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You searched for: Author/Creator Badell, Isabel

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1. A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network. Issue 4 (14th November 2006)

2. A novel gain-of-function STAT1 mutation resulting in basal phosphorylation of STAT1 and increased distal IFN-γ-mediated responses in chronic mucocutaneous candidiasis. Issue 2 (December 2015)

3. Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact. Issue 4 (7th January 2011)

4. Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose‐6‐phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm. (20th September 2019)

5. Combined cord blood and bone marrow transplantation from the same human leucocyte antigen‐identical sibling donor for children with malignant and non‐malignant diseases. (18th December 2014)

6. Defibrotide in hematopoietic stem cell transplantation: A multicenter survey study of the Spanish Hematopoietic Stem Cell Transplantation Group (GETH). (30th March 2021)

7. Genome‐wide DNA methylation profiling predicts relapse in childhood B‐cell acute lymphoblastic leukaemia. (30th October 2012)

9. 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). Issue 1 (5th November 2019)

10. Initial report on Spanish pediatric oncologic, hematologic, and post stem cell transplantation patients during SARS‐CoV‐2 pandemic. Issue 9 (16th July 2020)