CADASIL and CARASIL-Reference-Cited by-同舟云学术

CADASIL and CARASIL

Published:2014-09 Issue:5 Volume:24 Page:525-544
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Tikka Saara¹,Baumann Marc¹,Siitonen Maija²,Pasanen Petra²,Pöyhönen Minna³,Myllykangas Liisa⁴,Viitanen Matti⁵⁶,Fukutake Toshio⁷,Cognat Emmanuel⁸⁹,Joutel Anne⁸⁹,Kalimo Hannu⁴¹⁰

Affiliation:

1. Protein Chemistry Unit, Institute of Biomedicine/Anatomy University of Helsinki Helsinki Finland

2. Department of Medical Biochemistry and Genetics, Institute of Biomedicine University of Turku Turku Finland

3. Department of Clinical Genetics Helsinki University Hospital, HUSLAB Helsinki Finland

4. Department of Pathology Haartman Institute University of Helsinki Helsinki Finland

5. Turku City Hospital Turku Finland

6. Division of Clinical Geriatrics Department of Neurobiology Care Sciences and Society Karolinska Institutet Stockholm Sweden

7. Department of Neurology Kameda Medical Center Kamogawa Chiba Japan

8. INSERM U1161 Paris France

9. Université Paris Diderot Sorbonne Paris Cité UMRS 1161 Paris France

10. Institute of Biomedicine Department of Forensic Medicine University of Turku Turku Finland

Funder

Fondation Leducq

Finnish Cultural Foundation

Sigrid Juselius Foundation

Swedish Research Council

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.12181

Reference136 articles.

1. Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations

2. Clinical Spectrum of CADASIL and the Effect of Cardiovascular Risk Factors on Phenotype

3. Insidious Cognitive Decline in CADASIL

4. CADASIL mutations impair Notch3 glycosylation by Fringe

5. Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease

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1. Progress to Clarify How NOTCH3 Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease;Biomolecules;2024-01-18

2. CADASIL: A NOTCH3-associated cerebral small vessel disease;Journal of Advanced Research;2024-01

3. Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy;Frontiers in Genetics;2023-09-18

4. Value of Quantitative Susceptibility Mapping in Clinical Neuroradiology;Journal of Magnetic Resonance Imaging;2023-09-08

5. Alzheimer's disease with a CADASIL twist - neuropathological examination proves its value in clarifying the genetics behind familial dementia;Journal of the Neurological Sciences;2023-09