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Shared Metabolic Profile of Caffeine in Parkinsonian Disorders 35 8

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Shared Metabolic Profile of Caffeine in Parkinsonian Disorders 35 8
デジタル博士論文障害者向け資料あり
竹重, 遥香2020Movement Disorders
国立国会図書館
  • ISSN0885-3185

Clinical heterogeneityoffrontotemporal dementiaand Parkinsonism linked to chromosome 17caused byMAPTN279Kmutationinrelationtotaupositron emission tomographyfeatures 34 4

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Clinical heterogeneityoffrontotemporal dementiaand Parkinsonism linked to chromosome 17caused byMAPTN279Kmutationinrelationtotaupositron emission tomographyfeatures 34 4
デジタル博士論文障害者向け資料あり
池田, 彩2019Movement Disorders
国立国会図書館
  • ISSN0885-3185

VPS35 Mutation in Japanese Patients with Typical Parkinson's Disease 27 11

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VPS35 Mutation in Japanese Patients with Typical Parkinson's Disease 27 11
デジタル博士論文障害者向け資料あり
安藤, 真矢2012Movement disorders
国立国会図書館
  • ISSN0885-3185

Morphologic changes of dendritic spines of striatal neurons in the levodopa-induced dyskinesia model 29 3

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Morphologic changes of dendritic spines of striatal neurons in the levodopa-induced dyskinesia model 29 3
デジタル博士論文障害者向け資料あり
Nishijima, HaruoWiley2014-03Movement Disorders
国立国会図書館
  • ISSN0885-3185

Natural History and Phenotypic Spectrum of <scp>GAA‐<i>FGF14</i></scp> Sporadic Late‐Onset Cerebellar Ataxia (<scp>SCA27B</scp>)

Natural History and Phenotypic Spectrum of <scp>GAA‐<i>FGF14</i></scp> Sporadic Late‐Onset Cerebellar Ataxia (<scp>SCA27B</scp>)
デジタル記事
2023-07-20Movement Disorders38 10p.1950-1956
全国の図書館

Ca²⁺–Calmodulin–Calcineurin Signaling Modulates α‐Synuclein Transmission

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デジタル記事
上田, 潤, 上村, 紀仁, 石本, 智之, 田口, 智之, 澤村, 正典, 中西, 悦郎, 生野, 真嗣, 松澤, 秀一, 山門, 穂高, 髙橋, 良輔Wiley2023-06Movement Disorders38 6p.1056-1067
インターネットで読める全国の図書館
  • 掲載誌（ISSN）0885-3185 1531-8257

Ca²⁺–Calmodulin–Calcineurin Signaling Modulates α‐Synuclein Transmission

Ca²⁺–Calmodulin–Calcineurin Signaling Modulates α‐Synuclein Transmission
デジタル記事
2023-06Movement Disorders38 6p.1056-1067
インターネットで読める全国の図書館

Embracing Monogenic Parkinson's Disease: The <scp>MJFF</scp> Global Genetic <scp>PD</scp> Cohort

Embracing Monogenic Parkinson's Disease: The <scp>MJFF</scp> Global Genetic <scp>PD</scp> Cohort
デジタル記事
2023-01-24Movement Disorders38 2p.286-303
インターネットで読める全国の図書館

Lewy Body Disease Primate Model with α‐Synuclein Propagation from the Olfactory Bulb

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デジタル記事
澤村, 正典, 尾上, 浩隆, 塚田, 秀夫, 伊佐, かおる, 山門, 穂高, 奥田, 真也, 生野, 真嗣, 畑中, 悠佑, 村山, 繁雄, 上村, 紀仁, 伊佐, 正, 髙橋, 良輔Wiley2022-10Movement Disorders37 10p.2033-2044
インターネットで読める全国の図書館
  • 掲載誌（ISSN）0885-3185 1531-8257

Lewy Body Disease Primate Model with α‐Synuclein Propagation from the Olfactory Bulb

