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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
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논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
Progressive Cognitive and Behavioral Changes With Leukodystrophy due to ABCD1 Gene Mutation
Dementia and Neurocognitive Disorders(대한치매학회지)
2022 .10
A novel mutation in the DNMT1 gene in a patient presenting with pure cerebellar ataxia
Journal of genetic medicine
2017 .01
A Little-Known Brain Imaging Feature in Neuromyelitis Optica Spectrum Disorder: A Leukodystrophy-Like Pattern
Journal of Clinical Neurology
2019 .01
The Etiologies of Chronic Progressive Cerebellar Ataxia in a Korean Population
Journal of Clinical Neurology
2018 .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
Novel Germline Mutations of BRCA1 and BRCA2 in Korean Familial Breast Cancer Patients
전남의대학술지
2019 .01
Effect of Korean Red Ginseng on the motor performance and ataxia
Journal of Ginseng Research
2024 .07
The R278I Mutation of PSEN1 in the Familial Alzheimer Disease
Dementia and Neurocognitive Disorders(대한치매학회지)
2020 .01
The Rise of Cerebellar Ataxia in South Korea: 2002–2016
Journal of Clinical Neurology
2020 .01
Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan
Cancer Research and Treatment
2019 .01
Expanding the Clinical Spectrum of RFC1 Gene Mutations
Journal Of Movement Disorders
2022 .05
New Nonsense Variant c.2983G>T; p.Glu995* in the CACNA1A Gene Causes Progressive Autosomal Dominant Ataxia
Journal Of Movement Disorders
2021 .01
Ataxia and Myoclonus with a Cherry-Red Spot Unfurling an Unusual Phenotypic Presentation of Sialidosis Type 1
Journal Of Movement Disorders
2021 .09
Treatable Ataxias: How to Find the Needle in the Haystack?
Journal Of Movement Disorders
2022 .09
Role of Cortico-ponto-cerebellar Tract from Supplementary Motor Area in Ataxic Hemiparesis of Supratentorial Stroke Patients
뇌신경재활
2021 .11
A Case of AOA2 With Compound Heterozygous SETX Mutations
Journal Of Movement Disorders
2022 .05
A Case of Familial Cold Autoinflammatory Syndrome with De Novo NLRP3 Mutation
Annals of Dermatology
2021 .01
A Novel KCNA1 Mutation in an Episodic Ataxia Type 1 Patient with Asterixis and Falls
Journal of Clinical Neurology
2021 .01
Primary Familial Brain Calcification With XPR1 Mutation Presenting With Cognitive Dysfunction
Journal of Clinical Neurology
2024 .03
A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2
Journal of Clinical Neurology
2018 .01
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