about
Exome sequencing identifies MPL as a causative gene in familial aplastic anemiaMissing Cells: Pathophysiology, Diagnosis, and Management of (Pan)Cytopenia in ChildhoodPathophysiology and management of thrombocytopenia in bone marrow failure: possible clinical applications of TPO receptor agonists in aplastic anemia and myelodysplastic syndromesPluripotent stem cells reveal the developmental biology of human megakaryocytes and provide a source of platelets for clinical applicationEltrombopag for the treatment of aplastic anemia: current perspectivesSuppressive effects of anthrax lethal toxin on megakaryopoiesisThe genomics of inherited bone marrow failure: from mechanism to the clinic.Bone marrow transplantation versus immunosuppressive therapy in patients with acquired severe aplastic anemia.A neonate with congenital amegakaryocytic thrombocytopenia associated with a chromosomal microdeletion at 21q22.11 including the gene RUNX1.Inherited thrombocytopenias frequently diagnosed in adults.Genomic characterization of the inherited bone marrow failure syndromes.Severe Clinical Course in a Patient with Congenital Amegakaryocytic Thrombocytopenia Due to a Missense Mutation of the c-MPL GeneDurable engraftment and correction of hematological abnormalities in children with congenital amegakaryocytic thrombocytopenia following myeloablative umbilical cord blood transplantation.Neonatal manifestations of inherited bone marrow failure syndromes.Recent advances in treatment of aplastic anemia.Eltrombopag Added to Standard Immunosuppression for Aplastic Anemia.Eltrombopag and improved hematopoiesis in refractory aplastic anemia.Current insights into the diagnosis and treatment of inherited bone marrow failure syndromes in China.Genetic predispositions to childhood leukemia.Prospects and challenges of reprogrammed cells in hematology and oncology.The optimal immunosuppressive therapy for aplastic anemia.Genetic Alterations of the Thrombopoietin/MPL/JAK2 Axis Impacting Megakaryopoiesis.Unexplained thrombocytosis: association of Baltimore polymorphism with germline MPL nonsense mutation.Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim.Use of Eltrombopag in Improving Poor Graft Function after Allogeneic Hematopoietic Stem Cell Transplantation.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Congenital amegakaryocytic thrombocytopenia.
@ast
Congenital amegakaryocytic thrombocytopenia.
@en
type
label
Congenital amegakaryocytic thrombocytopenia.
@ast
Congenital amegakaryocytic thrombocytopenia.
@en
prefLabel
Congenital amegakaryocytic thrombocytopenia.
@ast
Congenital amegakaryocytic thrombocytopenia.
@en
P2860
P356
P1476
Congenital amegakaryocytic thrombocytopenia.
@en
P2093
Amy E Geddis
P2860
P304
P356
10.1002/PBC.22927
P577
2011-02-18T00:00:00Z