Millington DS - Search Results

1

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: millington ds. 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.

2

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: millington ds. Genet Med. 2006 May;8(5):302-6. doi: 10.1097/01.gim.0000217781.66786.9b. Genet Med. 2006. PMID: 16702880 Free 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: millington ds. Genet Med. 2009 Jul;11(7):536-41. doi: 10.1097/GIM.0b013e3181a87867. Genet Med. 2009. PMID: 19521244 Free article. Clinical Trial.

4

Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease.

An Y, Young SP, Kishnani PS, Millington DS, Amalfitano A, Corz D, Chen YT. An Y, et al. Among authors: millington ds. Mol Genet Metab. 2005 Aug;85(4):247-54. doi: 10.1016/j.ymgme.2005.03.010. Mol Genet Metab. 2005. PMID: 15886040

5

Screening for Pompe disease using a rapid dried blood spot method: experience of a clinical diagnostic laboratory.

Goldstein JL, Young SP, Changela M, Dickerson GH, Zhang H, Dai J, Peterson D, Millington DS, Kishnani PS, Bali DS. Goldstein JL, et al. Among authors: millington ds. Muscle Nerve. 2009 Jul;40(1):32-6. doi: 10.1002/mus.21376. Muscle Nerve. 2009. PMID: 19533645

6

Assessing disease severity in Pompe disease: the roles of a urinary glucose tetrasaccharide biomarker and imaging techniques.

Young SP, Piraud M, Goldstein JL, Zhang H, Rehder C, Laforet P, Kishnani PS, Millington DS, Bashir MR, Bali DS. Young SP, et al. Among authors: millington ds. Am J Med Genet C Semin Med Genet. 2012 Feb 15;160C(1):50-8. doi: 10.1002/ajmg.c.31320. Epub 2012 Jan 17. Am J Med Genet C Semin Med Genet. 2012. PMID: 22252961

7

Misinformation regarding tandem mass spectrometric vs fluorometric assays to screen newborns for LSDs.

Millington DS, Bali DM. Millington DS, et al. Mol Genet Metab Rep. 2017 May 10;11:72-73. doi: 10.1016/j.ymgmr.2017.04.009. eCollection 2017 Jun. Mol Genet Metab Rep. 2017. PMID: 28529890 Free PMC article. No abstract available.

8

Current State of the Art of Newborn Screening for Lysosomal Storage Disorders.

Millington DS, Bali DS. Millington DS, et al. Int J Neonatal Screen. 2018 Jul 18;4(3):24. doi: 10.3390/ijns4030024. eCollection 2018 Sep. Int J Neonatal Screen. 2018. PMID: 33072946 Free PMC article. Review.

9

Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate.

Ahmad A, Kahler SG, Kishnani PS, Artigas-Lopez M, Pappu AS, Steiner R, Millington DS, Van Hove JL. Ahmad A, et al. Among authors: millington ds. Am J Med Genet. 1999 Dec 3;87(4):331-8. doi: 10.1002/(sici)1096-8628(19991203)87:4<331::aid-ajmg10>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10588840

10

Development of a fluorometric microtiter plate based enzyme assay for MPS IVA (Morquio type A) using dried blood spots.

Ullal AJ, Millington DS, Bali DS. Ullal AJ, et al. Among authors: millington ds. Mol Genet Metab Rep. 2014 Oct 22;1:461-464. doi: 10.1016/j.ymgmr.2014.10.004. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896123 Free PMC article.

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