Hemoglobin E Disease
What's New
Last Posted: Jan 31, 2024
- CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease.
N R C Cruz, et al. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2024 0 e12879 - [Characteristics of Silent Alpha Thalassemia Gene in Child-Bearing Adults in Guangdong].
Ge Huang, et al. Zhongguo shi yan xue ye xue za zhi 2023 0 (6) 1811-1814 - Detecting rare thalassemia in children with anemia using third-generation sequencing.
Zhen-Min Ren, et al. Hematology (Amsterdam, Netherlands) 2023 0 (1) 2241226 - Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype.
Michael D Diamantidis, et al. Journal of molecular medicine (Berlin, Germany) 2023 0 - Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare ?-Globin Mutations.
Yuling Qiu, et al. Hemoglobin 2023 0 1-4 - Alpha-Hemoglobin Stabilizing Protein Gene Polymorphism (rs4499252 A/G) and its Association with Beta-Thalassemia Major in Iraqi Patients.
Adnan Khalaf M, et al. Archives of Razi Institute 2023 0 (3) 1033-1039 - Proliferative retinopathy and maculopathy are two independent conditions in sickle cell disease: Is there a role of blood rheology?1.
Beral Laurence, et al. Clinical hemorheology and microcirculation 2018 0 (3) 337-345 - Progressive Decline in Estimated GFR in Patients With Sickle Cell Disease: An Observational Cohort Study.
Derebail Vimal K, et al. American journal of kidney diseases : the official journal of the National Kidney Foundation 2019 0 (1) 47-55 - Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province.
Huang Ti-Long, et al. Frontiers in pediatrics 2020 0 159 - Telomere shortening correlates with disease severity in hemoglobin H disease patients.
Panjawatanan Panadeekarn, et al. Blood cells, molecules & diseases 2021 0 102563
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About Rare Diseases PHGKB
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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