Author

Shinichiro Arashima

Observed names: S Arashima, S. Arashima, SHINICHIRO ARASHIMA, Shin-ichiro ARASHIMA, Shinichiro ARASHIMA, Shinichirou Arashima, Shin‐Ichiro Arashima

Institutions: Hokkaido University of Education, Hokkaido University

Observed institutions: Mukogawa Women's University, Hokkaido University of Education, Hokkaido University, Hokkaido University Hospital, Kumamoto University

OpenAlex ID: A5110099641

Urinary Oligosaccharides of Fucosidosis

1978 · Masanori NISHIGAKI, Katsuko YAMASHITA, et al. · The Journal of Biochemistry · 108

Urinary glycopeptides of fucosidosis.

1979 · K. Yamashita, Y. Tachibana, et al. · Journal of Biological Chemistry · 77

PDF

Hyperammonemia Due to a Mutant Enzyme of Ornithine Transcarbamylase

1971 · Ichiro Matsuda, Shinichiro Arashima, et al. · PEDIATRICS · 48

Mass screening for Wilson's disease: Results and recommendations

1999 · Yukitoshi Yamaguchi, Tsugutoshi Aoki, et al. · Pediatrics International · 45

PDF

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

1999 · T. Ohura, D. Abukawa, et al. · Journal of Inherited Metabolic Disease · 41

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

1976 · Ichiro Matsuda, Yogo Oka, et al. · The Journal of Pediatrics · 40

A Case of Carbamyl Phosphate Synthetase Deficiency

1972 · SHINICHIRO ARASHIMA, ICHIRO MATSUDA · The Tohoku Journal of Experimental Medicine · 35

PDF

Ultrastructural Studies in Fetal I-cell Disease

1976 · Kazuhiro Abe, Ichiro Matsuda, et al. · Pediatric Research · 32

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

1998 · Akihiro Yamaguchi, Akihiro Matsuura, et al. · Human Mutation · 29

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

1974 · T. Kajii, I. Matsuda, et al. · Clinical Genetics · 28

Fucosidosis

1973 · ICHIRO MATSUDA, SHINICHIRO ARASHIMA, et al. · The Tohoku Journal of Experimental Medicine · 26

PDF

Prenatal diagnosis of I-cell disease

1975 · Ichiro Matsuda, Shinichiro Arashima, et al. · Human Genetics · 24

Digestion of Asparagine-Linked Oligosaccharides by Endo-β-N-Acetylglucosaminidase in the Human Skin Fibroblasts Obtained from Fucosidosis Patients1

1981 · Yoko TACHIBANA, Katsuko YAMASHITA, et al. · The Journal of Biochemistry · 22

Renal tubular acidosis and skeletal demineralization in patients on long-term anticonvulsant therapy

1975 · Ichiro Matsuda, Yasuo Takekoshi, et al. · The Journal of Pediatrics · 22

Impaired monocyte function in glycogen storage disease type Ib

1986 · N. Ueno, M. Tomita, et al. · European Journal of Pediatrics · 20

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

1973 · Ichiro Matsuda, Shinichiro Arashima, et al. · Clinica Chimica Acta · 18

Determination of triethylenetetramine in plasma of patients by high-performance liquid chromatography.

1990 · Katsumi MIYAZAKI, Satoshi KISHINO, et al. · Chemical and Pharmaceutical Bulletin · 17

PDF

Mutation in a Putative Glycosylation Site (N489T) of Biotinidase in the Only Known Japanese Child with Biotinidase Deficiency

1998 · Robert J. Pomponio, Akihiro Yamaguchi, et al. · Molecular Genetics and Metabolism · 16

Citrate Treatment in a Patient with Pyruvate Decarboxylase Deficiency

1976 · YOGO OKA, ICHIRO MATSUDA, et al. · The Tohoku Journal of Experimental Medicine · 11

PDF

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

1971 · Shinichiro Arashima, Ichiro Matsuda · Biochemical and Biophysical Research Communications · 11

Characterization of neutral glycolipids in Tay‐Sachs brain

1979 · Akira Inagawa, Akira Makita, et al. · Journal of Neurochemistry · 9

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

1982 · K Abe, S Arashima, et al. · Journal of Clinical Pathology · 7

PDF

A defective enzyme in hyperphenylalaninaemia due to biopterin deficiency

1983 · S. Yoshioka, M. Masada, et al. · Journal of Inherited Metabolic Disease · 5

Lysine Intolerance in a Variant Form of Citrullinemia

1979 · Ichro Matsuda, Shinichiro Arashima, et al. · Pediatric Research · 5

Cerebro‐hepato‐renal Syndrome of Zellweger

1986 · Kyoji Nakamura, Toshinao Takenouchi, et al. · Acta Pathologica Japonica · 4

Works count: 37

Citation count: 713

H-index: 17

I10-index: 20