Kyoko Kiyota

Metabolome Characteristics of Liver Autophagy Deficiency under Starvation Conditions in Infancy

K. Ihara, T. Hanada, K. Sakai, 2021, Nutrients.

Auto-immune disorders in a child with PIK3CD variant and 22q13 deletion.

K. Ihara, K. Yoshiura, S. Korematsu, 2018, European journal of medical genetics.

Leucyl-tRNA synthetase deficiency systemically induces excessive autophagy in zebrafish

K. Ihara, T. Ishitani, H. Shiraishi, 2021, Scientific Reports.

A transient myelodysplastic/myeloproliferative neoplasm in a patient with cardio‐facio‐cutaneous syndrome and a germline BRAF mutation

T. Maeda, Y. Matsubara, Y. Aoki, 2013, American journal of medical genetics. Part A.

Renal lesions mimicking acute focal bacterial nephritis in pediatric leukemia.

K. Ihara, S. Suenobu, Kyoko Kiyota, 2021, Pediatrics International.

A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess

K. Ihara, K. Ozono, T. Kubota, 2020, CEN Case Reports.

Rituximab-induced serum sickness in a girl with nephrotic syndrome

K. Ihara, K. Sekiguchi, Kyoko Kiyota, 2022, CEN Case Reports.