Ryuta Morihara
Okayama, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 88 publications
Ketogenic diet reintroduction in an adult patient with glucose transporter type 1 deficiency syndrome
Journal: Rinsho shinkeigaku = Clinical neurology
Published: August 10, 2026
Direct glia-to-neuron conversion mitigates hippocampal damage in a vascular dementia mouse model.
Journal: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
Published: April 11, 2026
The utility of Gold Coast criteria for amyotrophic lateral sclerosis.
Journal: Journal of the neurological sciences
Published: October 10, 2025
Retraction notice to "Injection of exogenous amyloid-ß oligomers aggravated cognitive deficits, and activated necroptosis, in APP23 transgenic mice". [Brain Res. 1821 (2023) 148565].
Journal: Brain research
Published: October 10, 2025
Real-world evaluation of Armstrong's criteria in corticobasal degeneration: Phenotypic overlap and diagnostic challenges.
Journal: Parkinsonism & related disorders
Published: October 03, 2025
Biallelic CAG repeat expansion in the ATXN2 gene presenting with parkinsonism and spasticity.
Journal: Parkinsonism & related disorders
Published: September 08, 2025
A Case of Retinopathy-Sensory Neuropathy Syndrome With a Novel Compound Heterozygous FLVCR1 Variant.
A Case of Retinopathy-Sensory Neuropathy Syndrome With a Novel Compound Heterozygous FLVCR1 Variant.
Journal: Journal of the peripheral nervous system : JPNS
Published: July 02, 2025
Two Cases of Autosomal Recessive Spinocerebellar Ataxia-8 Showing Two Novel Variants of SYNE1 in Japanese Families.
Journal: Internal medicine (Tokyo, Japan)
Published: June 04, 2025
Comparison of Anatomical Landmarks and Atlas- and Automated Atlas Segmentation Application-Based Targeting in Magnetic Resonance Imaging-Guided Focused Ultrasound Ventralis Intermedius Thalamotomy.
Journal: Operative neurosurgery (Hagerstown, Md.)
Published: May 14, 2025
Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathology.
Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathology.
Journal: Acta neuropathologica
Published: January 23, 2025
Last Updated: 09/26/2026