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Fukai, Ryoko
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1

Molecular diagnosis of 405 individuals with autism spectrum..:

Miyake, Noriko ; Tsurusaki, Yoshinori ; Fukai, Ryoko...
European Journal of Human Genetics.  , 2023
Link: https://doi.org/10.1038/..
 
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2

SGTA associates with intracellular aggregates in neurodegen..:

Kubota, Shun ; Doi, Hiroshi ; Koyano, Shigeru...
Molecular Brain.  14 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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3

Case Report: Anti-MOG Antibody Seroconversion Accompanied b..:

Takahashi, Keita ; Takeuchi, Hideyuki ; Fukai, Ryoko...
Frontiers in Immunology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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4

Reply to "GGCRepeat Expansion ofNOTCH2NLCis Rare in Europea..:

Doi, Hiroshi ; Okubo, Masaki ; Fukai, Ryoko...
Annals of Neurology.  88 (2020)  3 - p. 642-643 , 2020
Link: https://doi.org/10.1002/..
 
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5

An acute encephalopathy with reduced diffusion in BRAF-asso..:

Okuzono, Sayaka ; Fukai, Ryoko ; Noda, Marie...
Brain and Development.  41 (2019)  4 - p. 378-381 , 2019
Link: https://doi.org/10.1016/..
 
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6

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Le..:

Okubo, Masaki ; Doi, Hiroshi ; Fukai, Ryoko...
Annals of Neurology.  86 (2019)  6 - p. 962-968 , 2019
Link: https://doi.org/10.1002/..
 
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7

Non-traumatic Acute Epidural Hematoma in Multiple Sclerosis..:

Fukai, Ryoko ; Takahashi, Keita ; Abe, Hiroyuki...
Frontiers in Neurology.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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8

A Case of McLeod Syndrome with A Novel XK Missense Mutation:

Komiya, Hiroyasu ; Takasu, Mutsuki ; Hashiguchi, Shunta...
Movement Disorders Clinical Practice.  5 (2018)  3 - p. 333-336 , 2018
Link: https://doi.org/10.1002/..
 
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9

A male case with CDKL5-associated encephalopathy manifestin..:

Akamine, Satoshi ; Ishizaki, Yoshito ; Sakai, Yasunari...
European Journal of Medical Genetics.  61 (2018)  8 - p. 451-454 , 2018
Link: https://doi.org/10.1016/..
 
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10

Cerebellar ataxia-dominant phenotype in patients with ERCC4..:

Doi, Hiroshi ; Koyano, Shigeru ; Miyatake, Satoko...
Journal of Human Genetics.  63 (2018)  4 - p. 417-423 , 2018
Link: https://doi.org/10.1038/..
 
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11

Cerebrospinal fluid level of Nogo receptor 1 antagonist lat..:

Takahashi, Keita ; Takeuchi, Hideyuki ; Kurihara, Yuji...
Journal of Neuroinflammation.  15 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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12

Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions ..:

Tada, Mikiko ; Doi, Hiroshi ; Koyano, Shigeru...
The American Journal of Pathology.  188 (2018)  2 - p. 507-514 , 2018
Link: https://doi.org/10.1016/..
 
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13

Integrative Analyses of De Novo Mutations Provide Deeper Bi..:

Takata, Atsushi ; Miyake, Noriko ; Tsurusaki, Yoshinori...
Cell Reports.  22 (2018)  3 - p. 734-747 , 2018
Link: https://doi.org/10.1016/..
 
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14

A case of severe movement disorder with GNAO1 mutation resp..:

Sakamoto, Saori ; Monden, Yukifumi ; Fukai, Ryoko...
Brain and Development.  39 (2017)  5 - p. 439-443 , 2017
Link: https://doi.org/10.1016/..
 
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15

De novo missense mutations in NALCN cause developmental and..:

Fukai, Ryoko ; Saitsu, Hirotomo ; Okamoto, Nobuhiko...
Journal of Human Genetics.  61 (2016)  5 - p. 451-455 , 2016
Link: https://doi.org/10.1038/..
 
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