Michael Clemente
Overview
Explore the profile of Michael Clemente including associated specialties, affiliations and a list of published articles.
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13
Citations
438
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0
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Recent Articles
1.
Lundgren S, Huuhtanen J, Keranen M, Feng X, Patel B, Ryland G, et al.
Sci Transl Med
. 2025 Feb;
17(787):eadl6758.
PMID: 40009697
Immune aplastic anemia (AA) is a life-threatening bone marrow failure disorder driven by an autoimmune T cell attack against hematopoietic stem and progenitor cells (HSPCs). However, the exact autoantigen targets...
2.
Lundgren S, Keranen M, Kankainen M, Huuhtanen J, Walldin G, Kerr C, et al.
Leukemia
. 2021 Mar;
35(5):1365-1379.
PMID: 33785863
The prevalence and functional impact of somatic mutations in nonleukemic T cells is not well characterized, although clonal T-cell expansions are common. In immune-mediated aplastic anemia (AA), cytotoxic T-cell expansions...
3.
Przychodzen B, Makishima H, Sekeres M, Balasubramanian S, Thota S, Patel B, et al.
Oncotarget
. 2018 Feb;
9(2):2050-2057.
PMID: 29416752
Using next generation sequencing we have systematically analyzed a large cohort of 489 patients with bone marrow failure (BMF), including myelodysplastic syndrome (MDS), acute myeloid leukemia (AML), aplastic anemia (AA),...
4.
Bat T, Abdelhamid O, Balasubramanian S, Mai A, Radivoyevitch T, Clemente M, et al.
Br J Haematol
. 2017 Aug;
182(5):730-733.
PMID: 28804905
No abstract available.
5.
Polprasert C, Schulze I, Sekeres M, Makishima H, Przychodzen B, Hosono N, et al.
Cancer Cell
. 2015 Apr;
27(5):658-70.
PMID: 25920683
Most cases of adult myeloid neoplasms are routinely assumed to be sporadic. Here, we describe an adult familial acute myeloid leukemia (AML) syndrome caused by germline mutations in the DEAD/H-box...
6.
Patel B, Hirsch C, Clemente M, Sekeres M, Makishima H, Maciejewski J
Int J Hematol
. 2015 Feb;
101(3):213-8.
PMID: 25690487
Whole exome next generation sequencing systematically applied as a discovery tool in myelodysplastic syndromes (MDS) has led to the identification of a large number of novel mutations. Despite hundreds of...
7.
Afable 2nd M, Shaik M, Sugimoto Y, Elson P, Clemente M, Makishima H, et al.
Haematologica
. 2011 May;
96(9):1269-75.
PMID: 21606164
Background: A combination of horse anti-thymocyte globulin and cyclosporine produces responses in 60-70% of patients with severe aplastic anemia. We performed a phase II study of rabbit anti-thymocyte globulin and...
8.
Jankowska A, Szpurka H, Calabro M, Mohan S, Schade A, Clemente M, et al.
Haematologica
. 2011 May;
96(7):954-62.
PMID: 21546506
Background: A deficiency of specific glycosylphosphatidyl inositol-anchored proteins in paroxysmal nocturnal hemoglobinuria may be responsible for most of the clinical features of this disease, but some functional consequences may be...
9.
Poggio E, Augustine J, Clemente M, Danzig J, Volokh N, Zand M, et al.
Transplantation
. 2007 Apr;
83(7):847-52.
PMID: 17460554
Background: The panel reactive antibody test (PRA) is an established method for assessing posttransplant risk of immune-mediated graft injury. The panel of reactive T cell assay (PRT) in which transplant...
10.
Augustine J, Poggio E, Clemente M, Aeder M, Bodziak K, Schulak J, et al.
J Am Soc Nephrol
. 2007 Mar;
18(5):1602-6.
PMID: 17389735
Prolonged exposure to dialysis before transplantation and black ethnicity are known risk factors for acute rejection and graft loss in kidney transplant recipients. Because the strength of the primed antidonor...