Search research articles
Contact Us
Filters
Showing results (31-40 of 37) with videos related to
Page
of 4
Sort By:
You have reached the last page of results.
This site can display upto 37 results.
Brain & Development
|
February 12, 2019
MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNA<sup>Met</sup> gene
Mari Kuwajima, Masahide Goto, Koyuru Kurane, et al.
Brain & Development
|
September 19, 2013
Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8
Hidekazu Kato, Fuyu Miyake, Hiroko Shimbo, et al.
Molecular Genetics and Metabolism
|
April 5, 2012
Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness
Hitoshi Osaka, Atsushi Takagi, Yu Tsuyusaki, et al.
Pediatric Neurology
|
September 27, 2020
Pyridoxal in the Cerebrospinal Fluid May Be a Better Indicator of Vitamin B6-dependent Epilepsy Than Pyridoxal 5'-Phosphate
Tomoyuki Akiyama, Yuki Hyodo, Kosei Hasegawa, et al.
Science Advances
|
November 10, 2021
High-sucrose diets contribute to brain angiopathy with impaired glucose uptake and psychosis-related higher brain dysfunctions in mice
Shinobu Hirai, Hideki Miwa, Tomoko Tanaka, et al.
The Tohoku Journal of Experimental Medicine
|
June 30, 2015
Mitochonic Acid 5 (MA-5), a Derivative of the Plant Hormone Indole-3-Acetic Acid, Improves Survival of Fibroblasts from Patients with Mitochondrial Diseases
Takehiro Suzuki, Hiroaki Yamaguchi, Motoi Kikusato, et al.
Ebiomedicine
|
June 6, 2017
Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases
Tetsuro Matsuhashi, Takeya Sato, Shin-Ichiro Kanno, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Brain & Development
|
February 12, 2019
MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNA<sup>Met</sup> gene
Mari Kuwajima, Masahide Goto, Koyuru Kurane, et al.
Brain & Development
|
September 19, 2013
Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8
Hidekazu Kato, Fuyu Miyake, Hiroko Shimbo, et al.
Molecular Genetics and Metabolism
|
April 5, 2012
Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness
Hitoshi Osaka, Atsushi Takagi, Yu Tsuyusaki, et al.
Pediatric Neurology
|
September 27, 2020
Pyridoxal in the Cerebrospinal Fluid May Be a Better Indicator of Vitamin B6-dependent Epilepsy Than Pyridoxal 5'-Phosphate
Tomoyuki Akiyama, Yuki Hyodo, Kosei Hasegawa, et al.
Science Advances
|
November 10, 2021
High-sucrose diets contribute to brain angiopathy with impaired glucose uptake and psychosis-related higher brain dysfunctions in mice
Shinobu Hirai, Hideki Miwa, Tomoko Tanaka, et al.
The Tohoku Journal of Experimental Medicine
|
June 30, 2015
Mitochonic Acid 5 (MA-5), a Derivative of the Plant Hormone Indole-3-Acetic Acid, Improves Survival of Fibroblasts from Patients with Mitochondrial Diseases
Takehiro Suzuki, Hiroaki Yamaguchi, Motoi Kikusato, et al.
Ebiomedicine
|
June 6, 2017
Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases
Tetsuro Matsuhashi, Takeya Sato, Shin-Ichiro Kanno, et al.
Page
of 4