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1991 1
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Page 1
Autoimmune hemolytic anemia.
Gehrs BC, Friedberg RC. Gehrs BC, et al. Am J Hematol. 2002 Apr;69(4):258-71. doi: 10.1002/ajh.10062. Am J Hematol. 2002. PMID: 11921020 Free article. Review.
Red blood cell (RBC) autoantibodies are a relatively uncommon cause of anemia. However, autoimmune hemolytic anemia (AIHA) must be considered in the differential diagnosis of hemolytic anemias, especially if the patient has a concomitant lymphoproliferative disorder …
Red blood cell (RBC) autoantibodies are a relatively uncommon cause of anemia. However, autoimmune hemolytic anemia (AIHA) must be co …
Cryoglobulinemia.
Tedeschi A, Baratè C, Minola E, Morra E. Tedeschi A, et al. Blood Rev. 2007 Jul;21(4):183-200. doi: 10.1016/j.blre.2006.12.002. Epub 2007 Feb 7. Blood Rev. 2007. PMID: 17289231 Review.
Cryoglobulinemia refers to the presence in serum of immunoglobulins that precipitate at a cold temperature. Type I cryoglobulins are single monoclonal immunoglobulins usually associated with haematological disorders. ...The relation between MC and HCV infection shows new i …
Cryoglobulinemia refers to the presence in serum of immunoglobulins that precipitate at a cold temperature. Type I cryoglobulins are …
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 hyperreactivity man …
Sjogren's syndrome (SS) is a chronic, slowly progressive, inflammatory, autoimmune disease characterized by (1) lymphocytic in …
Diagnosis and management of Evans syndrome in adults: first consensus recommendations.
Fattizzo B, Marchetti M, Michel M, Cantoni S, Frederiksen H, Giordano G, Glenthøj A, González-López TJ, Murakhovskaya I, Napolitano M, Mingot ME, Arguello M, Patriarca A, Raso S, Vianelli N, Barcellini W. Fattizzo B, et al. Lancet Haematol. 2024 Aug;11(8):e617-e628. doi: 10.1016/S2352-3026(24)00144-3. Epub 2024 Jul 2. Lancet Haematol. 2024. PMID: 38968944 Review.
Evans syndrome is a rare disease marked by a severe clinical course, high relapse rate, infectious and thrombotic complications, and sometimes fatal outcome. ...The panellists recommended extensive clinical and laboratory diagnostic tests, including bone marrow evaluation …
Evans syndrome is a rare disease marked by a severe clinical course, high relapse rate, infectious and thrombotic complications, and …
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. Some authors have referred to ALPS …
Autoimmune Lymphoproliferative Syndrome (ALPS) is a recently recognized disease in which a genetic defect in programmed …
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.
However, a defect in the mechanisms of control of self-reactive B and T cells may favour these manifestations. Three PID are defined by the occurrence of autoimmune manifestations: APECED (Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy), autoimmun …
However, a defect in the mechanisms of control of self-reactive B and T cells may favour these manifestations. Three PID are defined by the …
Prevalence of mixed cryoglobulinaemia syndrome and circulating cryoglobulins in a population-based survey: the Origgio study.
Monti G, Saccardo F, Castelnovo L, Novati P, Sollima S, Riva A, Sarzi-Puttini P, Quartuccio L, De Vita S, Galli M. Monti G, et al. Autoimmun Rev. 2014 Jun;13(6):609-14. doi: 10.1016/j.autrev.2013.11.005. Epub 2014 Jan 10. Autoimmun Rev. 2014. PMID: 24418294 Review.
Mixed cryoglobulinaemia syndrome (MCS) is associated with a number of infectious, autoimmune and lymphoproliferative disorders, particularly chronic hepatitis C infection. ...Of the 266 randomly selected subjects invited to undergo a clinical examination and …
Mixed cryoglobulinaemia syndrome (MCS) is associated with a number of infectious, autoimmune and lymphoproliferative di …
Regulatory T cells: development, function and role in autoimmunity.
Lan RY, Ansari AA, Lian ZX, Gershwin ME. Lan RY, et al. Autoimmun Rev. 2005 Jul;4(6):351-63. doi: 10.1016/j.autrev.2005.01.007. Epub 2005 Mar 7. Autoimmun Rev. 2005. PMID: 16081026 Review.
Much focus has been placed on thymically derived CD4(+)CD25(+) regulatory T cells, given that the depletion of this subset in murine models results in the spontaneous development of autoimmune diseases. These naturally occurring regulatory T cells are found to be functiona …
Much focus has been placed on thymically derived CD4(+)CD25(+) regulatory T cells, given that the depletion of this subset in murine models …
Hepatitis C virus, Sjogren's syndrome and B-cell lymphoma: linking infection, autoimmunity and cancer.
Ramos-Casals M, De Vita S, Tzioufas AG. Ramos-Casals M, et al. Autoimmun Rev. 2005 Jan;4(1):8-15. doi: 10.1016/j.autrev.2004.04.004. Autoimmun Rev. 2005. PMID: 15652773 Review.
An increased prevalence of hematologic malignancies is often described in patients with Sjogren's syndrome (SS). Viruses have been proposed as possible etiologic or triggering agents of systemic autoimmune diseases (SADs), with hepatitis C virus (HCV) being one of t …
An increased prevalence of hematologic malignancies is often described in patients with Sjogren's syndrome (SS). Viruses have been pr …
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 …
12 results