K. Wagatsuma

Prenatal diagnosis of Hurler's syndrome—Biochemical studies on the affected fetus

K. Abo, T. Nakao, S. Tsugawa, 2004, Human Genetics.

A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling

A. Tsuchiyama, N. Tachi, T. Nakao, 1983, Journal of Inherited Metabolic Disease.

Comparative enzymology of eleven acid hydrolases in cultured amniotic fluid cells, skin fibroblasts and embryonic lung fibroblasts, and the respective changes with the increasing age of the cell cultures.

Y. Ishikawa, T. Nakao, S. Tsugawa, 1985, The Tohoku journal of experimental medicine.

A new type of hyperlysinaemia due to a transport defect of lysine into mitochondria

A. Tsuchiyama, T. Nakao, S. Tsugawa, 1986, Journal of Inherited Metabolic Disease.

Heparan sulfate and dermatan sulfate from the liver of a patient with Hurler syndrome: high performance liquid chromatography of their degradation products after incubation with alpha-L-iduronidase-deficient fibroblasts.

Y. Ishikawa, C. Igarashi, T. Nakao, 1984, Clinica chimica acta; international journal of clinical chemistry.

Activities of sulfatases for the degradation of acidic glycosaminoglycans in cultured skin fibroblasts from two siblings with multiple sulfatase deficiency.

N. Tachi, T. Orii, T. Nakao, 1983, Clinica chimica acta; international journal of clinical chemistry.

Properties of α-l-iduronidase in cultured skin fibroblasts from α-l-iduronidase-deficient patients

Y. Ishikawa, T. Nakao, S. Tsugawa, 2004, Human Genetics.

The mechanism of hyperammonaemia and hyperornithinaemia in the syndrome of hyperornithinaemia, hyperammonaemia with homocitrullinuria

A. Tsuchiyama, Y. Itakura, T. Nakao, 1983, Journal of Inherited Metabolic Disease.

Complementation analysis of beta-galactosidase deficiency by means of histochemical method.

Y. Ishikawa, T. Nakao, S. Tsugawa, 1985, The Tohoku journal of experimental medicine.