Roos D - Search Results

1

Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family.

Köker MY, Sanal O, de Boer M, Tezcan I, Metin A, Tan C, Ersoy F, Roos D. Köker MY, et al. Among authors: roos d. Eur J Clin Invest. 2006 Apr;36(4):257-64. doi: 10.1111/j.1365-2362.2006.01619.x. Eur J Clin Invest. 2006. PMID: 16620288

2

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

3

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

4

Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reaction.

De Boer M, Bolscher BG, Sijmons RH, Scheffer H, Weening RS, Roos D. De Boer M, et al. Among authors: roos d. Prenat Diagn. 1992 Sep;12(9):773-7. doi: 10.1002/pd.1970120910. Prenat Diagn. 1992. PMID: 1438069

5

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: roos d. Blood. 1992 Sep 15;80(6):1553-8. Blood. 1992. PMID: 1520880 Free article.

6

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: roos d. Blood. 1991 Jun 1;77(11):2482-7. Blood. 1991. PMID: 1710153 Free article.

7

A phosphoprotein of Mr 47,000, defective in autosomal chronic granulomatous disease, copurifies with one of two soluble components required for NADPH:O2 oxidoreductase activity in human neutrophils.

Bolscher BG, van Zwieten R, Kramer IM, Weening RS, Verhoeven AJ, Roos D. Bolscher BG, et al. Among authors: roos d. J Clin Invest. 1989 Mar;83(3):757-63. doi: 10.1172/JCI113954. J Clin Invest. 1989. PMID: 2537848 Free PMC article.

8

Metabolic comparison between basophils and other leukocytes from human blood.

de Boer M, Roos D. de Boer M, et al. Among authors: roos d. J Immunol. 1986 May 1;136(9):3447-54. J Immunol. 1986. PMID: 3007619

9

Developments in the treatment of patients with chronic granulomatous disease.

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

10

Purification and cryopreservation of phagocytes from human blood.

Roos D, de Boer M. Roos D, et al. Methods Enzymol. 1986;132:225-43. doi: 10.1016/s0076-6879(86)32010-x. Methods Enzymol. 1986. PMID: 3821511 No abstract available.

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