Owada M - Search Results

1

Subcellular localization of acid sphingomyelinase and lipid in Niemann-Pick mice.

Sakiyama T, Akashi K, Akatsuka A, Owada M, Miyawaki S, Kitagawa T. Sakiyama T, et al. Among authors: owada m. J Inherit Metab Dis. 1987;10(3):301-4. doi: 10.1007/BF01800087. J Inherit Metab Dis. 1987. PMID: 2828764 No abstract available.

2

Lack of acid sphingomyelinase in the mitochondria-lysosome fraction of brain from Niemann-Pick mice.

Tsuda M, Owada M, Kitagawa T, Miyawaki S. Tsuda M, et al. Among authors: owada m. J Inherit Metab Dis. 1985;8(3):147-8. doi: 10.1007/BF01819301. J Inherit Metab Dis. 1985. PMID: 3027450 No abstract available.

3

Bone marrow transplantation in Niemann-Pick mice.

Sakiyama T, Tsuda M, Owada M, Kitagawa T, Miyawaki S, Shinagawa T, Tadokoro M. Sakiyama T, et al. Among authors: owada m. J Inherit Metab Dis. 1986;9(3):305-8. doi: 10.1007/BF01799671. J Inherit Metab Dis. 1986. PMID: 3099079 No abstract available.

4

A survey on prenatal diagnosis of inherited metabolic diseases in Japan.

Tada K, Aikawa J, Igarashi Y, Hayasaka K, Narisawa K, Owada M, Kitagawa T. Tada K, et al. Among authors: owada m. J Inherit Metab Dis. 1989;12 Suppl 2:260-2. doi: 10.1007/BF03335392. J Inherit Metab Dis. 1989. PMID: 2512420 No abstract available.

5

Successful treatment of maternal phenylketonuria with a formula consisting of low phenylalanine peptide as a protein source.

Owada M, Abe M, Ono M, Kitagawa T, Sato Y. Owada M, et al. J Inherit Metab Dis. 1988;11(3):341-4. doi: 10.1007/BF01800389. J Inherit Metab Dis. 1988. PMID: 3148086 No abstract available.

6

Bone marrow transplantation for Niemann-Pick mice.

Sakiyama T, Tsuda M, Owada M, Joh K, Miyawaki S, Kitagawa T. Sakiyama T, et al. Among authors: owada m. Biochem Biophys Res Commun. 1983 Jun 15;113(2):605-10. doi: 10.1016/0006-291x(83)91769-2. Biochem Biophys Res Commun. 1983. PMID: 6347196

7

Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis.

Matsuura T, Hoshide R, Fukushima M, Sakiyama T, Owada M, Matsuda I. Matsuura T, et al. Among authors: owada m. J Inherit Metab Dis. 1993;16(1):31-8. doi: 10.1007/BF00711312. J Inherit Metab Dis. 1993. PMID: 8487501

8

[Biochemical diagnosis and mass screening for hereditary amino acid disorders].

Owada M, Kitagawa T. Owada M, et al. Nihon Rinsho. 1992 Jul;50(7):1522-9. Nihon Rinsho. 1992. PMID: 1404880 Japanese.

9

Prenatal diagnosis of I-cell disease by measuring altered alpha-mannosidase activity in amniotic fluid.

Owada M, Nishiya O, Sakiyama T, Kitagawa T. Owada M, et al. J Inherit Metab Dis. 1980;3(4):117-21. doi: 10.1007/BF02312545. J Inherit Metab Dis. 1980. PMID: 6787332

10

[Lysosomal storage diseases].

Owada M, Kitagawa T. Owada M, et al. Nihon Rinsho. 2001 Dec;59 Suppl 8:317-27. Nihon Rinsho. 2001. PMID: 11808243 Review. Japanese. No abstract available.

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