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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
A Novel KCNA1 Mutation in an Episodic Ataxia Type 1 Patient with Asterixis and Falls
Journal of Clinical Neurology
2021 .01
Vertical Saccadic Slowing in Episodic Ataxia Type 2
Journal of Clinical Neurology
2022 .11
성별에 따른 일화기억 차이에 대한 체계적 고찰
재활치료과학
2020 .01
A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2
Journal of Clinical Neurology
2018 .01
New Nonsense Variant c.2983G>T; p.Glu995* in the CACNA1A Gene Causes Progressive Autosomal Dominant Ataxia
Journal Of Movement Disorders
2021 .01
The Etiologies of Chronic Progressive Cerebellar Ataxia in a Korean Population
Journal of Clinical Neurology
2018 .01
Spinocerebellar Ataxia 48 Patient With a Novel De Novo Variant of STUB1
Journal of Clinical Neurology
2022 .11
Effect of Korean Red Ginseng on the motor performance and ataxia
Journal of Ginseng Research
2024 .07
Treatable Ataxias: How to Find the Needle in the Haystack?
Journal Of Movement Disorders
2022 .09
The Rise of Cerebellar Ataxia in South Korea: 2002–2016
Journal of Clinical Neurology
2020 .01
Anti-CASPR2-Antibody-Positive Isaacs’ Syndrome Presenting with Myokymia, Neuropathic Pain, and Hyperhidrosis
Journal of Clinical Neurology
2020 .01
Variants of Lipolysis-Related Genes in Korean Patients with Very High Triglycerides
Yonsei Medical Journal
2018 .01
Role of Cortico-ponto-cerebellar Tract from Supplementary Motor Area in Ataxic Hemiparesis of Supratentorial Stroke Patients
뇌신경재활
2021 .11
A Novel APTX Variant and Ataxia with Oculomotor Apraxia Type 1
Journal of Clinical Neurology
2017 .07
Ataxia and Myoclonus with a Cherry-Red Spot Unfurling an Unusual Phenotypic Presentation of Sialidosis Type 1
Journal Of Movement Disorders
2021 .09
Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses
Annals of Laboratory Medicine
2019 .01
젊은 성인의 성별에 따른 일화기억과 공간인지의 차이
재활치료과학
2021 .01
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review A Case Report and Literature Review
Journal Of Movement Disorders
2023 .05
소뇌 뇌졸중 환자에서 실조로 인한 균형장애에 대한 시각적 피드백 훈련 기반 테트락스의 치료적 효과: 후향적 연구
대한물리의학회지
2016 .01
Validity and Reliability of the Korean-Translated Version of the International Cooperative Ataxia Rating Scale in Cerebellar Ataxia
Journal Of Movement Disorders
2023 .01
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