Acute Promyelocytic Leukemia
What's New
Last Posted: Jan 02, 2025
- A distinct subgroup of AML resembling the APL immunophenotype is associated with DIC.
Pan Li, et al. BMC cancer 2024 0 (1) 1576 - Cytogenetic and Molecular Characteristics in Adult Hispanic Acute Myeloid Leukemia Patients From Puerto Rico.
Daniel H Jiang, et al. Cureus 2024 0 (9) e70388 - Characteristics and Prognosis of "Acute Promyelocytic Leukemia-like" Nucleophosmin-1-Mutated Acute Myeloid Leukemia in a Retrospective Patient Cohort.
Vasiliki Papadopoulou, et al. Biomedicines 2024 0 (10) - [Analysis of the clinical characteristics of acute myeloid leukemia related to the treatment of hematological and solid tumors].
Y Jiao, et al. Zhonghua zhong liu za zhi [Chinese journal of oncology] 2024 0 (1) 86-95 - No Association of AS3MT Gene Polymorphisms with Susceptibility to Hepatotoxicity in APL Patients Treated with AS2O3: A Single-Center Study.
Zeinab Joneidi, et al. International journal of hematology-oncology and stem cell research 2023 0 (4) 281-290 - Analysis of the clinical characteristics and prognosis of adult de novo acute myeloid leukemia (none APL) with PTPN11 mutations.
Li Sheng, et al. Open medicine (Warsaw, Poland) 2023 0 (1) 20230830 - Influence on therapeutic outcome of platelet count at diagnosis in patients with de novo non-APL acute myeloid leukemia.
Yujiao Zhang, et al. BMC cancer 2023 0 (1) 1030 - [Characteristics of genetic variants in 134 patients with Acute myeloid leukemia].
Miao He, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 0 (10) 1222-1227 - Prognostic value of the mutation types and dynamics of FLT3-ITD in acute myeloid leukemia.
Mosae Koo, et al. European journal of haematology 2023 0 - Acute myeloid leukemia with NUP98::RARG resembling acute promyelocytic leukemia accompanying ARID1B gene mutation.
Danyang Wu, et al. Hematology (Amsterdam, Netherlands) 2023 0 (1) 2227495
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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