 Immunologic Deficiency Syndromes
"Immunologic Deficiency Syndromes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.
| Descriptor ID |
D007153
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| MeSH Number(s) |
C20.673
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| Concept/Terms |
Immunologic Deficiency Syndromes- Immunologic Deficiency Syndromes
- Deficiency Syndromes, Immunologic
- Immunological Deficiency Syndromes
- Deficiency Syndrome, Immunological
- Deficiency Syndromes, Immunological
- Immunological Deficiency Syndrome
- Syndrome, Immunological Deficiency
- Syndromes, Immunological Deficiency
- Deficiency Syndrome, Immunologic
- Syndrome, Immunologic Deficiency
- Syndromes, Immunologic Deficiency
- Immunologic Deficiency Syndrome
Antibody Deficiency Syndrome- Antibody Deficiency Syndrome
- Deficiency Syndromes, Antibody
- Antibody Deficiency Syndromes
- Deficiency Syndrome, Antibody
- Syndrome, Antibody Deficiency
- Syndromes, Antibody Deficiency
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Below are MeSH descriptors whose meaning is more general than "Immunologic Deficiency Syndromes".
Below are MeSH descriptors whose meaning is more specific than "Immunologic Deficiency Syndromes".
This graph shows the total number of publications written about "Immunologic Deficiency Syndromes" by people in this website by year, and whether "Immunologic Deficiency Syndromes" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 1 | 0 | 1 | | 2015 | 2 | 0 | 2 | | 2018 | 2 | 0 | 2 | | 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Immunologic Deficiency Syndromes" by people in Profiles.
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Searing DA, Dutmer CM, Fleischer DM, Shaker MS, Oppenheimer J, Grayson MH, Stukus D, Hartog N, Hsieh EWY, Rider NL, Vander Leek TK, Kim H, Chan ES, Mack D, Ellis AK, Abrams EM, Bansal P, Lang DM, Lieberman J, Golden DB, Wallace D, Portnoy J, Mosnaim G, Greenhawt M. A Phased Approach to Resuming Suspended Allergy/Immunology Clinical Services. J Allergy Clin Immunol Pract. 2020 Jul - Aug; 8(7):2125-2134.
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Mowrer C, Lee BR, Goyal R, Selvarangan R, Schuster JE. Outcome of children with rhinovirus detection prior to allogeneic hematopoietic cell transplant. Pediatr Transplant. 2018 12; 22(8):e13301.
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Cadieux-Dion M, Safina NP, Engleman K, Saunders C, Repnikova E, Raje N, Canty K, Farrow E, Miller N, Zellmer L, Thiffault I. Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report. BMC Med Genet. 2018 03 09; 19(1):41.
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Giardino G, Gallo V, Somma D, Farrow EG, Thiffault I, D'Assante R, Donofrio V, Paciolla M, Ursini MV, Leonardi A, Saunders CJ, Pignata C. Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis. J Allergy Clin Immunol. 2016 05; 137(5):1591-1595.e4.
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Bonilla FA, Khan DA, Ballas ZK, Chinen J, Frank MM, Hsu JT, Keller M, Kobrynski LJ, Komarow HD, Mazer B, Nelson RP, Orange JS, Routes JM, Shearer WT, Sorensen RU, Verbsky JW, Bernstein DI, Blessing-Moore J, Lang D, Nicklas RA, Oppenheimer J, Portnoy JM, Randolph CR, Schuller D, Spector SL, Tilles S, Wallace D. Practice parameter for the diagnosis and management of primary immunodeficiency. J Allergy Clin Immunol. 2015 Nov; 136(5):1186-205.e1-78.
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Raje N, Soden S, Swanson D, Ciaccio CE, Kingsmore SF, Dinwiddie DL. Utility of next generation sequencing in clinical primary immunodeficiencies. Curr Allergy Asthma Rep. 2014 Oct; 14(10):468.
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Fischer RT, Friend B, Talmon GA, Grant WJ, Quiros-Tejeira RE, Langnas AN, Coccia PF. Intestinal transplantation in children with multiple intestinal atresias and immunodeficiency. Pediatr Transplant. 2014 Mar; 18(2):190-6.
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Singhi AD, Goyal A, Davison JM, Regueiro MD, Roche RL, Ranganathan S. Pediatric autoimmune enteropathy: an entity frequently associated with immunodeficiency disorders. Mod Pathol. 2014 Apr; 27(4):543-53.
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Dinwiddie DL, Kingsmore SF, Caracciolo S, Rossi G, Moratto D, Mazza C, Sabelli C, Bacchetta R, Passerini L, Magri C, Bell CJ, Miller NA, Hateley SL, Saunders CJ, Zhang L, Schroth GP, Barlati S, Badolato R. Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections. J Allergy Clin Immunol. 2013 Feb; 131(2):594-7.e1-3.
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Badolato R, Prandini A, Caracciolo S, Colombo F, Tabellini G, Giacomelli M, Cantarini ME, Pession A, Bell CJ, Dinwiddie DL, Miller NA, Hateley SL, Saunders CJ, Zhang L, Schroth GP, Plebani A, Parolini S, Kingsmore SF. Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome. Blood. 2012 Mar 29; 119(13):3185-7.
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