Seger RA - Search Results

1

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: seger ra. J Leukoc Biol. 1992 Feb;51(2):164-71. doi: 10.1002/jlb.51.2.164. J Leukoc Biol. 1992. PMID: 1431553

2

156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox.

Leusen JH, Bolscher BG, Hilarius PM, Weening RS, Kaulfersch W, Seger RA, Roos D, Verhoeven AJ. Leusen JH, et al. Among authors: seger ra. J Exp Med. 1994 Dec 1;180(6):2329-34. doi: 10.1084/jem.180.6.2329. J Exp Med. 1994. PMID: 7964505 Free PMC article.

3

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. Am J Hum Genet. 1992 Nov;51(5):1127-35. Am J Hum Genet. 1992. PMID: 1415254 Free PMC article.

4

Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers.

de Boer M, Hilarius-Stokman PM, Hossle JP, Verhoeven AJ, Graf N, Kenney RT, Seger R, Roos D. de Boer M, et al. Blood. 1994 Jan 15;83(2):531-6. Blood. 1994. PMID: 8286749 Free article.

5

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. PLoS One. 2009;4(4):e5234. doi: 10.1371/journal.pone.0005234. Epub 2009 Apr 21. PLoS One. 2009. PMID: 19381301 Free PMC article.

6

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

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

7

Analysis of the gene and gene product in patients with X linked chronic granulomatous disease (XL-CGD).

Frey D, Mühlebach T, Seger R. Frey D, et al. Acta Paediatr Hung. 1988-1989;29(1-2):185-9. Acta Paediatr Hung. 1988. PMID: 3255401 No abstract available.

8

Treatment of patients with chronic granulomatous disease with recombinant human interferon-gamma does not improve neutrophil oxidative metabolism, cytochrome b558 content or levels of four anti-microbial proteins.

Mühlebach TJ, Gabay J, Nathan CF, Erny C, Dopfer G, Schroten H, Wahn V, Seger RA. Mühlebach TJ, et al. Among authors: seger ra. Clin Exp Immunol. 1992 May;88(2):203-6. doi: 10.1111/j.1365-2249.1992.tb03062.x. Clin Exp Immunol. 1992. PMID: 1572085 Free PMC article. Clinical Trial.

9

Granulocyte-macrophage colony stimulating factor does not improve neutrophil oxidative metabolism in a patient with variant X-linked chronic granulomatous disease.

Mühlebach TJ, Feickert HJ, Welte K, Seger RA. Mühlebach TJ, et al. Among authors: seger ra. Eur J Pediatr. 1991 Jun;150(8):575-8. doi: 10.1007/BF02072210. Eur J Pediatr. 1991. PMID: 1659535

10

Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.

Dinauer MC, Pierce EA, Erickson RW, Muhlebach TJ, Messner H, Orkin SH, Seger RA, Curnutte JT. Dinauer MC, et al. Among authors: seger ra. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11231-5. doi: 10.1073/pnas.88.24.11231. Proc Natl Acad Sci U S A. 1991. PMID: 1763037 Free PMC article.

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