144 related articles for article (PubMed ID: 16138344)
1. Acute lymphoblastic leukemia in a patient with chronic granulomatous disease and a novel mutation in CYBB: first report.
Wolach B; Ash S; Gavrieli R; Stark B; Yaniv I; Roos D
Am J Hematol; 2005 Sep; 80(1):50-4. PubMed ID: 16138344
[TBL] [Abstract][Full Text] [Related]
2. X-linked chronic granulomatous disease: first report of mutations in patients of Argentina.
Barese C; Copelli S; Zandomeni R; Oleastro M; Zelazko M; Rivas EM
J Pediatr Hematol Oncol; 2004 Oct; 26(10):656-60. PubMed ID: 15454837
[TBL] [Abstract][Full Text] [Related]
3. Characterization of 17 new cases of X-linked chronic granulomatous disease with seven novel mutations in the CYBB gene.
von Goessel H; Hossle JP; Seger R; Gungor T
Exp Hematol; 2006 Apr; 34(4):528-35. PubMed ID: 16569599
[TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of a novel splice site mutation within the CYBB gene leading to X-linked chronic granulomatous disease.
Barese CN; Copelli SB; De Matteo E; Zandomeni R; Salgueiro F; Di Giovanni D; Heyworth P; Rivas EM
Pediatr Blood Cancer; 2005 Apr; 44(4):420-2. PubMed ID: 15468310
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of chronic granulomatous disease in a male fetus.
Yavuz Köker M; Metin A; Ozgür TT; de Boer M; Roos D
Iran J Allergy Asthma Immunol; 2009 Mar; 8(1):57-61. PubMed ID: 19279361
[TBL] [Abstract][Full Text] [Related]
6. A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD).
Rump A; Rösen-Wolff A; Gahr M; Seidenberg J; Roos C; Walter L; Günther V; Roesler J
Gene; 2006 Apr; 371(2):174-81. PubMed ID: 16516412
[TBL] [Abstract][Full Text] [Related]
7. Mutations of chronic granulomatous disease in Turkish families.
Köker MY; Sanal O; De Boer M; Tezcan I; Metin A; Ersoy F; Roos D
Eur J Clin Invest; 2007 Jul; 37(7):589-95. PubMed ID: 17576211
[TBL] [Abstract][Full Text] [Related]
8. 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
Eur J Clin Invest; 2006 Apr; 36(4):257-64. PubMed ID: 16620288
[TBL] [Abstract][Full Text] [Related]
9. Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics.
Agudelo-Flórez P; Prando-Andrade CC; López JA; Costa-Carvalho BT; Quezada A; Espinosa FJ; de Souza Paiva MA; Roxo P; Grumach A; Jacob CA; Carneiro-Sampaio MM; Newburger PE; Condino-Neto A
Pediatr Blood Cancer; 2006 Feb; 46(2):243-52. PubMed ID: 16123991
[TBL] [Abstract][Full Text] [Related]
10. Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox.
Patiño PJ; Perez JE; Lopez JA; Condino-Neto A; Grumach AS; Botero JH; Curnutte JT; García de Olarte D
Hum Mutat; 1999; 13(1):29-37. PubMed ID: 9888386
[TBL] [Abstract][Full Text] [Related]
11. The search for a genetic defect in Polish patients with chronic granulomatous disease.
Jurkowska M; Kurenko-Deptuch M; Bal J; Roos D
Arch Immunol Ther Exp (Warsz); 2004; 52(6):441-6. PubMed ID: 15577746
[TBL] [Abstract][Full Text] [Related]
12. Severe clinical forms of cytochrome b-negative chronic granulomatous disease (X91-) in 3 brothers with a point mutation in the promoter region of CYBB.
Stasia MJ; Brion JP; Boutonnat J; Morel F
J Infect Dis; 2003 Nov; 188(10):1593-604. PubMed ID: 14624387
[TBL] [Abstract][Full Text] [Related]
13. Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB gene).
Gérard B; El Benna J; Alcain F; Gougerot-Pocidalo MA; Grandchamp B; Chollet-Martin S
Hum Mutat; 2001 Aug; 18(2):163. PubMed ID: 11462241
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.
van de Vosse E; van Wengen A; van Geelen JA; de Boer M; Roos D; van Dissel JT
J Hum Genet; 2009 Jun; 54(6):313-6. PubMed ID: 19329991
[TBL] [Abstract][Full Text] [Related]
15. X-linked chronic granulomatous disease in a male child with an X-CGD carrier, Klinefelter brother.
Gill HK; Kumar HC; Cheng CK; Ming CC; Nallusamy R; Yusoff NM; Mohamad SB; Ripen AM; Dhaliwal JS; Murad S
Asian Pac J Allergy Immunol; 2013 Jun; 31(2):167-72. PubMed ID: 23859418
[TBL] [Abstract][Full Text] [Related]
16. Genetic and biochemical background of chronic granulomatous disease.
Jurkowska M; Bernatowska E; Bal J
Arch Immunol Ther Exp (Warsz); 2004; 52(2):113-20. PubMed ID: 15179325
[TBL] [Abstract][Full Text] [Related]
17. Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections.
Agudelo-Flórez P; Costa-Carvalho BT; López JA; Redher J; Newburger PE; Olalla-Saad ST; Condino-Neto A
Am J Hematol; 2004 Mar; 75(3):151-6. PubMed ID: 14978696
[TBL] [Abstract][Full Text] [Related]
18. Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease.
Köker MY; van Leeuwen K; de Boer M; Celmeli F; Metin A; Ozgür TT; Tezcan I; Sanal O; Roos D
Eur J Clin Invest; 2009 Apr; 39(4):311-9. PubMed ID: 19292887
[TBL] [Abstract][Full Text] [Related]
19. Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease.
Yu G; Hong DK; Dionis KY; Rae J; Heyworth PG; Curnutte JT; Lewis DB
Clin Immunol; 2008 Aug; 128(2):117-26. PubMed ID: 18625437
[TBL] [Abstract][Full Text] [Related]
20. Fatal hemophagocytic lymphohistiocytosis in X-linked chronic granulomatous disease associated with a perforin gene variant.
van Montfrans JM; Rudd E; van de Corput L; Henter JI; Nikkels P; Wulffraat N; Boelens JJ
Pediatr Blood Cancer; 2009 Apr; 52(4):527-9. PubMed ID: 19058215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]