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2000 1
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2004 2
2005 2
2006 3
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2008 3
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68 results

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Page 1
The diagnosis and management of the haematologic manifestations of lupus.
Velo-García A, Castro SG, Isenberg DA. Velo-García A, et al. J Autoimmun. 2016 Nov;74:139-160. doi: 10.1016/j.jaut.2016.07.001. Epub 2016 Jul 25. J Autoimmun. 2016. PMID: 27461045 Review.
Haematological manifestations in systemic lupus erythematosus (SLE) are frequently observed. They are diverse and range from mild to severe. Therefore, different treatment approaches are needed from simply keeping vigilant to significant immunosuppression. ...
Haematological manifestations in systemic lupus erythematosus (SLE) are frequently observed. They are diverse and range from mild to …
Clinical Applications of Hemolytic Markers in the Differential Diagnosis and Management of Hemolytic Anemia.
Barcellini W, Fattizzo B. Barcellini W, et al. Dis Markers. 2015;2015:635670. doi: 10.1155/2015/635670. Epub 2015 Dec 27. Dis Markers. 2015. PMID: 26819490 Free PMC article. Review.
Increased reticulocytes, lactate dehydrogenase, and bilirubin, as well as reduced haptoglobin, are observed in conditions other than hemolysis that may confound the clinical picture. Hemoglobin defines the clinical severity of hemolysis, and thrombocytopenia suggests a pos …
Increased reticulocytes, lactate dehydrogenase, and bilirubin, as well as reduced haptoglobin, are observed in conditions other than …
Daratumumab as a novel treatment option in refractory ITP.
Vernava I, Schmitt CA. Vernava I, et al. Blood Cells Mol Dis. 2023 Mar;99:102724. doi: 10.1016/j.bcmd.2023.102724. Epub 2023 Jan 13. Blood Cells Mol Dis. 2023. PMID: 36669360
Several single-patient reports and case series have demonstrated successful treatment with daratumumab in ITP, autoimmune thrombocytopenia in Evans syndrome as well as other cytopenias or pure red cell aplasia after allogeneic stem cell transplantation or in congeni …
Several single-patient reports and case series have demonstrated successful treatment with daratumumab in ITP, autoimmune thrombocytopenia i …
Evans syndrome and systemic lupus erythematosus: clinical presentation and outcome.
Costallat GL, Appenzeller S, Costallat LT. Costallat GL, et al. Joint Bone Spine. 2012 Jul;79(4):362-4. doi: 10.1016/j.jbspin.2011.07.004. Epub 2011 Sep 23. Joint Bone Spine. 2012. PMID: 21944976
OBJECTIVE: To review the clinical, laboratory and outcome features of Evans syndrome (ES) in systemic lupus erythematosus (SLE) patients. ...Treatment strategies frequently used in SLE contribute to longer disease remission and less frequent exacerbation than obs …
OBJECTIVE: To review the clinical, laboratory and outcome features of Evans syndrome (ES) in systemic lupus erythematosus (SLE …
Evans syndrome in adults: an observational multicenter study.
Fattizzo B, Michel M, Giannotta JA, Hansen DL, Arguello M, Sutto E, Bianchetti N, Patriarca A, Cantoni S, Mingot-Castellano ME, McDonald V, Capecchi M, Zaninoni A, Consonni D, Vos JM, Vianelli N, Chen F, Glenthøj A, Frederiksen H, González-López TJ, Barcellini W. Fattizzo B, et al. Blood Adv. 2021 Dec 28;5(24):5468-5478. doi: 10.1182/bloodadvances.2021005610. Blood Adv. 2021. PMID: 34592758 Free PMC article.
Evans syndrome (ES) is a rare condition, defined as the presence of 2 autoimmune cytopenias, most frequently autoimmune hemolytic anemia and immune thrombocytopenia (ITP) and rarely autoimmune neutropenia. ...
Evans syndrome (ES) is a rare condition, defined as the presence of 2 autoimmune cytopenias, most frequently autoimmune hemoly …
Pathobiology of secondary immune thrombocytopenia.
