Roos D - Search Results

1

A missense mutation in the heavy subunit of gamma-glutamylcysteine synthetase gene causes hemolytic anemia.

Ristoff E, Augustson C, Geissler J, de Rijk T, Carlsson K, Luo JL, Andersson K, Weening RS, van Zwieten R, Larsson A, Roos D. Ristoff E, et al. Among authors: roos d. Blood. 2000 Apr 1;95(7):2193-6. Blood. 2000. PMID: 10733484 Free article.

2

Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.

Roos D, van Zwieten R, Wijnen JT, Gómez-Gallego F, de Boer M, Stevens D, Pronk-Admiraal CJ, de Rijk T, van Noorden CJ, Weening RS, Vulliamy TJ, Ploem JE, Mason PJ, Bautista JM, Khan PM, Beutler E. Roos D, et al. Blood. 1999 Nov 1;94(9):2955-62. Blood. 1999. PMID: 10556177 Free article.

3

Familial deficiency of glutathione reductase in human blood cells.

Loos H, Roos D, Weening R, Houwerzijl J. Loos H, et al. Among authors: roos d. Blood. 1976 Jul;48(1):53-62. Blood. 1976. PMID: 947404 Free article.

4

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.

5

Neutrophil Fc gamma RIIIb deficiency, nature, and clinical consequences: a study of 21 individuals from 14 families.

de Haas M, Kleijer M, van Zwieten R, Roos D, von dem Borne AE. de Haas M, et al. Among authors: roos d. Blood. 1995 Sep 15;86(6):2403-13. Blood. 1995. PMID: 7662988 Free article.

6

A single dose of granulocyte-macrophage colony-stimulating factor induces systemic interleukin-8 release and neutrophil activation in healthy volunteers.

van Pelt LJ, Huisman MV, Weening RS, von dem Borne AE, Roos D, van Oers RH. van Pelt LJ, et al. Among authors: roos d. Blood. 1996 Jun 15;87(12):5305-13. Blood. 1996. PMID: 8652846 Free article.

7

Seven new mutations in the nicotinamide adenine dinucleotide reduced-cytochrome b(5) reductase gene leading to methemoglobinemia type I.

Dekker J, Eppink MH, van Zwieten R, de Rijk T, Remacha AF, Law LK, Li AM, Cheung KL, van Berkel WJ, Roos D. Dekker J, et al. Among authors: roos d. Blood. 2001 Feb 15;97(4):1106-14. doi: 10.1182/blood.v97.4.1106. Blood. 2001. PMID: 11159544 Free article.

8

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.

9

Induction of neutrophil FC-gamma receptor I expression can be used as a marker for biologic activity of recombinant interferon-gamma in vivo.

Huizinga TW, Van der Schoot CE, Roos D, Weening RS. Huizinga TW, et al. Among authors: roos d. Blood. 1991 May 1;77(9):2088-90. Blood. 1991. PMID: 1902126 Free article. Clinical Trial. No abstract available.

10

Molecular basis of glutathione reductase deficiency in human blood cells.

Kamerbeek NM, van Zwieten R, de Boer M, Morren G, Vuil H, Bannink N, Lincke C, Dolman KM, Becker K, Schirmer RH, Gromer S, Roos D. Kamerbeek NM, et al. Among authors: roos d. Blood. 2007 Apr 15;109(8):3560-6. doi: 10.1182/blood-2006-08-042531. Epub 2006 Dec 21. Blood. 2007. PMID: 17185460 Free article.

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