Mika Hayashi

High-resolution photoreceptor imaging analysis of patients with autosomal dominant retinitis pigmentosa (adRP) caused by HK1 mutation

K. Yamaki, S. Kameya, Hiroshi Takahashi, 2020, Ophthalmic genetics.

Metabolomics for improved treatment monitoring of phenylketonuria: urinary biomarkers for non-invasive assessment of dietary adherence and nutritional deficiencies.

P. Britz‐McKibbin, Mika Hayashi, M. Shanmuganathan, 2019, The Analyst.

The Role of miR-217-5p in the Puromycin Aminonucleoside-Induced Morphological Change of Podocytes

H. Owada, O. Ishibashi, T. Inui, 2022, Non-coding RNA.

Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation

K. Yamaki, S. Kameya, Hiroshi Takahashi, 2021, Ophthalmic genetics.