Mika Ishige

Unique and abnormal subependymal pseudocysts in a newborn with mitochondrial disease

K. Murayama, N. Nagano, I. Morioka, 2021, Science progress.

Effect of Dedifferentiated Fat Cell Transplantation in a Mouse Model of Acute Graft-Versus-Host Disease

Taro Matsumoto, H. Mugishima, T. Kazama, 2017 .

Blood glucose trends in glycogen storage disease type Ia: A cross‐sectional study

T. Hamazaki, Hironori Kobayashi, Yoriko Watanabe, 2023, Journal of inherited metabolic disease.

Successful cord blood transplantation in a 42-day-old boy with infantile Krabbe disease

H. Mugishima, H. Shichino, M. Chin, 2011, International journal of hematology.

Neonatal Sepsis-Like Syndrome with Human Parechovirus Type 4

H. Ushijima, T. Fuchigami, T. Urakami, 2021, Journal of Nihon University Medical Association.

Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity.

O. Ohara, T. Awaya, E. Naito, 2017, Molecular genetics and metabolism.

Severe rotavirus gastroenteritis in children older than 5 years after vaccine introduction.

S. Okitsu, S. Hayakawa, H. Ushijima, 2020, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Safety, efficacy and pharmacokinetics of palivizumab in off-label neonates, infants, and young children at risk for serious respiratory syncytial virus infection: a multicenter phase II clinical trial

S. Kusuda, Akinari Hinoki, T. Hatata, 2023, The Lancet regional health. Western Pacific.

Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

Y. Kinosada, T. Fukao, Toshiyuki Yamamoto, 2015, International journal of molecular medicine.

Biallelic GALM pathogenic variants cause a novel type of galactosemia

O. Ohara, K. Nakayama, R. Funayama, 2018, Genetics in Medicine.

Clinical perspective on the use of human amniotic epithelial cells to treat congenital metabolic diseases with a focus on maple syrup urine disease

S. Hayakawa, B. Grubbs, I. Morioka, 2021, Stem cells translational medicine.