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New Nonsense Variant c.2983G>T; p.Glu995* in the CACNA1A Gene Causes Progressive Autosomal Dominant Ataxia
Yannic Saathoff, Saskia Biskup, Claudia Funke, Christian Roth
J Mov Disord. 2021;14(1):70-74.   Published online October 31, 2020    DOI: https://doi.org/10.14802/jmd.20082
                              
  Cited By 1
Sialidosis Type I without a Cherry Red Spot— Is There a Genetic Basis?
Koti Neeraja, Vikram Venkappayya Holla, Shweta Prasad, Bharath Kumar Surisetti, Kempaiah Rakesh, Nitish Kamble, Ravi Yadav, Pramod Kumar Pal
J Mov Disord. 2021;14(1):65-69.   Published online October 31, 2020    DOI: https://doi.org/10.14802/jmd.20083
                              Supplementary
Immune-Mediated Cerebellar Ataxias: Clinical Diagnosis and Treatment Based on Immunological and Physiological Mechanisms
Hiroshi Mitoma, Mario Manto, Marios Hadjivassiliou
J Mov Disord. 2021;14(1):10-28.   Published online January 12, 2021    DOI: https://doi.org/10.14802/jmd.20040
                              
  Cited By 1
Progressive Supranuclear Palsy with Predominant Cerebellar Ataxia
Shoichiro Ando, Masato Kanazawa, Osamu Onodera
J Mov Disord. 2020;13(1):20-26.   Published online December 19, 2019    DOI: https://doi.org/10.14802/jmd.19061
                              
  Cited By 4
Assessment of Bone Mineral Density of Patients with Spinocerebellar Ataxia Type 3
Aline MS Farias, Simone Appenzeller, Marcondes C França, Alberto RM Martinez, Elba E Etchebehere, Thiago F Souza, Allan O Santos
J Mov Disord. 2019;12(1):43-46.   Published online January 30, 2019    DOI: https://doi.org/10.14802/jmd.18041
                              
  Cited By 1
The ‘Hot Cross Bun’ Sign Is Not Always Multiple System Atrophy: Etiologies of 11 Cases
Christopher Way, David Pettersson, Amie Hiller
J Mov Disord. 2019;12(1):27-30.   Published online December 19, 2018    DOI: https://doi.org/10.14802/jmd.18031
                              
  Cited By 6
Abnormal Eye Movements in Parkinsonism and Movement Disorders
Ileok Jung, Ji-Soo Kim
J Mov Disord. 2019;12(1):1-13.   Published online January 30, 2019    DOI: https://doi.org/10.14802/jmd.18034
                              Supplementary
  Cited By 8
Genetic Screening for Spinocerebellar Ataxia Genes in a Japanese Single-Hospital Cohort
Ryuji Sakakibara, Fuyuki Tateno, Masahiko Kishi, Yohei Tsuyusaki, Yosuke Aiba, Hitoshi Terada, Tsutomu Inaoka, Setsu Sawai, Satoshi Kuwabara, Fumio Nomura
J Mov Disord. 2017;10(3):116-122.   Published online August 8, 2017    DOI: https://doi.org/10.14802/jmd.17011
                              
  Cited By 2
Progressive Supranuclear Gaze Palsy with Predominant Cerebellar Ataxia: A Case Series with Videos
Zheyu Xu, Tchoyoson C.C. Lim, Wing Lok Au, Louis C.S. Tan
J Mov Disord. 2017;10(2):87-91.   Published online April 18, 2017    DOI: https://doi.org/10.14802/jmd.16059
                              Supplementary
  Cited By 2
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
                              
  Cited By 34
Hereditary Cerebellar Ataxias: A Korean Perspective
Ji Sun Kim, Jin Whan Cho
J Mov Disord. 2015;8(2):67-75.   Published online May 31, 2015    DOI: https://doi.org/10.14802/jmd.15006
                              
  Cited By 11
Ataxia with Vitamin E Deficiency in Norway
Areej Elkamil, Krisztina K. Johansen, Jan Aasly
J Mov Disord. 2015;8(1):33-36.   Published online January 31, 2015    DOI: https://doi.org/10.14802/jmd.14030
                              
  Cited By 8
A Case of Multiple System Atrophy-Cerebellar Type Preceded by Dementia
Eun Hye Jang, Joo Kyung Lee, Hyun Jung Jang, Mi-Jung Kim, Sun Ju Chung
J Mov Disord. 2012;5(2):48-52. DOI: https://doi.org/10.14802/jmd.12011
                              
  Cited By 3
Preliminary Study of Intravenous Amantadine Treatment for Ataxia Management in Patients with Probable Multiple System Atrophy with Predominant Cerebellar Ataxia
Jinyoung Youn, Hyeeun Shin, Ji Sun Kim, Jin Whan Cho
J Mov Disord. 2012;5(1):1-4. DOI: https://doi.org/10.14802/jmd.12001
                              
  Cited By 2
MicroRNAs in Experimental Models of Movement Disorders
Soon-Tae Lee, Manho Kim
J Mov Disord. 2011;4(2):55-59. DOI: https://doi.org/10.14802/jmd.11011
                              
  Cited By 3
A Case of Genetically Confirmed Spinocerebellar Ataxia Type 8
Gyoungim Suh, Won Chan Kim, Myung Sik Lee
J Mov Disord. 2008;1(2):90-92. DOI: https://doi.org/10.14802/jmd.08017
                              
Reliability of Serum Anti-thyroid Antibody Screening in the Diagnosis of Parkinson’s Disease and Multiple System Atrophy
Taek-Jun Lee, Hee-Young Shin, Won Tae Yoon, Won Yong Lee
J Mov Disord. 2008;1(2):75-81. DOI: https://doi.org/10.14802/jmd.08014
                              
Myoclonus-Ataxia Syndrome Associated with COVID-19
Kuldeep Shetty, Atul Manchakrao Jadhav, Ranjith Jayanthakumar, Seema Jamwal, Tejaswini Shanubhogue, Mallepalli Prabhakar Reddy, Gopal Krishna Dash, Radhika Manohar, Vivek Jacob Philip, Vikram Huded
Received September 9, 2020  Accepted December 24, 2020  Published online April 6, 2021
DOI: https://doi.org/10.14802/jmd.20106    [Epub ahead of print]
                              Supplementary
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