Tada K - Search Results

1

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yao YQ, Danks DM, Green A, McCabe ER. Matsubara Y, et al. Among authors: tada k. Lancet. 1991 Aug 31;338(8766):552-3. doi: 10.1016/0140-6736(91)91110-g. Lancet. 1991. PMID: 1678810

2

Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiency.

Matsubara Y, Narisawa K, Miyabayashi S, Tada K, Coates PM. Matsubara Y, et al. Among authors: tada k. Lancet. 1990 Jun 30;335(8705):1589. doi: 10.1016/0140-6736(90)91413-5. Lancet. 1990. PMID: 1972503 No abstract available.

3

Simple and rapid detection of phenylketonuria mutation tightly linked to haplotype 2 by modified polymerase chain reaction.

Matsubara Y, Narisawa K, Tada K. Matsubara Y, et al. Among authors: tada k. J Inherit Metab Dis. 1990;13(5):775-9. doi: 10.1007/BF01799586. J Inherit Metab Dis. 1990. PMID: 2246864 No abstract available.

4

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.

Matsubara Y, Narisawa K, Miyabayashi S, Tada K, Coates PM, Bachmann C, Elsas LJ 2nd, Pollitt RJ, Rhead WJ, Roe CR. Matsubara Y, et al. Among authors: tada k. Biochem Biophys Res Commun. 1990 Aug 31;171(1):498-505. doi: 10.1016/0006-291x(90)91421-n. Biochem Biophys Res Commun. 1990. PMID: 2393404

5

Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yeqi Y, Danks DM, Green A, McCabe ER. Matsubara Y, et al. Among authors: tada k. Prog Clin Biol Res. 1992;375:453-62. Prog Clin Biol Res. 1992. PMID: 1359564 No abstract available.

6

Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspects.

Matsubara Y, Narisawa K, Tada K. Matsubara Y, et al. Among authors: tada k. Eur J Pediatr. 1992 Mar;151(3):154-9. doi: 10.1007/BF01954373. Eur J Pediatr. 1992. PMID: 1601002 Review.

7

A novel splicing mutation in propionic acidemia associated with a tetranucleotide direct repeat in the PCCB gene.

Ohura T, Narisawa K, Tada K, Iinuma K. Ohura T, et al. Among authors: tada k. Hum Genet. 1995 Jun;95(6):707-8. doi: 10.1007/BF00209492. Hum Genet. 1995. PMID: 7789958

8

The molecular defect in propionic acidemia: exon skipping caused by an 8-bp deletion from an intron in the PCCB allele.

Ohura T, Ogasawara M, Ikeda H, Narisawa K, Tada K. Ohura T, et al. Among authors: tada k. Hum Genet. 1993 Oct;92(4):397-402. doi: 10.1007/BF01247343. Hum Genet. 1993. PMID: 8225321

9

Propionic acidaemia: sequence analysis of mutant mRNAs from Japanese beta subunit-deficient patients.

Ohura T, Narisawa K, Tada K. Ohura T, et al. Among authors: tada k. J Inherit Metab Dis. 1993;16(5):863-7. doi: 10.1007/BF00714279. J Inherit Metab Dis. 1993. PMID: 8295402 No abstract available.

10

A four-nucleotide insertion at the E1 alpha gene in a patient with pyruvate dehydrogenase deficiency.

Endo H, Miyabayashi S, Tada K, Narisawa K. Endo H, et al. Among authors: tada k. J Inherit Metab Dis. 1991;14(5):793-9. doi: 10.1007/BF01799952. J Inherit Metab Dis. 1991. PMID: 1779625 No abstract available.

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

1,244 results

Search Page

Filters