Kuijper EJ - Search Results

1

Linkage analysis in properdin deficiency families: refined location in proximal Xp.

Wadelius C, Pigg M, Sundvall M, Sjöholm AG, Goonewardena P, Kuijper EJ, Tijssen CC, Jansz A, Späth PJ, Schaad UB, et al. Wadelius C, et al. Among authors: kuijper ej. Clin Genet. 1992 Jul;42(1):8-12. doi: 10.1111/j.1399-0004.1992.tb03126.x. Clin Genet. 1992. PMID: 1516231

2

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: kuijper ej. J Immunol. 1996 Oct 15;157(8):3666-71. J Immunol. 1996. PMID: 8871668

3

Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatellite.

Agardi D, Pigg M, Sjöholm AG, Truedsson L, Späth PJ, Kuijper EJ, Tijssen CC, Tranebjaerg L, Gustavson KH, Ulfendahl PJ, et al. Agardi D, et al. Among authors: kuijper ej. Exp Clin Immunogenet. 1995;12(2):111-4. Exp Clin Immunogenet. 1995. PMID: 7576715

4

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: kuijper ej. Immunopharmacology. 1997 Dec;38(1-2):203-6. doi: 10.1016/s0162-3109(97)00087-8. Immunopharmacology. 1997. PMID: 9476131 Review. No abstract available.

5

Dysfunctional properdin in a Dutch family with meningococcal disease.

Sjöholm AG, Kuijper EJ, Tijssen CC, Jansz A, Bol P, Spanjaard L, Zanen HC. Sjöholm AG, et al. Among authors: kuijper ej. N Engl J Med. 1988 Jul 7;319(1):33-7. doi: 10.1056/NEJM198807073190106. N Engl J Med. 1988. PMID: 3380115 No abstract available.

6

Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.

van den Bogaard R, Fijen CA, Schipper MG, de Galan L, Kuijper EJ, Mannens MM. van den Bogaard R, et al. Among authors: kuijper ej. Eur J Hum Genet. 2000 Jul;8(7):513-8. doi: 10.1038/sj.ejhg.5200496. Eur J Hum Genet. 2000. PMID: 10909851

7

Complement deficiencies in patients over ten years old with meningococcal disease due to uncommon serogroups.

Fijen CA, Kuijper EJ, Hannema AJ, Sjöholm AG, van Putten JP. Fijen CA, et al. Among authors: kuijper ej. Lancet. 1989 Sep 9;2(8663):585-8. doi: 10.1016/s0140-6736(89)90712-5. Lancet. 1989. PMID: 2570284

8

Properdin deficiency: molecular basis and disease association.

Fijen CA, van den Bogaard R, Schipper M, Mannens M, Schlesinger M, Nordin FG, Dankert J, Daha MR, Sjöholm AG, Truedsson L, Kuijper EJ. Fijen CA, et al. Among authors: kuijper ej. Mol Immunol. 1999 Sep-Oct;36(13-14):863-7. doi: 10.1016/s0161-5890(99)00107-8. Mol Immunol. 1999. PMID: 10698340 Review. No abstract available.

9

[A family with meningococcal infections].

Tersmette-Steenstra HM, Kuijper EJ, Tijssen CC, Bol P, Zanen HC, Jansz A. Tersmette-Steenstra HM, et al. Among authors: kuijper ej. Ned Tijdschr Geneeskd. 1986 Dec 6;130(49):2213-6. Ned Tijdschr Geneeskd. 1986. PMID: 3543701 Dutch. No abstract available.

10

Application of whole-cell DNA restriction endonuclease profiles to the epidemiology of Clostridium difficile-induced diarrhea.

Kuijper EJ, Oudbier JH, Stuifbergen WN, Jansz A, Zanen HC. Kuijper EJ, et al. J Clin Microbiol. 1987 Apr;25(4):751-3. doi: 10.1128/jcm.25.4.751-753.1987. J Clin Microbiol. 1987. PMID: 3033017 Free PMC article.

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