Detalhe da pesquisa
1.
Burkitt-like lymphoma with 11q aberration: a germinal center-derived lymphoma genetically unrelated to Burkitt lymphoma.
Haematologica
; 104(9): 1822-1829, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30733272
2.
Etiopathological mechanisms and clinical characteristics of hyperhemolysis syndrome in Spanish patients with thalassemia.
Ann Hematol
; 95(9): 1419-27, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27392662
3.
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).
Front Pediatr
; 11: 1140637, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37020654
4.
Venous thromboembolism in pediatric patients with acute lymphoblastic leukemia under chemotherapy treatment. Risk factors and usefulness of thromboprophylaxis. Results of LAL-SEHOP-PETHEMA-2013.
J Thromb Haemost
; 20(6): 1390-1399, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35289066
5.
Methotrexate-induced subacute neurotoxicity in a child with acute lymphoblastic leukemia carrying genetic polymorphisms related to folate homeostasis.
Am J Hematol
; 86(1): 98-101, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21064136
6.
C>A substitution in NT 46 of the 3' UTR region (the α complex protected region) of the alpha-1 globin gene: a non-deletional mutation or polymorphism?
J Clin Pathol
; 73(1): 14-16, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31434698
7.
Measurable Residual Disease Assessed by Flow-Cytometry Is a Stable Prognostic Factor for Pediatric T-Cell Acute Lymphoblastic Leukemia in Consecutive SEHOP Protocols Whereas the Impact of Oncogenetics Depends on Treatment.
Front Pediatr
; 8: 614521, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33614543
8.
Thalassemia diagnosis in a blood donor from a unique trimorphic red blood cell population observed in the recipient.
Clin Chem Lab Med
; 52(9): e205-6, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24781676
9.
Expanding the Clinical and Genetic Spectra of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected and Unexpected Findings.
Front Immunol
; 10: 2325, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31681265
10.
Retinal toxic reactions following photopheresis.
Arch Dermatol
; 143(5): 622-5, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17515512
11.
Resolution of disseminated fusariosis in a child with acute leukemia treated with combined antifungal therapy: a case report.
BMC Infect Dis
; 7: 40, 2007 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-17493279
12.
Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
Eur J Haematol
; 84(1): 89-90, 2010 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19758413
13.
Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3.
Mol Genet Genomic Med
; 3(3): 221-32, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26029709
14.
Diagnostic and therapeutic challenges of primary autoimmune haemolytic anaemia in children.
Arch Dis Child
; 99(7): 668-73, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24599068
15.
Ethylenediaminetetraacetic acid-dependent pseudomacrocytosis.
J Clin Pathol
; 66(9): 811-4, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23723302
16.
Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia.
Gene
; 514(1): 31-5, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23178241
17.
Central nervous system chemotoxicity during treatment of pediatric acute lymphoblastic leukemia/lymphoma.
Crit Rev Oncol Hematol
; 84(2): 274-86, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22578745