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

Year Number of Results
1959 1
1964 2
1965 1
1969 1
1971 1
1972 3
1973 1
1974 2
1975 6
1976 5
1977 20
1978 15
1979 16
1980 16
1981 20
1982 16
1983 22
1984 21
1985 20
1986 23
1987 15
1988 16
1989 29
1990 10
1991 22
1992 17
1993 38
1994 25
1995 44
1996 54
1997 68
1998 56
1999 79
2000 56
2001 67
2002 57
2003 58
2004 46
2005 86
2006 98
2007 101
2008 103
2009 97
2010 115
2011 123
2012 112
2013 151
2014 156
2015 152
2016 142
2017 173
2018 173
2019 159
2020 73
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2,703 results
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Page 1
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. It occurs in approximately 1:4000 births, and the incidence is increasing due to affected parents bearing their own affected …
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. ...
Chromosome 22q11.2 deletion syndrome is the most common microdeletion syndrome in humans. The effects are protean and highly v …
Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome).
Kuo CY, Signer R, Saitta SC. Kuo CY, et al. Curr Allergy Asthma Rep. 2018 Oct 30;18(12):75. doi: 10.1007/s11882-018-0823-5. Curr Allergy Asthma Rep. 2018. PMID: 30377837 Review.
PURPOSE OF REVIEW: This review provides an update on the progress in identifying the range of immunological dysfunction seen in DiGeorge syndrome and on more recent diagnostic and treatment approaches. ...DiGeorge syndrome reflects a clinical phenotype …
PURPOSE OF REVIEW: This review provides an update on the progress in identifying the range of immunological dysfunction seen in DiGeorge
DiGeorge syndrome : Relevance of psychiatric symptoms in undiagnosed adult patients.
Kraus C, Vanicek T, Weidenauer A, Khanaqa T, Stamenkovic M, Lanzenberger R, Willeit M, Kasper S. Kraus C, et al. Wien Klin Wochenschr. 2018 Apr;130(7-8):283-287. doi: 10.1007/s00508-018-1335-y. Epub 2018 Apr 18. Wien Klin Wochenschr. 2018. PMID: 29671046 Free PMC article.
DiGeorge syndrome or 22q11.2 deletion syndrome is one of the most common genetic microdeletion syndromes in humans. In addition to physical manifestations, DiGeorge syndrome is associated with a high prevalence of psychiatric disorders, such as
DiGeorge syndrome or 22q11.2 deletion syndrome is one of the most common genetic microdeletion syndromes in humans. In
Follicular Helper T Cells in DiGeorge Syndrome.
Klocperk A, Paračková Z, Bloomfield M, Rataj M, Pokorný J, Unger S, Warnatz K, Šedivá A. Klocperk A, et al. Front Immunol. 2018 Jul 23;9:1730. doi: 10.3389/fimmu.2018.01730. eCollection 2018. Front Immunol. 2018. PMID: 30083170 Free PMC article.
The population of CXCR5(+) memory CD4(+) T cells (cTFHs) was significantly expanded in patients with DiGeorge syndrome, but only healthy controls and not DiGeorge syndrome patients showed gradual increase of CXCR5 expression on cTFHs with age. ...Thus, …
The population of CXCR5(+) memory CD4(+) T cells (cTFHs) was significantly expanded in patients with DiGeorge syndrome, but on …
The immune deficiency of chromosome 22q11.2 deletion syndrome.
Morsheimer M, Brown Whitehorn TF, Heimall J, Sullivan KE. Morsheimer M, et al. Am J Med Genet A. 2017 Sep;173(9):2366-2372. doi: 10.1002/ajmg.a.38319. Epub 2017 Jun 19. Am J Med Genet A. 2017. PMID: 28627729 Review.
The syndrome originally described by Dr. Angelo DiGeorge had immunodeficiency as a central component. When a 22q11.2 deletion was identified as the cause in the majority of patients with DiGeorge syndrome, the clinical features of 22q11.2 deletion s
The syndrome originally described by Dr. Angelo DiGeorge had immunodeficiency as a central component. When a 22q11.2 deletion …
[DiGeorge syndrome].
Hamada H, Terai M. Hamada H, et al. Nihon Rinsho. 2006 Jun 28;Suppl 2:46-8. Nihon Rinsho. 2006. PMID: 16817347 Review. Japanese. No abstract available.
Immune system defects in DiGeorge syndrome and association with clinical course.
Nain E, Kiykim A, Ogulur I, Kasap N, Karakoc-Aydiner E, Ozen A, Baris S. Nain E, et al. Scand J Immunol. 2019 Nov;90(5):e12809. doi: 10.1111/sji.12809. Epub 2019 Sep 9. Scand J Immunol. 2019. PMID: 31322747
We evaluated 18 DiGeorge syndrome (DGS) patients and aimed to investigate the immunological changes in this population. DGS patients with low naive CD4(+) T and CD8(+) T cells were defined as high-risk (HR) patients, whereas patients with normal numbers of naive CD4 …
We evaluated 18 DiGeorge syndrome (DGS) patients and aimed to investigate the immunological changes in this population. DGS pa …
DiGeorge syndrome: an update.
Baldini A. Baldini A. Curr Opin Cardiol. 2004 May;19(3):201-4. doi: 10.1097/00001573-200405000-00002. Curr Opin Cardiol. 2004. PMID: 15096950 Review.
PURPOSE OF REVIEW: This article is an update on DiGeorge syndrome research focusing on the synergy of human and model systems genetics toward the understanding of conotruncal and aortic arch defects. ...SUMMARY: The Tbx1 genetic pathway and the cell biology of tissu …
PURPOSE OF REVIEW: This article is an update on DiGeorge syndrome research focusing on the synergy of human and model systems …
Schizophrenia in DiGeorge Syndrome: A Unique Case Report.
Rizvi S, Khan AM, Saeed H, Aribara AM, Carrington A, Griffiths A, Mohit A. Rizvi S, et al. Cureus. 2018 Aug 14;10(8):e3142. doi: 10.7759/cureus.3142. Cureus. 2018. PMID: 30345199 Free PMC article.
Genetic testing performed revealed the deletion of 22q11.2, thus establishing the diagnosis of DiGeorge syndrome. This case highlights the importance of noticing subtle physical exam findings along with laboratory findings as this led to the diagnosis of DiGeorge
Genetic testing performed revealed the deletion of 22q11.2, thus establishing the diagnosis of DiGeorge syndrome. This case hi …
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