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

Year Number of Results
1991 1
1996 1
1999 1
2001 2
2002 1
2003 1
2005 3
2007 1
2008 3
2009 3
2011 5
2013 1
2014 2
2015 2
2016 1
2017 1
2018 2
2019 1
2020 1
2024 0

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29 results

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Page 1
Mixed cryoglobulinemia.
Ferri C. Ferri C. Orphanet J Rare Dis. 2008 Sep 16;3:25. doi: 10.1186/1750-1172-3-25. Orphanet J Rare Dis. 2008. PMID: 18796155 Free PMC article. Review.
The prevalence of 'essential' MC is reported as approximately 1:100,000 (with a female-to-male ratio 3:1), but this term is now used to refer to a minority of MC patients only. ...Differential diagnoses include a wide range of systemic, infectious and neoplastic dis …
The prevalence of 'essential' MC is reported as approximately 1:100,000 (with a female-to-male ratio 3:1), but this term is no …
Sjogren's Syndrome.
Papiris SA, Tsonis IA, Moutsopoulos HM. Papiris SA, et al. Semin Respir Crit Care Med. 2007 Aug;28(4):459-71. doi: 10.1055/s-2007-985667. Semin Respir Crit Care Med. 2007. PMID: 17764063 Review.
Sjogren's syndrome (SS) is a chronic, slowly progressive, inflammatory, autoimmune disease characterized by (1) lymphocytic infiltration of the exocrine glands leading to diminished or absent glandular secretion, and (2) marked B-lymphocytic cell hyperreactiv …
Sjogren's syndrome (SS) is a chronic, slowly progressive, inflammatory, autoimmune disease characterized by (1) lymphoc …
Nonapoptotic functions of Fas/CD95 in the immune response.
Guégan JP, Legembre P. Guégan JP, et al. FEBS J. 2018 Mar;285(5):809-827. doi: 10.1111/febs.14292. Epub 2017 Nov 16. FEBS J. 2018. PMID: 29032605 Free article. Review.
Mutations in this receptor are associated with a loss of apoptotic signaling and have been detected in an autoimmune disorder called autoimmune lymphoproliferative syndrome (ALPS) type Ia, which shares some clinical features with systemic lupus …
Mutations in this receptor are associated with a loss of apoptotic signaling and have been detected in an autoimmune disorder called …
Acquired immune-mediated thrombophilia in lymphoproliferative disorders.
Lechner K, Simonitsch I, Haselböck J, Jäger U, Pabinger I. Lechner K, et al. Leuk Lymphoma. 2011 Oct;52(10):1836-43. doi: 10.3109/10428194.2011.580474. Epub 2011 Jul 18. Leuk Lymphoma. 2011. PMID: 21767105 Review.
Sixty-one cases had a lupus anticoagulant, three an antibody to protein S, one to protein C, and one to ADAMTS 13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13). Lupus anticoagulants occurred in all histological subtypes of non-H …
Sixty-one cases had a lupus anticoagulant, three an antibody to protein S, one to protein C, and one to ADAMTS 13 (a disintegrin and metallo …
After 95 years, it's time to eRASe JMML.
Meynier S, Rieux-Laucat F. Meynier S, et al. Blood Rev. 2020 Sep;43:100652. doi: 10.1016/j.blre.2020.100652. Epub 2020 Jan 16. Blood Rev. 2020. PMID: 31980238 Review.
The available genetic and clinical data have enabled researchers to establish relationships between JMML and several clinical conditions, including Noonan syndrome, Ras-associated lymphoproliferative disease, and Moyamoya disease. ...
The available genetic and clinical data have enabled researchers to establish relationships between JMML and several clinical conditions, in …
The epidemiology of non-Hodgkin lymphoma.
Grulich AE, Vajdic CM. Grulich AE, et al. Pathology. 2005 Dec;37(6):409-19. doi: 10.1080/00313020500370192. Pathology. 2005. PMID: 16373224 Review.
These include immune-deficiency-associated central nervous system NHL (Epstein-Barr virus); gastric mucosa-associated lymphoid tissue NHL (Helicobacter pylori); adult T-cell leukemia/lymphoma (human T-lymphotrophic virus type 1) and body cavity-based lymphoma (human …
These include immune-deficiency-associated central nervous system NHL (Epstein-Barr virus); gastric mucosa-associated lymphoid tissue NHL (H …
Molecular mechanisms in genetically defined autoinflammatory diseases: disorders of amplified danger signaling.
de Jesus AA, Canna SW, Liu Y, Goldbach-Mansky R. de Jesus AA, et al. Annu Rev Immunol. 2015;33:823-74. doi: 10.1146/annurev-immunol-032414-112227. Epub 2015 Feb 20. Annu Rev Immunol. 2015. PMID: 25706096 Free PMC article. Review.
Studying such patients has revealed genetic defects that have helped unravel key innate immune pathways, including excessive IL-1 signaling, constitutive NF-kappaB activation, and, more recently, chronic type I IFN signaling. Discoveries of monogenic defects that le …
Studying such patients has revealed genetic defects that have helped unravel key innate immune pathways, including excessive IL-1 sig …
Double negative (DN) αβ T cells: misperception and overdue recognition.
Martina MN, Noel S, Saxena A, Rabb H, Hamad AR. Martina MN, et al. Immunol Cell Biol. 2015 Mar;93(3):305-10. doi: 10.1038/icb.2014.99. Epub 2014 Nov 25. Immunol Cell Biol. 2015. PMID: 25420721 Free PMC article. Review.
However, they are poorly understood and largely ignored by immunologists because of their historical association with the lymphoproliferation that occurs in mice (lpr and gld) and humans (autoimmune lymphoproliferative syndromes patients) with impaired Fas-mediated …
However, they are poorly understood and largely ignored by immunologists because of their historical association with the lymphoproliferatio …
Immune response in progressive multifocal leukoencephalopathy: an overview.
Weber T, Weber F, Petry H, Lüke W. Weber T, et al. J Neurovirol. 2001 Aug;7(4):311-7. doi: 10.1080/13550280152537166. J Neurovirol. 2001. PMID: 11517409 Review.
By far the most common underlying immunosuppressive illness is the acquired immune deficiency syndrome, accounting for about 85% of PML cases currently seen in clinical practice. PML may occur in patients with deficits in the humoral and/or cellular immune response such as …
By far the most common underlying immunosuppressive illness is the acquired immune deficiency syndrome, accounting for about 85% of P …
von Willebrand factor: clinical features of inherited and acquired disorders.
Bloom AL. Bloom AL. Mayo Clin Proc. 1991 Jul;66(7):743-51. doi: 10.1016/s0025-6196(12)62088-6. Mayo Clin Proc. 1991. PMID: 2072762 Review.
Three broad types of vWD are recognized; in addition, a platelet-type vWD (pseudo-vWD) is due to an abnormal platelet receptor for vWF. ...Acquired vWD may complicate lymphoproliferative and autoimmune disorders, and proteolytic degradation of vWF complicates …
Three broad types of vWD are recognized; in addition, a platelet-type vWD (pseudo-vWD) is due to an abnormal platelet receptor for vW …
29 results