SCOPUS 정보 검색 플랫폼

Volumn 18, Issue 1, 1998, Pages 48-51

The phenotype of SLE associated with complete deficiency of complement isotype C4A

(7) Welch, Thomas R a,b Brickman, Chaim c Bishof, Nancy d Maringhini, Silvio e Rutkowski, Mark f Frenzke, Marie a Kantor, Nancy c

a CINCINNATI CHILDREN S HOSPITAL RESEARCH FOUNDATION (United States)

b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER (United States)

c SINAI GRACE HOSPITAL (United States)

d UNIVERSITY OF KENTUCKY (United States)

e Ospedale dei Bambini di Palermo (Italy)

f UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE (United States)

Author keywords

Complement; Deficiency; Genetics; Systemic lupus erythematosus

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4A;

ADULT; ARTICLE; COMPLEMENT DEFICIENCY; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; HUMAN; KIDNEY DISEASE; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SYSTEMIC LUPUS ERYTHEMATOSUS;

ADULT; AFRICAN CONTINENTAL ANCESTRY GROUP; ALLELES; COMPLEMENT C3; COMPLEMENT C4A; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; MALE; MIDDLE AGED; MULTICENTER STUDIES; PHENOTYPE; SEVERITY OF ILLNESS INDEX;

EID: 0031888367 PISSN: 02719142 EISSN: None Source Type: Journal
DOI: 10.1023/A:1023287820786 Document Type: Article

Times cited : (25)

References (18)

1
- 0020471136
- Disease states in genetic complement deficiencies
- Tappeiner G: Disease states in genetic complement deficiencies. Int J Dermatol 21:175-191, 1982
- (1982) Int J Dermatol , vol.21 , pp. 175-191
- Tappeiner, G.¹

2
- 0024211944
- Inherited deficiency of the fourth component of human complement
- Hauptmann G, Tappeiner G, Schifferli JA: Inherited deficiency of the fourth component of human complement. Immunodefic Rev 1:3-22, 1988
- (1988) Immunodefic Rev , vol.1 , pp. 3-22
- Hauptmann, G.¹ Tappeiner, G.² Schifferli, J.A.³

3
- 0022539141
- Polymorphism of the human complement C4 and steroid 21-hydroxylase genes
- Schneider PM, Carroll MC, Alper CA, Rittner C, Whitehead AS: Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. J Clin Invest 78:650-657, 1986
- (1986) J Clin Invest , vol.78 , pp. 650-657
- Schneider, P.M.¹ Carroll, M.C.² Alper, C.A.³ Rittner, C.⁴ Whitehead, A.S.⁵

4
- 0025089362
- Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A
- Carroll MC, Fathallah DM, Bergamaschini L, Alicot EM, Isenman DE: Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A. Proc Natl Acad Sci USA 87:6868-6872, 1990
- (1990) Proc Natl Acad Sci USA , vol.87 , pp. 6868-6872
- Carroll, M.C.¹ Fathallah, D.M.² Bergamaschini, L.³ Alicot, E.M.⁴ Isenman, D.E.⁵

5
- 0024310747
- Molecular genetics of C4B deficiency in IgA nephropathy
- Welch TR, Beischel LS, Choi EM: Molecular genetics of C4B deficiency in IgA nephropathy. Hum Immunol 26:353-363, 1989
- (1989) Hum Immunol , vol.26 , pp. 353-363
- Welch, T.R.¹ Beischel, L.S.² Choi, E.M.³

6
- 0025022528
- Null alleles of human complement C4
- Braun L, Schneider PM, Giles CM, Bertrams J, Rittner C: Null alleles of human complement C4. J Exp Med 171:129-140, 1990
- (1990) J Exp Med , vol.171 , pp. 129-140
- Braun, L.¹ Schneider, P.M.² Giles, C.M.³ Bertrams, J.⁴ Rittner, C.⁵

7
- 0023771690
- Major histocompatibility complex extended haplotypes in systemic lupus erythematosus
- Welch TR, Beischel LS, Balakrishnan K, Quinlan M, West CD: Major histocompatibility complex extended haplotypes in systemic lupus erythematosus. Dis Markers 6:247-255, 1988
- (1988) Dis Markers , vol.6 , pp. 247-255
- Welch, T.R.¹ Beischel, L.S.² Balakrishnan, K.³ Quinlan, M.⁴ West, C.D.⁵

8
- 0022496377
- Clinical aspects of systemic lupus erythematosus in childhood
- Emery H: Clinical aspects of systemic lupus erythematosus in childhood. Pediatr Clin North Am 33:1177-1190, 1986
- (1986) Pediatr Clin North Am , vol.33 , pp. 1177-1190
- Emery, H.¹

