Kimitoshi Hirayanagi

发表

Noninvasive and quantitative evaluation of movement disorder disability using an infrared depth sensor

Y. Ikeda, Y. Yuminaka, Minori Furuta, 2019, Journal of Clinical Neuroscience.

Putaminal iron deposition precedes MSA-P onset by 2 years

Y. Ikeda, B. Mihara, K. Nagashima, 2018, Neurology.

Encephalopathy with amyloid angiopathy and numerous amyloid plaques with low levels of CSF Aβ1–40/Aβ1–42

K. Okamoto, M. Amari, M. Takatama, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Juvenile-onset Sporadic Amyotrophic Lateral Sclerosis with a Frameshift FUS Gene Mutation Presenting Unique Neuroradiological Findings and Cognitive Impairment.

K. Makioka, Y. Ikeda, N. Furuta, 2016, Internal medicine.

Suppression of the yeast elongation factor Spt4 ortholog reduces expanded SCA36 GGCCUG repeat aggregation and cytotoxicity

Y. Ikeda, N. Furuta, S. Tsukagoshi, 2019, Brain Research.

A middle-aged male suffering from encephalopathy with cerebral amyloid angiopathy (CAA) with amyloid beta (Aβ) presented with initial symptoms of transient consciousness disturbance and left visual field photophobia. Lesions with aberrantly high signal on T2-weighted magnetic resonance imaging (MRI)

K. Okamoto, M. Amari, M. Takatama, 2012 .

Porphyrins ameliorate spinocerebellar ataxia type 36 GGCCTG repeat expansion-mediated cytotoxicity

Y. Ikeda, N. Furuta, S. Tsukagoshi, 2021, Neuroscience Research.

Reversal of leukoencephalopathy induced by liposomal amphotericin B in a patient with cryptococcal meningitis

K. Makioka, Y. Ikeda, Kimitoshi Hirayanagi, 2015, Journal of the Neurological Sciences.

Bilateral striatal necrosis caused by a founder mitochondrial 14459G>A mutation in two independent Japanese families

K. Makioka, Y. Ikeda, H. Takashima, 2017, Journal of the Neurological Sciences.

Response to the letter to the editor regarding an article “Bilateral striatal necrosis caused by a founder mitochondrial 14459G>A mutation in two independent Japanese families”

Y. Ikeda, Kimitoshi Hirayanagi, 2017, Journal of the Neurological Sciences.

Clinical, radiological, and molecular analyses of neuronal intranuclear inclusion disease with polyglycine inclusions

Y. Ikeda, Minori Furuta, S. Tsukagoshi, 2023, Journal of the Neurological Sciences.

Cerebral Microbleeds, Cerebrospinal Fluid, and Neuroimaging Markers in Clinical Subtypes of Alzheimer's Disease

K. Ishii, N. Hattori, Y. Tsushima, 2021, Frontiers in Neurology.

Progressive Pseudolithiasis Associated with the Intravenous Administration of Ceftriaxone in Patients with Central Nervous System Infections

K. Makioka, Y. Ikeda, Kunihiko Ishizawa, 2017, Internal medicine.

A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits.

K. Okamoto, M. Ikeda, M. Amanuma, 2012, Internal medicine.

An Autopsy Case of Fulminant Hepatitis in a Patient with Multiple Sclerosis Treated by Interferon-Beta-1a

M. Yamada, M. Kusano, S. Nobusawa, 2017, Internal medicine.

[A case of neurolymphomatosis presenting extended involvement of spinal nerve roots].

K. Makioka, Y. Ikeda, Minori Furuta, 2015, Rinsho shinkeigaku = Clinical neurology.