4.5 Article

Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype

Related references

Note: Only part of the references are listed.
Review Clinical Neurology

Imaging of MELAS

Konark Malhotra et al.

CURRENT PAIN AND HEADACHE REPORTS (2016)

Review Clinical Neurology

Neuroimaging of stroke-like episodes in MELAS

Hiromichi Ito et al.

BRAIN & DEVELOPMENT (2011)

Article Clinical Neurology

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan

Yi-Chung Lee et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2007)

Article Clinical Neurology

CT and MRI rating of white matter lesions

F Fazekas et al.

CEREBROVASCULAR DISEASES (2002)