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Pediatric secondary chronic myelogenous leukemia in a patient with hemophagocytic lymphohistiocytosis carrying UNC13D, LYST, and ITK variants.
- Source :
-
Pediatric blood & cancer [Pediatr Blood Cancer] 2024 Oct; Vol. 71 (10), pp. e31166. Date of Electronic Publication: 2024 Jul 19. - Publication Year :
- 2024
- Subjects :
- Humans
Male
Child
Protein-Tyrosine Kinases genetics
Neoplasms, Second Primary pathology
Neoplasms, Second Primary genetics
Female
Prognosis
Lymphohistiocytosis, Hemophagocytic genetics
Lymphohistiocytosis, Hemophagocytic pathology
Lymphohistiocytosis, Hemophagocytic complications
Lymphohistiocytosis, Hemophagocytic etiology
Leukemia, Myelogenous, Chronic, BCR-ABL Positive genetics
Leukemia, Myelogenous, Chronic, BCR-ABL Positive drug therapy
Leukemia, Myelogenous, Chronic, BCR-ABL Positive pathology
Leukemia, Myelogenous, Chronic, BCR-ABL Positive complications
Membrane Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1545-5017
- Volume :
- 71
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Pediatric blood & cancer
- Publication Type :
- Report
- Accession number :
- 39030925
- Full Text :
- https://doi.org/10.1002/pbc.31166