Copyright © 2014 Anna Karastaneva et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Although bone marrow transplantation (BMT) from an HLA identical sibling is considered as treatment of choice in pediatric patients with severe aplastic anemia (SAA), a significant number of them experience graft failure (GF) after BMT.We report a case of an 8-year-old male patient with SAA who presented with a complicated posttransplant course due to parvovirus B19 infection and GF. A subsequent attempt to support the graft by antithymocyte globulin (ATG) and a peripheral stem cell boost ...
BACKGROUND AND OBJECTIVE: After allogeneic bone marrow transplantation (BMT) it is important to be a...
A small population of CD55CD59 blood cells was detected in a patient who devel-oped donor-type late...
The role of mixed hematopoietic chimerism in engraftment and relapse after allogeneic BMT remains un...
Although bone marrow transplantation (BMT) from an HLA identical sibling is considered as treatment ...
Background: For peripheral blood stem cell transplantation (PSCT), several engraftment analysis meth...
Ninety-one patients were studied serially for chimeric status following allogeneic stem cell transpl...
We report a girl with severe combined immunodeficiency (SCID) who had a paternal T-depleted bone mar...
Bone marrow transplantation (BMT) using HLA‐partially matched family donors has produced disappointi...
There have been sporadic reports of the development of delayed disease recurrence after bone marrow ...
We analyzed the clinical course and risk factors of 18 patients with poor engraftment after allogene...
Summary: Clonal hematopoiesis of indeterminate potential (CHIP) is caused by recurrent somatic mutat...
Bone marrow transplantation (BMT) using HLA-partially matched family donors has produced disappointi...
Mismatched related donors of hematopoietic SCT (HSCT) for severe aplastic anemia (SAA) present chall...
An immune basis for most patients with aplastic anemia (AA) provides a rationale for immunosuppressi...
It is important to be able to assess the contribution of donor cells to the graft followmg bone marr...
BACKGROUND AND OBJECTIVE: After allogeneic bone marrow transplantation (BMT) it is important to be a...
A small population of CD55CD59 blood cells was detected in a patient who devel-oped donor-type late...
The role of mixed hematopoietic chimerism in engraftment and relapse after allogeneic BMT remains un...
Although bone marrow transplantation (BMT) from an HLA identical sibling is considered as treatment ...
Background: For peripheral blood stem cell transplantation (PSCT), several engraftment analysis meth...
Ninety-one patients were studied serially for chimeric status following allogeneic stem cell transpl...
We report a girl with severe combined immunodeficiency (SCID) who had a paternal T-depleted bone mar...
Bone marrow transplantation (BMT) using HLA‐partially matched family donors has produced disappointi...
There have been sporadic reports of the development of delayed disease recurrence after bone marrow ...
We analyzed the clinical course and risk factors of 18 patients with poor engraftment after allogene...
Summary: Clonal hematopoiesis of indeterminate potential (CHIP) is caused by recurrent somatic mutat...
Bone marrow transplantation (BMT) using HLA-partially matched family donors has produced disappointi...
Mismatched related donors of hematopoietic SCT (HSCT) for severe aplastic anemia (SAA) present chall...
An immune basis for most patients with aplastic anemia (AA) provides a rationale for immunosuppressi...
It is important to be able to assess the contribution of donor cells to the graft followmg bone marr...
BACKGROUND AND OBJECTIVE: After allogeneic bone marrow transplantation (BMT) it is important to be a...
A small population of CD55CD59 blood cells was detected in a patient who devel-oped donor-type late...
The role of mixed hematopoietic chimerism in engraftment and relapse after allogeneic BMT remains un...