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

Year Number of Results
2001 2
2002 1
2005 1
2008 1
2009 1
2011 1
2013 1
2017 1
2018 1
2019 1
2020 1
2021 1
2022 1
2024 0

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11 results

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Page 1
Autosomal-dominant primary immunodeficiencies.
Lawrence T, Puel A, Reichenbach J, Ku CL, Chapgier A, Renner E, Minard-Colin V, Ouachée M, Casanova JL. Lawrence T, et al. Curr Opin Hematol. 2005 Jan;12(1):22-30. doi: 10.1097/01.moh.0000149609.37309.0a. Curr Opin Hematol. 2005. PMID: 15604887 Review.
The vast majority of known primary immunodeficiencies (PIDs) are autosomal or X-linked recessive Mendelian traits. Only four classical primary immunodeficiencies are thought to be autosomal-dominant, three of which still lack a well-defined genetic etiology: …
The vast majority of known primary immunodeficiencies (PIDs) are autosomal or X-linked recessive Mendelian traits. Only four c …
The Robustness of Cellular Immunity Determines the Fate of SARS-CoV-2 Infection.
Moga E, Lynton-Pons E, Domingo P. Moga E, et al. Front Immunol. 2022 Jun 27;13:904686. doi: 10.3389/fimmu.2022.904686. eCollection 2022. Front Immunol. 2022. PMID: 35833134 Free PMC article. Review.
Two years after the appearance of the SARS-CoV-2 virus, the causal agent of the current global pandemic, it is time to analyze the evolution of the immune protection that infection and vaccination provide. Cellular immunity plays an important role in limiting disease sever …
Two years after the appearance of the SARS-CoV-2 virus, the causal agent of the current global pandemic, it is time to analyze the ev …
Evaluation of B lymphocyte deficiencies.
Vickery JD, Michael CF, Lew DB. Vickery JD, et al. Cardiovasc Hematol Disord Drug Targets. 2013 Aug;13(2):133-43. doi: 10.2174/1871529x11313020006. Cardiovasc Hematol Disord Drug Targets. 2013. PMID: 23988001 Review.
An arrest in B cell development at the pre-B cell stage leads to agammaglobulinemia and an insignificant number of B cells. X-linked agammaglobulinemia is the most common of these developmental arrests while the autosomal recessive agammaglobulinemi …
An arrest in B cell development at the pre-B cell stage leads to agammaglobulinemia and an insignificant number of B cells. X-linked …
Primary immunodeficiency diseases associated with increased susceptibility to viral infections and malignancies.
Rezaei N, Hedayat M, Aghamohammadi A, Nichols KE. Rezaei N, et al. J Allergy Clin Immunol. 2011 Jun;127(6):1329-41.e2; quiz 1342-3. doi: 10.1016/j.jaci.2011.02.047. Epub 2011 Apr 22. J Allergy Clin Immunol. 2011. PMID: 21514636 Review.
Here we review the clinical and biologic features of several PIDs associated with enhanced susceptibility to viral infections and cancer, including X-linked lymphoproliferative disease; IL-2-inducible T-cell kinase deficiency; epidermodysplasia verruciformis; warts, hypoga …
Here we review the clinical and biologic features of several PIDs associated with enhanced susceptibility to viral infections and cancer, in …
Early defects in B cell development.
Conley ME. Conley ME. Curr Opin Allergy Clin Immunol. 2002 Dec;2(6):517-22. doi: 10.1097/00130832-200212000-00007. Curr Opin Allergy Clin Immunol. 2002. PMID: 14752335 Review.
PURPOSE OF REVIEW: Recent clinical studies in patients with genetically proven X-linked or autosomal recessive agammaglobulinemia provide some guidelines that should influence our management of patients with suspected immunodeficiency. ...Because the physical …
PURPOSE OF REVIEW: Recent clinical studies in patients with genetically proven X-linked or autosomal recessive agammaglobul …
The same mutation in a family with adenosine deaminase 2 deficiency.
Sozeri B, Ercan G, Dogan OA, Yıldız J, Demir F, Doğanay L. Sozeri B, et al. Rheumatol Int. 2021 Jan;41(1):227-233. doi: 10.1007/s00296-019-04444-z. Epub 2019 Sep 20. Rheumatol Int. 2021. PMID: 31541281 Review.
The deficiency of adenosine deaminase 2 (DADA2) has recently been defined as a monogenetic autosomal recessive autoinflammatory disease. ...
The deficiency of adenosine deaminase 2 (DADA2) has recently been defined as a monogenetic autosomal recessive autoinfl …
Defects in Jak-STAT-mediated cytokine signals cause hyper-IgE syndrome: lessons from a primary immunodeficiency.
Minegishi Y, Karasuyama H. Minegishi Y, et al. Int Immunol. 2009 Feb;21(2):105-12. doi: 10.1093/intimm/dxn134. Epub 2008 Dec 15. Int Immunol. 2009. PMID: 19088064 Review.
Recent studies have demonstrated that hypomorphic mutations in signal transducer and activator of transcription 3 result in the classical multisystem form of HIES, whereas a null mutation in tyrosine kinase 2 causes the autosomal recessive form of HIES that i …
Recent studies have demonstrated that hypomorphic mutations in signal transducer and activator of transcription 3 result in the classical mu …
[Common variable immunodeficiency. Review].
Iglesias Alzueta J, Matamoros Florí N. Iglesias Alzueta J, et al. Allergol Immunopathol (Madr). 2001 May-Jun;29(3):113-8. doi: 10.1016/s0301-0546(01)79029-5. Allergol Immunopathol (Madr). 2001. PMID: 11434884 Review. Spanish.
The age at which clinical manifestations appear, the absence of familial antecedents and the presence of circulating B lymphocytes form the basis of the differential diagnosis between X-linked agammaglobulinemia and autosomal recessive forms. The treatment of …
The age at which clinical manifestations appear, the absence of familial antecedents and the presence of circulating B lymphocytes form the …
[Multiple facets of ADA2 deficiency: Vasculitis, auto-inflammatory disease and immunodeficiency: A literature review of 135 cases from literature].
Fayand A, Sarrabay G, Belot A, Hentgen V, Kone-Paut I, Grateau G, Melki I, Georgin-Lavialle S. Fayand A, et al. Rev Med Interne. 2018 Apr;39(4):297-306. doi: 10.1016/j.revmed.2017.11.006. Epub 2017 Dec 19. Rev Med Interne. 2018. PMID: 29273180 Review. French.
Deficiency of adenosine deaminase 2 (DADA2) is a recently described auto-inflammatory disorder. It is an autosomal recessive inherited disease, caused by mutations in the ADA2 gene (formerly known as CECR1) encoding ADA2 enzyme. ...
Deficiency of adenosine deaminase 2 (DADA2) is a recently described auto-inflammatory disorder. It is an autosomal recessiv …
[Primary immunodeficiencies. Clinical features and variant forms].
Fontán Casariego G. Fontán Casariego G. Allergol Immunopathol (Madr). 2001 May-Jun;29(3):101-7. doi: 10.1016/s0301-0546(01)79027-1. Allergol Immunopathol (Madr). 2001. PMID: 11434882 Review. Spanish.
Furthermore, new forms of severe combined immunodeficiency (SCID) and of recessive autosomal agammaglobulinemia are described. From the publication of this classification until the end of the year 2000 a minimum of three new PIDs have been described and a fur …
Furthermore, new forms of severe combined immunodeficiency (SCID) and of recessive autosomal agammaglobulinemia are des …
11 results