Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1992 1
1994 1
1998 1
2003 1
2005 1
2007 2
2009 1
2011 1
2012 1
2015 1
2017 2
2018 2
2019 3
2020 1
2021 1
2022 3
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

21 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Recurrent infections associated with rare immunoglobulin isotypes deficiency"
Page 1
Truly selective primary IgM deficiency is probably very rare.
Janssen LMA, Macken T, Creemers MCW, Pruijt JFM, Eijk JJJ, de Vries E. Janssen LMA, et al. Clin Exp Immunol. 2018 Feb;191(2):203-211. doi: 10.1111/cei.13065. Epub 2017 Oct 27. Clin Exp Immunol. 2018. PMID: 28984901 Free PMC article. Review.
Isolated decreased serum-immunoglobulin (Ig)M has been associated with severe and/or recurrent infections, atopy and autoimmunity. ...Also, many papers on IgM deficiency have included patients with more abnormalities than simply IgM-deficienc …
Isolated decreased serum-immunoglobulin (Ig)M has been associated with severe and/or recurrent infections, atopy …
Treating secondary antibody deficiency in patients with haematological malignancy: European expert consensus.
Jolles S, Michallet M, Agostini C, Albert MH, Edgar D, Ria R, Trentin L, Lévy V. Jolles S, et al. Eur J Haematol. 2021 Apr;106(4):439-449. doi: 10.1111/ejh.13580. Epub 2021 Feb 2. Eur J Haematol. 2021. PMID: 33453130 Review.
OBJECTIVES: Secondary antibody deficiency (SAD), associated with severe, recurrent or persistent infections, is common in patients with haematological malignancies (HM), but unifying guidance on immunoglobulin replacement therapy (IgRT) in these …
OBJECTIVES: Secondary antibody deficiency (SAD), associated with severe, recurrent or persistent infections, is …
Immunodeficiency with hyper-IgM (HIM).
Notarangelo LD, Duse M, Ugazio AG. Notarangelo LD, et al. Immunodefic Rev. 1992;3(2):101-21. Immunodefic Rev. 1992. PMID: 1554497 Review.
Immunodeficiency with hyper-IgM (HIM) is a rare disorder characterized by recurrent infections associated with low IgG and IgA, and normal to increased IgM serum levels. ...Recurrent neutropaenia is a frequent finding. Immunological abnormalitie …
Immunodeficiency with hyper-IgM (HIM) is a rare disorder characterized by recurrent infections associated with l …
Clinical, genetic and immunological characteristics of 40 Chinese patients with CD40 ligand deficiency.
Du X, Tang W, Chen X, Zeng T, Wang Y, Chen Z, Xu T, Zhou L, Tang X, An Y, Zhao X. Du X, et al. Scand J Immunol. 2019 Oct;90(4):e12798. doi: 10.1111/sji.12798. Epub 2019 Jul 21. Scand J Immunol. 2019. PMID: 31179555 Free article.
CD40 ligand (CD40L) deficiency is a rare but life-threatening primary immunodeficiency caused by mutations in the CD40L gene. ...Opportunistic infections, including Pneumocystis carinii pneumonia and invasive fungal disease associated with Talaromyces …
CD40 ligand (CD40L) deficiency is a rare but life-threatening primary immunodeficiency caused by mutations in the CD40L gene. …
Somatic hypermutation defects in two adult hyper immunoglobulin M patients.
Yilmaz H, Fırtına S, Sarıtaş M, Sayitoğlu M, Ar MC. Yilmaz H, et al. Immunol Res. 2022 Dec;70(6):811-816. doi: 10.1007/s12026-022-09310-y. Epub 2022 Jul 25. Immunol Res. 2022. PMID: 35879489
Hyper immunoglobulin M (HIGM) syndrome is a rare disorder of the immune system with impaired antibody functions. ...It should be suspected in patients with a history of early-onset recurrent respiratory infections, enlarged lymph nodes, and autoimmune …
Hyper immunoglobulin M (HIGM) syndrome is a rare disorder of the immune system with impaired antibody functions. ...It should …
Case Report: Susceptibility to viral infections and secondary hemophagocytic lymphohistiocytosis responsive to intravenous immunoglobulin as primary manifestations of adenosine deaminase 2 deficiency.
