Alexandra Regueiro
0000-0003-3156-4784
21 papers found
Refreshing results…
Treosulfan-Based Conditioning Regimen In Pediatric Hematopoietic Stem Cell Transplantation: A Retrospective Analysis on Behalf of the Spanish Group for Hematopoietic Transplantation and Cellular Therapy (GETH-TC)
Haploidentical vs. HLA-matched donor hematopoietic stem-cell transplantation for pediatric patients with acute lymphoblastic leukemia in second remission: A collaborative retrospective study of the Spanish Group for Bone Marrow Transplantation in Children (GETMON/GETH) and the Spanish Childhood Relapsed ALL Board (ReALLNet)
Haploidentical hematopoietic stem cell transplantation in pediatric and adolescent patients: A study of the Spanish hematopoietic stem cell transplantation group (GETH)
Síndrome de plaquetas grises, algo más que un trastorno hemorrágico
Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma
Defibrotide in hematopoietic stem cell transplantation: A multicenter survey study of the Spanish Hematopoietic Stem Cell Transplantation Group (GETH)
Cost-effectiveness analysis of defibrotide in the treatment of patients with severe veno-occlusive disease/sinusoidal obstructive syndrome with multiorgan dysfunction following hematopoietic cell transplantation in Spain
Haploidentical transplantation in pediatric non‐malignant diseases: a retrospective analysis on behalf of the Spanish Group for Hematopoietic Transplantation (GETH)
Haploidentical transplantation in high‐risk pediatric leukemia: A retrospective comparative analysis on behalf of the Spanish working Group for bone marrow transplantation in children (GETMON) and the Spanish Grupo for hematopoietic transplantation (GETH)
Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies
Haploidentical stem cell transplantation in a boy with chronic granulomatous disease
Intraepithelial lymphocyte immunophenotype: a useful tool in the diagnosis of celiac disease
Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene
Bioética y Oncología.
Suction entrapment of an upper limb in a swimming pool
Clinical case: Refractory hypercalcemia associated to B-cell lymphoma, an oncological emergency
Quality of chest compressions by Down syndrome people: A pilot trial
Hypertrophic osteoarthropathy and Hodgkin's disease
Osteosarcoma and ATR-16 syndrome: association or coincidence?
Assessment of chest compressions quality performed by residents before and after pediatric cardiopulmonary resuscitation training
Missing publications? Search for publications with a matching author name.