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

Year Number of Results
1975 1
1978 1
1980 1
1981 1
1983 4
1984 3
1985 3
1986 4
1987 3
1988 2
1989 4
1990 5
1991 4
1992 8
1993 16
1994 29
1995 17
1996 19
1997 14
1998 20
1999 17
2000 25
2001 23
2002 16
2003 26
2004 28
2005 20
2006 18
2007 33
2008 26
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2010 22
2011 28
2012 29
2013 25
2014 30
2015 25
2016 28
2017 28
2018 43
2019 33
2020 33
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674 results
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Page 1
The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management.
Yazdani R, Fekrvand S, Shahkarami S, Azizi G, Moazzami B, Abolhassani H, Aghamohammadi A. Yazdani R, et al. Clin Immunol. 2019 Jan;198:19-30. doi: 10.1016/j.clim.2018.11.007. Epub 2018 Nov 13. Clin Immunol. 2019. PMID: 30439505 Review.
Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by low or absent levels of serum IgG, IgA, IgE and normal or increased levels of serum IgM. ...Herein, the epidemiology, pathogenesis, clinical manifestati
Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency disorder characterized by low or absent level
Clinical Phenotypes of Hyper-IgM Syndromes.
de la Morena MT. de la Morena MT. J Allergy Clin Immunol Pract. 2016 Nov-Dec;4(6):1023-1036. doi: 10.1016/j.jaip.2016.09.013. J Allergy Clin Immunol Pract. 2016. PMID: 27836054 Review.
Technical advancements in whole-genome, whole-exome, and RNA-sequencing have seen the explosion of genetic discoveries in the field of PIDs. The present review aims to focus on a group of immunodeficiency disorders associated with elevated levels of IgM (hyper
Technical advancements in whole-genome, whole-exome, and RNA-sequencing have seen the explosion of genetic discoveries in the field of PIDs. …
X-Linked Hyper IgM Syndrome.
Dunn CP, de la Morena MT. Dunn CP, et al. 2007 May 31 [updated 2020 Feb 20]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301576 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: X-linked hyper IgM syndrome (HIGM1), a disorder of abnormal T- and B-cell function, is characterized by low serum concentrations of IgG, IgA, and IgE with normal or elevated serum concentrations of IgM. ...Liver disease, a ser …
CLINICAL CHARACTERISTICS: X-linked hyper IgM syndrome (HIGM1), a disorder of abnormal T- and B-cell function, is charac …
Comprehensive review of autoantibodies in patients with hyper-IgM syndrome.
Barbouche MR, Chen Q, Carbone M, Ben-Mustapha I, Shums Z, Trifa M, Malinverno F, Bernuzzi F, Zhang H, Agrebi N, Norman GL, Chang C, Gershwin ME, Invernizzi P. Barbouche MR, et al. Cell Mol Immunol. 2018 Jun;15(6):610-617. doi: 10.1038/cmi.2017.140. Epub 2018 Feb 5. Cell Mol Immunol. 2018. PMID: 29400703 Free PMC article. Review.
Hyper-immunoglobulin M syndrome is an X-linked primary immunodeficiency disease caused by mutations in the CD40 ligand gene. ...Half of the hyperimmunoglobulin M syndrome patients were found to be anti-MIT3 IgM positive vs none of the controls (
Hyper-immunoglobulin M syndrome is an X-linked primary immunodeficiency disease caused by mutations in the CD40 ligand
The hyper IgM syndromes.
Qamar N, Fuleihan RL. Qamar N, et al. Clin Rev Allergy Immunol. 2014 Apr;46(2):120-30. doi: 10.1007/s12016-013-8378-7. Clin Rev Allergy Immunol. 2014. PMID: 23797640 Review.
The hyper IgM syndromes are a group of rare inherited immune deficiency disorders characterized by impairment of immunoglobulin isotype switching resulting from defects in the CD40 ligand/CD40 signaling pathway. X-linked forms of hyper IgM are caused b …
The hyper IgM syndromes are a group of rare inherited immune deficiency disorders characterized by impairment of immunoglobuli …
Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.
