Chen YT - Search Results

1

Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c.

Lei KJ, Shelly LL, Lin B, Sidbury JB, Chen YT, Nordlie RC, Chou JY. Lei KJ, et al. Among authors: chen yt. J Clin Invest. 1995 Jan;95(1):234-40. doi: 10.1172/JCI117645. J Clin Invest. 1995. PMID: 7814621 Free PMC article.

2

Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus.

Lei KJ, Chen YT, Chen H, Wong LJ, Liu JL, McConkie-Rosell A, Van Hove JL, Ou HC, Yeh NJ, Pan LY, et al. Lei KJ, et al. Among authors: chen h, chen yt. Am J Hum Genet. 1995 Oct;57(4):766-71. Am J Hum Genet. 1995. PMID: 7573034 Free PMC article.

3

Type I glycogen storage disease: nine years of management with cornstarch.

Chen YT, Bazzarre CH, Lee MM, Sidbury JB, Coleman RA. Chen YT, et al. Eur J Pediatr. 1993;152 Suppl 1:S56-9. doi: 10.1007/BF02072090. Eur J Pediatr. 1993. PMID: 8319727

4

Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle.

Shen J, Bao Y, Liu HM, Lee P, Leonard JV, Chen YT. Shen J, et al. Among authors: chen yt. J Clin Invest. 1996 Jul 15;98(2):352-7. doi: 10.1172/JCI118799. J Clin Invest. 1996. PMID: 8755644 Free PMC article.

5

Renal disease in type I glycogen storage disease.

Chen YT, Coleman RA, Scheinman JI, Kolbeck PC, Sidbury JB. Chen YT, et al. N Engl J Med. 1988 Jan 7;318(1):7-11. doi: 10.1056/NEJM198801073180102. N Engl J Med. 1988. PMID: 3422104

6

Cornstarch therapy in type I glycogen-storage disease.

Chen YT, Cornblath M, Sidbury JB. Chen YT, et al. N Engl J Med. 1984 Jan 19;310(3):171-5. doi: 10.1056/NEJM198401193100306. N Engl J Med. 1984. PMID: 6581385 No abstract available.

7

The role of raw starches in the treatment of type I glycogenosis.

Sidbury JB, Chen YT, Roe CR. Sidbury JB, et al. Among authors: chen yt. Arch Intern Med. 1986 Feb;146(2):370-3. Arch Intern Med. 1986. PMID: 3456223 No abstract available.

8

Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.

Bao Y, Kishnani P, Wu JY, Chen YT. Bao Y, et al. Among authors: chen yt. J Clin Invest. 1996 Feb 15;97(4):941-8. doi: 10.1172/JCI118517. J Clin Invest. 1996. PMID: 8613547 Free PMC article.

9

Delivery of glucose-6-phosphatase in a canine model for glycogen storage disease, type Ia, with adeno-associated virus (AAV) vectors.

Beaty RM, Jackson M, Peterson D, Bird A, Brown T, Benjamin DK Jr, Juopperi T, Kishnani P, Boney A, Chen YT, Koeberl DD. Beaty RM, et al. Among authors: chen yt. Gene Ther. 2002 Aug;9(15):1015-22. doi: 10.1038/sj.gt.3301728. Gene Ther. 2002. PMID: 12101432

10

Clinical and metabolic correction of pompe disease by enzyme therapy in acid maltase-deficient quail.

Kikuchi T, Yang HW, Pennybacker M, Ichihara N, Mizutani M, Van Hove JL, Chen YT. Kikuchi T, et al. Among authors: chen yt. J Clin Invest. 1998 Feb 15;101(4):827-33. doi: 10.1172/JCI1722. J Clin Invest. 1998. PMID: 9466978 Free PMC article.

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

3,458 results

Search Page

Filters