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Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
October 10, 2022
Calcifying pseudoneoplasm of the neuraxis (CAPNON) associated with neurenteric cyst. An autopsy case showing unusual fatal outcome
Shojiro Ichimata, Yukiko Hata, Akane Aikawa, et al.
Biological & Pharmaceutical Bulletin
|
May 8, 2015
The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors
Nozomi Hisajima, Yukiko Hata, Koshi Kinoshita, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
September 7, 2022
Pathological and Comprehensive Genetic Investigation of Autopsy Cases of Idiopathic Bradyarrhythmia
Yukiko Hata, Shojiro Ichimata, Keiichi Hirono, et al.
The Tohoku Journal of Experimental Medicine
|
November 3, 2012
Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene
Takamichi Uchiyama, Ken Yoshimura, Kazunari Kaneko, et al.
International Journal of Clinical and Experimental Pathology
|
July 18, 2014
An autopsy case of infantile-onset vanishing white matter disease related to an EIF2B2 mutation (V85E) in a hemizygous region
Yukiko Hata, Koshi Kinoshita, Kazushi Miya, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
November 29, 2005
Simple and sensitive determination of free and total morphine in human liver and kidney using gas chromatography-mass spectrometry
Keiko Kudo, Tomomi Ishida, Naoki Nishida, et al.
Neuropathology and Applied Neurobiology
|
March 24, 2021
An autopsy case of pure nigropathy with TUBA4A nonsense mutation
Keitaro Okada, Yukiko Hata, Shojiro Ichimata, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
July 3, 2018
[A pedigree of hereditary hyperekplexia]
Hideyuki Moriyoshi, Yukiko Hata, Ryosuke Inagaki, et al.
Journal of Forensic and Legal Medicine
|
February 27, 2007
The sudden and unexpected death of a female-to-male transsexual patient
Hiromasa Inoue, Naoki Nishida, Noriaki Ikeda, et al.
Brain & Development
|
November 4, 2019
Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants
Yukiko Hata, Yuko Oku, Hiromichi Taneichi, et al.
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Search research articles
Search
Showing results (91-100 of 144) with videos related to
Sort By:
Page
of 15
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
October 10, 2022
Calcifying pseudoneoplasm of the neuraxis (CAPNON) associated with neurenteric cyst. An autopsy case showing unusual fatal outcome
Shojiro Ichimata, Yukiko Hata, Akane Aikawa, et al.
Biological & Pharmaceutical Bulletin
|
May 8, 2015
The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors
Nozomi Hisajima, Yukiko Hata, Koshi Kinoshita, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
September 7, 2022
Pathological and Comprehensive Genetic Investigation of Autopsy Cases of Idiopathic Bradyarrhythmia
Yukiko Hata, Shojiro Ichimata, Keiichi Hirono, et al.
The Tohoku Journal of Experimental Medicine
|
November 3, 2012
Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene
Takamichi Uchiyama, Ken Yoshimura, Kazunari Kaneko, et al.
International Journal of Clinical and Experimental Pathology
|
July 18, 2014
An autopsy case of infantile-onset vanishing white matter disease related to an EIF2B2 mutation (V85E) in a hemizygous region
Yukiko Hata, Koshi Kinoshita, Kazushi Miya, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
November 29, 2005
Simple and sensitive determination of free and total morphine in human liver and kidney using gas chromatography-mass spectrometry
Keiko Kudo, Tomomi Ishida, Naoki Nishida, et al.
Neuropathology and Applied Neurobiology
|
March 24, 2021
An autopsy case of pure nigropathy with TUBA4A nonsense mutation
Keitaro Okada, Yukiko Hata, Shojiro Ichimata, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
July 3, 2018
[A pedigree of hereditary hyperekplexia]
Hideyuki Moriyoshi, Yukiko Hata, Ryosuke Inagaki, et al.
Journal of Forensic and Legal Medicine
|
February 27, 2007
The sudden and unexpected death of a female-to-male transsexual patient
Hiromasa Inoue, Naoki Nishida, Noriaki Ikeda, et al.
Brain & Development
|
November 4, 2019
Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants
Yukiko Hata, Yuko Oku, Hiromichi Taneichi, et al.
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of 15