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Year Number of Results
1986 1
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Page 1
CD40 Ligand Deficiency.
Leite LFB, Máximo TA, Mosca T, Forte WCN. Leite LFB, et al. Allergol Immunopathol (Madr). 2020 Jul-Aug;48(4):409-413. doi: 10.1016/j.aller.2019.08.005. Epub 2019 Dec 9. Allergol Immunopathol (Madr). 2020. PMID: 31831191 Review.
It manifests itself as a decrease in serum IgG, IgA and IgE, with normal or high IgM, defects in T cell proliferation, and decrease in soluble CD40L. ...Thus, its differential diagnosis with other inborn errors of immunity is essential, especially CD40 deficiency and varia …
It manifests itself as a decrease in serum IgG, IgA and IgE, with normal or high IgM, defects in T cell proliferation, and decrease i …
X-linked hyper IgM syndrome with severe eosinophilia: a case report and review of the literature.
Li H, Cao Y, Ma J, Li C. Li H, et al. BMC Pediatr. 2022 Apr 4;22(1):178. doi: 10.1186/s12887-022-03251-z. BMC Pediatr. 2022. PMID: 35379217 Free PMC article. Review.
BACKGROUND: Hyper IgM syndromes (HIGMS) are a group of rare primary immunodeficiency disorders. ...The absolute eosinophil count (AEC) also returned to normal range. X-linked hyper IgM syndrome was confirmed by gene test. Two months after …
BACKGROUND: Hyper IgM syndromes (HIGMS) are a group of rare primary immunodeficiency disorders. ...The absolute eosinop …
Autoimmune manifestations in primary immune deficiencies.
Bussone G, Mouthon L. Bussone G, et al. Autoimmun Rev. 2009 Feb;8(4):332-6. doi: 10.1016/j.autrev.2008.11.004. Epub 2008 Nov 24. Autoimmun Rev. 2009. PMID: 19028607 Review.
In these conditions, organ specific autoimmune diseases such as type 1 diabetes mellitus or Hashimoto's thyroiditis are prominently encountered. Several other PID such as common variable immunodeficiency (CVID), Good syndrome and hyper-IgM …
In these conditions, organ specific autoimmune diseases such as type 1 diabetes mellitus or Hashimoto's thyroiditis are promin …
CD40 ligand deficiency: treatment strategies and novel therapeutic perspectives.
França TT, Barreiros LA, Al-Ramadi BK, Ochs HD, Cabral-Marques O, Condino-Neto A. França TT, et al. Expert Rev Clin Immunol. 2019 May;15(5):529-540. doi: 10.1080/1744666X.2019.1573674. Epub 2019 Feb 18. Expert Rev Clin Immunol. 2019. PMID: 30681380 Review.
CD40 ligand (CD40L) deficiency or X-linked Hyper-IgM syndrome is a severe primary immunodeficiency caused by mutations in the CD40L gene. ...
CD40 ligand (CD40L) deficiency or X-linked Hyper-IgM syndrome is a severe primary immunodeficiency caused by mut …
Pediatric allergy and immunology in Brazil.
Rosario-Filho NA, Jacob CM, Sole D, Condino-Neto A, Arruda LK, Costa-Carvalho B, Cocco RR, Camelo-Nunes I, Chong-Neto HJ, Wandalsen GF, Castro AP, Yang AC, Pastorino AC, Sarinho ES. Rosario-Filho NA, et al. Pediatr Allergy Immunol. 2013 Jun;24(4):402-9. doi: 10.1111/pai.12069. Epub 2013 Apr 11. Pediatr Allergy Immunol. 2013. PMID: 23578336 Review.
Molecular diagnosis of primary immunodeficiencies (PID) showed a high incidence of fungal infections including paracoccidioidomycosis in X-linked hyper-IgM syndrome, and the occurrence of BCG adverse reactions or other mycobacterial infections in patients wit …
Molecular diagnosis of primary immunodeficiencies (PID) showed a high incidence of fungal infections including paracoccidioidomycosis in X-l …
Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature.
Romani L, Williamson PR, Di Cesare S, Di Matteo G, De Luca M, Carsetti R, Figà-Talamanca L, Cancrini C, Rossi P, Finocchi A. Romani L, et al. Front Immunol. 2021 Jul 15;12:708837. doi: 10.3389/fimmu.2021.708837. eCollection 2021. Front Immunol. 2021. PMID: 34335625 Free PMC article. Review.
The hyper IgM syndromes are a rare group of primary immunodeficiency. The X-linked Hyper IgM syndrome (HIGM), due to a gene defect in CD40L, is the commonest variant; it is characterized by an increased susceptibility to a narrow spectrum …
The hyper IgM syndromes are a rare group of primary immunodeficiency. The X-linked Hyper IgM syndrome …
Inherited and acquired clinical phenotypes associated with neuroendocrine tumors.
Nicolaides RE, de la Morena MT. Nicolaides RE, et al. Curr Opin Allergy Clin Immunol. 2017 Dec;17(6):431-442. doi: 10.1097/ACI.0000000000000406. Curr Opin Allergy Clin Immunol. 2017. PMID: 29040209 Review.
PURPOSE OF REVIEW: Overview of neuroendocrine neoplasms in the context of their associations with primary and secondary immunodeficiency states. RECENT FINDINGS: Malignancies of neuroendocrine origin are well known to be associated with hereditary syndromes, including mult …
PURPOSE OF REVIEW: Overview of neuroendocrine neoplasms in the context of their associations with primary and secondary immunodeficiency …
Infectious complications of the primary immunodeficiencies.
Stiehm ER, Chin TW, Haas A, Peerless AG. Stiehm ER, et al. Clin Immunol Immunopathol. 1986 Jul;40(1):69-86. doi: 10.1016/0090-1229(86)90070-x. Clin Immunol Immunopathol. 1986. PMID: 3521971 Review.
This means too many, too severe, too prolonged, too complicated and too unusual infections. Infections in immunodeficiency have a characteristic cause depending on the nature of the immune deficiency. ...Infections can also be induced by live vaccines given in immunodef …
This means too many, too severe, too prolonged, too complicated and too unusual infections. Infections in immunodeficiency have a cha …
Immunoglobulin class switch recombination deficiency type 1 or CD40 ligand deficiency: from bedside to bench and back again.
Hirbod-Mobarakeh A, Aghamohammadi A, Rezaei N. Hirbod-Mobarakeh A, et al. Expert Rev Clin Immunol. 2014 Jan;10(1):91-105. doi: 10.1586/1744666X.2014.864554. Epub 2013 Nov 26. Expert Rev Clin Immunol. 2014. PMID: 24308834 Review.
The immunoglobulin class switch recombination deficiency or hyper-IgM syndrome is characterized by normal or elevated serum IgM and low serum levels of other immunoglobulins. Since the first reported patient with hyper-IgM, more than 200 …
The immunoglobulin class switch recombination deficiency or hyper-IgM syndrome is characterized by normal or elevated s …
Flow cytometry assays in primary immunodeficiency diseases.
O'Gorman MR, Zollett J, Bensen N. O'Gorman MR, et al. Methods Mol Biol. 2011;699:317-35. doi: 10.1007/978-1-61737-950-5_15. Methods Mol Biol. 2011. PMID: 21116990 Review.
The primary immunodeficiency diseases (PIDs) encompass an extremely large and diverse number of clinical disorders caused by mutations in genes that affect virtually every measurable component of our immune systems. ...The flow cytometry procedures that have been developed …
The primary immunodeficiency diseases (PIDs) encompass an extremely large and diverse number of clinical disorders caused by mutation …
17 results