Goetz J - Search Results

1

HLA A*, B*-BF* and C4 A*, B* allele associations, with special reference to BF*S07, in the Tunisian population.

Helal AN, Lefranc G, Hauptmann G, Goetz J, Tongio MM, Davrinche C, Rivat C, Cavelier B, Chibani J, Chaabani H. Helal AN, et al. Among authors: goetz j. J Immunogenet. 1983 Jun;10(3):205-8. doi: 10.1111/j.1744-313x.1983.tb00796.x. J Immunogenet. 1983. PMID: 6576063

2

[Polymorphism of C4 and factor B in type I diabetes].

Blickle JF, Hauptmann G, Goetz J, Tongio MM, Mayer S, Brogard JM, Dorner M. Blickle JF, et al. Among authors: goetz j. Pathol Biol (Paris). 1988 Jun;36(6):791-4. Pathol Biol (Paris). 1988. PMID: 3047638 French.

3

C4 haplotypes with duplications at the C4A or C4B loci: frequency and associations with BF, C2, and HLA-A, B, C, DR alleles.

Uring-Lambert B, Goetz J, Tongio MM, Mayer S, Hauptmann G. Uring-Lambert B, et al. Among authors: goetz j. Tissue Antigens. 1984 Jul;24(1):70-2. doi: 10.1111/j.1399-0039.1984.tb00403.x. Tissue Antigens. 1984. PMID: 6592795 No abstract available.

4

Association of the C2-deficiency gene (C2*QO) with the C4A*4, C4B*2 genes.

Hauptmann G, Tongio MM, Goetz J, Mayer S, Fauchet R, Sobel A, Griscel C, Berthoux F, Rivat C, Rother U. Hauptmann G, et al. Among authors: goetz j. J Immunogenet. 1982 Apr;9(2):127-32. doi: 10.1111/j.1744-313x.1982.tb00972.x. J Immunogenet. 1982. PMID: 7086154 No abstract available.

5

Molecular basis of complete C4 deficiency. A study of three patients.

Uring-Lambert B, Mascart-Lemone F, Tongio MM, Goetz J, Hauptmann G. Uring-Lambert B, et al. Among authors: goetz j. Hum Immunol. 1989 Feb;24(2):125-32. doi: 10.1016/0198-8859(89)90052-9. Hum Immunol. 1989. PMID: 2784426

6

Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysis.

Uring-Lambert B, Vegnaduzzi N, Carroll MC, Tongio MM, Goetz J, Hauptmann G. Uring-Lambert B, et al. Among authors: goetz j. FEBS Lett. 1987 Jun 8;217(1):65-8. doi: 10.1016/0014-5793(87)81244-9. FEBS Lett. 1987. PMID: 2885219 Free article.

7

Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic model.

Giles CM, Uring-Lambert B, Goetz J, Hauptmann G, Fielder AH, Ollier W, Rittner C, Robson T. Giles CM, et al. Among authors: goetz j. Immunogenetics. 1988;27(6):442-8. doi: 10.1007/BF00364431. Immunogenetics. 1988. PMID: 2453461

8

Complement C4 phenotypes in dementia of the Alzheimer type.

Eikelenboom P, Goetz J, Pronk JC, Hauptmann G. Eikelenboom P, et al. Among authors: goetz j. Hum Hered. 1988;38(1):48-51. doi: 10.1159/000153754. Hum Hered. 1988. PMID: 3350531

9

An estimate on the frequency of duplicated haplotypes and silent alleles of human C4 protein polymorphism. I. Investigations in healthy Caucasoid families.

Steuer M, Mauff G, Adam C, Baur MP, Bender K, Goetz J, Goldmann SF, Hauptmann G, Neugebauer M, Tongio MM, et al. Steuer M, et al. Among authors: goetz j. Tissue Antigens. 1989 May;33(5):501-10. doi: 10.1111/j.1399-0039.1989.tb01701.x. Tissue Antigens. 1989. PMID: 2799804

10

Partial deficiency of the fourth component of human complement (C4) and autoantibody directed against C4 in a patient with SLE.

Ripoche J, Fontaine M, Godin M, Hauptmann G, Goetz J. Ripoche J, et al. Among authors: goetz j. Ann Immunol (Paris). 1983 Sep-Oct;134D(2):233-45. doi: 10.1016/s0771-050x(83)80089-8. Ann Immunol (Paris). 1983. PMID: 6559049

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