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1973
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1982 2
1983 1
1984 1
1987 2
1988 2
1989 4
1990 3
1991 2
1992 3
1993 2
1995 2
1996 3
1997 1
1999 4
2000 3
2001 4
2002 1
2003 1
2004 5
2005 1
2006 3
2007 7
2008 5
2009 3
2010 9
2011 6
2012 3
2013 9
2014 6
2015 3
2016 6
2017 7
2018 7
2019 3
2020 1
2021 5
2022 1
2023 4
2024 2
2025 1

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131 results

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Page 1
Chronic Granulomatous Disease: a Comprehensive Review.
Yu HH, Yang YH, Chiang BL. Yu HH, et al. Clin Rev Allergy Immunol. 2021 Oct;61(2):101-113. doi: 10.1007/s12016-020-08800-x. Clin Rev Allergy Immunol. 2021. PMID: 32524254 Review.
Chronic granulomatous disease (CGD) is a primary immunodeficiency of phagocyte function due to defective NADPH oxidase (phox). ...The hyper-activation of NF-qB and inflammasome in CGD phagocytes also lead to long-lasting production of pro-inflammatory cytokin
Chronic granulomatous disease (CGD) is a primary immunodeficiency of phagocyte function due to defective NADPH oxidase
Flow cytometry-based diagnosis of primary immunodeficiency diseases.
Kanegane H, Hoshino A, Okano T, Yasumi T, Wada T, Takada H, Okada S, Yamashita M, Yeh TW, Nishikomori R, Takagi M, Imai K, Ochs HD, Morio T. Kanegane H, et al. Allergol Int. 2018 Jan;67(1):43-54. doi: 10.1016/j.alit.2017.06.003. Epub 2017 Jul 3. Allergol Int. 2018. PMID: 28684198 Free article. Review.
Flow cytometry effectively identifies major forms of PIDs, including severe combined immunodeficiency, X-linked agammaglobulinemia, hyper IgM syndromes, Wiskott-Aldrich syndrome, X-linked lymphoproliferative syndrome, familial hemophagocytic lymphohist …
Flow cytometry effectively identifies major forms of PIDs, including severe combined immunodeficiency, X-linked agammaglobulin …
Gene Therapies for Primary Immune Deficiencies.
Kohn LA, Kohn DB. Kohn LA, et al. Front Immunol. 2021 Feb 25;12:648951. doi: 10.3389/fimmu.2021.648951. eCollection 2021. Front Immunol. 2021. PMID: 33717203 Free PMC article. Review.
Gene therapy has successfully treated several PIDs including Adenosine Deaminase Severe Combined Immunodeficiency (SCID), X-linked SCID, Artemis SCID, Wiskott-Aldrich Syndrome, X-linked Chronic Granulomatous Disease and Leukocyte A …
Gene therapy has successfully treated several PIDs including Adenosine Deaminase Severe Combined Immunodeficiency (SCID), X-linked
Chronic Granulomatous Disease.
Rawat A, Bhattad S, Singh S. Rawat A, et al. Indian J Pediatr. 2016 Apr;83(4):345-53. doi: 10.1007/s12098-016-2040-3. Epub 2016 Feb 11. Indian J Pediatr. 2016. PMID: 26865172 Review.
Chronic granulomatous disease (CGD) is the most common symptomatic phagocytic defect. It is caused by mutations in genes encoding protein subunits of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. ...Evidence for white cell tr
Chronic granulomatous disease (CGD) is the most common symptomatic phagocytic defect. It is caused by mutations in g
Immunodeficiency Presenting as an Undiagnosed Disease.
Routes JM, Verbsky JW. Routes JM, et al. Pediatr Clin North Am. 2017 Feb;64(1):27-37. doi: 10.1016/j.pcl.2016.08.007. Pediatr Clin North Am. 2017. PMID: 27894450 Review.
Although primary immunodeficiencies typically present with recurrent, chronic, or severe infections, autoimmune manifestations frequently accompany these disorders and may be the initial clinical manifestations. The presence of 2 or more autoimmune disorders, unusual sever …
Although primary immunodeficiencies typically present with recurrent, chronic, or severe infections, autoimmune manifestations freque …
Hematologically important mutations: X-linked chronic granulomatous disease (fourth update).
Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Stasia MJ, Bakri FG, Köker N, Köker MY, Madkaika M, de Boer M, Garcia-Morato MB, Shephard JLV, Roesler J, Kanegane H, Kawai T, Di Matteo G, Shahrooei M, Bustamante J, Rawat A, Vignesh P, Mortaz E, Fayezi A, Cagdas D, Tezcan I, Kitcharoensakkul M, Dinauer MC, Meyts I, Wolach B, Condino-Neto A, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Roos D, et al. Blood Cells Mol Dis. 2021 Sep;90:102587. doi: 10.1016/j.bcmd.2021.102587. Epub 2021 Jun 2. Blood Cells Mol Dis. 2021. PMID: 34175765 Review.
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. CGD patients suffer from severe bacterial and fungal infections. The disease is caused by a lack of superoxide production by the leukocyte enz
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. CGD patie
Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology and British Society of Paediatric Gastroenterology, Hepatology and Nutrition.
Kammermeier J, Lamb CA, Jones KDJ, Anderson CA, Baple EL, Bolton C, Braggins H, Coulter TI, Gilmour KC, Gregory V, Hambleton S, Hartley D, Hawthorne AB, Hearn S, Laurence A, Parkes M, Russell RK, Speight RA, Travis S, Wilson DC, Uhlig HH. Kammermeier J, et al. Lancet Gastroenterol Hepatol. 2023 Mar;8(3):271-286. doi: 10.1016/S2468-1253(22)00337-5. Epub 2023 Jan 9. Lancet Gastroenterol Hepatol. 2023. PMID: 36634696 Review.
Genomic medicine enables the identification of patients with rare or ultra-rare monogenic forms of inflammatory bowel disease (IBD) and supports clinical decision making. Patients with monogenic IBD frequently experience extremely early onset of treatment-refractory dis
Genomic medicine enables the identification of patients with rare or ultra-rare monogenic forms of inflammatory bowel disease (IBD) a …
Chronic granulomatous disease.
Holland SM. Holland SM. Clin Rev Allergy Immunol. 2010 Feb;38(1):3-10. doi: 10.1007/s12016-009-8136-z. Clin Rev Allergy Immunol. 2010. PMID: 19504359 Review.
Chronic granulomatous disease (CGD) was first described in the 1950s and has become a paradigm for genetic neutrophil diseases. ...With X-linked and autosomal recessive forms, it has been an important disease for the development of bone m
Chronic granulomatous disease (CGD) was first described in the 1950s and has become a paradigm for genetic neutrophil d
131 results