Katsuya Nakamura

Senior Assistant Professor

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Articles (16)

Collaborators (3)

Makoto Urushitani

Shiga University of Medical Science

Takayoshi Shimohata

Gifu University

Koichiro Kuwahara

Shinshu University

Katsuya Nakamura

Research Interests

Explore related searches

Contact this professor

Articles (16)

Collaborators (3)

Makoto Urushitani

Takayoshi Shimohata

Koichiro Kuwahara

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Katsuya Nakamura

Research Interests

Explore related searches

Contact this professor

Articles (16)

HTRA1-related cerebral small-vessel disease causes cerebral microbleeds on the brainstem surface

A unique electro-contact-free sensing for illegal drug methamphetamine determination by electrochemiluminescence based on wireless power transmission technology

Auditory Neuropathy Spectrum Disorder Progressing with Motor and Sensory Neuropathy Caused by an <i>ATP1A1</i> Variant

Functional evaluation of novel variants of <i>B4GALNT1</i> in a patient with hereditary spastic paraplegia and the general population

Genetic counselling for at-risk family members with hereditary transthyretin amyloidosis: data from a single-centre study

Lysinuric protein intolerance exhibiting renal tubular acidosis/Fanconi syndrome in a Japanese woman

Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease

Severe Cerebral Small Vessel Disease Caused by the Uniallelic p.A252T Variant ofHTRA1

Long-term Observation of a Japanese Patient with a Multiple-system Neurodegenerative Disorder with a Uniallelic de novo Missense Variant in KIF1A

Tongue Hemiatrophy in Multifocal Motor Neuropathy

Tongue Hemiatrophy in Multifocal Motor Neuropathy

Clinical Features and Neuroimaging Findings of Neuropil Antibody–Positive Idiopathic Sporadic Ataxia of Unknown Etiology

Moyamoya Disease-like Cerebrovascular Stenotic Lesions Are an Important Phenotype of POEMS Syndrome-associated Vasculopathy

Genetic counseling and predictive testing for hereditary neuromuscular diseases,遺伝性神経疾患の遺伝カウンセリングと発症前診断

Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis

Collaborators (3)

Makoto Urushitani

Takayoshi Shimohata

Koichiro Kuwahara

How do I reach out?

Meet Kite AI