These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Molecular basis of the autosomal recessive forms of chronic granulomatous disease. Curnutte JT Immunodefic Rev; 1992; 3(2):149-72. PubMed ID: 1554499 [TBL] [Abstract][Full Text] [Related]
5. Chronic granulomatous disease: diagnosis and classification at the molecular level. Hopkins PJ; Bemiller LS; Curnutte JT Clin Lab Med; 1992 Jun; 12(2):277-304. PubMed ID: 1611821 [TBL] [Abstract][Full Text] [Related]
6. Delineation of the phagocyte NADPH oxidase through studies of chronic granulomatous diseases of childhood. Gallin JI Int J Tissue React; 1993; 15(3):99-103. PubMed ID: 8188451 [TBL] [Abstract][Full Text] [Related]
13. Cytochrome b-245 and its involvement in the molecular pathology of chronic granulomatous disease. Segal AW Hematol Oncol Clin North Am; 1988 Jun; 2(2):213-23. PubMed ID: 3292507 [TBL] [Abstract][Full Text] [Related]
14. The human NADPH oxidase: primary and secondary defects impairing the respiratory burst function and the microbicidal ability of phagocytes. de Oliveira-Junior EB; Bustamante J; Newburger PE; Condino-Neto A Scand J Immunol; 2011 May; 73(5):420-7. PubMed ID: 21204900 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Adenovirus-mediated gene transfer into monocyte-derived macrophages of patients with X-linked chronic granulomatous disease: ex vivo correction of deficient respiratory burst. Schneider SD; Rusconi S; Seger RA; Hossle JP Gene Ther; 1997 Jun; 4(6):524-32. PubMed ID: 9231068 [TBL] [Abstract][Full Text] [Related]
17. A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox. Leusen JH; de Boer M; Bolscher BG; Hilarius PM; Weening RS; Ochs HD; Roos D; Verhoeven AJ J Clin Invest; 1994 May; 93(5):2120-6. PubMed ID: 8182143 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Chronic granulomatous disease: mutations in cytochrome b558. Roos D; De Boer M; De Klein A; Bolscher BG; Weening RS Immunodeficiency; 1993; 4(1-4):289-301. PubMed ID: 8167720 [No Abstract] [Full Text] [Related] [Next] [New Search]