Chen YT - Search Results

1

Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage disease.

McConkie-Rosell A, Wilson C, Piccoli DA, Boyle J, DeClue T, Kishnani P, Shen JJ, Boney A, Brown B, Chen YT. McConkie-Rosell A, et al. Among authors: chen yt. J Inherit Metab Dis. 1996;19(1):51-8. doi: 10.1007/BF01799348. J Inherit Metab Dis. 1996. PMID: 8830177

2

Definitive prenatal diagnosis for type III glycogen storage disease.

Yang BZ, Ding JH, Brown BI, Chen YT. Yang BZ, et al. Among authors: chen yt. Am J Hum Genet. 1990 Oct;47(4):735-9. Am J Hum Genet. 1990. PMID: 2220811 Free PMC article.

3

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.

4

Pulmonary hypertension in glycogen storage disease type I.

Kishnani P, Bengur AR, Chen YT. Kishnani P, et al. Among authors: chen yt. J Inherit Metab Dis. 1996;19(2):213-6. doi: 10.1007/BF01799432. J Inherit Metab Dis. 1996. PMID: 8739968 No abstract available.

5

Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers.

Shen J, Liu HM, McConkie-Rosell A, Chen YT. Shen J, et al. Among authors: chen yt. Prenat Diagn. 1998 Jan;18(1):61-4. doi: 10.1002/(sici)1097-0223(199801)18:1<61::aid-pd223>3.0.co;2-i. Prenat Diagn. 1998. PMID: 9483641

6

Nutritional deficiencies in a patient with glycogen storage disease type Ib.

Kishnani PS, Boney A, Chen YT. Kishnani PS, et al. Among authors: chen yt. J Inherit Metab Dis. 1999 Oct;22(7):795-801. doi: 10.1023/a:1005549823146. J Inherit Metab Dis. 1999. PMID: 10518279

7

Prenatal diagnosis of glycogen storage disease type IV using PCR-based DNA mutation analysis.

Shen J, Liu HM, McConkie-Rosell A, Chen YT. Shen J, et al. Among authors: chen yt. Prenat Diagn. 1999 Sep;19(9):837-9. doi: 10.1002/(sici)1097-0223(199909)19:9<837::aid-pd652>3.0.co;2-g. Prenat Diagn. 1999. PMID: 10521841

8

Glycogen storage disease types I and II: treatment updates.

Koeberl DD, Kishnani PS, Chen YT. Koeberl DD, et al. Among authors: chen yt. J Inherit Metab Dis. 2007 Apr;30(2):159-64. doi: 10.1007/s10545-007-0519-9. Epub 2007 Feb 16. J Inherit Metab Dis. 2007. PMID: 17308886 Free PMC article. Review.

9

Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III.

Ding JH, de Barsy T, Brown BI, Coleman RA, Chen YT. Ding JH, et al. Among authors: chen yt. J Pediatr. 1990 Jan;116(1):95-100. doi: 10.1016/s0022-3476(05)81652-x. J Pediatr. 1990. PMID: 2295969

10

Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.

Chen YT, He JK, Ding JH, Brown BI. Chen YT, et al. Am J Hum Genet. 1987 Dec;41(6):1002-15. Am J Hum Genet. 1987. PMID: 2961257 Free PMC article.

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