9
- 0021948453
- The effect of null C4 alleles on complement function
- Welch TR, Beischel L, Berry A, Forristal J, West CD: The effect of null C4 alleles on complement function. Clin Immunol Immunopathol 34:316-325, 1985
- (1985) Clin Immunol Immunopathol , vol.34 , pp. 316-325
- Welch, T.R.¹ Beischel, L.² Berry, A.³ Forristal, J.⁴ West, C.D.⁵

10
- 0022235453
- Genetic deficiency of C4, C2 or C1q and lupus syndromes
- Meyer O, Hauptmann G, Tappeiner G, Ochs HD, Mascart-Lemone F: Genetic deficiency of C4, C2 or C1q and lupus syndromes. Clin Exp Immunol 62:678-684, 1985
- (1985) Clin Exp Immunol , vol.62 , pp. 678-684
- Meyer, O.¹ Hauptmann, G.² Tappeiner, G.³ Ochs, H.D.⁴ Mascart-Lemone, F.⁵

11
- 0029157307
- Glomerulonephritis associated with complete deficiency of the fourth component of complement
- Welch TR, McAdams JA, Beischel LS: Glomerulonephritis associated with complete deficiency of the fourth component of complement. Arth Rheum 38:1333-1337, 1995
- (1995) Arth Rheum , vol.38 , pp. 1333-1337
- Welch, T.R.¹ McAdams, J.A.² Beischel, L.S.³

12
- 0023574736
- C4 isotype deficiency in IgA nephropathy
- Welch TR, Berry A, Beischel LS: C4 isotype deficiency in IgA nephropathy. Pediatr Nephr 1:136-139, 1987
- (1987) Pediatr Nephr , vol.1 , pp. 136-139
- Welch, T.R.¹ Berry, A.² Beischel, L.S.³

13
- 0025367541
- C4B deficiency: A risk factor for bacteremia with encapsulated organisms
- Bishof NA, Welch TR, Beischel LS: C4B deficiency: A risk factor for bacteremia with encapsulated organisms. J Infect Dis 162:248-250, 1990
- (1990) J Infect Dis , vol.162 , pp. 248-250
- Bishof, N.A.¹ Welch, T.R.² Beischel, L.S.³

14
- 0020687287
- Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: Importance of null alleles of C4A and C4B in determining disease susceptibility
- Fielder AHL, Walport MJ, Batchelor JR, Rynes RI, Black CM, Dodi IA, Hughes GRV: Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: Importance of null alleles of C4A and C4B in determining disease susceptibility. Br Med J 286:425-428, 1983
- (1983) Br Med J , vol.286 , pp. 425-428
- Fielder, A.H.L.¹ Walport, M.J.² Batchelor, J.R.³ Rynes, R.I.⁴ Black, C.M.⁵ Dodi, I.A.⁶ Hughes, G.R.V.⁷

15
- 0020688126
- Extended HLA/ complement allele haplotypes: Evidence for T/t-like complex in man
- Awdeh ZL, Raum D, Yunis EJ, Alper CA: Extended HLA/ complement allele haplotypes: Evidence for T/t-like complex in man. Proc Natl Acad Sci USA 80:259-263, 1983
- (1983) Proc Natl Acad Sci USA , vol.80 , pp. 259-263
- Awdeh, Z.L.¹ Raum, D.² Yunis, E.J.³ Alper, C.A.⁴

16
- 0022632377
- Major-histocompatibility-complex extended haplotypes in membranoproliferative glomerulonephritis
- Welch TR, Beischel LS, Balakrishnan BS, Quinlan M, West CD: Major-histocompatibility-complex extended haplotypes in membranoproliferative glomerulonephritis. N Engl J Med 314:1476-1481, 1986
- (1986) N Engl J Med , vol.314 , pp. 1476-1481
- Welch, T.R.¹ Beischel, L.S.² Balakrishnan, B.S.³ Quinlan, M.⁴ West, C.D.⁵

17
- 0022472150
- Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black Americans
- Howard PF, Hochberg MC, Bias WB, Arnett FC, McLean RH: Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black Americans. Am J Med 81:187-193, 1986
- (1986) Am J Med , vol.81 , pp. 187-193
- Howard, P.F.¹ Hochberg, M.C.² Bias, W.B.³ Arnett, F.C.⁴ McLean, R.H.⁵

18
- 0030059140
- Comparative analysis of the disease-associated complement C4 gene from the HLA-A1, B8, DR3 haplotype
- Ulgiati D, Abraham LJ: Comparative analysis of the disease-associated complement C4 gene from the HLA-A1, B8, DR3 haplotype. Exp Clin Immunogenet 13:43-54, 1996
- (1996) Exp Clin Immunogenet , vol.13 , pp. 43-54
- Ulgiati, D.¹ Abraham, L.J.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.