Siderosis
What's New
Last Posted: Jan 09, 2024
- Genome-Wide Association Studies of ARIA From the Aducanumab Phase 3 ENGAGE and EMERGE Studies.
Stephanie J Loomis, et al. Neurology 2024 0 (3) e207919 - Clinical Characteristics, Neuroimaging Markers, and Outcomes in Patients with Cerebral Amyloid Angiopathy: A Prospective Cohort Study.
Aikaterini Theodorou, et al. Journal of clinical medicine 2023 0 (17) - Association of candidate genetic variants and circulating levels of ApoE/ApoJ with common neuroimaging features of cerebral amyloid angiopathy.
Anna Bonaterra-Pastra, et al. Frontiers in aging neuroscience 2023 0 1134399 - Cortical superficial siderosis multifocality in cerebral amyloid angiopathy: A prospective study.
Charidimou Andreas, et al. Neurology 2017 0 (21) 2128-2135 - Prevalence and Natural History of Superficial Siderosis: A Population-Based Study.
Pichler Michael, et al. Stroke 2017 0 (12) 3210-3214 - Correlation of Pancreatic Iron Overload Measured by T2*-Weighted Magnetic Resonance Imaging in Diabetic Patients with ?-Thalassemia Major.
Kosaryan Mehrnoush, et al. Hemoglobin 2017 0 (3) 151-156 - Increased cerebral microbleeds and cortical superficial siderosis in pediatric patients with Down syndrome.
Schoeppe Franziska, et al. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2018 0 (1) 158-164 - Atrophy patterns in cerebral amyloid angiopathy with and without cortical superficial siderosis.
Kim Joonho, et al. Neurology 2018 0 (20) e1751-e1758 - Pathologically Confirmed Cerebral Amyloid Angiopathy with No Radiological Sign in a Patient with Early Onset Alzheimer's Disease.
Kim Seung Joo, et al. Yonsei medical journal 2018 0 (6) 801-805 - APOE and cortical superficial siderosis in CAA: Meta-analysis and potential mechanisms.
Charidimou Andreas, et al. Neurology 2019 0 (4) e358-e371
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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
- Page last updated:Apr 18, 2024
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