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

Year Number of Results
1968 1
1972 2
1973 1
1974 1
1975 5
1976 3
1977 4
1978 7
1979 4
1980 5
1981 7
1982 7
1983 6
1984 5
1985 8
1986 7
1987 2
1988 6
1989 11
1990 2
1991 2
1992 1
1993 5
1994 5
1995 1
1996 7
1997 6
1998 8
1999 7
2000 12
2001 8
2002 6
2003 6
2004 10
2005 8
2006 6
2007 14
2008 14
2009 7
2010 10
2011 16
2012 10
2013 11
2014 13
2015 17
2016 9
2017 10
2018 12
2019 19
2020 21
2021 23
2022 26
2023 32
2024 6

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428 results

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Page 1
DiGeorge Syndrome.
Lackey AE, Muzio MR. Lackey AE, et al. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 31747205 Free Books & Documents.
DiGeorge Syndrome (DGS) is a combination of signs and symptoms caused by defects in the development of structures derived from the pharyngeal arches during embryogenesis. ...DGS is one of several syndromes that has historically grouped under a bigger umbrella called
DiGeorge Syndrome (DGS) is a combination of signs and symptoms caused by defects in the development of structures derived from
Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
McDonald-McGinn DM, Sullivan KE. McDonald-McGinn DM, et al. Medicine (Baltimore). 2011 Jan;90(1):1-18. doi: 10.1097/MD.0b013e3182060469. Medicine (Baltimore). 2011. PMID: 21200182 Free article. Review.
Chromosome 22q11.2 deletion syndrome is a common syndrome also known as DiGeorge syndrome and velocardiofacial syndrome. ...Many patients have a mild to moderate immune deficiency, and the majority of patients have a cardiac anomaly
Chromosome 22q11.2 deletion syndrome is a common syndrome also known as DiGeorge syndrome and velocardiofacial …
Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome.
Sullivan KE. Sullivan KE. Immunol Rev. 2019 Jan;287(1):186-201. doi: 10.1111/imr.12701. Immunol Rev. 2019. PMID: 30565249 Review.
Chromosome 22q11.2 deletion syndrome is the most common microdeletion syndrome in humans. The effects are protean and highly variable, making a unified approach difficult. ...A brief discussion of the other organ system involvement will be provided for context. The …
Chromosome 22q11.2 deletion syndrome is the most common microdeletion syndrome in humans. The effects are protean and highly v …
22q11.2 Deletion Syndrome.
McDonald-McGinn DM, Hain HS, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. 1999 Sep 23 [updated 2020 Feb 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1999 Sep 23 [updated 2020 Feb 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301696 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families. ...Agents/circumstances to avoid: Infants with lymphocyte abnormalities should not be immunized
CLINICAL CHARACTERISTICS: Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are h …
Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management.
Biggs SE, Gilchrist B, May KR. Biggs SE, et al. Curr Allergy Asthma Rep. 2023 Apr;23(4):213-222. doi: 10.1007/s11882-023-01071-4. Epub 2023 Mar 10. Curr Allergy Asthma Rep. 2023. PMID: 36897497 Free PMC article. Review.
PURPOSE OF REVIEW: This review focuses on immunologic findings, relationships among immunologic findings and associated conditions of autoimmunity and atopy, and management of immunologic disease in chromosome 22q11.2 deletion syndrome (22q11.2DS, historically known as …
PURPOSE OF REVIEW: This review focuses on immunologic findings, relationships among immunologic findings and associated conditions of autoim …
Immunodeficiency.
Justiz Vaillant AA, Qurie A. Justiz Vaillant AA, et al. 2023 Jun 26. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jun 26. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 29763203 Free Books & Documents.
Treatment should not include gammaglobulin preparations to prevent hypersensitivity reactions. . T-cell Immunodeficiencies Congenital thymic aplasia (DiGeorge syndrome): Tetany is present. Fungal and viral infections are common. ...Acquired Immune Deficiency …
Treatment should not include gammaglobulin preparations to prevent hypersensitivity reactions. . T-cell Immunodeficiencies Congenital thymic …
Thymus transplantation.
Markert ML, Devlin BH, McCarthy EA. Markert ML, et al. Clin Immunol. 2010 May;135(2):236-46. doi: 10.1016/j.clim.2010.02.007. Epub 2010 Mar 16. Clin Immunol. 2010. PMID: 20236866 Free PMC article. Review.
Although thymic hypoplasia or aplasia is characteristic of DiGeorge anomaly, in "complete" DiGeorge anomaly, there is no detectable thymus as determined by the absence of naive (CD45RA(+), CD62L(+)) T cells. Transplantation of postnatal allogeneic cult …
Although thymic hypoplasia or aplasia is characteristic of DiGeorge anomaly, in "complete" DiGeorge anomaly, the …
Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.
Mustillo PJ, Sullivan KE, Chinn IK, Notarangelo LD, Haddad E, Davies EG, de la Morena MT, Hartog N, Yu JE, Hernandez-Trujillo VP, Ip W, Franco J, Gambineri E, Hickey SE, Varga E, Markert ML. Mustillo PJ, et al. J Clin Immunol. 2023 Feb;43(2):247-270. doi: 10.1007/s10875-022-01418-y. Epub 2023 Jan 17. J Clin Immunol. 2023. PMID: 36648576 Free PMC article. Review.
Current practices vary widely regarding the immunological work-up and management of patients affected with defects in thymic development (DTD), which include chromosome 22q11.2 microdeletion syndrome (22q11.2del) and other causes of DiGeorge syndrome (DGS) an …
Current practices vary widely regarding the immunological work-up and management of patients affected with defects in thymic development (DT …
Lymphatic endothelial transcription factor Tbx1 promotes an immunosuppressive microenvironment to facilitate post-myocardial infarction repair.
Wang W, Li X, Ding X, Xiong S, Hu Z, Lu X, Zhang K, Zhang H, Hu Q, Lai KS, Chen Z, Yang J, Song H, Wang Y, Wei L, Xia Z, Zhou B, He Y, Pu J, Liu X, Ke R, Wu T, Huang C, Baldini A, Zhang M, Zhang Z. Wang W, et al. Immunity. 2023 Oct 10;56(10):2342-2357.e10. doi: 10.1016/j.immuni.2023.07.019. Epub 2023 Aug 24. Immunity. 2023. PMID: 37625409
Here, we reveal an unknown intramyocardial immunosuppressive program driven by Tbx1, a DiGeorge syndrome disease gene that encodes a T-box transcription factor (TF). ...The activated LECs penetrated the infarcted area and functioned as intramyocardial immune
Here, we reveal an unknown intramyocardial immunosuppressive program driven by Tbx1, a DiGeorge syndrome disease gene that enc …
Regulation of the MIR155 host gene in physiological and pathological processes.
Elton TS, Selemon H, Elton SM, Parinandi NL. Elton TS, et al. Gene. 2013 Dec 10;532(1):1-12. doi: 10.1016/j.gene.2012.12.009. Epub 2012 Dec 14. Gene. 2013. PMID: 23246696 Review.
MiR-155-5p is one of the best characterized miRNAs and recent data indicate that miR-155-5p plays a critical role in various physiological and pathological processes such as hematopoietic lineage differentiation, immunity, inflammation, viral infections, cancer, cardiovasc …
MiR-155-5p is one of the best characterized miRNAs and recent data indicate that miR-155-5p plays a critical role in various physiological a …
428 results