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Journal of the Neurological Sciences
|
July 16, 2013
TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature
Keita Sonoda, Kensuke Sasaki, Takahisa Tateishi, et al.
Journal of Diabetes Investigation
|
June 23, 2016
Hypoglycemia and glycemic variability are associated with mortality in non-intensive care unit hospitalized infectious disease patients with diabetes mellitus
Soichi Takeishi, Akihiro Mori, Hiroki Hachiya, et al.
Biochemical and Biophysical Research Communications
|
May 31, 2016
Conformational divergence in the HA-33/HA-17 trimer of serotype C and D botulinum toxin complex
Yoshimasa Sagane, Shintaro Hayashi, Tomonori Akiyama, et al.
Rheumatology International
|
August 26, 2006
A possible variant of neuro-Behçet disease presenting chronic progressive ataxia without mucocutaneo-ocular symptoms
Masaki Hirose, Takeshi Ikeuchi, Shintaro Hayashi, et al.
Japanese Journal of Infectious Diseases
|
January 31, 2024
Proton-Pump Inhibitors and Risk of Bloodstream Infection without an Identifiable Source: a Hospital-Based Case-Control Study
Shintaro Hayashi, Tomohito Moriyama, Yuichiro Ito, et al.
Current Microbiology
|
March 19, 2013
Random phage display-based screening of peptides that bind to botulinum neurotoxin binding protein, nontoxic nonhemagglutinin
Yoshimasa Sagane, Keita Miyata, Sayuri Kurihara, et al.
Journal of Neuroinflammation
|
March 31, 2016
Morvan's syndrome and myasthenia gravis related to familial Mediterranean fever gene mutations
Junpei Koge, Shintaro Hayashi, Hiroyuki Murai, et al.
Journal of the Neurological Sciences
|
June 15, 2014
A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles
Takayuki Fujii, Shintaro Hayashi, Nobutoshi Kawamura, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
May 24, 2013
A case of hereditary diffuse leukoencephalopathy with axonal spheroids caused by a de novo mutation in CSF1R masquerading as primary progressive multiple sclerosis
Ban-yu Saitoh, Ryo Yamasaki, Shintaro Hayashi, et al.
Acta Neuropathologica
|
July 6, 2004
Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation
Chun-Feng Tan, Yue-Shan Piao, Shintaro Hayashi, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 60) with videos related to
Sort By:
Page
of 6
Journal of the Neurological Sciences
|
July 16, 2013
TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature
Keita Sonoda, Kensuke Sasaki, Takahisa Tateishi, et al.
Journal of Diabetes Investigation
|
June 23, 2016
Hypoglycemia and glycemic variability are associated with mortality in non-intensive care unit hospitalized infectious disease patients with diabetes mellitus
Soichi Takeishi, Akihiro Mori, Hiroki Hachiya, et al.
Biochemical and Biophysical Research Communications
|
May 31, 2016
Conformational divergence in the HA-33/HA-17 trimer of serotype C and D botulinum toxin complex
Yoshimasa Sagane, Shintaro Hayashi, Tomonori Akiyama, et al.
Rheumatology International
|
August 26, 2006
A possible variant of neuro-Behçet disease presenting chronic progressive ataxia without mucocutaneo-ocular symptoms
Masaki Hirose, Takeshi Ikeuchi, Shintaro Hayashi, et al.
Japanese Journal of Infectious Diseases
|
January 31, 2024
Proton-Pump Inhibitors and Risk of Bloodstream Infection without an Identifiable Source: a Hospital-Based Case-Control Study
Shintaro Hayashi, Tomohito Moriyama, Yuichiro Ito, et al.
Current Microbiology
|
March 19, 2013
Random phage display-based screening of peptides that bind to botulinum neurotoxin binding protein, nontoxic nonhemagglutinin
Yoshimasa Sagane, Keita Miyata, Sayuri Kurihara, et al.
Journal of Neuroinflammation
|
March 31, 2016
Morvan's syndrome and myasthenia gravis related to familial Mediterranean fever gene mutations
Junpei Koge, Shintaro Hayashi, Hiroyuki Murai, et al.
Journal of the Neurological Sciences
|
June 15, 2014
A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles
Takayuki Fujii, Shintaro Hayashi, Nobutoshi Kawamura, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
May 24, 2013
A case of hereditary diffuse leukoencephalopathy with axonal spheroids caused by a de novo mutation in CSF1R masquerading as primary progressive multiple sclerosis
Ban-yu Saitoh, Ryo Yamasaki, Shintaro Hayashi, et al.
Acta Neuropathologica
|
July 6, 2004
Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation
Chun-Feng Tan, Yue-Shan Piao, Shintaro Hayashi, et al.
Page
of 6