Bali D - Search Results

1

Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects.

Herzeg A, Borges B, Lianoglou BR, Gonzalez-Velez J, Canepa E, Munar D, Young SP, Bali D, Gelb MH, Chakraborty P, Kishnani PS, Harmatz P, Cohen JL, MacKenzie TC. Herzeg A, et al. Among authors: bali d. Prenat Diagn. 2023 Dec;43(13):1638-1649. doi: 10.1002/pd.6460. Epub 2023 Nov 13. Prenat Diagn. 2023. PMID: 37955580 Review.

2

In Utero Enzyme-Replacement Therapy for Infantile-Onset Pompe's Disease.

Cohen JL, Chakraborty P, Fung-Kee-Fung K, Schwab ME, Bali D, Young SP, Gelb MH, Khaledi H, DiBattista A, Smallshaw S, Moretti F, Wong D, Lacroix C, El Demellawy D, Strickland KC, Lougheed J, Moon-Grady A, Lianoglou BR, Harmatz P, Kishnani PS, MacKenzie TC. Cohen JL, et al. Among authors: bali d. N Engl J Med. 2022 Dec 8;387(23):2150-2158. doi: 10.1056/NEJMoa2200587. Epub 2022 Nov 9. N Engl J Med. 2022. PMID: 36351280 Free PMC article.

3

Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker.

Young SP, Zhang H, Corzo D, Thurberg BL, Bali D, Kishnani PS, Millington DS. Young SP, et al. Among authors: bali d. Genet Med. 2009 Jul;11(7):536-41. doi: 10.1097/GIM.0b013e3181a87867. Genet Med. 2009. PMID: 19521244 Free article. Clinical Trial.

4

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.

5

β2 Agonists enhance the efficacy of simultaneous enzyme replacement therapy in murine Pompe disease.

Koeberl DD, Li S, Dai J, Thurberg BL, Bali D, Kishnani PS. Koeberl DD, et al. Among authors: bali d. Mol Genet Metab. 2012 Feb;105(2):221-7. doi: 10.1016/j.ymgme.2011.11.005. Epub 2011 Nov 11. Mol Genet Metab. 2012. PMID: 22154081 Free PMC article.

6

Characterization of immune response in Cross-Reactive Immunological Material (CRIM)-positive infantile Pompe disease patients treated with enzyme replacement therapy.

Desai AK, Kazi ZB, Bali DS, Kishnani PS. Desai AK, et al. Mol Genet Metab Rep. 2019 May 10;20:100475. doi: 10.1016/j.ymgmr.2019.100475. eCollection 2019 Sep. Mol Genet Metab Rep. 2019. PMID: 31193175 Free PMC article.

7

The electrodiagnostic characteristics of Glycogen Storage Disease Type III.

Hobson-Webb LD, Austin SL, Bali DS, Kishnani PS. Hobson-Webb LD, et al. Among authors: bali ds. Genet Med. 2010 Jul;12(7):440-5. doi: 10.1097/GIM.0b013e3181cd735b. Genet Med. 2010. PMID: 20071996 Free article.

8

Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERT.

Banugaria SG, Prater SN, Patel TT, Dearmey SM, Milleson C, Sheets KB, Bali DS, Rehder CW, Raiman JA, Wang RA, Labarthe F, Charrow J, Harmatz P, Chakraborty P, Rosenberg AS, Kishnani PS. Banugaria SG, et al. PLoS One. 2013 Jun 25;8(6):e67052. doi: 10.1371/journal.pone.0067052. Print 2013. PLoS One. 2013. PMID: 23825616 Free PMC article.

9

Development of a clinically validated in vitro functional assay to assess pathogenicity of novel GAA variants in patients with Pompe disease identified via newborn screening.

Goomber S, Huggins E, Rehder CW, Cohen JL, Bali DS, Kishnani PS. Goomber S, et al. Front Genet. 2022 Sep 30;13:1001154. doi: 10.3389/fgene.2022.1001154. eCollection 2022. Front Genet. 2022. PMID: 36246652 Free PMC article.

10

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: bali d. Genet Med. 2006 May;8(5):302-6. doi: 10.1097/01.gim.0000217781.66786.9b. Genet Med. 2006. PMID: 16702880 Free article.

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