Kikuchi M - Search Results

1

Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut0 patients.

Mikami H, Ogasawara M, Matsubara Y, Kikuchi M, Miyabayashi S, Kure S, Narisawa K. Mikami H, et al. Among authors: kikuchi m. J Hum Genet. 1999;44(1):35-9. doi: 10.1007/s100380050103. J Hum Genet. 1999. PMID: 9929975

2

Assay of methylmalonyl CoA mutase with high-performance liquid chromatography.

Kikuchi M, Hanamizu H, Narisawa K, Tada K. Kikuchi M, et al. Clin Chim Acta. 1989 Oct 16;184(3):307-13. doi: 10.1016/0009-8981(89)90064-8. Clin Chim Acta. 1989. PMID: 2575466

3

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. Clin Chim Acta. 1990 Aug 31;189(3):297-301. doi: 10.1016/0009-8981(90)90311-f. Clin Chim Acta. 1990. PMID: 2225461

4

Enzymatic analysis in lymphocytes and erythrocytes from six patients with different phenotypes of phosphorylase kinase deficiency.

Kikuchi M, Aikawa J, Ishizawa S, Igarashi Y, Narisawa K, Tada K. Kikuchi M, et al. J Inherit Metab Dis. 1988;11(3):315-8. doi: 10.1007/BF01800383. J Inherit Metab Dis. 1988. PMID: 3148080 No abstract available.

5

[Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy].

Murotsuki J, Uehara S, Okamura K, Yajima A, Kikuchi M, Oura T, Miyabayashi S. Murotsuki J, et al. Among authors: kikuchi m. Nihon Sanka Fujinka Gakkai Zasshi. 1991 Dec;43(12):1613-6. Nihon Sanka Fujinka Gakkai Zasshi. 1991. PMID: 1744457 Japanese.

6

Secondary amyloidosis in glycogen storage disease type Ib.

Kikuchi M, Haginoya K, Miyabayashi S, Igarashi Y, Narisawa K, Tada K. Kikuchi M, et al. Eur J Pediatr. 1990 Feb;149(5):344-5. doi: 10.1007/BF02171563. Eur J Pediatr. 1990. PMID: 2311631

7

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: kikuchi m. Eur J Pediatr. 1987 Jul;146(4):370-2. doi: 10.1007/BF00444940. Eur J Pediatr. 1987. PMID: 3308467

8

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. Eur J Pediatr. 1991 Oct;150(12):852-3. doi: 10.1007/BF01955007. Eur J Pediatr. 1991. PMID: 1743219

9

Type 4 renal tubular acidosis (subtype 2) in a patient with methylmalonic acidaemia.

Ohura T, Kikuchi M, Abukawa D, Hanamizu H, Aikawa J, Narisawa K, Tada K, Yunoki H. Ohura T, et al. Among authors: kikuchi m. Eur J Pediatr. 1990 Dec;150(2):115-8. doi: 10.1007/BF02072052. Eur J Pediatr. 1990. PMID: 2279506

10

An acute form of tyrosinemia type I with multiple intrahepatic mass lesions.

Tazawa Y, Kikuchi M, Kurobane I, Watanabe A, Nakai H, Narisawa K, Tada K. Tazawa Y, et al. Among authors: kikuchi m. J Pediatr Gastroenterol Nutr. 1990 May;10(4):536-9. doi: 10.1097/00005176-199005000-00018. J Pediatr Gastroenterol Nutr. 1990. PMID: 1694241

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