Y. Mizuno

Hereditary antithrombin III deficiency with a superior sagittal sinus thrombosis: evidence for a possible mutation starting in the mother of the propositus.

S. Ikemoto, S. Muramatsu, Y. Mizuno, 1990, Thrombosis research.

A novel threonine to proline mutation in the helix termination motif of keratin 1 in epidermolytic hyperkeratosis with severe palmoplantar hyperkeratosis and contractures of the digits

Y. Suga, H. Yaguchi, H. Ogawa, 2005, The British journal of dermatology.

A Japanese case of naevoid basal cell carcinoma syndrome associated with segmental vitiligo

S. Imakado, Y. Suga, H. Ogawa, 2005, The British journal of dermatology.

A case of a Japanese neonate with congenital ichthyosiform erythroderma diagnosed as Netherton syndrome

T. Shimizu, Y. Suga, S. Ikeda, 2006, Clinical and experimental dermatology.

A Japanese infant with localized ichthyosis linearis circumflexa on the palms and soles harbouring a compound heterozygous mutation in the SPINK5 gene

T. Shimizu, Toshiaki Shimizu, Y. Suga, 2005, The British journal of dermatology.

Multiple ulcers of the ileum due toCytomegalovirus infection in a patient who showed no evidence of an immunocompromised state

M. Hirose, Hironori Tanaka, S. Taniwaki, 1997, Journal of Gastroenterology.