Curnutte J - Search Results

1

Chronic granulomatous disease. Report on a national registry of 368 patients.

Winkelstein JA, Marino MC, Johnston RB Jr, Boyle J, Curnutte J, Gallin JI, Malech HL, Holland SM, Ochs H, Quie P, Buckley RH, Foster CB, Chanock SJ, Dickler H. Winkelstein JA, et al. Among authors: curnutte j. Medicine (Baltimore). 2000 May;79(3):155-69. doi: 10.1097/00005792-200005000-00003. Medicine (Baltimore). 2000. PMID: 10844935 Free article.

2

Genetic variants of chronic granulomatous disease: prevalence of deficiencies of two cytosolic components of the NADPH oxidase system.

Clark RA, Malech HL, Gallin JI, Nunoi H, Volpp BD, Pearson DW, Nauseef WM, Curnutte JT. Clark RA, et al. Among authors: curnutte jt. N Engl J Med. 1989 Sep 7;321(10):647-52. doi: 10.1056/NEJM198909073211005. N Engl J Med. 1989. PMID: 2770793

3

Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease.

Foster CB, Lehrnbecher T, Mol F, Steinberg SM, Venzon DJ, Walsh TJ, Noack D, Rae J, Winkelstein JA, Curnutte JT, Chanock SJ. Foster CB, et al. Among authors: curnutte jt. J Clin Invest. 1998 Dec 15;102(12):2146-55. doi: 10.1172/JCI5084. J Clin Invest. 1998. PMID: 9854050 Free PMC article.

4

Phosphorylation of the oxidase-related 48K phosphoprotein family in the unusual autosomal cytochrome-negative and X-linked cytochrome-positive types of chronic granulomatous disease.

Okamura N, Malawista SE, Roberts RL, Rosen H, Ochs HD, Babior BM, Curnutte JT. Okamura N, et al. Among authors: curnutte jt. Blood. 1988 Aug;72(2):811-6. Blood. 1988. PMID: 3401601 Free article.

5

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease.

Roesler J, Curnutte JT, Rae J, Barrett D, Patino P, Chanock SJ, Goerlach A. Roesler J, et al. Among authors: curnutte jt. Blood. 2000 Mar 15;95(6):2150-6. Blood. 2000. PMID: 10706888 Free article.

6

Genomic structure of the human p47-phox (NCF1) gene.

Chanock SJ, Roesler J, Zhan S, Hopkins P, Lee P, Barrett DT, Christensen BL, Curnutte JT, Görlach A. Chanock SJ, et al. Among authors: curnutte jt. Blood Cells Mol Dis. 2000 Feb;26(1):37-46. doi: 10.1006/bcmd.2000.0274. Blood Cells Mol Dis. 2000. PMID: 10772875

7

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease.

Görlach A, Lee PL, Roesler J, Hopkins PJ, Christensen B, Green ED, Chanock SJ, Curnutte JT. Görlach A, et al. Among authors: curnutte jt. J Clin Invest. 1997 Oct 15;100(8):1907-18. doi: 10.1172/JCI119721. J Clin Invest. 1997. PMID: 9329953 Free PMC article.

8

Chronic granulomatous disease and glutathione peroxidase deficiency, revisited.

Newburger PE, Malawista SE, Dinauer MC, Gelbart T, Woodman RC, Chada S, Shen Q, van Blaricom G, Quie PG, Curnutte JT. Newburger PE, et al. Among authors: curnutte jt. Blood. 1994 Dec 1;84(11):3861-9. Blood. 1994. PMID: 7949143 Free article.

9

Chronic granulomatous disease.

Woodman RC, Curnutte JT. Woodman RC, et al. Among authors: curnutte jt. West J Med. 1991 Apr;154(4):460. West J Med. 1991. PMID: 1877191 Free PMC article. No abstract available.

10

Chronic granulomatous disease: diagnosis and classification at the molecular level.

Hopkins PJ, Bemiller LS, Curnutte JT. Hopkins PJ, et al. Among authors: curnutte jt. Clin Lab Med. 1992 Jun;12(2):277-304. Clin Lab Med. 1992. PMID: 1611821 Review.

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