Diamond-blackfan Anemia 3
What's New
Last Posted: May 29, 2023
- Prevalence and clinical expression of germline predisposition to myeloid neoplasms in adults with marrow hypocellularity.
Elisabetta Molteni, et al. Blood 2023 0 - Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.
Alter Blanche P, et al. Haematologica 2017 0 (1) 30-39 - Molecular analysis and genotype-phenotype correlation of Diamond-Blackfan anemia.
Arbiv O A, et al. Clinical genetics 2017 0 (2) 320-328 - The Genetic Landscape of Diamond-Blackfan Anemia.
Ulirsch Jacob C, et al. American journal of human genetics 2018 0 (6) 930-947 - Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
Russo Roberta, et al. American journal of hematology 2018 0 (5) 672-682 - A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2.
Özen Seza, et al. The Journal of rheumatology 2019 0 (1) 117-125 - Expansion of germline RPS20 mutation phenotype to include Diamond-Blackfan anemia.
Bhar Saleh, et al. Human mutation 2020 0 (11) 1918-1930 - Eltrombopag for patients with moderate aplastic anemia or uni-lineage cytopenias.
Fan Xing, et al. Blood advances 2020 0 (8) 1700-1710 - [Prevalence and risk factors of obesity in children with Diamond-Blackfan anemia].
Yi Mei-Hui, et al. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2022 0 (10) 1143-1148 - The Glucocorticoid Receptor Polymorphism Landscape in Patients With Diamond Blackfan Anemia Reveals an Association Between Two Clinically Relevant Single Nucleotide Polymorphisms and Time to Diagnosis.
Lonetti Annalisa, et al. Frontiers in physiology 2021 0 745032
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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
- Page last updated:May 18, 2024
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