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Results of search for 'au:"MATSUDA, I"', page 22 of 31
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Authors
Akaboshi, I
Arashima, S
Endo, F
Furuse, A
Hattori, S
Higashi, A
Hoshide, R
Indo, Y
Kitano, A
Matsuda, I
Matsuura, T
Mitsubuchi, H
Motohara, K
Nagata, N
Nishiyama, S
Nobukuni, Y
Nunoi, H
Ohta, T
Ohtani, Y
Tsuchiya, H
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421.
Carnitine status and blood ammonium levels in low birth weight infants.
[electronic resource]
by
Nakamura, T
Nakamura, S
Kondo, Y
Ikeda, T
Ogata, T
Endo, F
Matsuda, I
Producer:
19900518
In:
Journal of pediatric gastroenterology and nutrition
vol. 10
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422.
Unusual case of diffuse connective tissue disease with nodule formations in muscle, lung, kidney and brain.
[electronic resource]
by
Nobukuni, Y
Miike, T
Ohtani, Y
Tsuchiya, H
Nunoi, H
Hattori, S
Matsuda, I
Producer:
19860606
In:
Brain & development
vol. 8
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423.
Insulin receptor of erythrocytes and glucose metabolism in uremic children.
[electronic resource]
by
Namikawa, T
Namikawa, T
Fujimoto, S
Furuse, A
Hattori, S
Matsuda, I
Nakahara, C
Ito, H
Producer:
19830811
In:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
vol. 15
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424.
Measurement of blood holoceruloplasmin by EIA using a mouse monoclonal antibody directed to holoceruloplasmin. Implication for mass screening of Wilson disease.
[electronic resource]
by
Endo, F
Taketa, K
Nakamura, K
Awata, H
Tanoue, A
Eda, Y
Matsuda, I
Producer:
19950302
In:
Journal of inherited metabolic disease
vol. 17
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425.
Exogenously expressed granulocyte colony-stimulating factor (G-CSF) receptor on K562 cells can transduce G-CSF-triggered growth and differentiation signals.
[electronic resource]
by
el-Sonbaty, S S
Watanabe, M
Hochito, K
Yamaguchi, K
Matsuda, I
Tsuchiya, H
Producer:
19950606
In:
International journal of hematology
vol. 61
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426.
Irradiated fetal thymus transplantation in a patient with combined immunodeficiency with predominant T cell defect.
[electronic resource]
by
Higuchi, S
Yanabe, Y
Tsuchiya, H
Akahoshi, I
Udaka, K
Migita, M
Matsuda, I
Producer:
19930423
In:
Acta paediatrica Japonica : Overseas edition
vol. 35
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427.
Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria.
[electronic resource]
by
Nakazato, H
Yoshimuta, J
Karashima, S
Matsumoto, S
Endo, F
Matsuda, I
Hattori, S
Producer:
19990217
In:
Kidney international
vol. 55
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428.
Prenatal diagnosis of I-cell disease.
[electronic resource]
by
Matsuda, I
Arashima, S
Mitsuyama, T
Oka, Y
Ikeuchi, T
Kaneko, Y
Ishikawa, M
Producer:
19760126
In:
Humangenetik
vol. 30
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429.
Blood ammonium level in low birth weight infants in relation to arginine intake.
[electronic resource]
by
Nakamura, S
Kondo, Y
Ogata, T
Iribe, K
Kudo, Y
Ikeda, T
Matsuda, I
Producer:
19890508
In:
Acta paediatrica Japonica : Overseas edition
vol. 30
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430.
Primary structure and gene localization of human prolidase.
[electronic resource]
by
Endo, F
Tanoue, A
Nakai, H
Hata, A
Indo, Y
Titani, K
Matsuda, I
Producer:
19890425
In:
The Journal of biological chemistry
vol. 264
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431.
Clinicopathological correlation of IgA nephropathy in children.
[electronic resource]
by
Hattori, S
Karashima, S
Furuse, A
Terashima, T
Hiramatsu, M
Murakami, M
Matsuda, I
Producer:
19850726
In:
American journal of nephrology
vol. 5
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432.
Structural organization of the gene for CD40 ligand: molecular analysis for diagnosis of X-linked hyper-IgM syndrome.
[electronic resource]
by
Shimadzu, M
Nunoi, H
Terasaki, H
Ninomiya, R
Iwata, M
Kanegasaka, S
Matsuda, I
Producer:
19950126
In:
Biochimica et biophysica acta
vol. 1260
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433.
Prenatal diagnosis of ornithine transcarbamylase deficiency by using a single nucleated erythrocyte from maternal blood.
[electronic resource]
by
Watanabe, A
Sekizawa, A
Taguchi, A
Saito, H
Yanaihara, T
Shimazu, M
Matsuda, I
Producer:
19980818
In:
Human genetics
vol. 102
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434.
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiency.
[electronic resource]
by
Hata, A
Matsuura, T
Setoyama, C
Shimada, K
Yokoi, T
Akaboshi, I
Matsuda, I
Producer:
19910702
In:
Human genetics
vol. 87
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435.
Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene.
[electronic resource]
by
Hata, A
Setoyama, C
Shimada, K
Takeda, E
Kuroda, Y
Akaboshi, I
Matsuda, I
Producer:
19890809
In:
American journal of human genetics
vol. 45
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436.
[Effects of halothane on sensory evoked potentials].
[electronic resource]
by
Miyamoto, T
Ryu, H
Yokoyama, T
Uemura, K
Nakajima, S
Matsuda, I
Ikeda, K
Producer:
19861103
In:
No to shinkei = Brain and nerve
vol. 38
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437.
Effect of pyridoxal 5-phosphate on the activity of GOT isozyme in plasma from patients with Duchenne muscular dystrophy.
[electronic resource]
by
Ohno, H
Taniguchi, N
Terayama, K
Hirata, F
Kawarabayashi, T
Miyoshino, S
Matsuda, I
Producer:
19820212
In:
The Tohoku journal of experimental medicine
vol. 135
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438.
Structural and functional differences of subspecies of apoA-I-containing lipoprotein in patients with plasma cholesteryl ester transfer protein deficiency.
[electronic resource]
by
Ohta, T
Nakamura, R
Takata, K
Saito, Y
Yamashita, S
Horiuchi, S
Matsuda, I
Producer:
19950818
In:
Journal of lipid research
vol. 36
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439.
The heparin-bound fraction of human lipoprotein-deficient serum inhibits endocytic uptake of oxidized low density lipoprotein by macrophages.
[electronic resource]
by
Suginohara, Y
Miyazaki, A
Hakamata, H
Sakamoto, Y
Ohta, T
Matsuda, I
Horiuchi, S
Producer:
19960718
In:
Atherosclerosis
vol. 120
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440.
Deficiency of the E1 beta subunit in the branched-chain alpha-keto acid dehydrogenase complex due to a single base substitution of the intron 5, resulting in two alternatively spliced mRNAs in a patient with maple syrup urine disease.
[electronic resource]
by
Hayashida, Y
Mitsubuchi, H
Indo, Y
Ohta, K
Endo, F
Wada, Y
Matsuda, I
Producer:
19940322
In:
Biochimica et biophysica acta
vol. 1225
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