Akaboshi I - Search Results

1

Simultaneous dual infection of herpes simplex virus type 1 and Epstein-Barr virus in an immunocompetent patient.

Akaboshi I, Hata A, Katsuki T, Matsuda I. Akaboshi I, et al. Pediatr Infect Dis J. 1988 Sep;7(9):655-8. doi: 10.1097/00006454-198809000-00011. Pediatr Infect Dis J. 1988. PMID: 2845350 No abstract available.

2

Unique pattern of Epstein-Barr virus specific antibodies in recurrent parotitis.

Akaboshi I, Katsuki T, Jamamoto J, Matsuda I. Akaboshi I, et al. Lancet. 1983 Nov 5;2(8358):1049-51. doi: 10.1016/s0140-6736(83)91038-3. Lancet. 1983. PMID: 6138599

3

Study of a female patient with ornithine transcarbamylase deficiency: detection of a nonsense mutation.

Hata A, Matsuura T, Setoyama C, Shimada K, Takeda E, Kuroda Y, Akaboshi I, Matsuda I. Hata A, et al. Among authors: akaboshi i. J Inherit Metab Dis. 1989;12(3):347-50. doi: 10.1007/BF01799239. J Inherit Metab Dis. 1989. PMID: 2515388 No abstract available.

4

A structural abnormality of E1 component of the branched-chain alpha-keto acid dehydrogenase complex in maple syrup urine disease.

Indo Y, Kitano A, Akaboshi I, Endo F, Matsuda I. Indo Y, et al. Among authors: akaboshi i. J Inherit Metab Dis. 1987;10(3):281-3. doi: 10.1007/BF01800082. J Inherit Metab Dis. 1987. PMID: 3123794 No abstract available.

5

Immunochemical evidence of pyruvate dehydrogenase (E1) deficiency.

Kitano A, Akaboshi I, Endo F, Matsuda I, Okano Y, Hase Y, Nagao Y, Kamoshita S, Miyabayashi S, Narisawa K. Kitano A, et al. Among authors: akaboshi i. J Inherit Metab Dis. 1988;11(3):329-32. doi: 10.1007/BF01800386. J Inherit Metab Dis. 1988. PMID: 3148083 No abstract available.

6

Maple syrup urine disease: clinical and biochemical significance of gene analysis.

Nobukuni Y, Mitsubuchi H, Akaboshi I, Indo Y, Endo F, Matsuda I. Nobukuni Y, et al. Among authors: akaboshi i. J Inherit Metab Dis. 1991;14(5):787-92. doi: 10.1007/BF01799951. J Inherit Metab Dis. 1991. PMID: 1664011 No abstract available.

7

A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiency.

Hata A, Matsuura T, Setoyama C, Shimada K, Yokoi T, Akaboshi I, Matsuda I. Hata A, et al. Among authors: akaboshi i. Hum Genet. 1991 May;87(1):28-32. doi: 10.1007/BF01213087. Hum Genet. 1991. PMID: 2037279

8

Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene.

Hata A, Setoyama C, Shimada K, Takeda E, Kuroda Y, Akaboshi I, Matsuda I. Hata A, et al. Among authors: akaboshi i. Am J Hum Genet. 1989 Jul;45(1):123-7. Am J Hum Genet. 1989. PMID: 2741942 Free PMC article.

9

Molecular diagnosis of maple syrup urine disease: screening and identification of gene mutations in the branched-chain alpha-ketoacid dehydrogenase multienzyme complex.

Nobukuni Y, Mitsubuchi H, Ohta K, Akaboshi I, Indo Y, Endo F, Matsuda I. Nobukuni Y, et al. Among authors: akaboshi i. J Inherit Metab Dis. 1992;15(5):827-33. doi: 10.1007/BF01800029. J Inherit Metab Dis. 1992. PMID: 1434524 No abstract available.

10

Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneity.

Indo Y, Akaboshi I, Nobukuni Y, Endo F, Matsuda I. Indo Y, et al. Among authors: akaboshi i. Hum Genet. 1988 Sep;80(1):6-10. doi: 10.1007/BF00451447. Hum Genet. 1988. PMID: 3417306

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