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Nobuhiro Arai

Tohoku University

13

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269

Citations

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Diagnosis of variant forms of hyperphenylalaninemia using filter paper spots of urine

1983 The Journal of Pediatrics
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Citations (12)
Glycogen Storage Disease Type 1b: Microsomal Glucose-6-Phosphatase System in Two Patients with Different Clinical Findings

1983 Pediatric Research
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Citations (32)
Differential diagnosis of variant forms of hyperphenylalaninaemia by urinary pterins

1983 Journal of Inherited Metabolic Disease
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Pyruvate decarboxylase deficiency in a patient with Leigh's encephalomyelopathy.

1982 Tohoku Journal of Experimental Medicine
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Citations (18)
Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase

1982 Journal of Inherited Metabolic Disease
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Citations (6)
Diagnosis of Dihydropteridine Reductase Deficiency by Erythrocyte Enzyme Assay

1981 Pediatrics
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Citations (19)
Dihydropteridine reductase deficiency: diagnosis by leukocyte enzyme assay

1980 Clinica Chimica Acta
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Citations (26)
Effect of adenosine deaminase replacement therapy on a child of adenosine deaminase deficiency with severe combined immunodeficiency disease.

1979 Tohoku Journal of Experimental Medicine
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Citations (3)
INCLUSION BODIES IN PANETH CELLS IN ZINC DEFICIENCY

1979 The Lancet
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Citations (8)
[A case of autoimmune hemolytic anemia with anti-D specificity in an infant].

1976 The Japanese journal of clinical hematology
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Citations (1)