H. Kusaka

R. Takahashi, H. Kusaka, T. Horibe, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

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

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

Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case

A. Shinde, H. Kusaka, T. Kitamoto, 2021, Neuropathology : official journal of the Japanese Society of Neuropathology.

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.

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan

I. Nishino, R. Kaji, S. Nakano, 2016, Orphanet Journal of Rare Diseases.

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.

Mutations of optineurin in amyotrophic lateral

Takeo Kato, T. Takumi, S. Matsuura, 2010 .

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.

Adult-onset motor neuron disease with basophilic intraneuronal inclusion bodies.

H. Kusaka, T. Imai, S. Matsumoto, 1993, Clinical neuropathology.

Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease

S. Hirai, E. Matsubara, K. Okamoto, 1992, Journal of Neurology.

Mutations of optineurin in amyotrophic lateral sclerosis

Takeo Kato, T. Takumi, S. Matsuura, 2010, Nature.

Optineurin immunoreactivity in neuronal and glial intranuclear inclusions in adult-onset neuronal intranuclear inclusion disease.

M. Murray, D. Dickson, H. Kusaka, 2014, American journal of neurodegenerative disease.

Chordoid meningioma in a child. Case report.

H. Ito, H. Kusaka, A. Kondo, 1998, Journal of neurosurgery.

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

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

Autopsy case of desminopathy involving skeletal and cardiac muscle

A. Shinde, H. Kusaka, R. Tsukamoto, 2007, Pathology international.

Messenger RNA degradation may be inhibited in sporadic inclusion body myositis

S. Nakano, A. Shinde, H. Ito, 2005, Neurology.

Localization of O-GlcNAc-modified proteins in neuromuscular diseases

S. Nakano, H. Kusaka, S. Kaneko, 2012, Medical Molecular Morphology.

Primary interosseous meningioma associated with pregnancy--case report.

H. Kusaka, T. Nishioka, K. Shimotake, 1989, Neurologia medico-chirurgica.

Expression of caveolar components in primary desminopathy

S. Nakano, A. Shinde, H. Kusaka, 2008, Neuromuscular Disorders.

JC virus granule cell neuronopathy associated with Ruxolitinib: A case report and review of the literature

M. Saijo, H. Kusaka, Y. Yakushiji, 2020, eNeurologicalSci.

A case of MOG antibody-positive bilateral optic neuritis and meningoganglionitis following a genital herpes simplex virus infection.

H. Kusaka, I. Nakashima, T. Kunieda, 2017, Multiple sclerosis and related disorders.

Activation of Transforming Growth Factor-beta/Smad Signaling Reduces Aggregate Formation of Mislocalized TAR DNA Binding Protein-43 (P03.182)

J. Fujisawa, H. Kusaka, Hidefumi Ito, 2012 .

α-Tocopherol transfer protein gene: Exon skipping of all transcripts causes ataxia

H. Ito, H. Kusaka, T. Imai, 1997, Neurology.

Nucleolar characteristics of reducing bodies in reducing body myopathy

H. Shibasaki, H. Sawada, S. Nakano, 2004, Acta Neuropathologica.

In situ identification of hepatitis C virus RNA in muscle

S. Nakano, H. Ito, H. Kusaka, 2005, Neurology.

Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial

Y. Itoyama, S. Tsuji, G. Sobue, 2017, The Lancet Neurology.

GCH1 mutations in dopa-responsive dystonia and Parkinson’s disease

Y. Shimo, G. Oyama, N. Hattori, 2018, Journal of Neurology.

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.

Olaf Ansorge, Christian Haass, H. Kretzschmar, 2011, Brain : a journal of neurology.

FUS pathology in basophilic inclusion body disease

D. Munoz, I. Mackenzie, S. Terada, 2009, Acta Neuropathologica.

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

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

Prednisolone-sparing effect of cyclosporin A therapy for very elderly patients with myasthenia gravis

S. Nakano, A. Shinde, H. Kusaka, 2013, Neuromuscular Disorders.

Endodermal epithelial cyst in the prepontine cistern extending into the fourth ventricle--case report.

H. Kusaka, O. Hirai, A. Kondo, 1991, Neurologia medico-chirurgica.

The updated retrospective questionnaire study of sporadic inclusion body myositis in Japan

I. Nishino, R. Kaji, H. Nodera, 2019, Orphanet Journal of Rare Diseases.

An unusual cervical chordoma: CT and MRI

H. Kusaka, K. Hashimoto, K. Yamamoto, 1996, Neuroradiology.

Myouclear Breakdown in Sporadic Inclusion Body Myositis

S. Nakano, H. Kusaka, 2011 .

Epithelium-lined cyst of the pretectal region: case report and electron microscope study.

H. Kusaka, T. Imai, T. Nishioka, 1989, Surgical neurology.

Intracisternal inclusions in Schwann cells of the sural nerve

H. Kusaka, T. Imai, 1992, Acta Neuropathologica.

Histone H1 is released from myonuclei and present in rimmed vacuoles with DNA in inclusion body myositis

Kengo Fujita, S. Nakano, A. Shinde, 2008, Neuromuscular Disorders.

