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Kentaro Shirai

Showing results (21-30 of 28) with videos related to

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Pediatric Blood & Cancer|March 28, 2023
A male with ganglioneuroblastoma cerebrospinal hemorrhages, cardiomyopathy, and retinopathy due to severe hypertensionTakuma Deguchi, Hiroko Fukushima, Ryoko Suzuki, et al.
Lab on a Chip|October 28, 2022
Hybrid double-spiral microfluidic chip for RBC-lysis-free enrichment of rare cells from whole bloodKentaro Shirai, Guofeng Guan, Tan Meihui, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
A patient with peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and severe hypoganglionosis associated with a novel SOX10 mutationYuko Akutsu, Kentaro Shirai, Akira Takei, et al.
Brain : a Journal of Neurology|September 27, 2018
De novo PHACTR1 mutations in West syndrome and their pathophysiological effectsNanako Hamada, Shunsuke Ogaya, Mitsuko Nakashima, et al.
Annals of Neurology|April 16, 2023
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological PropertiesMaria Cristina Cioclu, Ilaria Mosca, Paolo Ambrosino, et al.
Acta Neuropathologica Communications|March 2, 2023
An integrated genetic analysis of epileptogenic brain malformed lesionsAtsushi Fujita, Mitsuhiro Kato, Hidenori Sugano, et al.
NPJ Genomic Medicine|August 26, 2025
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delayKohei Hamanaka, Atsushi Fujita, Satoko Miyatake, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2022
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophyMasamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Pediatric Blood & Cancer|March 28, 2023
A male with ganglioneuroblastoma cerebrospinal hemorrhages, cardiomyopathy, and retinopathy due to severe hypertensionTakuma Deguchi, Hiroko Fukushima, Ryoko Suzuki, et al.
Lab on a Chip|October 28, 2022
Hybrid double-spiral microfluidic chip for RBC-lysis-free enrichment of rare cells from whole bloodKentaro Shirai, Guofeng Guan, Tan Meihui, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
A patient with peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and severe hypoganglionosis associated with a novel SOX10 mutationYuko Akutsu, Kentaro Shirai, Akira Takei, et al.
Brain : a Journal of Neurology|September 27, 2018
De novo PHACTR1 mutations in West syndrome and their pathophysiological effectsNanako Hamada, Shunsuke Ogaya, Mitsuko Nakashima, et al.
Annals of Neurology|April 16, 2023
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological PropertiesMaria Cristina Cioclu, Ilaria Mosca, Paolo Ambrosino, et al.
Acta Neuropathologica Communications|March 2, 2023
An integrated genetic analysis of epileptogenic brain malformed lesionsAtsushi Fujita, Mitsuhiro Kato, Hidenori Sugano, et al.
NPJ Genomic Medicine|August 26, 2025
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delayKohei Hamanaka, Atsushi Fujita, Satoko Miyatake, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2022
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophyMasamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, et al.
Pageof 3