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1981 1
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338 results

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Page 1
Autoimmune Lymphoproliferative Syndrome: An Overview.
Matson DR, Yang DT. Matson DR, et al. Arch Pathol Lab Med. 2020 Feb;144(2):245-251. doi: 10.5858/arpa.2018-0190-RS. Epub 2019 Apr 8. Arch Pathol Lab Med. 2020. PMID: 30958694 Free PMC article. Review.
Autoimmune lymphoproliferative syndrome (ALPS) is an inherited nonmalignant lymphoproliferative disorder characterized by heterozygous mutations within the first apoptosis signal receptor (FAS) signaling pathway. Defects in FAS-mediated apoptosis cause …
Autoimmune lymphoproliferative syndrome (ALPS) is an inherited nonmalignant lymphoproliferative disorder charact …
Presentation and diagnosis of autoimmune lymphoproliferative syndrome (ALPS).
Lambert MP. Lambert MP. Expert Rev Clin Immunol. 2021 Nov;17(11):1163-1173. doi: 10.1080/1744666X.2021.1978842. Epub 2021 Sep 17. Expert Rev Clin Immunol. 2021. PMID: 34503378 Review.
INTRODUCTION: Autoimmune lymphoproliferative syndrome (ALPS) is a rare disorder of immune dysregulation characterized by derangements in first apoptosis signal-mediated apoptosis and elevations in CD3(+)TCRalphabeta(+)CD4(-)CD8(-) 'double negative' T cells. . …
INTRODUCTION: Autoimmune lymphoproliferative syndrome (ALPS) is a rare disorder of immune dysregulation characterized b …
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 …
Current concepts on Sjogren's syndrome - classification criteria and biomarkers.
Jonsson R, Brokstad KA, Jonsson MV, Delaleu N, Skarstein K. Jonsson R, et al. Eur J Oral Sci. 2018 Oct;126 Suppl 1(Suppl Suppl 1):37-48. doi: 10.1111/eos.12536. Eur J Oral Sci. 2018. PMID: 30178554 Free PMC article. Review.
Sjogren's syndrome is a lymphoproliferative disease with autoimmune features characterized by mononuclear cell infiltration of exocrine glands, notably the lacrimal and salivary glands. ...Current treatments are mainly symptomatic. As a result of the diverse …
Sjogren's syndrome is a lymphoproliferative disease with autoimmune features characterized by mononuclear cell infiltra …
The Changing Landscape of Autoimmune Hemolytic Anemia.
Barcellini W, Fattizzo B. Barcellini W, et al. Front Immunol. 2020 Jun 3;11:946. doi: 10.3389/fimmu.2020.00946. eCollection 2020. Front Immunol. 2020. PMID: 32655543 Free PMC article. Review.
Autoimmune hemolytic anemia (AIHA) is a greatly heterogeneous disease due to autoantibodies directed against erythrocytes, with or without complement activation. ...AIHAs may be primary/idiopathic or secondary to infections, autoimmune diseases, malignancies, partic …
Autoimmune hemolytic anemia (AIHA) is a greatly heterogeneous disease due to autoantibodies directed against erythrocytes, with or wi …
New insights in cryoglobulinemic vasculitis.
Silva F, Pinto C, Barbosa A, Borges T, Dias C, Almeida J. Silva F, et al. J Autoimmun. 2019 Dec;105:102313. doi: 10.1016/j.jaut.2019.102313. Epub 2019 Aug 2. J Autoimmun. 2019. PMID: 31383568 Review.
Cryoglobulinemia is classified into three types (I, II and III) on the basis of immunoglobulin composition. Predisposing conditions include lymphoproliferative, autoimmune diseases and hepatitis C virus infection. The diagnosis of cryoglobulinemic syndrome is …
Cryoglobulinemia is classified into three types (I, II and III) on the basis of immunoglobulin composition. Predisposing conditions include …
Sjogren's syndrome.
Fox RI. Fox RI. Lancet. 2005 Jul 23-29;366(9482):321-31. doi: 10.1016/S0140-6736(05)66990-5. Lancet. 2005. PMID: 16039337 Review.
Sjogren's syndrome is a chronic autoimmune disorder of the exocrine glands with associated lymphocytic infiltrates of the affected glands. ...The accessibility of these glands to biopsy enables study of the molecular biology of a tissue-specific autoimmune pr …
Sjogren's syndrome is a chronic autoimmune disorder of the exocrine glands with associated lymphocytic infiltrates of the affe …
Epstein-Barr Virus and Cytomegalovirus Infections of the Liver.
Bunchorntavakul C, Reddy KR. Bunchorntavakul C, et al. Gastroenterol Clin North Am. 2020 Jun;49(2):331-346. doi: 10.1016/j.gtc.2020.01.008. Gastroenterol Clin North Am. 2020. PMID: 32389366 Review.
Atypical manifestations, such as cholestasis, chronic hepatitis, precipitation of acute-on-chronic liver failure, and autoimmune hepatitis, are reported with EBV infection, whereas cholestasis, portal vein thrombosis, and Budd-Chiari syndrome are reported with CMV i …
Atypical manifestations, such as cholestasis, chronic hepatitis, precipitation of acute-on-chronic liver failure, and autoimmune hepa …
Lung complications of Sjogren syndrome.
Luppi F, Sebastiani M, Sverzellati N, Cavazza A, Salvarani C, Manfredi A. Luppi F, et al. Eur Respir Rev. 2020 Aug 18;29(157):200021. doi: 10.1183/16000617.0021-2020. Print 2020 Sep 30. Eur Respir Rev. 2020. PMID: 32817113 Free PMC article. Review.
Primary Sjogren syndrome (pSS) is a systemic autoimmune disease characterised by lymphocytic infiltration of exocrine glands and by a number of systemic manifestations, including those regarding the lung. Pulmonary involvement in pSS includes interstitial lung disea …
Primary Sjogren syndrome (pSS) is a systemic autoimmune disease characterised by lymphocytic infiltration of exocrine glands a …
Polyclonal hypergammaglobulinaemia: assessment, clinical interpretation, and management.
Zhao EJ, Cheng CV, Mattman A, Chen LYC. Zhao EJ, et al. Lancet Haematol. 2021 May;8(5):e365-e375. doi: 10.1016/S2352-3026(21)00056-9. Lancet Haematol. 2021. PMID: 33894171 Review.
Polyclonal hypergammaglobulinaemia is most commonly caused by liver disease, immune dysregulation, or inflammation, but can also provide an important diagnostic clue of rare diseases such as histiocyte disorders, autoimmune lymphoproliferative syndrome, Castl …
Polyclonal hypergammaglobulinaemia is most commonly caused by liver disease, immune dysregulation, or inflammation, but can also provide an …
338 results