Acute Promyelocytic Leukemia
What's New
Last Posted: Jan 29, 2024
- [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 - Comprehensive genetic analyses of childhood acute leukemia in Iraq using next-generation sequencing.
Lika'a Fasih Y Al-Kzayer, et al. Translational pediatrics 2023 0 (5) 827-844 - Molecular Heterogeneity of Pediatric AML with Atypical Promyelocytes Accumulation in Children-A Single Center Experience.
Aleksandra Borkovskaia et al. Genes 2023 14(3) - A global study for acute myeloid leukemia with RARG rearrangement.
Zhu Honghu, et al. Blood advances 2023 0
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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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