Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications.
about
Master regulatory GATA transcription factors: mechanistic principles and emerging links to hematologic malignanciesInborn errors of the development of human natural killer cellsGATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndromeExome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.Genetic predisposition syndromes: when should they be considered in the work-up of MDS?Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults.Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.GATA2 deficiency-associated bone marrow disorder differs from idiopathic aplastic anemia.GATA2 deficiency.Bone marrow immunophenotyping by flow cytometry in refractory cytopenia of childhood.Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency.Haematopoietic and immune defects associated with GATA2 mutation.Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrityWarts and all: human papillomavirus in primary immunodeficiencies.A genetic perspective on granulomatous diseases with an emphasis on mycobacterial infections.Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset.Genetic predispositions to childhood leukemia.MonoMAC syndrome in a patient with a GATA2 mutation: case report and review of the literatureGATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity.The evolution of cellular deficiency in GATA2 mutationProposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes.Rheumatologic manifestations of the "MonoMAC" syndrome. a systematic review.Dendritic cell analysis in primary immunodeficiencyClinical characteristics and factors predicting respiratory failure in adenovirus pneumonia.GATA2 deficiency and related myeloid neoplasms.Mycobacterium avium complex disseminated infection in a kidney transplant recipient.Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.Mutations in GATA2 are rare in juvenile myelomonocytic leukemia.Presence of hypogammaglobulinemia and abnormal antibody responses in GATA2 deficiencyDendritic cell, monocyte, B and NK lymphoid deficiency defines the lost lineages of a new GATA-2 dependent myelodysplastic syndrome.MonoMAC versus idiopathic CD4+ lymphocytopenia. Comment to Haematologica. 2011;96(8):1221-5.MonoMAC and GATA2 deficiency: overlapping clinical and pathological features with aplastic anemia and idiopathic CD4+ lymphocytopenia. Reply to Haematologica 2012;97(4):058669.GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients
P2860
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P2860
Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications.
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին 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
Myelodysplasia in autosomal do ...... res and clinical implications.
@ast
Myelodysplasia in autosomal do ...... res and clinical implications.
@en
type
label
Myelodysplasia in autosomal do ...... res and clinical implications.
@ast
Myelodysplasia in autosomal do ...... res and clinical implications.
@en
prefLabel
Myelodysplasia in autosomal do ...... res and clinical implications.
@ast
Myelodysplasia in autosomal do ...... res and clinical implications.
@en
P2093
P2860
P1433
P1476
Myelodysplasia in autosomal do ...... res and clinical implications.
@en
P2093
Amalia Dutra
Dennis D Hickstein
Diane C Arthur
Donald C Vinh
Evgenia Pak
Irina Maric
Katherine R Calvo
Kyungjae Myung
Mark Raffeld
P2860
P304
P356
10.3324/HAEMATOL.2011.041152
P577
2011-04-20T00:00:00Z