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Results of search for 'au:"MATSUDA, I"', page 20 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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381.
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this region.
[electronic resource]
by
Mitsubuchi, H
Nobukuni, Y
Akaboshi, I
Indo, Y
Endo, F
Matsuda, I
Producer:
19910507
In:
The Journal of clinical investigation
vol. 87
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382.
Isolation and characterization of the human ornithine transcarbamylase gene: structure of the 5'-end region.
[electronic resource]
by
Hata, A
Tsuzuki, T
Shimada, K
Takiguchi, M
Mori, M
Matsuda, I
Producer:
19870109
In:
Journal of biochemistry
vol. 100
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383.
Analysis of cell proteins in lymphoblasts of acute lymphocytic leukemia by two-dimensional gel electrophoresis.
[electronic resource]
by
Tsuchiya, H
Migita, M
Nunoi, H
Adachi, N
Matsuda, I
Takeda, T
Producer:
19870730
In:
Acta haematologica
vol. 77
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384.
Zinc status of untreated histidinemic children.
[electronic resource]
by
Kitano, A
Higashi, A
Nagata, N
Matsuda, I
Hase, Y
Oura, T
Producer:
19851101
In:
Journal of pediatric gastroenterology and nutrition
vol. 4
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385.
Biochemical nature of pyruvate dehydrogenase complex in the patient with primary lactic acidaemia.
[electronic resource]
by
Kitano, A
Endo, F
Kuroda, Y
Aso, S
Kawasaki, T
Matsuda, I
Producer:
19900322
In:
Journal of inherited metabolic disease
vol. 12
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386.
Sex-determining region Y (SRY) in a patient with 46,XX true hermaphroditism.
[electronic resource]
by
Tanoue, A
Nakamura, T
Endo, F
Nishiyama, S
Sakiyama, H
Matsuda, I
Producer:
19930506
In:
The Japanese journal of human genetics
vol. 37
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387.
Lactose intolerance associated with cataracts.
[electronic resource]
by
Hirashima, Y
Shinozuka, S
Ieiri, T
Matsuda, I
Ono, Y
Murata, T
Producer:
19790324
In:
European journal of pediatrics
vol. 130
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388.
Extravascular iodine in contrast enhancement with computed tomography.
[electronic resource]
by
Handa, J
Matsuda, I
Handa, H
Nakano, Y
Komuro, H
Nakajima, K
Producer:
19780925
In:
Neuroradiology
vol. 15
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389.
Dramatic response to corticosteroid therapy of nephrotic syndrome associated with IgA nephropathy.
[electronic resource]
by
Furuse, A
Hiramatsu, M
Adachi, N
Karashima, S
Hattori, S
Matsuda, I
Producer:
19851219
In:
The International journal of pediatric nephrology
vol. 6
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390.
[A nation-wide survey for neurologic and hepato-neurologic type of Wilson disease: clinical features and hepatic copper content].
[electronic resource]
by
Shimizu, N
Suzuki, M
Yamaguchi, Y
Aoki, T
Matsuda, I
Arima, M
Producer:
19961203
In:
No to hattatsu = Brain and development
vol. 28
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391.
Zinc absorption and its correlation with results of oral zinc tolerance testing in nonalcoholic liver cirrhosis; kinetic study.
[electronic resource]
by
Gohshi, K
Fujiyama, S
Shibata, J
Sato, T
Higashi, A
Matsuda, I
Producer:
19961204
In:
Hepato-gastroenterology
vol. 42
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392.
Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis.
[electronic resource]
by
Matsuura, T
Hoshide, R
Fukushima, M
Sakiyama, T
Owada, M
Matsuda, I
Producer:
19930607
In:
Journal of inherited metabolic disease
vol. 16
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393.
Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiency.
[electronic resource]
by
Tuchman, M
Matsuda, I
Munnich, A
Malcolm, S
Strautnieks, S
Briede, T
Producer:
19950504
In:
American journal of medical genetics
vol. 55
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394.
Specificity of PCR-SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency.
[electronic resource]
by
Hoshide, R
Matsuura, T
Komaki, S
Koike, E
Ueno, I
Matsuda, I
Producer:
19940303
In:
Journal of inherited metabolic disease
vol. 16
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395.
[The influence of exercise loading for a long period on the renal function of the children with mesangial proliferative glomerulonephritis].
[electronic resource]
by
Furuse, A
Ushijima, T
Terashima, T
Karashima, S
Hattori, S
Matsuda, I
Producer:
19920518
In:
Nihon Jinzo Gakkai shi
vol. 33
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396.
Amplification of human argininosuccinate synthetase pseudogenes.
[electronic resource]
by
Nomiyama, H
Obaru, K
Jinno, Y
Matsuda, I
Shimada, K
Miyata, T
Producer:
19870506
In:
Journal of molecular biology
vol. 192
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397.
Isolation of apolipoprotein A-I-containing lipoproteins by immunoaffinity chromatography using a formylated derivative of cellulose gel.
[electronic resource]
by
Ohta, T
Hattori, S
Murakami, M
Horiuchi, S
Nishiyama, S
Matsuda, I
Producer:
19890419
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 179
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398.
Late neonatal vitamin K deficiency associated with subclinical liver dysfunction in human milk-fed infants.
[electronic resource]
by
Matsuda, I
Nishiyama, S
Motohara, K
Endo, F
Ogata, T
Futagoishi, Y
Producer:
19890505
In:
The Journal of pediatrics
vol. 114
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399.
Stereoselective analysis of the enantiomers of ethotoin in human serum using chiral stationary phase liquid chromatography and gas chromatography-mass spectrometry.
[electronic resource]
by
Inotsume, N
Fujii, J
Honda, M
Nakano, M
Higashi, A
Matsuda, I
Producer:
19890309
In:
Journal of chromatography
vol. 428
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400.
Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndrome.
[electronic resource]
by
Kitano, A
Nishiyama, S
Miike, T
Hattori, S
Ohtani, Y
Matsuda, I
Producer:
19861114
In:
Brain & development
vol. 8
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