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Page 1
Emerging therapies for glycogen storage disease type I.
Koeberl DD, Kishnani PS, Bali D, Chen YT. Koeberl DD, et al. Among authors: bali d. Trends Endocrinol Metab. 2009 Jul;20(5):252-8. doi: 10.1016/j.tem.2009.02.003. Epub 2009 Jun 21. Trends Endocrinol Metab. 2009. PMID: 19541498 Review.
Prenatal diagnosis in glycogen storage diseases.
Chen YT, Bali D, Sullivan J. Chen YT, et al. Among authors: bali d. Prenat Diagn. 2002 May;22(5):357-9. doi: 10.1002/pd.166. Prenat Diagn. 2002. PMID: 12001186 Review. No abstract available.
Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.
Koeberl DD, Young SP, Gregersen NS, Vockley J, Smith WE, Benjamin DK Jr, An Y, Weavil SD, Chaing SH, Bali D, McDonald MT, Kishnani PS, Chen YT, Millington DS. Koeberl DD, et al. Among authors: bali d. Pediatr Res. 2003 Aug;54(2):219-23. doi: 10.1203/01.PDR.0000074972.36356.89. Epub 2003 May 7. Pediatr Res. 2003. PMID: 12736383
Hepatocellular carcinoma in glycogen storage disease type Ia: a case series.
Franco LM, Krishnamurthy V, Bali D, Weinstein DA, Arn P, Clary B, Boney A, Sullivan J, Frush DP, Chen YT, Kishnani PS. Franco LM, et al. Among authors: bali d. J Inherit Metab Dis. 2005;28(2):153-62. doi: 10.1007/s10545-005-7500-2. J Inherit Metab Dis. 2005. PMID: 15877204
Pompe disease diagnosis and management guideline.
Kishnani PS, Steiner RD, Bali D, Berger K, Byrne BJ, Case LE, Crowley JF, Downs S, Howell RR, Kravitz RM, Mackey J, Marsden D, Martins AM, Millington DS, Nicolino M, O'Grady G, Patterson MC, Rapoport DM, Slonim A, Spencer CT, Tifft CJ, Watson MS. Kishnani PS, et al. Among authors: bali d. Genet Med. 2006 May;8(5):267-88. doi: 10.1097/01.gim.0000218152.87434.f3. Genet Med. 2006. PMID: 16702877 Free PMC article. No abstract available.
176 results