Chen YT - Search Results

1

Non-lethal congenital hypotonia due to glycogen storage disease type IV.

Burrow TA, Hopkin RJ, Bove KE, Miles L, Wong BL, Choudhary A, Bali D, Li SC, Chen YT. Burrow TA, et al. Among authors: chen yt. Am J Med Genet A. 2006 Apr 15;140(8):878-82. doi: 10.1002/ajmg.a.31166. Am J Med Genet A. 2006. PMID: 16528737

2

Prenatal diagnosis in glycogen storage diseases.

Chen YT, Bali D, Sullivan J. Chen YT, et al. Prenat Diagn. 2002 May;22(5):357-9. doi: 10.1002/pd.166. Prenat Diagn. 2002. PMID: 12001186 Review. No abstract available.

3

Glycogen storage disease type I: diagnosis and phenotype/genotype correlation.

Matern D, Seydewitz HH, Bali D, Lang C, Chen YT. Matern D, et al. Among authors: chen yt. Eur J Pediatr. 2002 Oct;161 Suppl 1:S10-9. doi: 10.1007/s00431-002-0998-5. Epub 2002 Jul 27. Eur J Pediatr. 2002. PMID: 12373566

4

Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.

Zhang H, Kallwass H, Young SP, Carr C, Dai J, Kishnani PS, Millington DS, Keutzer J, Chen YT, Bali D. Zhang H, et al. Among authors: chen yt. Genet Med. 2006 May;8(5):302-6. doi: 10.1097/01.gim.0000217781.66786.9b. Genet Med. 2006. PMID: 16702880 Free article.

5

Glycogen storage disease type IIIa in curly-coated retrievers.

Gregory BL, Shelton GD, Bali DS, Chen YT, Fyfe JC. Gregory BL, et al. Among authors: chen yt. J Vet Intern Med. 2007 Jan-Feb;21(1):40-6. doi: 10.1892/0891-6640(2007)21[40:gsdtii]2.0.co;2. J Vet Intern Med. 2007. PMID: 17338148 Free article.

6

Sibling phenotype concordance in classical infantile Pompe disease.

Smith WE, Sullivan-Saarela JA, Li JS, Cox GF, Corzo D, Chen YT, Kishnani PS. Smith WE, et al. Among authors: chen yt. Am J Med Genet A. 2007 Nov 1;143A(21):2493-501. doi: 10.1002/ajmg.a.31936. Am J Med Genet A. 2007. PMID: 17853454 Review.

7

A case of congenital glycogen storage disease type IV with a novel GBE1 mutation.

Raju GP, Li HC, Bali DS, Chen YT, Urion DK, Lidov HG, Kang PB. Raju GP, et al. Among authors: chen yt. J Child Neurol. 2008 Mar;23(3):349-52. doi: 10.1177/0883073807309248. Epub 2008 Jan 29. J Child Neurol. 2008. PMID: 18230843

8

Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease.

Kishnani PS, Chuang TP, Bali D, Koeberl D, Austin S, Weinstein DA, Murphy E, Chen YT, Boyette K, Liu CH, Chen YT, Li LH. Kishnani PS, et al. Among authors: chen yt. Hum Mol Genet. 2009 Dec 15;18(24):4781-90. doi: 10.1093/hmg/ddp441. Epub 2009 Sep 16. Hum Mol Genet. 2009. PMID: 19762333

9

Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder.

Li SC, Chen CM, Goldstein JL, Wu JY, Lemyre E, Burrow TA, Kang PB, Chen YT, Bali DS. Li SC, et al. Among authors: chen cm, chen yt. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S83-90. doi: 10.1007/s10545-009-9026-5. Epub 2010 Jan 8. J Inherit Metab Dis. 2010. PMID: 20058079

10

Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV.

Lee YC, Chang CJ, Bali D, Chen YT, Yan YT. Lee YC, et al. Among authors: chen yt. Hum Mol Genet. 2011 Feb 1;20(3):455-65. doi: 10.1093/hmg/ddq492. Epub 2010 Nov 12. Hum Mol Genet. 2011. PMID: 21075835

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