Drago E, Garbarino F, Signa S, Grossi A, Schena F, Penco F, Santori E, Candotti F, Boztug K, Volpi S, Gattorno M, Caorsi R. Drago E, et al. Front Immunol. 2022 Sep 9;13:937108. doi: 10.3389/fimmu.2022.937108. eCollection 2022. Front Immunol. 2022. PMID: 36159847 Free PMC article.
Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disease associated with a highly variable clinical presentation, including systemic vasculitis, immunodeficiency, and cytopenia. We report a case of a 16-year-old girl affected by recurrent …
Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disease associated with a highly variable clinical prese …
Isolated growth hormone deficiency in a patient with immunoglobulin class switch recombination deficiency.
Kashef S, Ghaedian MM, Rezaei N, Karamizadeh Z, Aghamohammadi A, Durandy A, Pan-Hammarstrom Q, Hammarstrom L. Kashef S, et al. J Investig Allergol Clin Immunol. 2009;19(3):233-6. J Investig Allergol Clin Immunol. 2009. PMID: 19610268 Free article.
Growth hormone deficiency (GHD) may be associated with a number of immunodeficiency diseases, but its association with immunoglobulin class switch recombination (Ig CSR) deficiencies is very rare. We report the case of a patient with a hi …
Growth hormone deficiency (GHD) may be associated with a number of immunodeficiency diseases, but its association with …
Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review.
Wu J, Chen J, Tian ZQ, Zhang H, Gong RL, Chen TX, Hong L. Wu J, et al. J Clin Immunol. 2017 Feb;37(2):166-179. doi: 10.1007/s10875-017-0369-7. Epub 2017 Feb 14. J Clin Immunol. 2017. PMID: 28197791 Review.
The distribution of AD-HIES patients with STAT3 deficiency in the Chinese population is not clear. Herein, we retrospectively report 17 AD-HIES patients with STAT3 deficiency and demonstrate their clinical, immunological, and genetic features. ...Routine laboratory …
The distribution of AD-HIES patients with STAT3 deficiency in the Chinese population is not clear. Herein, we retrospectively report …
Severe T- and B-cell immune deficiency associated with malignant thymoma.
Yel L, Liao O, Lin F, Gupta S. Yel L, et al. Ann Allergy Asthma Immunol. 2003 Nov;91(5):501-5. doi: 10.1016/S1081-1206(10)61522-0. Ann Allergy Asthma Immunol. 2003. PMID: 14692437
METHODS: The patient presented with a superior vena cava syndrome caused by a malignant thymoma. During chemotherapy and radiotherapy, he experienced recurrent episodes of pulmonary infections due to Haemophilus influenza and Serratia marcescens and persistent oral …
METHODS: The patient presented with a superior vena cava syndrome caused by a malignant thymoma. During chemotherapy and radiotherapy, he ex …
Complex phenotypes in ALG12-congenital disorder of glycosylation (ALG12-CDG): Case series and review of the literature.
Tahata S, Gunderson L, Lanpher B, Morava E. Tahata S, et al. Mol Genet Metab. 2019 Dec;128(4):409-414. doi: 10.1016/j.ymgme.2019.08.007. Epub 2019 Aug 26. Mol Genet Metab. 2019. PMID: 31481313 Review.
ALG12-congenital disorder of glycosylation (ALG12-CDG) is a rare disorder caused by a deficiency of dolichol-P-mannose:Man(7)GlcNAc(2)-PP-dolichyl-alpha-6-mannosyltransferase which presents with intellectual disability, hypotonia, dysmorphic features, low IgG levels …
ALG12-congenital disorder of glycosylation (ALG12-CDG) is a rare disorder caused by a deficiency of dolichol-P-mannose:Man(7)G …
21 results