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1 . Academic Journal
Myosin Va, a Novel Interaction Partner of STXBP1, Is Required to Transport Syntaxin1A to the Plasma Membrane
저자
by
Taura, Yoshihiro
;
Tozawa, Takenori
;
Fujimoto, Takahiro
;
Ichise, Eisuke
;
Chiyonobu, Tomohiro
, et al.
소스
In
Neuroscience
May 2023
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7 . Academic Journal
Quantitative pretreatment EEG predicts efficacy of ACTH therapy in infantile epileptic spasms syndrome
저자
by
Kanai, Sotaro
;
Oguri, Masayoshi
;
Okanishi, Tohru
;
Miyamoto, Yosuke
;
Maeda, Masanori
, et al.
소스
In
Clinical Neurophysiology
December 2022 144:83-90
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7 . Academic Journal
Phenotypes of SMA patients retaining SMN1 with intragenic mutation
저자
by
Wijaya, Yogik Onky Silvana
;
Ar Rohmah, Mawaddah
;
Niba, Emma Tabe Eko
;
Morisada, Naoya
;
Noguchi, Yoriko
, et al.
소스
In
Brain and Development
August 2021 43(7):745-758
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7 . Academic Journal
Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene
저자
by
Niba, Emma Tabe Eko
;
Nishio, Hisahide
;
Wijaya, Yogik Onky Silvana
;
Lai, Poh San
;
Tozawa, Takenori
, et al.
소스
In
Brain and Development
February 2021 43(2):294-302
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7 . Academic Journal
Cerebellar peduncle injury predicts motor impairments in preterm infants: A quantitative tractography study at term-equivalent age
저자
by
Hasegawa, Tatsuji
;
Yamada, Kei
;
Tozawa, Takenori
;
Chiyonobu, Tomohiro
;
Tokuda, Sachiko
, et al.
소스
In
Brain and Development
October 2018 40(9):743-752
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7 . Academic Journal
Bilateral choroid plexus resection in a 9p hexasomy/tetrasomy mosaic patient.
저자
by
Takada, Rei
;
Tozawa, Takenori
;
Yamanaka, Takumi
;
Moroto, Masaharu
;
Iehara, Tomoko
, et al.
소스
Human Genome Variation; 2/26/2024, Vol. 11 Issue 1, p1-4, 4p
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7 . Academic Journal
Leigh-like syndrome with progressive cerebellar atrophy caused by novel HIBCH variants.
저자
by
Taura, Yoshihiro
;
Tozawa, Takenori
;
Isoda, Kenichi
;
Hirai, Satori
;
Chiyonobu, Tomohiro
, et al.
소스
Human Genome Variation; 10/16/2023, Vol. 10 Issue 1, p1-4, 4p
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7 .
FGFR1 related Encephalocraniocutaneous lipomatosis in a neonate with congenital hydrocephalus
저자
by
Zuiki, Masashi
;
Chiyonobu, Tomohiro
;
Morimoto, Hidechika
;
Sawada, Hiroko
;
Tozawa, Takenori
, et al.
소스
In
Brain and Development Case Reports
March 2024 2(1)
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7 . Academic Journal
Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformation.
저자
by
Mori, Jun
;
Hasegawa, Tatsuji
;
Miyamoto, Yosuke
;
Kitamura, Kazumasa
;
Morimoto, Hidechika
, et al.
소스
Human Genome Variation; 6/3/2022, Vol. 9 Issue 1, p1-4, 4p
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7 . Academic Journal
Low‐grade IVH in preterm infants causes cerebellar damage, motor, and cognitive impairment.
저자
by
Sakaue, Satoshi
;
Hasegawa, Tatsuji
;
Sakai, Koji
;
Zen, Yui
;
Tozawa, Takenori
, et al.
소스
Pediatrics International
. Nov2021, Vol. 63 Issue 11, p1327-1333. 7p.
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