R. Wate

发表

Regionally different immunoreactivity for Smurf2 and pSmad2/3 in TDP‐43‐positive inclusions of amyotrophic lateral sclerosis

H. Ito, H. Kusaka, S. Kaneko, 2013, Neuropathology and applied neurobiology.

Smad ubiquitination regulatory factor‐2 in progressive supranuclear palsy

S. Nakano, H. Ito, H. Kusaka, 2011, Neuropathology and applied neurobiology.

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis

T. Miki, R. Kaji, H. Nodera, 2009, Journal of the Neurological Sciences.

Expression of an endoplasmic reticulum-resident chaperone, glucose-regulated stress protein 78, in the spinal cord of a mouse model of amyotrophic lateral sclerosis

S. Nakano, H. Kusaka, Hidefumi Ito, 2005, Acta Neuropathologica.

Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis

S. Nakano, H. Kusaka, Hidefumi Ito, 2006, Acta Neuropathologica.

Radio-sensitivity of the cells from amyotrophic lateral sclerosis model mice transfected with human mutant SOD1.

R. Okayasu, H. Kusaka, Hidefumi Ito, 2005, Journal of radiation research.

Intra-bone marrow-bone marrow transplantation slows disease progression and prolongs survival in G93A mutant SOD1 transgenic mice, an animal model mouse for amyotrophic lateral sclerosis

S. Nakano, H. Kusaka, S. Ikehara, 2009, Brain Research.

Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model

S. Nakano, H. Kusaka, Hidefumi Ito, 2008, Acta Neuropathologica.

The first Japanese patient with variant Creutzfeldt‐Jakob disease (vCJD)

S. Nakano, A. Shinde, H. Kusaka, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation

H. Kusaka, H. Kawakami, H. Maruyama, 2014, Neuropathology (Kyoto. 1993).

Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease

R. Takahashi, T. Mizutani, N. Shibata, 2011, Acta Neuropathologica.

Activation of Transforming Growth Factor-β/Smad Signaling Reduces Aggregate Formation of Mislocalized TAR DNA-Binding Protein-43

J. Fujisawa, S. Nakano, H. Kusaka, 2012, Neurodegenerative Diseases.

Efficacy and safety of tacrolimus as long-term monotherapy for myasthenia gravis

H. Kusaka, Y. Yakushiji, T. Kunieda, 2021, Neuromuscular Disorders.

Diagnostic clues and more from photographs

A. Hirano, R. Wate, 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.

Zonisamide ameliorates levodopa-induced dyskinesia and reduces expression of striatal genes in Parkinson model rats

H. Kusaka, S. Morise, Masataka Nakamura, 2017, Neuroscience Research.

Nuclear Contour Irregularity and Abnormal Transporter Protein Distribution in Anterior Horn Cells in Amyotrophic Lateral Sclerosis

S. Nakano, H. Kusaka, Hidefumi Ito, 2009, Journal of neuropathology and experimental neurology.

Treatment with edaravone, initiated at symptom onset, slows motor decline and decreases SOD1 deposition in ALS mice

S. Nakano, H. Ito, H. Kusaka, 2008, Experimental Neurology.

Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats

H. Ito, H. Kusaka, H. Kawakami, 2006, Neurology.

Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation

R. Takahashi, R. Kaji, H. Kusaka, 2011, Acta Neuropathologica.

Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease

S. Nakano, H. Kusaka, Hidefumi Ito, 2008, Acta Neuropathologica.

Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations

R. Takahashi, H. Kusaka, H. Kawakami, 2018, Journal of neuropathology and experimental neurology.

[A case of cerebellar syndrome associated with HIV infection].

S. Nakano, A. Shinde, H. Kusaka, 2009, Rinsho shinkeigaku = Clinical neurology.

Successful treatment of paroxysmal tonic spasms with topiramate in a patient with neuromyelitis optica.

H. Kusaka, S. Iida, Masataka Nakamura, 2015, Multiple sclerosis and related disorders.

Weight loss in the early stage of progressive supranuclear palsy

H. Kusaka, A. Saito, K. Fujita, 2016, Brain and behavior.

Myonuclear breakdown in sporadic inclusion body myositis is accompanied by DNA double strand breaks

S. Nakano, A. Shinde, H. Kusaka, 2011, Neuromuscular Disorders.

Early-onset Parkinson's Disease Associated with Chromosome 22q11.2 Deletion Syndrome.

H. Kusaka, S. Kaneko, R. Wate, 2016, Internal medicine.