Focal epilepsy as first symptom in CADASIL
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,General Medicine
Reference5 articles.
1. Notch3 mutations in CADASIL, a hereditary adult onset condition causing stroke and dementia;Joutel;Nature,1996
2. The phenotypic spectrum of CADASIL: clinical findings in 102 cases;Dichgans;Ann Neurol,1998
3. The natural history of CADASIL: a pooled analysis of previously published cases;Desmond;Stroke,1999
4. Epilepsy in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy;Haan;Cerebrovasc Dis,2007
5. Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study;Baudrimont;Stroke,1993
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Case report: CADASIL with cysteine-sparing P572L mutation on exon 11 presenting as focal onset epilepsy;2023-11-25
2. A Case of CADASIL with <i>NOTCH3</i> Gene Mutation Presenting with Focal Epileptic Seizure: A Case of CADASIL Presenting with Focal Epileptic Seizure;Archives Of Epilepsy;2023-03-01
3. Recurrent generalized seizures as the prominent manifestation in a patient with CADASIL: a case report and literature review;BMC Neurology;2022-09-30
4. Cerebral autosomo-dominant arteriopathy with subcortical infarctions and leukoencephalopathy;Russian neurological journal;2021-11-12
5. A large number of cerebral microbleeds in CADASIL patients presenting with recurrent seizures: a case report;BMC Neurology;2019-05-30
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