Cines DB, Liebman H, Stasi R. Cines DB, et al. Semin Hematol. 2009 Jan;46(1 Suppl 2):S2-14. doi: 10.1053/j.seminhematol.2008.12.005. Semin Hematol. 2009. PMID: 19245930 Free PMC article. Review.
Immune thrombocytopenia can be secondary to medications or to a concurrent disease, such as an autoimmune condition (eg, systemic lupus erythematosus [SLE], antiphospholipid antibody syndrome [APS], immune thyroid disease, or Evans syndrome), a lymphoproliferative d …
Immune thrombocytopenia can be secondary to medications or to a concurrent disease, such as an autoimmune condition (eg, systemic lupus eryt …
Monogenic inborn errors of immunity in autoimmune disorders.
Venkatachari IV, Chougule A, Gowri V, Taur P, Bodhanwala M, Prabhu S, Madkaikar M, Desai M. Venkatachari IV, et al. Immunol Res. 2023 Oct;71(5):771-780. doi: 10.1007/s12026-023-09391-3. Epub 2023 May 18. Immunol Res. 2023. PMID: 37199901
Hematological AID was the most common AID (75%) in children with PIRD. Positive predictive value (PPV) of abnormal immunological tests was 50% and sensitivity of 70%. ...Age at presentation, number of autoimmunity, routine immunological tests, and JMF criteria are not p …
Hematological AID was the most common AID (75%) in children with PIRD. Positive predictive value (PPV) of abnormal immunological test …
New advances in the diagnosis and treatment of autoimmune lymphoproliferative syndrome.
Teachey DT. Teachey DT. Curr Opin Pediatr. 2012 Feb;24(1):1-8. doi: 10.1097/MOP.0b013e32834ea739. Curr Opin Pediatr. 2012. PMID: 22157362 Free PMC article. Review.
These will be discussed in this review. RECENT FINDINGS: A number of key observations have been made recently that better define the pathophysiology of ALPS, including the characterization of somatic FAS variant ALPS, the identification of haploinsufficiency as a mechanism …
These will be discussed in this review. RECENT FINDINGS: A number of key observations have been made recently that better define the …
Infrequent Thrombotic Complications in Japanese Patients with Warm Autoimmune Hemolytic Anemia.
Higuchi T, Hoshi T, Toriyama M, Nakajima A, Haruki K. Higuchi T, et al. Intern Med. 2023 May 15;62(10):1441-1447. doi: 10.2169/internalmedicine.0541-22. Epub 2022 Sep 28. Intern Med. 2023. PMID: 36171129 Free PMC article.
Twenty-nine patients were diagnosed as primary cases and 18 as secondary cases, and 10 patients were diagnosed with Evans syndrome. Results No patient presented with thrombosis, and over a median observation period of 15 months, 3 patients had ischemic cerebr …
Twenty-nine patients were diagnosed as primary cases and 18 as secondary cases, and 10 patients were diagnosed with Evans syndrome …
Current clinical spectrum of common variable immunodeficiency in Spain: The multicentric nationwide GTEM-SEMI-CVID registry.
Cabañero-Navalon MD, Garcia-Bustos V, Nuñez-Beltran M, Císcar Fernández P, Mateu L, Solanich X, Carrillo-Linares JL, Robles-Marhuenda Á, Puchades-Gimeno F, Pelaez Ballesta A, López-Osle N, Torralba-Cabeza MÁ, Bielsa Masdeu AM, Diego Gil J, Tornador Gaya N, Pascual Castellanos G, Sánchez-Martínez R, Barragán-Casas JM, González-García A, Patier de la Peña JL, López-Wolf D, Mora Rufete A, Canovas Mora A, Forner Giner MJ, Moral Moral P. Cabañero-Navalon MD, et al. Front Immunol. 2022 Oct 28;13:1033666. doi: 10.3389/fimmu.2022.1033666. eCollection 2022. Front Immunol. 2022. PMID: 36389743 Free PMC article.
More than one-third of the patients in our cohort showed lymphadenopathies and splenomegaly in their follow-up, and more than 33% presented immune cytopenias, especially Evans' syndrome. Gastrointestinal disease was observed in more than 40% of the patients. …
More than one-third of the patients in our cohort showed lymphadenopathies and splenomegaly in their follow-up, and more than 33% presented …
68 results