TETSUO ASHIZAWA to Magnetic Resonance Imaging
This is a "connection" page, showing publications TETSUO ASHIZAWA has written about Magnetic Resonance Imaging.
Connection Strength
0.328
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Sensitivity of Advanced Magnetic Resonance Imaging to Progression over Six?Months in Early Spinocerebellar Ataxia. Mov Disord. 2024 Oct; 39(10):1856-1867.
Score: 0.096
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Proton magnetic resonance spectroscopy: an in vivo window to study neurodegenerative disorders. Arch Neurol. 1999 Dec; 56(12):1446-7.
Score: 0.070
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Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias. Neurology. 2025 Sep 09; 105(5):e213980.
Score: 0.026
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Clinically Meaningful Magnetic Resonance Endpoints Sensitive to Preataxic Spinocerebellar Ataxia Types 1 and 3. Ann Neurol. 2023 04; 93(4):686-701.
Score: 0.022
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Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10. Arch Neurol. 2002 Aug; 59(8):1285-90.
Score: 0.021
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Clinical and genomic analysis of a large Chinese family with familial cortical myoclonic tremor with epilepsy and SAMD12 intronic repeat expansion. Epilepsia Open. 2021 03; 6(1):102-111.
Score: 0.019
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[A case report of volatile solvent psychosis]. Nihon Arukoru Yakubutsu Igakkai Zasshi. 1996 Oct; 31(5):475-82.
Score: 0.014
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Sensory and motor cortex function contributes to symptom severity in spinocerebellar ataxia type 6. Brain Struct Funct. 2017 03; 222(2):1039-1052.
Score: 0.014
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Comprehensive phenotype of the p.Arg420his allelic form of spinocerebellar ataxia type 13. Cerebellum. 2013 Dec; 12(6):932-6.
Score: 0.011
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Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders. Neurobiol Aging. 2013 Oct; 34(10):2442.e11-7.
Score: 0.011
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Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids. Arq Neuropsiquiatr. 2013 Jan; 71(1):66.
Score: 0.011
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Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10. Ann Neurol. 2001 Aug; 50(2):234-9.
Score: 0.005
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An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia. Neurology. 2000 Jan 25; 54(2):491-3.
Score: 0.004
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Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype. Neurology. 1998 Oct; 51(4):1081-6.
Score: 0.004