Lewy Body Disease Primate Model with α‐Synuclein Propagation from the Olfactory Bulb
デジタル記事
2022-10Movement Disorders37 10p.2033-2044
インターネットで読める全国の図書館

Putaminal Recombinant Glucocerebrosidase Delivery with Magnetic Resonance<scp>–</scp>Guided Focused Ultrasound in Parkinson's Disease: A Phase I Study

Putaminal Recombinant Glucocerebrosidase Delivery with Magnetic Resonance<scp>–</scp>Guided Focused Ultrasound in Parkinson's Disease: A Phase I Study
デジタル記事
2022-09-11Movement Disorders37 10p.2134-2139
全国の図書館

High‐Contrast Imaging of α‐Synuclein Pathologies in Living Patients with Multiple System Atrophy

High‐Contrast Imaging of α‐Synuclein Pathologies in Living Patients with Multiple System Atrophy
デジタル記事
2022-08-30Movement Disorders37 10p.2159-2161
インターネットで読める全国の図書館

A Machine Learning–Based Approach to Discrimination of Tauopathies Using [<scp><sup>18</sup>F</scp>]<scp>PM‐PBB3 PET</scp> Images

A Machine Learning–Based Approach to Discrimination of Tauopathies Using [<scp><sup>18</sup>F</scp>]<scp>PM‐PBB3 PET</scp> Images
デジタル記事
2022-08-28Movement Disorders37 11p.2236-2246
インターネットで読める全国の図書館

<scp>HOMER</scp>‐3 Antibodies Were Not Detected in Two German Cohorts of Patients with Multiple System Atrophy

<scp>HOMER</scp>‐3 Antibodies Were Not Detected in Two German Cohorts of Patients with Multiple System Atrophy
デジタル記事
2022-08-17Movement Disorders37 10p.2165-2166
全国の図書館

Repeat‐Associated Non‐<scp>AUG</scp> Translation of <scp>AGAGGG</scp> Repeats that Cause <scp>X</scp>‐Linked Dystonia‐Parkinsonism

Repeat‐Associated Non‐<scp>AUG</scp> Translation of <scp>AGAGGG</scp> Repeats that Cause <scp>X</scp>‐Linked Dystonia‐Parkinsonism
デジタル記事
2022-08-16Movement Disorders37 11p.2284-2289
インターネットで読める全国の図書館

Phase 1/1b Studies of <scp>UCB0599</scp>, an Oral Inhibitor of α‐Synuclein Misfolding, Including a Randomized Study in Parkinson's Disease

Phase 1/1b Studies of <scp>UCB0599</scp>, an Oral Inhibitor of α‐Synuclein Misfolding, Including a Randomized Study in Parkinson's Disease
デジタル記事
2022-08-12Movement Disorders37 10p.2045-2056
全国の図書館

<scp>α‐Synuclein V15A</scp> Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid‐Binding Property

<scp>α‐Synuclein V15A</scp> Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid‐Binding Property
デジタル記事
2022-07-27Movement Disorders37 10p.2075-2085
インターネットで読める全国の図書館

<i>MED27</i>, <i>SLC6A7,</i> and <i>MPPE1</i> Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia

<i>MED27</i>, <i>SLC6A7,</i> and <i>MPPE1</i> Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia
デジタル記事
2022-07-25Movement Disorders37 10p.2139-2146
全国の図書館

Middle Cerebellar Peduncle in Early Stage of Multiple System Atrophy: A <scp>THK5351 PET</scp> Study

Middle Cerebellar Peduncle in Early Stage of Multiple System Atrophy: A <scp>THK5351 PET</scp> Study
デジタル記事
2022-07-15Movement Disorders37 9p.1957-1959
全国の図書館

Striatal <scp>Blood–Brain</scp> Barrier Opening in Parkinson's Disease Dementia: A Pilot Exploratory Study

Striatal <scp>Blood–Brain</scp> Barrier Opening in Parkinson's Disease Dementia: A Pilot Exploratory Study
デジタル記事
2022-06-28Movement Disorders37 10p.2057-2065
全国の図書館