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1991
2025

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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
2025 0

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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.
Mixed cryoglobulinemia (MC), type II and type III, refers to the presence of circulating cryoprecipitable immune complexes in the serum and manifests clinically by a classical triad of purpura, weakness and arthralgias. ...The prevalence of 'essential' MC is reporte …
Mixed cryoglobulinemia (MC), type II and type III, refers to the presence of circulating cryoprecipitable immune complexes in …
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 …
Autoimmune lymphoproliferative syndrome, a disorder of apoptosis.
Jackson CE, Puck JM. Jackson CE, et al. Curr Opin Pediatr. 1999 Dec;11(6):521-7. doi: 10.1097/00008480-199912000-00009. Curr Opin Pediatr. 1999. PMID: 10590910 Review.
Autoimmune Lymphoproliferative Syndrome (ALPS) is a recently recognized disease in which a genetic defect in programmed cell death, or apoptosis, leads to breakdown of lymphocyte homeostasis and normal immunologic tolerance. ...ALPS is subdivided into: 1
Autoimmune Lymphoproliferative Syndrome (ALPS) is a recently recognized disease in which a genetic defect in programmed
Cellular and molecular mechanisms of immune dysregulation and autoimmunity.
Azizi G, Pouyani MR, Abolhassani H, Sharifi L, Dizaji MZ, Mohammadi J, Mirshafiey A, Aghamohammadi A. Azizi G, et al. Cell Immunol. 2016 Dec;310:14-26. doi: 10.1016/j.cellimm.2016.08.012. Epub 2016 Aug 27. Cell Immunol. 2016. PMID: 27614846 Review.
A specific group of PIDs entitled "diseases of immune dysregulation" are developed due to mutation in the genes which have critical roles in the regulation of immune responses and immunological tolerance. This group of PID patients develop autoimmune and inflammatory disor …
A specific group of PIDs entitled "diseases of immune dysregulation" are developed due to mutation in the genes which have critical roles in …
Recent advances in the concept and diagnosis of autoimmune pancreatitis and IgG4-related disease.
Okazaki K, Uchida K, Koyabu M, Miyoshi H, Takaoka M. Okazaki K, et al. J Gastroenterol. 2011 Mar;46(3):277-88. doi: 10.1007/s00535-011-0386-x. Epub 2011 Mar 11. J Gastroenterol. 2011. PMID: 21452084 Review.
Recent studies have suggested the existence of two subtypes of autoimmune pancreatitis (AIP): type 1 AIP, related to IgG4 (lymphoplasmacytic sclerosing pancreatitis); and type 2 AIP, related to a granulocytic epithelial lesion (idiopathic duct-centric …
Recent studies have suggested the existence of two subtypes of autoimmune pancreatitis (AIP): type 1 AIP, related to Ig …
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.
Three PID are defined by the occurrence of autoimmune manifestations: APECED (Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy), autoimmune lymphoproliferative syndrome (ALPS) and IPEX syndrome (immunodysregulation, polyendo …
Three PID are defined by the occurrence of autoimmune manifestations: APECED (Autoimmune Polyendocrinopathy-Candidiasis-Ectode …
Promotion and prevention of autoimmune disease by CD8+ T cells.
Gravano DM, Hoyer KK. Gravano DM, et al. J Autoimmun. 2013 Sep;45:68-79. doi: 10.1016/j.jaut.2013.06.004. Epub 2013 Jul 17. J Autoimmun. 2013. PMID: 23871638 Review.
Until recently, little was known about the importance of CD8+ T effectors in promoting and preventing autoimmune disease development. CD8+ T cells can oppose or promote autoimmune disease through activities as suppressor cells and as cytotoxic effectors. ...Defining …
Until recently, little was known about the importance of CD8+ T effectors in promoting and preventing autoimmune disease development. …
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. Despite scientific progress and the …
The available genetic and clinical data have enabled researchers to establish relationships between JMML and several clinical conditions, in …
Rare diseases that mimic Systemic Lupus Erythematosus (Lupus mimickers).
Chasset F, Richez C, Martin T, Belot A, Korganow AS, Arnaud L. Chasset F, et al. Joint Bone Spine. 2019 Mar;86(2):165-171. doi: 10.1016/j.jbspin.2018.10.007. Epub 2018 Oct 26. Joint Bone Spine. 2019. PMID: 30837156 Review.
Some of these "SLE mimickers" are very common, such as rosacea which can be mistaken for the butterfly rash, while others such as Kikuchi disease, type-1 interferonopathies, Castleman's disease, prolidase deficiency, angioimmunoblastic T-cell lymphoma, Evans' syn
Some of these "SLE mimickers" are very common, such as rosacea which can be mistaken for the butterfly rash, while others such as Kikuchi di …
29 results