- Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease
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Hertz E, Lopez G, Lichtenberg J, Haubenberger D, Tayebi N, Hallett M, Sidransky E
- KMID: 2545928
- J Mov Disord.
- 2023 Sep;16(3):321-324.
- doi: 10.14802/jmd.23074
Biallelic mutations in GBA1 cause the lysosomal storage disorder Gaucher disease, and carriers of GBA1 variants have an increased risk of Parkinson’s disease (PD). It is still unknown whether GBA1... -
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- Pallidal Deep Brain Stimulation for Refractory Celiac-Related Myoclonus
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Youn J, Slow E, Chen R, Lozano AM, Fasano A
- KMID: 2545929
- J Mov Disord.
- 2023 Sep;16(3):325-327.
- doi: 10.14802/jmd.23006
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- From Evidence to the Dish: A Viewpoint of Implementing a Thai-Style Mediterranean Diet for Parkinson’s Disease
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Phokaewvarangkul O, Kantachadvanich N, Buranasrikul V, Phoumindr A, Phumphid S, Jagota P, Bhidayasiri R
- KMID: 2545924
- J Mov Disord.
- 2023 Sep;16(3):279-284.
- doi: 10.14802/jmd.23021
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- Pisa Syndrome in Subacute Sclerosing Panencephalitis: A Case Report and Review of the Literature
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Kaur S, Singh AS, Prabhakar S, Singhvi JP, Mann HS, Kaul A
- KMID: 2545933
- J Mov Disord.
- 2023 Sep;16(3):336-338.
- doi: 10.14802/jmd.23052
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- Historical and More Common Nongenetic Movement Disorders From Asia
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Ibrahim NM, Jagota P, Pal PK, Bhidayasiri R, Lim SY, Ugawa Y, Aldaajani Z, Jeon B, Fujioka S, Lee JY, Kukkle PL, Shang H, Phokaewvarangkul O, Diesta C, Shambetova C, Lin CH
- KMID: 2545922
- J Mov Disord.
- 2023 Sep;16(3):248-260.
- doi: 10.14802/jmd.22224
Nongenetic movement disorders are common throughout the world. The movement disorders encountered may vary depending on the prevalence of certain disorders across various geographical regions. In this paper, we review... -
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- Gravitational syncope induced by rising elevators in a Parkinson’s disease patient
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Sohn SW, Yoo D, Ahn TB
- KMID: 2545931
- J Mov Disord.
- 2023 Sep;16(3):331-332.
- doi: 10.14802/jmd.23076
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- Dystonic Opisthotonus in Kufor-Rakeb Syndrome: Expanding the Phenotypic and Genotypic Spectrum
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Gurram S, Holla VV, Kumari R, Dhar D, Kamble N, Yadav R, Muthusamy B, Pal PK
- KMID: 2545935
- J Mov Disord.
- 2023 Sep;16(3):343-346.
- doi: 10.14802/jmd.23098
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- A Novel Variant of GCH1 in Dopa-Responsive Dystonia With Oculogyric Crises and Intrafamilial Phenotypic Heterogeneity
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Kim T, Ha SH, Yoo D, Park KS, Ahn TB
- KMID: 2545934
- J Mov Disord.
- 2023 Sep;16(3):339-342.
- doi: 10.14802/jmd.23085
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- Apomorphine Monotherapy for Parkinson’s Disease: A Neglected Option?
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Desjardins C, Nilles C, Devos D, Roze E
- KMID: 2545930
- J Mov Disord.
- 2023 Sep;16(3):328-330.
- doi: 10.14802/jmd.23057
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- Clinical and Genetic Features of Huntington’s Disease Patients From Republic of Serbia: A Single-Center Experience
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Kresojević N, Perović I, Stanković I, Tomić A, Lukic´ MJ, Marković V, Stojković T, Mandić G, Janković M, Marjanović A, Branković M, Novaković I, Petrović I, Dragašević N, Stefanova E, Svetel M, Kostić V
- KMID: 2545932
- J Mov Disord.
- 2023 Sep;16(3):333-335.
- doi: 10.14802/jmd.23028
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- Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
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Jagota P, Ugawa Y, Aldaajani Z, Ibrahim NM, Ishiura H, Nomura Y, Tsuji S, Diesta C, Hattori N, Onodera O, Bohlega S, Al-Din A, Lim SY, Lee JY, Jeon B, Pal PK, Shang H, Fujioka S, Kukkle PL, Phokaewvarangkul O, Lin CH, Shambetova C, Bhidayasiri R
- KMID: 2545921
- J Mov Disord.
- 2023 Sep;16(3):231-247.
- doi: 10.14802/jmd.23065
Clinical case studies and reporting are important to the discovery of new disorders and the advancement of medical sciences. Both clinicians and basic scientists play equally important roles leading to... -
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- Cervical proprioception in Parkinson's disease and its correlation with manual dexterity function
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- KMID: 2545926
- J Mov Disord.
- 2023 Sep;16(3):295-306.
- doi: 10.14802/jmd.23039
ObjectiveaaCervical proprioception plays a crucial role in posture and movement control. This study aimed to determine the relationships of cervical proprioception, cervical muscle strength and endurance with manual dexterity and... -
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- KMT2B-Related Dystonia in Indian Patients With Literature Review and Emphasis on Asian Cohort
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Dhar D, Holla VV, Kumari R, Sriram N, Saini J, Yadav R, Pandey A, Kamble N, Muthusamy B, Pal PK
- KMID: 2545925
- J Mov Disord.
- 2023 Sep;16(3):285-294.
- doi: 10.14802/jmd.23035
ObjectiveaaMutations in the KMT2B gene have been identified in patients previously diagnosed with idiopathic dystonia. Literature on KMT2B-related dystonia is sparse in the Indian and Asian populations. MethodsaaWe report seven patients... -
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- GBA1 Variants and Parkinson’s Disease: Paving the Way for Targeted Therapy
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Huh YE, Usnich T, Scherzer CR, Klein C, Chung SJ
- KMID: 2545923
- J Mov Disord.
- 2023 Sep;16(3):261-278.
- doi: 10.14802/jmd.23023
Glucosylceramidase beta 1 (GBA1) variants have attracted enormous attention as the most promising and important genetic candidates for precision medicine in Parkinson’s disease (PD). A substantial correlation between GBA1 genotypes... -
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- Spatiotemporal Gait Parameters in Adults With Premanifest and Manifest Huntington’s Disease: A Systematic Review
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Browning S, Holland S, Wellwood I, Bilney B
- KMID: 2545927
- J Mov Disord.
- 2023 Sep;16(3):307-320.
- doi: 10.14802/jmd.23111
ObjectiveaaTo systematically review and critically evaluate literature on spatiotemporal gait deviations in individuals with premanifest and manifest Huntington’s Disease (HD) in comparison with healthy cohorts. MethodsaaWe conducted a systematic review, guided... -
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