Hereditary cerebral amyloid angiopathy mimicking CADASIL syndrome-Reference-Cited by-同舟云学术

Hereditary cerebral amyloid angiopathy mimicking CADASIL syndrome

Published:2021-10-16 Issue:11 Volume:28 Page:3866-3869
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Euro J of Neurology

Author:

Psychogios Klearchos¹²^ORCID,Xiromerisiou Georgia³,Kargiotis Odysseas¹^ORCID,Safouris Apostolos¹,Fiolaki Aidonio¹,Bonakis Anastasios²,Paraskevas Georgios P.²⁴,Giannopoulos Sotirios²^ORCID,Tsivgoulis Georgios²⁵^ORCID

Affiliation:

1. Stroke Unit Metropolitan Hospital Piraeus Greece

2. Second Department of Neurology School of Medicine “Attikon” University Hospital National and Kapodistrian University of Athens Athens Greece

3. Department of Neurology Faculty of Medicine School of Health Sciences University Hospital of Larissa University of Thessaly Larissa Greece

4. Neurogenetics Unit 1st Department of Neurology Eginition University Hospital National and Kapodistrian University of Athens Athens Greece

5. Department of Neurology The University of Tennessee Health Science Center Memphis TN USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.14981

Reference5 articles.

1. Monogenic cerebral small‐vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology

2. CADASIL

3. Occipital Cortical Calcifications in Cerebral Amyloid Angiopathy

4. Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy

5. Cerebral Amyloid Angiopathy With Vascular Iron Accumulation and Calcification

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1. The Genetics of Cerebral Microbleeds;Stroke Genetics;2024

2. Management of Inherited CNS Small Vessel Diseases: The CADASIL Example: A Scientific Statement From the American Heart Association;Stroke;2023-10

3. Clinical considerations in early-onset cerebral amyloid angiopathy;Brain;2023-06-06

4. Autopsy confirmed CADASIL with the c.1490C > T (p.S497L) variant of uncertain causal significance;Neurological Sciences;2022-01-13

5. The Greek Variant in APP Gene: The Phenotypic Spectrum of APP Mutations;International Journal of Molecular Sciences;2021-11-16