Mitochondrial DNA A4336G Mutation in Alzheimer’s and Parkinson’s Diseases

Publisher： Karger

E-ISSN： 1421-9913|48|1|34-36

ISSN： 0014-3022

Source： European Neurology, Vol.48, Iss.1, 2002-07, pp. : 34-36

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Mitochondrial DNA Variants in a Portuguese Population of Patients with Alzheimer’s Disease

By  

European Neurology, Vol. 53, Iss. 3, 2005-04 ,pp. : 121-124

Karger

Access to resources Recommend Favorite

Wernicke’s Encephalopathy in a Patient with Multiple Symmetrical Lipomatosis and the A8344G Mutation of Mitochondrial DNA

By  

European Neurology, Vol. 47, Iss. 2, 2002-02 ,pp. : 126-128

Karger

Access to resources Recommend Favorite

No Mutation of G209A in the Alpha-Synuclein Gene in Sporadic Parkinson’s Disease among Taiwan Chinese

By  

European Neurology, Vol. 41, Iss. 2, 1999-02 ,pp. : 85-87

Karger

Access to resources Recommend Favorite

Cognitive Dysfunctions in Mild Parkinson’s Disease Dementia: Comparison with Patients Having Mild Alzheimer’s Disease and Normal Controls

By  

European Neurology, Vol. 59, Iss. 1-2, 2007-10 ,pp. : 49-54

Karger

Access to resources Recommend Favorite

Clock Test Deficits Related to the Global Cognitive State in Alzheimer’s and Parkinson’s Disease

By  

Dementia and Geriatric Cognitive Disorders, Vol. 33, Iss. 1, 2012-03 ,pp. : 59-72

Karger

Access to resources Recommend Favorite