Sahai I - Search Results

1

The re-occurrence of cardiomyopathy in propionic acidemia after liver transplantation.

Berry GT, Blume ED, Wessel A, Singh T, Hecht L, Marsden D, Sahai I, Elisofon S, Ferguson M, Kim HB, Harris DJ, Demirbas D, Almuqbil M, Nyhan WL. Berry GT, et al. Among authors: sahai i. JIMD Rep. 2020 Apr 8;54(1):3-8. doi: 10.1002/jmd2.12119. eCollection 2020 Jul. JIMD Rep. 2020. PMID: 32685343 Free PMC article.

2

Beta-Ketothiolase Deficiency Presenting with Metabolic Stroke After a Normal Newborn Screen in Two Individuals.

Wojcik MH, Wierenga KJ, Rodan LH, Sahai I, Ferdinandusse S, Genetti CA, Towne MC, Peake RWA, James PM, Beggs AH, Brownstein CA, Berry GT, Agrawal PB. Wojcik MH, et al. Among authors: sahai i. JIMD Rep. 2018;39:45-54. doi: 10.1007/8904_2017_45. Epub 2017 Jul 20. JIMD Rep. 2018. PMID: 28726122 Free PMC article.

3

Newborn screening.

Sahai I, Marsden D. Sahai I, et al. Crit Rev Clin Lab Sci. 2009;46(2):55-82. doi: 10.1080/10408360802485305. Crit Rev Clin Lab Sci. 2009. PMID: 19255915 Review.

4

A retrospective study of adult patients with noncirrhotic hyperammonemia.

Stergachis AB, Mogensen KM, Khoury CC, Lin AP, Peake RW, Baker JJ, Barkoudah E, Sahai I, Sweetser DA, Berry GT, Krier JB. Stergachis AB, et al. Among authors: sahai i. J Inherit Metab Dis. 2020 Nov;43(6):1165-1172. doi: 10.1002/jimd.12292. Epub 2020 Aug 16. J Inherit Metab Dis. 2020. PMID: 32713002

5

A near-miss: very long chain acyl-CoA dehydrogenase deficiency with normal primary markers in the initial well-timed newborn screening specimen.

Sahai I, Bailey JC, Eaton RB, Zytkovicz T, Harris DJ. Sahai I, et al. J Pediatr. 2011 Jan;158(1):172; author reply 172-3. doi: 10.1016/j.jpeds.2010.09.026. Epub 2010 Nov 12. J Pediatr. 2011. PMID: 21074171 No abstract available.

6

Newborn Screening for Glutaric Aciduria-II: The New England Experience.

Sahai I, Garganta CL, Bailey J, James P, Levy HL, Martin M, Neilan E, Phornphutkul C, Sweetser DA, Zytkovicz TH, Eaton RB. Sahai I, et al. JIMD Rep. 2014;13:1-14. doi: 10.1007/8904_2013_262. Epub 2013 Nov 5. JIMD Rep. 2014. PMID: 24190796 Free PMC article.

7

Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update.

Bergmann AK, Sahai I, Falcone JF, Fleming J, Bagg A, Borgna-Pignati C, Casey R, Fabris L, Hexner E, Mathews L, Ribeiro ML, Wierenga KJ, Neufeld EJ. Bergmann AK, et al. Among authors: sahai i. J Pediatr. 2009 Dec;155(6):888-892.e1. doi: 10.1016/j.jpeds.2009.06.017. Epub 2009 Jul 29. J Pediatr. 2009. PMID: 19643445 Free PMC article.

8

Long-term follow-up to ensure quality care of individuals diagnosed with newborn screening conditions: early experience in New England.

Sahai I, Eaton RB, Hale JE, Mulcahy EA, Comeau AM. Sahai I, et al. Genet Med. 2010 Dec;12(12 Suppl):S220-7. doi: 10.1097/GIM.0b013e3181fe5d37. Genet Med. 2010. PMID: 21150368 Free article.

9

Neonatal screening for inborn errors of metabolism using tandem mass spectrometry: experience of the pilot study in Andhra Pradesh, India.

Sahai I, Zytkowicz T, Rao Kotthuri S, Lakshmi Kotthuri A, Eaton RB, Akella RR. Sahai I, et al. Indian J Pediatr. 2011 Aug;78(8):953-60. doi: 10.1007/s12098-011-0398-9. Epub 2011 Mar 17. Indian J Pediatr. 2011. PMID: 21416125

10

Newborn screening for hepatorenal tyrosinemia-I by tandem mass spectrometry using pooled samples: a four-year summary by the New England newborn screening program.

Zytkovicz TH, Sahai I, Rush A, Odewale A, Johnson D, Fitzgerald E, Britton D, Eaton RB. Zytkovicz TH, et al. Among authors: sahai i. Clin Biochem. 2013 May;46(7-8):681-4. doi: 10.1016/j.clinbiochem.2013.02.002. Epub 2013 Feb 24. Clin Biochem. 2013. PMID: 23462696

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