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Department Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Univers | 論文
- Consideration on the methodology of a simple and effective birth defect monitoring system
- Synaptotagmin I hypothalamic knockdown prevents amygdaloid seizure-induced damage of hippocampal neurons but not of entorhinal neurons
- Antisense in vivo knockdown of synaptotagmin I and synapsin I by HVJ-liposome mediated gene transfer modulates ischemic injury of hippocampus in opposing ways
- A Japanese girl with leukoencephalopathy with vanishing white matter
- Arthrogryposis multiplex congenita with callosal agenesis and dentato-olivary dysplasia
- A Japanese case of infantile sialic acid storage disease
- Activity of neurons in ventrolateral respiratory groups during swallowing in decerebrate rats
- Brainstem and spinal projections of augmenting expiratory neurons in the rat
- Morphology of the decrementing expiratory neurons in the brainstem of the rat
- Brain MRI findings of older patients with Pallister-Killian syndrome
- Laryngeal dystonia in xeroderma pigmentosum
- DETECTION OF REGIONAL CARDIAC WALL MOTION ABNORMALITIES BY CARDIAC WALL KYMOGRAPHY : Echocardiography II : IIIrd Auditorium : Proceedings of the 43rd Annual Meeting of the Japanese Circulation Society, Tokyo, 1979
- Cortical gray matter lesions in acute encephalopathy with febrile convulsive status epilepticus
- Immunohistochemical expression of fibroblast growth factor (FGF)-2 in epilepsy-associated malformations of cortical development (MCDs)
- Transcranial magnetic stimulation in an adrenoleukodystrophy patient
- Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
- Apoptosis Involved in Density-dependent Regulation of Rat Fibroblastic 3Y1 CellCulture
- Perspective of Child Neurology in Japan
- Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia
- Increased expression of β-hexosaminidase α chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I