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J

Julián Sevilla

fundación para la investigación biomédica del hospital infantil universitario niño jesús
H指数:34
被引数:4,548

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Prognostic significance of mutation type and chromosome fragility in Fanconi anemia

范可尼贫血中突变类型和染色体脆性的预后意义

2024-11-190
OAAI
Comparison of outcomes of immunosuppressive therapy with rabbit versus horse antithymocyte globulin and cyclosporine a in children with acquired severe aplastic anemia
2024-04-150
PRE
Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA (vol 12, 13057, 2022)
2024-03-280
OAAI
Gene therapy restores the transcriptional program of stem cells in Fanconi anemia
2023-04-068
OAAI
Access to gene therapy for rare diseases when commercialization is not fit for purpose

当商业化不适合目的时,获得罕见疾病的基因治疗

2023-02-1328
PRE
Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA
2022-07-2911
OAAI
Venous thromboembolism in pediatric patients with acute lymphoblastic leukemia under chemotherapy treatment. Risk factors and usefulness of thromboprophylaxis. Results of LAL-SEHOP-PETHEMA-2013
2022-06-018
OAAI
Next generation sequencing for diagnosis of hereditary anemia: Experience in a Spanish reference center
2022-06-014
PRE