C. Yonee

Association of Acute Cerebellar Ataxia and Human Papilloma Virus Vaccination: A Case Report

S. Kusunoki, Y. Maegaki, H. Hayami, 2013, Neuropediatrics.

Exploratory evaluation of an eye-tracking system in patients with advanced spinal muscular atrophy type I receiving nusinersen

M. Chinen, Minoru Shibata, K. Okanari, 2022, Frontiers in Neurology.

Quantitative computed tomography for enzyme replacement therapy in Pompe disease

E. Nanba, Y. Maegaki, I. Higuchi, 2012, Brain and Development.

A novel STXBP1 mutation causes typical Rett syndrome in a Japanese girl

T. Matsuishi, N. Matsumoto, Tomoko Saikusa, 2018, Brain and Development.

Systemic administration of the antisense oligonucleotide NS‐089/NCNP‐02 for skipping of exon 44 in patients with Duchenne muscular dystrophy: Study protocol for a phase I/II clinical trial

Y. Aoki, Y. Asahina, E. Hida, 2023, medRxiv.

Vertebral fusion in a patient with supernumerary‐der(22)t(11;22) syndrome

Y. Maegaki, Toshiyuki Yamamoto, Y. Kawano, 2009, American journal of medical genetics. Part A.

Somatic mosaicism for a SLC2A1 mutation: implications for genetic counseling for GLUT1 deficiency syndrome

H. Oguni, M. Matsufuji, N. Sano, 2017, Clinical genetics.

Effects of Vagus Nerve Stimulation on Sustained Seizure Clusters: A Case Report

T. Otsubo, K. Yoshimoto, R. Hanaya, 2021, NMC case report journal.