 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 |
|---|
| 1981 | 0 | 1 | 1 | | 1982 | 0 | 1 | 1 | | 1984 | 0 | 2 | 2 | | 1986 | 1 | 0 | 1 | | 1987 | 5 | 0 | 5 | | 1988 | 2 | 1 | 3 | | 1989 | 6 | 1 | 7 | | 1990 | 1 | 1 | 2 | | 1991 | 2 | 2 | 4 | | 1992 | 2 | 1 | 3 | | 1993 | 0 | 1 | 1 | | 1994 | 2 | 0 | 2 | | 1995 | 1 | 0 | 1 | | 1996 | 1 | 0 | 1 | | 1997 | 3 | 0 | 3 | | 1998 | 0 | 1 | 1 | | 2000 | 2 | 0 | 2 | | 2001 | 2 | 0 | 2 | | 2002 | 0 | 2 | 2 | | 2004 | 1 | 0 | 1 | | 2010 | 2 | 0 | 2 | | 2011 | 1 | 0 | 1 | | 2013 | 2 | 1 | 3 | | 2014 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2017 | 3 | 0 | 3 | | 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Immunologic Deficiency Syndromes" by people in Profiles.
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Pasparakis M, Kelliher M. Connecting immune deficiency and inflammation. Science. 2018 08 24; 361(6404):756-757.
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Rosen MJ, Ireland B, Narasimhan M, French C, Irwin RS. Cough in Ambulatory Immunocompromised Adults: CHEST Expert Panel Report. Chest. 2017 11; 152(5):1038-1042.
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Platt CD, Fried AJ, Hoyos-Bachiloglu R, Usmani GN, Schmidt B, Whangbo J, Chiarle R, Chou J, Geha RS. Combined immunodeficiency with EBV positive B cell lymphoma and epidermodysplasia verruciformis due to a novel homozygous mutation in RASGRP1. Clin Immunol. 2017 10; 183:142-144.
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Aubert G, Strauss KA, Lansdorp PM, Rider NL. Defects in lymphocyte telomere homeostasis contribute to cellular immune phenotype in patients with cartilage-hair hypoplasia. J Allergy Clin Immunol. 2017 Oct; 140(4):1120-1129.e1.
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Dobbs K, Domínguez Conde C, Zhang SY, Parolini S, Audry M, Chou J, Haapaniemi E, Keles S, Bilic I, Okada S, Massaad MJ, Rounioja S, Alwahadneh AM, Serwas NK, Capuder K, Çiftçi E, Felgentreff K, Ohsumi TK, Pedergnana V, Boisson B, Haskologlu S, Ensari A, Schuster M, Moretta A, Itan Y, Patrizi O, Rozenberg F, Lebon P, Saarela J, Knip M, Petrovski S, Goldstein DB, Parrott RE, Savas B, Schambach A, Tabellini G, Bock C, Chatila TA, Comeau AM, Geha RS, Abel L, Buckley RH, Ikinciogullari A, Al-Herz W, Helminen M, Dogu F, Casanova JL, Boztug K, Notarangelo LD. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections. N Engl J Med. 2015 Jun 18; 372(25):2409-22.
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Chakraborty PK, Schmitz-Abe K, Kennedy EK, Mamady H, Naas T, Durie D, Campagna DR, Lau A, Sendamarai AK, Wiseman DH, May A, Jolles S, Connor P, Powell C, Heeney MM, Giardina PJ, Klaassen RJ, Kannengiesser C, Thuret I, Thompson AA, Marques L, Hughes S, Bonney DK, Bottomley SS, Wynn RF, Laxer RM, Minniti CP, Moppett J, Bordon V, Geraghty M, Joyce PB, Markianos K, Rudner AD, Holcik M, Fleming MD. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD). Blood. 2014 Oct 30; 124(18):2867-71.
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Chen R, Giliani S, Lanzi G, Mias GI, Lonardi S, Dobbs K, Manis J, Im H, Gallagher JE, Phanstiel DH, Euskirchen G, Lacroute P, Bettinger K, Moratto D, Weinacht K, Montin D, Gallo E, Mangili G, Porta F, Notarangelo LD, Pedretti S, Al-Herz W, Alfahdli W, Comeau AM, Traister RS, Pai SY, Carella G, Facchetti F, Nadeau KC, Snyder M, Notarangelo LD. Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias. J Allergy Clin Immunol. 2013 Sep; 132(3):656-664.e17.
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Usmani GN, Woda BA, Newburger PE. Advances in understanding the pathogenesis of HLH. Br J Haematol. 2013 Jun; 161(5):609-22.
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Wiseman DH, May A, Jolles S, Connor P, Powell C, Heeney MM, Giardina PJ, Klaassen RJ, Chakraborty P, Geraghty MT, Major-Cook N, Kannengiesser C, Thuret I, Thompson AA, Marques L, Hughes S, Bonney DK, Bottomley SS, Fleming MD, Wynn RF. A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD). Blood. 2013 Jul 4; 122(1):112-23.
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Greenspan NS, Lu MA, Shipley JW, Ding X, Li Q, Sultana D, Kollaros M, Schreiber JR, Fu P, Putterman C, Emancipator SN. IgG3 deficiency extends lifespan and attenuates progression of glomerulonephritis in MRL/lpr mice. Biol Direct. 2012 Jan 16; 7:3.
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