Sjöholm AG - Search Results

1

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon.

Fredrikson GN, Gullstrand B, Schneider PM, Witzel-Schlömp K, Sjöholm AG, Alper CA, Awdeh Z, Truedsson L. Fredrikson GN, et al. Among authors: sjoholm ag. Hum Immunol. 1998 Nov;59(11):713-9. doi: 10.1016/s0198-8859(98)00068-8. Hum Immunol. 1998. PMID: 9796739

2

Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II genes.

Truedsson L, Alper CA, Awdeh ZL, Johansen P, Sjöholm AG, Sturfelt G. Truedsson L, et al. Among authors: sjoholm ag. J Immunol. 1993 Nov 15;151(10):5856-63. J Immunol. 1993. PMID: 7901282

3

Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency.

Westberg J, Fredrikson GN, Truedsson L, Sjöholm AG, Uhlén M. Westberg J, et al. Among authors: sjoholm ag. Genomics. 1995 Sep 1;29(1):1-8. doi: 10.1006/geno.1995.1208. Genomics. 1995. PMID: 8530058

4

Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.

Fredrikson GN, Westberg J, Kuijper EJ, Tijssen CC, Sjöholm AG, Uhlén M, Truedsson L. Fredrikson GN, et al. Among authors: sjoholm ag. J Immunol. 1996 Oct 15;157(8):3666-71. J Immunol. 1996. PMID: 8871668

5

Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutations.

Fredrikson GN, Gullstrand B, Westberg J, Sjöholm AG, Uhlén M, Truedsson L. Fredrikson GN, et al. Among authors: sjoholm ag. J Clin Immunol. 1998 Jul;18(4):272-82. doi: 10.1023/a:1027385806871. J Clin Immunol. 1998. PMID: 9710744

6

DNA analysis in a MHC heterozygous patient with complete C4 deficiency--homozygosity for C4 gene deletion and C4 pseudogene.

Nordin Fredrikson G, Truedsson L, Sjöholm AG, Kjellman M. Nordin Fredrikson G, et al. Among authors: sjoholm ag. Exp Clin Immunogenet. 1991;8(1):29-37. Exp Clin Immunogenet. 1991. PMID: 1910860

7

New procedure for the detection of complement deficiency by ELISA. Analysis of activation pathways and circumvention of rheumatoid factor influence.

Fredrikson GN, Truedsson L, Sjöholm AG. Fredrikson GN, et al. Among authors: sjoholm ag. J Immunol Methods. 1993 Dec 3;166(2):263-70. doi: 10.1016/0022-1759(93)90367-g. J Immunol Methods. 1993. PMID: 8288879

8

C4 phenotypes in IgA nephropathy: disease progression associated with C4A deficiency but not with C4 isotype concentrations.

Wopenka U, Thysell H, Sjöholm AG, Truedsson L. Wopenka U, et al. Among authors: sjoholm ag. Clin Nephrol. 1996 Mar;45(3):141-5. Clin Nephrol. 1996. PMID: 8706353

9

Human properdin deficiency has a heterogeneous genetic background.

Truedsson L, Westberg J, Fredrikson GN, Sjöholm AG, Kuijper EJ, Fijen CA, Späth PJ, Uhlén M. Truedsson L, et al. Among authors: sjoholm ag. Immunopharmacology. 1997 Dec;38(1-2):203-6. doi: 10.1016/s0162-3109(97)00087-8. Immunopharmacology. 1997. PMID: 9476131 Review. No abstract available.

10

Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n).

Späth PJ, Sjöholm AG, Fredrikson GN, Misiano G, Scherz R, Schaad UB, Uhring-Lambert B, Hauptmann G, Westberg J, Uhlén M, Wadelius C, Truedsson L. Späth PJ, et al. Among authors: sjoholm ag. Clin Exp Immunol. 1999 Nov;118(2):278-84. doi: 10.1046/j.1365-2249.1999.01056.x. Clin Exp Immunol. 1999. PMID: 10540191 Free PMC article.

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