S. Arashima

发表

Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics

H. Shiraishi, K. Tada, A. Yamaguchi, 1999, Journal of Inherited Metabolic Disease.

The effects of oral alanine administration on blood glucose, pyruvate, lactate, serum glucagon and insulin in human newborns

T. Mitsuyama, S. Arashima, I. Matsuda, 1977, European Journal of Pediatrics.

Inherited Copper Toxicity in Long-Evans Cinnamon Rats Exhibiting Spontaneous Hepatitis: A Model of Wilson's Disease

N. Kasai, N. Takeichi, T. Takahashi, 1992, Pediatric Research.

Mutation in a putative glycosylation site (N489T) of biotinidase in the only known Japanese child with biotinidase deficiency.

B. Wolf, J. Hymes, A. Yamaguchi, 1998, Molecular genetics and metabolism.

Ornithine transcarbamylase, an isoelectric point (pI) isozyme in human liver and its deficiency.

S. Arashima, I. Matsuda, 1971, Biochemical and biophysical research communications.

Ultrastructural Studies in Fetal I-cell Disease

K. Abe, M. Ishikawa, T. Mitsuyama, 1976, Pediatric Research.

A case of carbamyl phosphate synthetase deficiency.

S. Arashima, I. Matsuda, 1972, The Tohoku journal of experimental medicine.

CEREBRO‐HEPATO‐RENAL SYNDROME OF ZELLWEGER

T. Takenouchi, M. Aizawa, S. Arashima, 1986 .

Leukocyte glutathione peroxidase deficiency in a male patient with chronic granulomatous disease.

N. Taniguchi, T. Mitsuyama, S. Arashima, 1976, The Journal of pediatrics.

Urinary oligosaccharides of fucosidosis. Evidence of the occurrence of X-antigenic determinant in serum-type sugar chains of glycoproteins.

A. Kobata, K. Yamashita, M. Nishigaki, 1978, Journal of biochemistry.

α-l-Fucosidase and α-d-mannosidase activity in the white blood cells in the disease and carrier state of fucosidosis

S. Arashima, I. Matsuda, Y. Oka, 1973 .

Urinary glycopeptides of fucosidosis.

A. Kobata, K. Yamashita, Y. Tachibana, 1979, The Journal of biological chemistry.

Mass screening for Wilson’s disease: Results and recommendations

F. Endo, T. Kitagawa, G. Takada, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

Prenatal diagnosis of I-cell disease

Y. Kaneko, M. Ishikawa, T. Mitsuyama, 1975, Humangenetik.

Hyperlipidaemia during persistent peritoneal dialysis.

A. Takase, S. Arashima, I. Matsuda, 1972, Archives of disease in childhood.

Osmolalities of infant formulas in Japan.

S. Arashima, I. Matsuda, M. Kamimura, 1977, American journal of diseases of children.

Hurler/Scheie genetic compound (mucopolysaccharidosis IH/IS) in Japanese brothers

I. Matsuda, T. Ohsawa, T. Kajii, 1974, Clinical genetics.

Metabolic acidosis in patients receiving anticonvulsants

T. Kondo, N. Taniguchi, T. Mitsuyama, 1979, European Journal of Pediatrics.

Tricho-rhino-phalangeal syndrome

T. Ohsawa, Naoki Fukushima, S. Arashima, 1976, Human Genetics.

Mutations of ATP7B gene in wilson disease in Japan: Identification of nine mutations and lack of clear founder effect in a Japanese population

A. Yamaguchi, K. Kikuchi, A. Matsuura, 1998, Human mutation.

Histidinemia. Classical and atypical form in siblings.

S. Arashima, I. Matsuda, Y. Oka, 1975, American journal of diseases of children.

Transient Hyperalaninemia and Hyperpyruvic Acidemia

T. Mitsuyama, S. Arashima, I. Matsuda, 1975 .

Application of the New Oral Pancreatic Exocrine Function Test “PFD” Test in Children—Normal Values in Children—

Y. Yamashiro, T. Konno, Y. Tazawa, 1984 .

Distribution pattern of lysosomal granules in fibroblasts of the Chediak-Higashi syndrome.

S. Arashima, M. Honma, K. Abe, 1982, Journal of clinical pathology.

Chediak-Higashi syndrome . granules in fibroblasts of the Distribution pattern of lysosomal

S. Arashima, M. Honma, K. Abe, 2022 .

A variant form of citrullinemia.

Y. Saito, S. Arashima, I. Matsuda, 1976, The Journal of pediatrics.

Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.

Y. Takekoshi, S. Arashima, I. Matsuda, 1971, Pediatrics.

Lysine Intolerance in a Variant Form of Citrullinemia

I. Akaboshi, N. Nagata, S. Arashima, 1979, Pediatric Research.

Metabolic acidosis in patients receiving anticonvulsants

T. Kondo, M. Homma, N. Taniguchi, 1979, Pediatric Research.

[Diagnosis of biliary atresia].

S. Arashima, 1975, [Hokkaido igaku zasshi] The Hokkaido journal of medical science.

A defective enzyme in hyperphenylalaninaemia due to biopterin deficiency

T. Seki, M. Akino, M. Masada, 1983, Journal of Inherited Metabolic Disease.

Digestion of asparagine-linked oligosaccharides by endo-beta-N-acetylglucosaminidase in the human skin fibroblasts obtained from fucosidosis patients.

A. Kobata, K. Yamashita, Y. Tachibana, 1981, Journal of biochemistry.

Citrate treatment in a patient with pyruvate decarboxylase deficiency.

T. Mitsuyama, S. Arashima, I. Matsuda, 1976, Tohoku journal of experimental medicine.