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REVIEW ARTICLE 2016 September 21
Episodic Ataxias: Clinical and Genetic Features
Episodic ataxia (EA) is a clinically heterogeneous group of disorders that are characterized by recurrent spells of truncal ataxia and incoordination lasting minutes to hours. Most have an autosomal dominant inheritance pattern. To date, 8 subtypes have been defined according to...
REVIEW ARTICLE 2016 September 21
Applications of CRISPR/Cas9 for Gene Editing in Hereditary Movement Disorders
Gene therapy is a potential therapeutic strategy for treating hereditary movement disorders, including hereditary ataxia, dystonia, Huntington’s disease, and Parkinson’s disease. Genome editing is a type of genetic engineering in which DNA is inserted, deleted or replaced in ...
ORIGINAL ARTICLE 2016 September 21
Cognition and Visit-to-Visit Variability of Blood Pressure and Heart Rate in De Novo Patients with Parkinson’s Disease
Objective We sought to identify whether the characteristics of long-term visit-to-visit blood pressure (BP) and heart rate (HR) are related to baseline cognitive profiles in, Parkinson’s disease (PD). Methods We selected drug-naïve PD patients who visited our hospital at leas...
ORIGINAL ARTICLE 2016 September 21
The MMSE and MoCA for Screening Cognitive Impairment in Less Educated Patients with Parkinson’s Disease
Objective To explore whether the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA) can be used to screen for dementia or mild cognitive impairment (MCI) in less educated patients with Parkinson’s disease (PD). Methods We reviewed the medical records...
ORIGINAL ARTICLE 2016 September 21
Falls and Their Associated Risks in Parkinson’s Disease Patients in Nigeria
Objective Falls are a devastating consequence of Parkinson’s disease (PD) and are due to motor imbalance. However, the frequency of falls and their risk factors among Nigerians with PD is not known despite the significant increase in PD cases in the country. To assess fall risk...
ORIGINAL ARTICLE 2016 September 21
Survival of Korean Huntington’s Disease Patients
Objective The survival of Huntington’s disease (HD) patients is reported to be 15–20 years. However, most studies on the survival of HD have been conducted in patients without genetic confirmation with the possible inclusion of non-HD patients, and all studies have been condu...
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Current Issue
Volume 9(3); September 2016
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Review Articles
129 Episodic Ataxias: Clinical and Genetic Features
Kwang-Dong Choi, Jae-Hwan Choi
J Mov Disord. 2016;9(3):129-135.   Published online September 21, 2016    DOI: https://doi.org/10.14802/jmd.16028
                              
136 Applications of CRISPR/Cas9 for Gene Editing in Hereditary Movement Disorders
Wooseok Im, Jangsup Moon, Manho Kim
J Mov Disord. 2016;9(3):136-143.   Published online September 21, 2016    DOI: https://doi.org/10.14802/jmd.16029
                              
Original Articles
144 Cognition and Visit-to-Visit Variability of Blood Pressure and Heart Rate in De Novo Patients with Parkinson’s Disease
Kyum-Yil Kwon, Seon Jong Pyo, Hye Mi Lee, Woo-Keun Seo, Seong-Beom Koh
J Mov Disord. 2016;9(3):144-151.   Published online September 21, 2016    DOI: https://doi.org/10.14802/jmd.16012
                              Supplementary
152 The MMSE and MoCA for Screening Cognitive Impairment in Less Educated Patients with Parkinson’s Disease
Ji In Kim, Mun Kyung Sunwoo, Young H. Sohn, Phil Hyu Lee, Jin Y. Hong
J Mov Disord. 2016;9(3):152-159.   Published online September 21, 2016    DOI: https://doi.org/10.14802/jmd.16020
                              
160 Falls and Their Associated Risks in Parkinson’s Disease Patients in Nigeria
Temitope Hannah Farombi, Mayowa O Owolabi, Adesola Ogunniyi
J Mov Disord. 2016;9(3):160-165.   Published online September 21, 2016    DOI: https://doi.org/10.14802/jmd.16011
                              
166 Survival of Korean Huntington’s Disease Patients
Han-Joon Kim, Chae-Won Shin, Beomseok Jeon, Hyeyoung Park
J Mov Disord. 2016;9(3):166-170.   Published online September 21, 2016    DOI: https://doi.org/10.14802/jmd.16022
                              
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