- Neurophysiological Tests in a Myasthenia Gravis Patient With Muscle-Specific Kinase Antibody Accompanied by Myotonic Discharges
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Gökmen S, Fidancı H, Alaydın HC, Söker EB
- KMID: 2561654
- J Clin Neurol.
- 2024 Nov;20(6):624-626.
- doi: 10.3988/jcn.2024.0347
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- Solute Carrier Family 2 Member 1 Gene Mutation Presenting as Adult-Onset Paroxysmal Exercise-Induced Dyskinesia Without Epilepsy
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Hwang YS, Oh E
- KMID: 2561642
- J Clin Neurol.
- 2024 Nov;20(6):627-629.
- doi: 10.3988/jcn.2024.0349
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- Development and Validation of the Korean Version of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-K)
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Lee J, Kim A, Choi SJ, Cho E, Seo J, Oh Si, Jung J, Kim JS, Sung JJ, Abrahams S, Hong YH
- KMID: 2561645
- J Clin Neurol.
- 2024 Nov;20(6):637-637.
- doi: 10.3988/jcn.2022.0403e
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- Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome: The First Genetically Confirmed Case in South Korea
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Yun SY, Choi SY, Lee JO, Kim HJ, Kim JS
- KMID: 2561643
- J Clin Neurol.
- 2024 Nov;20(6):630-633.
- doi: 10.3988/jcn.2024.0232
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- Novel MYORG Variant Linked to Primary Familial Brain Calcification
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Cristea AC, Pérez-Castrillón JL, Usategui-Martin R
- KMID: 2561644
- J Clin Neurol.
- 2024 Nov;20(6):634-636.
- doi: 10.3988/jcn.2024.0252
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- Intellectual Disability in Episodic Ataxia Type 2: Beyond Paroxysmal Vertigo and Ataxia
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Kim S, Kim JS, Lee SH, Kim JM, Na S, Choi JH, Kim HJ
- KMID: 2561647
- J Clin Neurol.
- 2024 Nov;20(6):563-570.
- doi: 10.3988/jcn.2024.0274
Background and Purpose Episodic ataxia type 2 (EA2) is characterized by recurrent vertigo and ataxia due to mutations in CACNA1A that encodes the α 1A-subunit of the P/Q-type voltage-gated calcium... -
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- Cardiovascular Autonomic Dysfunction Before and After Chemotherapy in Cancer Patients
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Yoon SY, Oh J
- KMID: 2561646
- J Clin Neurol.
- 2024 Nov;20(6):551-562.
- doi: 10.3988/jcn.2024.0221
Complications that occur during cancer therapy have emerged as a major contributor to the poor quality of life experienced by cancer patients as they live longer due to improved treatments.... -
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- Clinical Cues for the Early Diagnosis of Transthyretin-Related Polyneuropathy
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Escolano-Lozano F, Dimova V, Baka P, Geber C, Birklein F
- KMID: 2561652
- J Clin Neurol.
- 2024 Nov;20(6):610-616.
- doi: 10.3988/jcn.2024.0246
Background and Purpose The estimated prevalence of hereditary transthyretin-related familial amyloid polyneuropathy (TTR-FAP) and the small number of known patients in Germany indicate that many patients with TTR-FAP remain undiagnosed,... -
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- Association Between Vertebral Arterial Tortuosity and Aneurysm Growth in Intracranial Vertebral Artery Dissection
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Park JY, Ha SH, Jeong S, Chang JY, Kang DW, Kwon SU, Kim BJ
- KMID: 2561653
- J Clin Neurol.
- 2024 Nov;20(6):617-623.
- doi: 10.3988/jcn.2024.0139
Background and Purpose An intracranial vertebral artery dissecting aneurysm (iVADA) increases the risk of future subarachnoid hemorrhage, which is a severe complication with high rebleeding rates and poor outcomes. Identifying... -
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- CGG Repeat Expansion in NOTCH2NLC Causing Overlapping Oculopharyngodistal Myopathy and Neuronal Intranuclear Inclusion Disease With Diffusion Weighted Imaging Abnormality in the Cerebellum
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Ma J, Zhang H, Meng B, Qin J, Liu H, Pang X, Zhao R, Wang J, Chang X, Guo J, Zhang W
- KMID: 2561649
- J Clin Neurol.
- 2024 Nov;20(6):580-590.
- doi: 10.3988/jcn.2023.0486
Background and Purpose CGG repeat expansion in the 5' untranslated region (5'UTR) of the Notch 2 N-terminal-like C gene (NOTCH2NLC) has been associated with neuronal intranuclear inclusion disease (NIID) and... -
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- Syncope in Migraine: A Genome-Wide Association Study Revealing Distinct Genetic Susceptibility Variants Across Subtypes
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Lin W, Liu Y, Liang CS, Yeh PK, Tsai CK, Hung KS, An YC, Yang FC
- KMID: 2561651
- J Clin Neurol.
- 2024 Nov;20(6):599-609.
- doi: 10.3988/jcn.2024.0156
Background and Purpose Syncope is characterized by the temporary loss of consciousness and is commonly associated with migraine. However, the genetic factors that contribute to this association are not well... -
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- Impact of Siponimod on Clinical and Radiological Parameters of Secondary Progressive Multiple Sclerosis: A Real-World Prospective Study
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Stavrogianni K, Kitsos DK, Giannopapas V, Stefanou MI, Christouli N, Smyrni V, Chasiotis AK, Akrivaki A, Dimitriadou E, Chondrogianni M, Tsivgoulis G, Giannopoulos S
- KMID: 2561650
- J Clin Neurol.
- 2024 Nov;20(6):591-598.
- doi: 10.3988/jcn.2024.0149
Background and Purpose Secondary progressive multiple sclerosis (SPMS) presents with a challenging clinical phenotype, and siponimod has a potential to treat the active clinical phenotype of this disease. This single-center... -
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- Blood Pressure Variability and Ocular Vestibular-Evoked Myogenic Potentials Are Independently Associated With Orthostatic Hypotension
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Kim KT, Lee JH, Hong JP, Park JW, Lee SU, Park E, Kim BJ, Kim JS
- KMID: 2561648
- J Clin Neurol.
- 2024 Nov;20(6):571-579.
- doi: 10.3988/jcn.2024.0092
Background and Purpose We delineated the association between otolithic dysfunction and blood pressure (BP) variability. Methods We prospectively recruited 145 consecutive patients (age=71 [59–79] years, median [interquartile range]; 76 females) with... -
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