Narisawa K - Search Results

1

3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal.

Gibson KM, Nyhan WL, Sweetman L, Narisawa K, Lehnert W, Divry P, Robinson BH, Roth KS, Beemer FA, van Sprang FJ, et al. Gibson KM, et al. Among authors: narisawa k. Eur J Pediatr. 1988 Oct;148(1):76-82. doi: 10.1007/BF00441821. Eur J Pediatr. 1988. PMID: 3197737

2

3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detection.

Narisawa K, Gibson KM, Sweetman L, Nyhan WL. Narisawa K, et al. Clin Chim Acta. 1989 Sep 15;184(1):57-64. doi: 10.1016/0009-8981(89)90256-8. Clin Chim Acta. 1989. PMID: 2480857

3

Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria.

Narisawa K, Gibson KM, Sweetman L, Nyhan WL, Duran M, Wadman SK. Narisawa K, et al. J Clin Invest. 1986 Apr;77(4):1148-52. doi: 10.1172/JCI112415. J Clin Invest. 1986. PMID: 3082934 Free PMC article.

4

Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatography.

Kikuchi M, Narisawa K, Tada K, Sweetman L. Kikuchi M, et al. Among authors: narisawa k. Clin Chim Acta. 1990 Aug 31;189(3):297-301. doi: 10.1016/0009-8981(90)90311-f. Clin Chim Acta. 1990. PMID: 2225461

5

Relationship between kinetic properties of mutant enzyme and biochemical and clinical responsiveness to biotin in holocarboxylase synthetase deficiency.

Sakamoto O, Suzuki Y, Li X, Aoki Y, Hiratsuka M, Suormala T, Baumgartner ER, Gibson KM, Narisawa K. Sakamoto O, et al. Among authors: narisawa k. Pediatr Res. 1999 Dec;46(6):671-6. doi: 10.1203/00006450-199912000-00004. Pediatr Res. 1999. PMID: 10590022

6

Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical method.

Hayasaka K, Metoki K, Ishiguro S, Kato S, Chiba T, Hirooka M, Kikuchi M, Kurobane I, Narisawa K, Tada K. Hayasaka K, et al. Among authors: narisawa k. Eur J Pediatr. 1987 Jul;146(4):370-2. doi: 10.1007/BF00444940. Eur J Pediatr. 1987. PMID: 3308467

7

Hyperamino-acidaemia and hyperammonaemia in epileptic children treated with valproic acid.

Iinuma K, Hayasaka K, Narisawa K, Tada K, Hori K. Iinuma K, et al. Among authors: narisawa k. Eur J Pediatr. 1988 Dec;148(3):267-9. doi: 10.1007/BF00441418. Eur J Pediatr. 1988. PMID: 3145882

8

Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations.

Yang X, Aoki Y, Li X, Sakamoto O, Hiratsuka M, Gibson KM, Kure S, Narisawa K, Matsubara Y, Suzuki Y. Yang X, et al. Among authors: narisawa k. J Hum Genet. 2000;45(6):358-62. doi: 10.1007/s100380070008. J Hum Genet. 2000. PMID: 11185745

9

Chronic pancreatitis in a child with glycogen storage disease type 1.

Kikuchi M, Hasegawa K, Handa I, Watabe M, Narisawa K, Tada K. Kikuchi M, et al. Among authors: narisawa k. Eur J Pediatr. 1991 Oct;150(12):852-3. doi: 10.1007/BF01955007. Eur J Pediatr. 1991. PMID: 1743219

10

Enzymatic diagnosis of holocarboxylase synthetase deficiency using apo-carboxyl carrier protein as a substrate.

Suzuki Y, Aoki Y, Sakamoto O, Li X, Miyabayashi S, Kazuta Y, Kondo H, Narisawa K. Suzuki Y, et al. Among authors: narisawa k. Clin Chim Acta. 1996 Jul 15;251(1):41-52. doi: 10.1016/0009-8981(96)06291-2. Clin Chim Acta. 1996. PMID: 8814349

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

242 results

Search Page

Filters