Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease-Reference-Cited by-同舟云学术

Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease

Published:1994 Issue:3 Volume:9 Page:305-310
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Hotamisligil Gokhan S.,Girmen A. Sule,Fink J. Stephen,Tivol Elizabeth,Shalish Christo,Trofatter James,Baenziger John,Diamond Shirley,Markham Charles,Sullivan Jack,Growdon John,Breakefield Xandra O.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference72 articles.

1. Principles of neurology. 3rd ed. New York: McGraw-Hill, 1985: 874-880.

2. The Endogenous Toxin Hypothesis of the Etiology of Parkinson's Disease and a Pilot Trial of High-Dosage Antioxidants in an Attempt to Slow the Progression of the Illness

3. Neuron numbers and sizes in aging brain: Comparisons of human, monkey, and rodent data

4. Striatal function in normal aging: Implications for Parkinson's disease

Cited by 68 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. B-Cell Receptor-Associated Protein 31 Negatively Regulates the Expression of Monoamine Oxidase A Via R1;Frontiers in Molecular Biosciences;2020-04-30

2. Androgen receptor and monoamine oxidase polymorphism in wild bonobos;Meta Gene;2014-12

3. Genomic and Pharmacogenomic Biomarkers of Parkinson’s Disease;Current Drug Metabolism;2014-03-31

4. Gene–environment interactions in Parkinson's disease: Specific evidence in humans and mammalian models;Neurobiology of Disease;2013-09

5. Neurodegeneration from Drugs and Aging-Derived Free Radicals;Molecular Basis of Oxidative Stress;2013-06-28