Meng X, Yang B, Suen WC. Meng X, et al. Innate Immun. 2018 Jan;24(1):4-10. doi: 10.1177/1753425917739681. Epub 2017 Nov 13. Innate Immun. 2018. PMID: 29132233 Free PMC article. Review.
The critical role of the CD40/CD40L pathway in B-cell proliferation, immunoglobulin (Ig) isotype switching and germinal center formation has been studied and described extensively in previous literature. Interruption of the CD40/CD40L signal causes hyper-IgM (HIGM) …
The critical role of the CD40/CD40L pathway in B-cell proliferation, immunoglobulin (Ig) isotype switching and germinal center formation has …
Primary B-cell immunodeficiencies.
Smith T, Cunningham-Rundles C. Smith T, et al. Hum Immunol. 2019 Jun;80(6):351-362. doi: 10.1016/j.humimm.2018.10.015. Epub 2018 Oct 22. Hum Immunol. 2019. PMID: 30359632 Free PMC article. Review.
Respiratory Complications in Patients with Hyper IgM Syndrome.
Moazzami B, Yazdani R, Azizi G, Kiaei F, Tafakori M, Modaresi M, Shirzadi R, Mahdaviani SA, Sohani M, Abolhassani H, Aghamohammadi A. Moazzami B, et al. J Clin Immunol. 2019 Aug;39(6):557-568. doi: 10.1007/s10875-019-00650-3. Epub 2019 Jun 11. J Clin Immunol. 2019. PMID: 31183658
PURPOSE: Hyper Immunoglobulin M (HIgM) syndrome is a heterogeneous group of primary immunodeficiency disorders, characterized by recurrent infections and associated with decreased serum IgG and IgA, but normal or increased IgM. The aim of the present s …
PURPOSE: Hyper Immunoglobulin M (HIgM) syndrome is a heterogeneous group of primary immunodeficiency disorders, charact …
Hyper IgM Syndrome: a Report from the USIDNET Registry.
Leven EA, Maffucci P, Ochs HD, Scholl PR, Buckley RH, Fuleihan RL, Geha RS, Cunningham CK, Bonilla FA, Conley ME, Ferdman RM, Hernandez-Trujillo V, Puck JM, Sullivan K, Secord EA, Ramesh M, Cunningham-Rundles C. Leven EA, et al. J Clin Immunol. 2016 Jul;36(5):490-501. doi: 10.1007/s10875-016-0291-4. Epub 2016 May 17. J Clin Immunol. 2016. PMID: 27189378 Free PMC article.
PURPOSE: The United States Immunodeficiency Network (USIDNET) patient registry was used to characterize the presentation, genetics, phenotypes, and treatment of patients with Hyper IgM Syndrome (HIGM). ...CONCLUSIONS: Analysis of the USIDNET Registry p …
PURPOSE: The United States Immunodeficiency Network (USIDNET) patient registry was used to characterize the presentation, genetics, p …
Haematopoietic stem cell transplant for hyper-IgM syndrome due to CD40 defects: a single-centre experience.
Al-Saud B, Al-Jomaie M, Al-Ghonaium A, Al-Ahmari A, Al-Mousa H, Al-Muhsen S, Al-Seraihy A, Arnaout R, Elshorbagi S, Al-Dhekri H, Ayas M. Al-Saud B, et al. Bone Marrow Transplant. 2019 Jan;54(1):63-67. doi: 10.1038/s41409-018-0219-0. Epub 2018 Jun 8. Bone Marrow Transplant. 2019. PMID: 29884852 Free article.
Hyper-IgM syndrome due to CD40 deficiency (HIGM3) is a rare disease with only a few reported cases of haematopoietic stem cell transplantation (HSCT). ...
Hyper-IgM syndrome due to CD40 deficiency (HIGM3) is a rare disease with only a few reported cases of haematopoietic st
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