Yukiko Mogami
Izumi, Japan
Last Updated: 09/26/2026
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Found 36 publications
Clinical characteristics and anti-ZSCAN1 antibody titer analysis in a nationwide survey of ROHHAD (-NET) syndrome.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 02, 2025
Efficacy and Safety of 5-Aminolevulinic Acid Hydrochloride Combined with Sodium Ferrous Citrate in Pediatric Patients with Leigh Syndrome and Central Nervous System Disorders: An Initial Exploratory Trial with a Double-Blind Placebo-Controlled Period, Followed by an Open-Label Period and a Subsequent Long-Term Administration Study.
Journal: Life (Basel, Switzerland)
Published: June 18, 2025
Contribution of activated complements and CD59 to the pathophysiology of Rasmussen syndrome.
Journal: Journal of neuroimmunology
Published: March 29, 2025
A case of spinal muscular atrophy type 0 treated with nusinersen without progression of early-onset scoliosis - possibility of preventing scoliosis with a rehabilitation program focusing on postural management.
Journal: Brain & development
Published: January 01, 2025
A case of MOG antibody-associated transverse myelitis preceded by headache, fever, and allodynia as early symptoms.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 07, 2024
Childhood-onset epilepsy in patients with dyskinetic cerebral palsy caused by basal ganglia and thalamic lesions.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: June 18, 2023
Newborn screening for spinal muscular atrophy in Osaka -challenges in a Japanese pilot study.
Journal: Brain & development
Published: December 20, 2022
A new diagnostic indication device of a biomarker growth differentiation factor 15 for mitochondrial diseases: From laboratory to automated inspection.
Journal: Journal of inherited metabolic disease
Published: March 22, 2020
Epilepsy in patients with advanced Fukuyama congenital muscular dystrophy.
Journal: Brain & development
Published: January 25, 2020
Vitamin B6 in acute encephalopathy with biphasic seizures and late reduced diffusion.
Journal: Brain & development
Published: November 08, 2019
De novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome.
Journal: Congenital anomalies
Published: October 30, 2018
Last Updated: 09/26/2026