Similar articles for PMID: 9454688

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1

Hematologically important mutations: X-linked chronic granulomatous disease--an update.

Heyworth PG, Curnutte JT, Noack D, Cross AR. Heyworth PG, et al. Blood Cells Mol Dis. 1997 Dec;23(3):443-50. doi: 10.1006/bcmd.1997.0163. Blood Cells Mol Dis. 1997. PMID: 9454688 No abstract available.

2

Hematologically important mutations: X-linked chronic granulomatous disease (second update).

Heyworth PG, Curnutte JT, Rae J, Noack D, Roos D, van Koppen E, Cross AR. Heyworth PG, et al. Blood Cells Mol Dis. 2001 Jan-Feb;27(1):16-26. doi: 10.1006/bcmd.2000.0347. Blood Cells Mol Dis. 2001. PMID: 11162142 No abstract available.

3

Hematologically important mutations: X-linked chronic granulomatous disease (third update).

Roos D, Kuhns DB, Maddalena A, Roesler J, Lopez JA, Ariga T, Avcin T, de Boer M, Bustamante J, Condino-Neto A, Di Matteo G, He J, Hill HR, Holland SM, Kannengiesser C, Köker MY, Kondratenko I, van Leeuwen K, Malech HL, Marodi L, Nunoi H, Stasia MJ, Ventura AM, Witwer CT, Wolach B, Gallin JI. Roos D, et al. Blood Cells Mol Dis. 2010 Oct 15;45(3):246-65. doi: 10.1016/j.bcmd.2010.07.012. Epub 2010 Aug 21. Blood Cells Mol Dis. 2010. PMID: 20729109 Free PMC article. Review.

4

X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.

Rae J, Newburger PE, Dinauer MC, Noack D, Hopkins PJ, Kuruto R, Curnutte JT. Rae J, et al. Am J Hum Genet. 1998 Jun;62(6):1320-31. doi: 10.1086/301874. Am J Hum Genet. 1998. PMID: 9585602 Free PMC article.

5

Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood.

Lun A, Roesler J, Renz H. Lun A, et al. Clin Chem. 2002 May;48(5):780-1. Clin Chem. 2002. PMID: 11978610 No abstract available.

6

Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease.

Roesler J, Heyden S, Burdelski M, Schäfer H, Kreth HW, Lehmann R, Paul D, Marzahn J, Gahr M, Rösen-Wolff A. Roesler J, et al. Exp Hematol. 1999 Mar;27(3):505-11. doi: 10.1016/s0301-472x(98)00024-1. Exp Hematol. 1999. PMID: 10089913 Free article.

7

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease.

Roos D, de Boer M, Kuribayashi F, Meischl C, Weening RS, Segal AW, Ahlin A, Nemet K, Hossle JP, Bernatowska-Matuszkiewicz E, Middleton-Price H. Roos D, et al. Blood. 1996 Mar 1;87(5):1663-81. Blood. 1996. PMID: 8634410 Free article. Review. No abstract available.

8

A novel polymorphism in the coding region of CYBB, the human gp91-phox gene.

Kuribayashi F, de Boer M, Leusen JH, Verhoeven AJ, Roos D. Kuribayashi F, et al. Hum Genet. 1996 May;97(5):611-3. doi: 10.1007/BF02281870. Hum Genet. 1996. PMID: 8655140

9

An in-frame triplet deletion within the gp91-phox gene in an adult X-linked chronic granulomatous disease patient with residual NADPH-oxidase activity.

Jendrossek V, Ritzel A, Neubauer B, Heyden S, Gahr M. Jendrossek V, et al. Eur J Haematol. 1997 Feb;58(2):78-85. doi: 10.1111/j.1600-0609.1997.tb00928.x. Eur J Haematol. 1997. PMID: 9111587

10

A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous disease.

Tsuda M, Kaneda M, Sakiyama T, Inana I, Owada M, Kiryu C, Shiraishi T, Kakinuma K. Tsuda M, et al. Hum Genet. 1998 Oct;103(4):377-81. doi: 10.1007/s004390050836. Hum Genet. 1998. PMID: 9856476

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