E-LIB Suche - Ergebnisse für: Okazaki, Tetsuya

1

An adolescent case of ASXL3-related disorder with delayed o..:

Arai, Yuto ; Okanishi, Tohru ; Okazaki, Tetsuya...
BMC Pediatrics. 24 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

2

First detailed case report of a pediatric patient with neur..:

Miyamoto, Yosuke ; Okazaki, Tetsuya ; Watanabe, Keisuke...
Brain and Development. 45 (2023) 1 - p. 70-76 , 2023

Link: https://doi.org/10.1016/..

3

Mastocytosis in a Case of Noonan Syndrome Caused by a De No..:

Kawaguchi, Tatsuya ; Okanishi, Tohru ; Okazaki, Tetsuya...
Yonago Acta Medica. 66 (2023) 4 - p. 463-466 , 2023

Link: https://doi.org/10.33160..

4

Phase Lag Analysis Scalp Electroencephalography May Predict..:

Oguri, Masayoshi ; Okazaki, Tetsuya ; Okanishi, Tohru...
Yonago Acta Medica. 66 (2023) 1 - p. 48-55 , 2023

Link: https://doi.org/10.33160..

5

Impaired neuronal integrity in traumatic brain injury detec..:

Kato, Hiroki ; Nakagawara, Jyoji ; Hachisuka, Kenji...
Journal of Cerebral Blood Flow & Metabolism. 42 (2022) 12 - p. 2245-2254 , 2022

Link: https://doi.org/10.1177/..

6

A case of ALG11-congenital disorders of glycosylation diagn..:

Arai, Yuto ; Okanishi, Tohru ; Kanai, Sotaro...
Brain and Development. 44 (2022) 10 - p. 732-736 , 2022

Link: https://doi.org/10.1016/..

7

Clinical course of a Japanese patient with developmental de..:

Okazaki, Tetsuya ; Kawaguchi, Tatsuya ; Saiki, Yusuke...
Human Genome Variation. 9 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

8

Gait disturbance in a patient with de novo 1.0-kb SOX2 micr..:

Yamada, Hiroyuki ; Okanishi, Tohru ; Okazaki, Tetsuya...
Brain and Development. 44 (2022) 1 - p. 68-72 , 2022

Link: https://doi.org/10.1016/..

9

Intractable startle epilepsy in Schuurs – Hoeijmakers syndr..:

Ohta, Kento ; Okanishi, Tohru ; Kanai, Sotaro...
Epileptic Disorders. 24 (2022) 3 - p. 606-608 , 2022

Link: https://doi.org/10.1684/..

10

FKRP mutations cause congenital muscular dystrophy 1C and l..:

Awano, Hiroyuki ; Saito, Yoshihiko ; Shimizu, Mamiko...
Journal of Clinical Neuroscience. 92 (2021) - p. 215-221 , 2021

Link: https://doi.org/10.1016/..

11

Progressive cerebral atrophies in three children with COL4A..:

Nakamura, Yuko ; Okanishi, Tohru ; Yamada, Hiroyuki...
Brain and Development. 43 (2021) 10 - p. 1033-1038 , 2021

Link: https://doi.org/10.1016/..

12

Clinical Characteristics of Fragile X Syndrome Patients inJ..:

Okazaki, Tetsuya ; Adachi, Kaori ; Matsuura, Kaori...
Yonago Acta Medica. 64 (2021) 1 - p. 30-33 , 2021

Link: https://doi.org/10.33160..

13

Clinical course of epilepsy and white matter abnormality li..:

Okazaki, Tetsuya ; Yamada, Hiroyuki ; Matsuura, Kaori...
Human Genome Variation. 8 (2021) 1 - p. , 2021

Link: https://doi.org/10.1038/..

14

Efficacy of long‐term adrenocorticotropic hormone therapy f..:

Baba, Shimpei ; Okanishi, Tohru ; Homma, Yoichiro...
Epilepsia Open. 6 (2021) 2 - p. 402-412 , 2021

Link: https://doi.org/10.1002/..

15

Duchenne muscular dystrophy–like phenotype in an LGMD2I pat..:

Okazaki, Tetsuya ; Matsuura, Kaori ; Kasagi, Noriko...
Human Genome Variation. 7 (2020) 1 - p. , 2020

Link: https://doi.org/10.1038/..