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Y Maegaki

Showing results (31-40 of 47) with videos related to

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No to Hattatsu = Brain and Development|June 8, 2001
[Mitochondrial DNA T to G mutation 8993 in Leigh encephalopathy and organic aciduria]M Ueno, A Oka, Y Maegaki, et al.
Neuropediatrics|February 6, 2010
Fulminant sepsis-associated encephalopathy in two children: serial neuroimaging findings and clinical courseA Kondo, C Sugiura, Y Fujii, et al.
Neuropediatrics|January 20, 2007
Late-onset neuropsychological symptoms in a Japanese patient with megalencephalic leukoencephalopathy with subcortical cystsC Sugiura, M Shiota, Y Maegaki, et al.
Neuropediatrics|June 1, 1997
Mechanisms of central motor reorganization in pediatric hemiplegic patientsY Maegaki, Y Maeoka, S Ishii, et al.
No to Hattatsu = Brain and Development|September 1, 1996
[Computed tomography and magnetic resonance imaging of the brain in congenital rubella syndrome]M Yoshimura, J Tohyama, Y Maegaki, et al.
No to Hattatsu = Brain and Development|July 1, 1995
[Two cases of post-encephalitic epilepsy characterized by auditory cognitive dysfunction; comparison with "a peculiar type of post-encephalitic/encephalopathic epilepsy"]T Yamamoto, Y Nanba, N Kodani, et al.
Biochemical and Biophysical Research Communications|August 5, 1996
A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathyI Nishino, A Seki, Y Maegaki, et al.
No to Hattatsu = Brain and Development|September 1, 1995
[Short somatosensory evoked potentials in patients with Fukuyama type congenital muscular dystrophy--a comparison with CT and MRI findings]Y Namba, Y Maegaki, Y Maeoka, et al.
Developmental Medicine and Child Neurology|March 1, 1997
A novel neurological disorder with progressive CNS calcification, deafness, renal tubular acidosis, and microcytic anemiaM Yoshimura, T Hara, Y Maegaki, et al.
Neuropediatrics|January 20, 2007
Clinical characteristics of acute encephalopathy of obscure origin: a biphasic clinical course is a common featureY Maegaki, A Kondo, R Okamoto, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
No to Hattatsu = Brain and Development|June 8, 2001
[Mitochondrial DNA T to G mutation 8993 in Leigh encephalopathy and organic aciduria]M Ueno, A Oka, Y Maegaki, et al.
Neuropediatrics|February 6, 2010
Fulminant sepsis-associated encephalopathy in two children: serial neuroimaging findings and clinical courseA Kondo, C Sugiura, Y Fujii, et al.
Neuropediatrics|January 20, 2007
Late-onset neuropsychological symptoms in a Japanese patient with megalencephalic leukoencephalopathy with subcortical cystsC Sugiura, M Shiota, Y Maegaki, et al.
Neuropediatrics|June 1, 1997
Mechanisms of central motor reorganization in pediatric hemiplegic patientsY Maegaki, Y Maeoka, S Ishii, et al.
No to Hattatsu = Brain and Development|September 1, 1996
[Computed tomography and magnetic resonance imaging of the brain in congenital rubella syndrome]M Yoshimura, J Tohyama, Y Maegaki, et al.
No to Hattatsu = Brain and Development|July 1, 1995
[Two cases of post-encephalitic epilepsy characterized by auditory cognitive dysfunction; comparison with "a peculiar type of post-encephalitic/encephalopathic epilepsy"]T Yamamoto, Y Nanba, N Kodani, et al.
Biochemical and Biophysical Research Communications|August 5, 1996
A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathyI Nishino, A Seki, Y Maegaki, et al.
No to Hattatsu = Brain and Development|September 1, 1995
[Short somatosensory evoked potentials in patients with Fukuyama type congenital muscular dystrophy--a comparison with CT and MRI findings]Y Namba, Y Maegaki, Y Maeoka, et al.
Developmental Medicine and Child Neurology|March 1, 1997
A novel neurological disorder with progressive CNS calcification, deafness, renal tubular acidosis, and microcytic anemiaM Yoshimura, T Hara, Y Maegaki, et al.
Neuropediatrics|January 20, 2007
Clinical characteristics of acute encephalopathy of obscure origin: a biphasic clinical course is a common featureY Maegaki, A Kondo, R Okamoto, et al.
Pageof 5