Hiroaki Hanafusa

Influence of UGT1A1 Genetic Variants on Free Bilirubin Levels in Japanese Newborns: A Preliminary Study

K. Nozu, Shohei Ohyama, K. Fujioka, 2022, International journal of environmental research and public health.

Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis

Y. Fukushima, Kyoko Takano, Y. Nakazawa, 2021, American journal of medical genetics. Part A.

A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy

K. Nozu, K. Iijima, N. Morisada, 2020, Human Genome Variation.

Dravet syndrome and hemorrhagic shock and encephalopathy syndrome associated with an intronic deletion of SCN1A

K. Nozu, H. Nagase, H. Yamaguchi, 2023, Brain and Development.

Impact after the Change from Voluntary to Universal Oral Rotavirus Vaccination on Consecutive Emergency Department Visits for Acute Gastroenteritis among Children in Kobe City, Japan (2016–2022)

H. Awano, K. Nozu, I. Morioka, 2022, Vaccines.

The smallest de novo 20q11.2 microdeletion causing intellectual disability and dysmorphic features

N. Okamoto, Toshiyuki Yamamoto, K. Nozu, 2017, Human Genome Variation.

Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease

Katsuya Nakamura, Y. Sekijima, K. Kuwahara, 2023, Molecular genetics and metabolism reports.