AbstractAutosomal recessive osteopetrosis (OP) is a rare, lethal disorder in which osteoclasts are absent or nonfunctional, resulting in a bone marrow cavity insufficient to support hematopoiesis. Because osteoclasts are derived from hematopoietic precursors, allogeneic hematopoietic cell transplantation can cure the bony manifestations of the disorder. However, high rates of graft failure have been observed in this population. It is not possible to harvest bone marrow from these patients for reinfusion should graft failure be observed. We report that 8 of 10 patients with OP had high numbers of circulating CD34+ cells (3% ± 0.9%). This increased proportion of peripheral CD34+ cells made it possible to harvest 2 × 106 CD34+ cells per kilogr...
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for most children with...
We report the international experience in outcomes after related and unrelated hematopoietic transpl...
Background: Osteopetrosis is a rare hereditary bone dysplasia characterized by insufficient osteocla...
AbstractAutosomal recessive osteopetrosis (OP) is a rare, lethal disorder in which osteoclasts are a...
Allogeneic hematopoietic stem cell transplantation is the treatment of choice for autosomal recessiv...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
In osteopetrosis, osteoclast dysfunction can lead to deafness, blindness, bone marrow failure, and d...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
Malignant autosomal recessive (AR) osteopetrosis represents an absolute indication for bone marrow t...
Autosomal recessive osteopetrosis is a human bone disease mainly caused by TCIRG1 gene mutations tha...
AbstractCD34+-selection of hematopoietic grafts for patients undergoing autologous hematopoietic ste...
This thesis focuses on developing stem cell targeted gene therapy for the severe hereditary disorder...
Allogeneic BMT has been reported to be the only curative therapy for children with juvenile autosoma...
Stem cells capable of restoring hematopoiesis following lethal bone marrow injury circulate in the b...
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for most children with...
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for most children with...
We report the international experience in outcomes after related and unrelated hematopoietic transpl...
Background: Osteopetrosis is a rare hereditary bone dysplasia characterized by insufficient osteocla...
AbstractAutosomal recessive osteopetrosis (OP) is a rare, lethal disorder in which osteoclasts are a...
Allogeneic hematopoietic stem cell transplantation is the treatment of choice for autosomal recessiv...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
In osteopetrosis, osteoclast dysfunction can lead to deafness, blindness, bone marrow failure, and d...
Infantile malignant osteopetrosis (IMO) is caused by lack of functional osteoclasts leading to skele...
Malignant autosomal recessive (AR) osteopetrosis represents an absolute indication for bone marrow t...
Autosomal recessive osteopetrosis is a human bone disease mainly caused by TCIRG1 gene mutations tha...
AbstractCD34+-selection of hematopoietic grafts for patients undergoing autologous hematopoietic ste...
This thesis focuses on developing stem cell targeted gene therapy for the severe hereditary disorder...
Allogeneic BMT has been reported to be the only curative therapy for children with juvenile autosoma...
Stem cells capable of restoring hematopoiesis following lethal bone marrow injury circulate in the b...
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for most children with...
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for most children with...
We report the international experience in outcomes after related and unrelated hematopoietic transpl...
Background: Osteopetrosis is a rare hereditary bone dysplasia characterized by insufficient osteocla...