I. Matsuda

发表

The effect of vitamin D on trasport of L-histidine by intestine.

M. Sugai, I. Matsuda, 1968, Biochimica et biophysica acta.

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.

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

K. Fujieda, N. Shida, Y. Takekoshi, 1975, The Journal of pediatrics.

Renal acid excretion in patients with hypogammaglobulinemia

N. Shida, Naoki Fukushima, Y. Takekoshi, 1972 .

Actinomycin D inhibition of intestinal transport of L-histidine and of vitamin D action

M. Sugai, I. Matsuda, 2005, Experientia.

Urinary hydroxyproline excretion and growth in children with congenital heart disease.

H. Kojima, I. Matsuda, K. Yamamoto, 1972, Clinica chimica acta; international journal of clinical chemistry.

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

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

INTRAVENOUS GAMMAGLOBULIN AND REDUCTION OF CORONARY ARTERY ABNORMALITIES IN CHILDREN WITH KAWASAKI DISEASE

K. Iribe, I. Matsuda, S. Nishihara, 1988, The Lancet.

Ultrastructural Studies in Fetal I-cell Disease

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

Effects of aspartic acid and orotic acid upon serum bilirubin level in newborn infants.

I. Matsuda, T. Shirahata, 1966, The Tohoku journal of experimental medicine.

Correspondence

F. Endo, T. Ueno, I. Matsuda, 1978 .

A case of carbamyl phosphate synthetase deficiency.

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

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.

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.

Red cell count in hereditary spherocytosis with nephrotic hypercholesterolemia.

A. Takase, I. Matsuda, 1975, The Tohoku journal of experimental medicine.

-glucruonidase activity in the stool of the newborn infant.

M. Takimoto, I. Matsuda, 1971, Biology of the neonate.

Osmolalities of infant formulas in Japan.

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

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.

Follow-up study of a nation-wide neonatal metabolic screening program in Japan

Y. Kuroda, K. Tada, T. Kitagawa, 1984, European Journal of Pediatrics.

Intellectual development in patients with untreated histidinemia

Y. Kuroda, K. Tada, T. Kitagawa, 1982 .

Intellectual development in patients with untreated histidinemia. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan.

Y. Kuroda, K. Tada, T. Kitagawa, 1982, Jornal de Pediatria.

Histidinemia. Classical and atypical form in siblings.

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

Intestinal disaccharidase activity in an infant with lactose intolerance.

I. Matsuda, H. Yoshioka, S. Arashima, 1971, Helvetica paediatrica acta.

Oculocerebrorenal syndrome in a child with a normal urinary acidification and a defect in bicarbonate reabsorption.

M. Sugai, I. Matsuda, T. Takeda, 1969, American journal of diseases of children.

Urinary acidification in children.

N. Shida, I. Matsuda, T. Takeda, 1968, Clinica chimica acta; international journal of clinical chemistry.

Mild renal tubular acidosis in a patient with short stature.

N. Shida, Y. Takekoshi, I. Matsuda, 1973, Tohoku journal of experimental medicine.

Ornithine loading test in Lowe's syndrome.

T. Kajii, M. Sugai, I. Matsuda, 1970, The Journal of pediatrics.

Renal reabsorption and excretion of bicarbonate in normal children.

N. Shida, I. Matsuda, 1969, Clinica chimica acta; international journal of clinical chemistry.

Urinary hydroxyproline excretion in normal Japanese children.

I. Matsuda, K. Yamamoto, 1968, Clinica chimica acta; international journal of clinical chemistry.

Treatment of phenylketonuria with a formula consisting of low-phenylalanine peptide. A collaborative study.

K. Tada, T. Kitagawa, M. Owada, 1987, Enzyme.

Transient Hyperalaninemia and Hyperpyruvic Acidemia

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

A case of renovascular hypertension with the nephrotic syndrome.

Y. Takekoshi, K. Itakura, I. Matsuda, 1971, Japanese circulation journal.

Nephrotic syndrome and spherocytosis.

N. Shida, A. Takase, I. Matsuda, 1969, Lancet.

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.

Metabolic acidosis in patients receiving anticonvulsants

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

Rapid detection of Pseudomonas glumae

I. Matsuda, 1990 .

Laboratory findings in a child with pseudo-vitamin D deficiency rickets.

T. Ohsawa, M. Sugai, I. Matsuda, 1969, Helvetica paediatrica acta.

Decreased carnitine and increased ammonia—Which comes first?

T. Nakamura, I. Matsuda, 1990 .

BILIRUBIN METABOLISM IN NEWBORNS

I. Matsuda, T. Shirahata, 1967 .

Phenobarbitone treatment in haemolytic jaundice.

A. Takase, I. Matsuda, 1969, Lancet.

Citrate treatment in a patient with pyruvate decarboxylase deficiency.

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

Glutaminase activity in the kidney of experimental nephrosis.

N. Shida, I. Matsuda, T. Takeda, 1974, The Tohoku journal of experimental medicine.