Found: 14
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Metabolic Syndrome Among Leukemia Survivors: Still Delineating the Risk.
- Published in:
- 2017
- By:
- Publication type:
- Editorial
A Novel Heterozygous Deletion Variant in KLOTHO Gene Leading to Haploinsufficiency and Impairment of Fibroblast Growth Factor 23 Signaling Pathway.
- Published in:
- Journal of Clinical Medicine, 2019, v. 8, n. 4, p. 500, doi. 10.3390/jcm8040500
- By:
- Publication type:
- Article
JC Virus Leuko-Encephalopathy in Reduced Intensity Conditioning Cord Blood Transplant Recipient with a Review of the Literature.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
Lethal ALAS2 mutation in males X-linked sideroblastic anaemia.
- Published in:
- British Journal of Haematology, 2017, v. 178, n. 4, p. 648, doi. 10.1111/bjh.14164
- By:
- Publication type:
- Article
Incidence and risk factors for cataract after haematopoietic stem cell transplantation for childhood leukaemia: an LEA study.
- Published in:
- British Journal of Haematology, 2015, v. 168, n. 4, p. 518, doi. 10.1111/bjh.13148
- By:
- Publication type:
- Article
Peripheral blood cells chimerism after unrelated cord blood transplantation in children: kinetics, predictive factors and impact on post-transplant outcome.
- Published in:
- British Journal of Haematology, 2014, v. 166, n. 4, p. 557, doi. 10.1111/bjh.12918
- By:
- Publication type:
- Article
Quality of life in minor siblings of childhood leukemia survivors, long-term after diagnosis: A LEA study (for Leucemies de l'Enfant et de l'Adolescent-childhood and adolescent leukemia).
- Published in:
- Psycho-Oncology, 2015, v. 24, n. 6, p. 661, doi. 10.1002/pon.3709
- By:
- Publication type:
- Article
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4479, doi. 10.1093/hmg/ddu160
- By:
- Publication type:
- Article
The expression of BIRC5 is correlated with loss of specific chromosomal regions in breast carcinomas.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 4, p. 299, doi. 10.1002/gcc.20533
- By:
- Publication type:
- Article
Acute GVHD is a strong predictor of full donor CD3+ T cell chimerism after reduced intensity conditioning allogeneic stem cell transplantation.
- Published in:
- American Journal of Hematology, 2012, v. 87, n. 12, p. 1074, doi. 10.1002/ajh.23319
- By:
- Publication type:
- Article
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
- Published in:
- Pediatric Diabetes, 2011, v. 12, n. 3pt1, p. 187, doi. 10.1111/j.1399-5448.2010.00679.x
- By:
- Publication type:
- Article
Two days of antithymocyte globulin are associated with a reduced incidence of acute and chronic graft-versus-host disease in reduced-intensity conditioning transplantation for hematologic diseases.
- Published in:
- Cancer (0008543X), 2013, v. 119, n. 5, p. 986, doi. 10.1002/cncr.27858
- By:
- Publication type:
- Article
Functional and Clinical Impact of Novel Tmprss6 Variants in Iron-Refractory Iron-Deficiency Anemia Patients and Genotype-Phenotype Studies.
- Published in:
- Human Mutation, 2014, v. 35, n. 11, p. 1321, doi. 10.1002/humu.22632
- By:
- Publication type:
- Article
Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activity.
- Published in:
- Human Mutation, 2012, v. 33, n. 9, p. 1388, doi. 10.1002/humu.22116
- By:
- Publication type:
- Article