Weening RS - Search Results

1

Chronic granulomatous disease: the European experience.

van den Berg JM, van Koppen E, Ahlin A, Belohradsky BH, Bernatowska E, Corbeel L, Español T, Fischer A, Kurenko-Deptuch M, Mouy R, Petropoulou T, Roesler J, Seger R, Stasia MJ, Valerius NH, Weening RS, Wolach B, Roos D, Kuijpers TW. van den Berg JM, et al. Among authors: weening rs. PLoS One. 2009;4(4):e5234. doi: 10.1371/journal.pone.0005234. Epub 2009 Apr 21. PLoS One. 2009. PMID: 19381301 Free PMC article.

2

Recombinant human interferon-gamma in patients with chronic granulomatous disease--European follow up study.

Weening RS, Leitz GJ, Seger RA. Weening RS, et al. Eur J Pediatr. 1995 Apr;154(4):295-8. doi: 10.1007/BF01957365. Eur J Pediatr. 1995. PMID: 7607280 Clinical Trial.

3

Point mutations in the promoter region of the CYBB gene leading to mild chronic granulomatous disease.

Weening RS, De Boer M, Kuijpers TW, Neefjes VM, Hack WW, Roos D. Weening RS, et al. Clin Exp Immunol. 2000 Dec;122(3):410-7. doi: 10.1046/j.1365-2249.2000.01405.x. Clin Exp Immunol. 2000. PMID: 11122248 Free PMC article.

4

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).

de Boer M, de Klein A, Hossle JP, Seger R, Corbeel L, Weening RS, Roos D. de Boer M, et al. Among authors: weening rs. Am J Hum Genet. 1992 Nov;51(5):1127-35. Am J Hum Genet. 1992. PMID: 1415254 Free PMC article.

5

Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease.

Roos D, de Boer M, Borregard N, Bjerrum OW, Valerius NH, Seger RA, Mühlebach T, Belohradsky BH, Weening RS. Roos D, et al. Among authors: weening rs. J Leukoc Biol. 1992 Feb;51(2):164-71. doi: 10.1002/jlb.51.2.164. J Leukoc Biol. 1992. PMID: 1431553

6

Splice site mutations are a common cause of X-linked chronic granulomatous disease.

de Boer M, Bolscher BG, Dinauer MC, Orkin SH, Smith CI, Ahlin A, Weening RS, Roos D. de Boer M, et al. Among authors: weening rs. Blood. 1992 Sep 15;80(6):1553-8. Blood. 1992. PMID: 1520880 Free article.

7

Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease.

Bolscher BG, de Boer M, de Klein A, Weening RS, Roos D. Bolscher BG, et al. Among authors: weening rs. Blood. 1991 Jun 1;77(11):2482-7. Blood. 1991. PMID: 1710153 Free article.

8

Developments in the treatment of patients with chronic granulomatous disease.

Weening RS, Verhoeven AJ, de Boer M, Roos D. Weening RS, et al. Acta Paediatr Hung. 1988-1989;29(1-2):223-7. Acta Paediatr Hung. 1988. PMID: 3151262 No abstract available.

9

Detection of carriers of the autosomal form of chronic granulomatous disease.

Verhoeven AJ, van Schaik ML, Roos D, Weening RS. Verhoeven AJ, et al. Among authors: weening rs. Blood. 1988 Feb;71(2):505-7. Blood. 1988. PMID: 3337910 Free article.

10

The management of chronic granulomatous disease.

Fischer A, Segal AW, Seger R, Weening RS. Fischer A, et al. Among authors: weening rs. Eur J Pediatr. 1993 Nov;152(11):896-9. doi: 10.1007/BF01957525. Eur J Pediatr. 1993. PMID: 8276018

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