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes

Kenji Nakashima, Eisaku Ohama, Shinsuke Kato, 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

Golgi apparatus and intraneuronal inclusions of anterior horn cells in amyotrophic lateral sclerosis: an immunohistochemical study

H. Kusaka, Hidefumi Ito, T. Imai, 1996, Acta Neuropathologica.

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.

CT, MRI, and autopsy findings in brain of a patient with MELAS.

H. Kusaka, M. Ito, T. Okuno, 1990, Pediatric neurology.

[Angiotropic lymphoma presenting with subacute dementia: treatment with combination chemotherapy (CHOP) based on antemortem diagnosis--a case report].

H. Kusaka, M. Matsuda, K. Fujiyoshi, 1993, Rinshō shinkeigaku Clinical neurology.

Aberrant Accumulation of BRCA1 in Alzheimer Disease and Other Tauopathies.

D. Dickson, H. Kusaka, Masataka Nakamura, 2019, 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.

Striatal efferent involvement and its correlation to levodopa efficacy in patients with multiple system atrophy

H. Kusaka, T. Imai, H Ito, 1996, Neurology.

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

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

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke‐like Episodes

H. Kusaka, T. Okuno, S. Hamazaki, 1989, Acta pathologica japonica.

Thymoma-associated Progressive Encephalomyelitis with Rigidity and Myoclonus (PERM) with Myasthenia Gravis

H. Kusaka, T. Kunieda, S. Morise, 2017, Internal medicine.

[A case of spontaneous superficial temporal artery aneurysm].

H. Kusaka, T. Nishioka, K. Shimotake, 1988, No shinkei geka. Neurological surgery.

Two cases of sporadic adult-onset neuronal intranuclear inclusion disease preceded by urinary disturbance for many years

H. Kusaka, I. Akiguchi, T. Kondo, 2018, Journal of the Neurological Sciences.

Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant

R. Matsumoto, R. Takahashi, S. Nakano, 2014, Acta neuropathologica communications.

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

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

Phrenic nerve conduction in the early stage of Guillain–Barre syndrome might predict the respiratory failure

H. Kusaka, K. Fujita, Y. Takanashi, 2007, Acta neurologica Scandinavica.

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.

Ultrastructural study of chromatolytic neurons in an adult-onset sporadic case of amyotrophic lateral sclerosis

H. Kusaka, T. Yamamoto, M. Yamasaki, 2004, Acta Neuropathologica.

Topographic involvement of the striatal efferents in basal ganglia of patients with adult-onset motor neuron disease with basophilic inclusions

H. Kusaka, Hidefumi Ito, T. Imai, 2004, Acta Neuropathologica.

An adult-onset case of sporadic motor neuron disease with basophilic inclusions

H. Kusaka, T. Imai, S. Matsumoto, 2004, Acta Neuropathologica.

[Successful treatment of neuromyelitis optica spectrum disorder by early initiation of plasma exchange].

H. Kusaka, K. Fujita, S. Kaneko, 2015, Rinshō 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.

Aberrant accumulation of ErbB4 in progressive supranuclear palsy

D. Dickson, H. Kusaka, S. Kaneko, 2018, Neuropathology and applied neurobiology.

Weight loss in the early stage of progressive supranuclear palsy

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

[A comparative immunohistochemical study of ubiquitin-positive skein-like inclusions in anterior horn neurons in subgroups of adult-onset motor neuron diseases].

H. Ito, H. Kusaka, M. Yamasaki, 1993, Rinsho shinkeigaku = Clinical neurology.

Pathology of motor neurons in amyotrophic lateral sclerosis with dementia.

H. Kusaka, T. Imai, 1993, Clinical Neuropathology.

Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-positive Lewy body-like inclusions.

N. Shibata, H. Ito, H. Kusaka, 1996, Clinical neuropathology.

Synaptic pathology of spinal anterior horn cells in amyotrophic lateral sclerosis: An immunohistochemical study

H. Kusaka, S. Goto, Hidefumi Ito, 1994, Journal of the Neurological Sciences.

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

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

Efficacy of pretreatment with the free radical scavenger, edaravone, for prevention of cerebral hyperperfusion after carotid artery stenting: A single-center randomized controlled trial

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

[A Patient with Acute Limbic Encephalitis Associated with Anti-Glutamate Receptor Antibodies and Subsequent Optic Neuritis].

H. Kusaka, Yukitoshi Takahashi, Masataka Nakamura, 2016, Brain and nerve = Shinkei kenkyu no shinpo.

[Neuropathology of the motor neuron disease--Bunina body].

H. Kusaka, 1999, Rinshō shinkeigaku Clinical neurology.

Zonisamide attenuates the severity of levodopa-induced dyskinesia via modulation of the striatal serotonergic system in a rat model of Parkinson's disease

H. Kusaka, Y. Yakushiji, S. Morise, 2021, Neuropharmacology.

Basophilic inclusions in sporadic juvenile amyotrophic lateral sclerosis: an immunocytochemical and ultrastructural study

N. Murakami, H. Kusaka, A. Hirano, 1992, Acta Neuropathologica.

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

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

Our Experience of Muscle Afferent Block for dystonia and spasticity

S. Nakano, H. Kusaka, Hisashi Ito, 2002 .