Hiroya Ono
Sendai, 9808574, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations.
Journal: Stem cell reports
Published: July 17, 2020
AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: September 13, 2019
The genetic profile of dysferlinopathy in a cohort of 209 cases: Genotype-phenotype relationship and a hotspot on the inner DysF domain.
Journal: Human mutation
Published: September 01, 2019
The updated retrospective questionnaire study of sporadic inclusion body myositis in Japan.
Journal: Orphanet journal of rare diseases
Published: February 10, 2019
Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons.
Journal: EBioMedicine
Published: November 30, 2018
Aberrant astrocytic expression of chondroitin sulfate proteoglycan receptors in a rat model of amyotrophic lateral sclerosis.
Journal: Journal of neuroscience research
Published: October 12, 2016
Multicenter questionnaire survey for sporadic inclusion body myositis in Japan.
Journal: Orphanet journal of rare diseases
Published: February 20, 2016
Case of cardiac tamponade during the treatment of acute cerebral infarction
Journal: Rinsho shinkeigaku = Clinical neurology
Published: April 08, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026