Alper, CA10
-
61
-
-
0023153960
-
Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency.
-
(1987)
Immunogenetics
, vol.25
, pp. 99-103
-
-
Layrisse, Z1
White, C2
Gunczler, P3
Gafaro Valera, L4
Arias, S5
Yunis, EJ6
Alper, CA7
Awdeh, ZL8
-
62
-
-
84996073778
-
-
Comparative study of HLA associations and C4A gene deletion in French‐Canadian and non‐French‐Canadian Caucasians with systemic lupus erythematosus (SLE), Fifteenth Annual Meeting of the American Society for Histocompatibility and Immunogenetics. Toronto, September
-
(1989)
, pp. 17-21
-
-
Goldstein, R1
Sengar, DPS2
|