Aoki Masashi | Department of Electrical and Electronic Engineering, National Defense Academy, 1-10-20 Hashirimizu, Yokosuka, Kanagawa 239-8686, Japan

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著作論文

Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome
Dysferlinopathy associated with rigid spine syndrome
Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMA
Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL)
Rapid Screening for Japanese Dysferlinopathy by Fluorescent Primer Extension
Development of a rat model of amyotrophic lateral sclerosis expressing a human SOD1 transgene
Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy
Up-Regulation of Insulin-Like Growth Factor-II Receptor in Reactive Astrocytes in the Spinal Cord of Amyotrophic Lateral Sclerosis Transgenic Rats
Therapeutic Efficacy of Transcranial Magnetic Stimulation for Hereditary Spinocerebellar Degeneration
HyperCKemia Related to the Initial and Recurrent Attacks of Neuromyelitis Optica
FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion
A Case of Late Onset Riboflavin-responsive Multiple Acyl-CoA Dehydrogenase Deficiency Manifesting as Recurrent Rhabdomyolysis and Acute Renal Failure
Neutralizing Antibodies Are Associated with a Reduction of Interferon-β Efficacy during the Treatment of Japanese Multiple Sclerosis Patients
Evaluation of Nematic Liquid Crystal Director Orientation in Vicinity of Glass Substrate Using Shear Horizontal Wave Propagation
Dynamic Response of Shear Horizontal Wave Propagating in Liquid Crystal Cell to Molecular Reorientation
T2-hyperintensity of the Middle Cerebellar Peduncles in a Patient with SCA7
Responses to Hemodynamic Stress in the Aged Heart.
Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure

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