Saori Kinjo

Vitamin D deficiency rickets caused by improper lifestyle in Japanese children

K. Miyako, H. Kohno, Saori Kinjo, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997–2017

K. Ihara, S. Ida, K. Ozono, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7

H. Okano, K. Ihara, T. Hara, 2016, Nature Genetics.

Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism.

T. Ogata, A. Umezawa, K. Hata, 2014, Fertility and sterility.

Two cases of Allgrove syndrome with mutations in the AAAS gene.

Toshiaki Tanaka, K. Miyako, H. Kohno, 2004, Endocrine journal.

Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease

N. Matsumoto, Y. Tsurusaki, M. Morimoto, 2015, Brain and Development.

Utility of point-of-care Gram stain by physicians for urinary tract infection in children ≤36 months

M. Matsushima, Toshifumi Yodoshi, T. Taniguchi, 2019, Medicine.