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11. A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia. (18th August 2019)

13. A novel homozygous disruptive PRF1 variant (K285Sfs*4) causes very early-onset of familial hemophagocytic lymphohystiocytosis type 2. (21st July 2020)

14. A Novel Karyotype in Acute Myeloid Leukemia with Basophilia. (1st March 2014)

16. A phase I study of panobinostat in children with relapsed and refractory hematologic malignancies. (17th August 2020)

19. A Prospective Study of Tubular Dysfunction in Pediatric Patients with Beta Thalassemia Major Receiving Deferasirox. (1st November 2013)