Different Clinical Phenotypes in Monozygotic CADASIL Twins With a Novel NOTCH3 Mutation-Reference-Cited by-同舟云学术

Different Clinical Phenotypes in Monozygotic CADASIL Twins With a Novel NOTCH3 Mutation

Published:2009-06 Issue:6 Volume:40 Page:2215-2218
ISSN:0039-2499
Container-title:Stroke
language:en
Short-container-title:Stroke

Author:

Mykkänen Kati¹,Junna Maija¹,Amberla Kaarina¹,Bronge Lena¹,Kääriäinen Helena¹,Pöyhönen Minna¹,Kalimo Hannu¹,Viitanen Matti¹

Affiliation:

1. From the Department of Medical Biochemistry and Genetics (K.M., M.J., H. Kääriäinen), University of Turku, Finland; the Division of Clinical Geriatrics (K.A., M.V.), Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden; the Division of Radiology, Department for Clinical Science (L.B.), Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden; the Department of Molecular Medicine (H. Kääriäinen), National Public Health Institute, Helsinki, Finland;...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialised Nursing,Cardiology and Cardiovascular Medicine,Clinical Neurology

Reference25 articles.

1. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

2. C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke

3. Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients

4. The phenotypic spectrum of CADASIL: Clinical findings in 102 cases

5. Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease

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