Kapoor S - Search Results

1

Detection of IEMs by Mass Spectrometry Techniques in High-Risk Children: A Pilot Study.

Patial A, Saini AG, Kaur R, Kapoor S, Sharda S, Kumar P, Singhi S, Singhi P, Dwivedi I, Malik VS, Tageja M, Didwal G, Kaur G, Varughese B, Attri SV. Patial A, et al. Among authors: kapoor s. Indian J Pediatr. 2022 Sep;89(9):885-893. doi: 10.1007/s12098-022-04207-y. Epub 2022 Jun 17. Indian J Pediatr. 2022. PMID: 35713767

2

Glycogen storage disease type III.

Kapoor S, Kumar PS, Mathur NB, Gondal R, Khalil A. Kapoor S, et al. Indian Pediatr. 1994 Oct;31(10):1288-91. Indian Pediatr. 1994. PMID: 7875798 No abstract available.

3

Newborn screening in India: current perspectives.

Kapoor S, Kabra M. Kapoor S, et al. Indian Pediatr. 2010 Mar;47(3):219-24. doi: 10.1007/s13312-010-0043-0. Indian Pediatr. 2010. PMID: 20371888 Free article. No abstract available.

4

Short syndrome-an expanding phenotype.

Singh A, Arora R, Singh P, Kapoor S. Singh A, et al. Among authors: kapoor s. Indian Pediatr. 2013 Apr;50(4):414-6. doi: 10.1007/s13312-013-0099-8. Indian Pediatr. 2013. PMID: 23665600 Free article.

5

National newborn screening program still a hype or a hope now?

Kapoor S, Gupta N, Kabra M. Kapoor S, et al. Indian Pediatr. 2013 Jul;50(7):639-43. doi: 10.1007/s13312-013-0187-9. Indian Pediatr. 2013. PMID: 23942430 Free article.

6

Genetic study of an Indian family with cherubism.

Singh A, Singh K, Goel R, Hu Y, Reichenberger E, Kapoor S. Singh A, et al. Among authors: kapoor s. Indian J Pediatr. 2014 Mar;81(3):299-301. doi: 10.1007/s12098-013-1195-4. Epub 2013 Sep 5. Indian J Pediatr. 2014. PMID: 24005878

7

Liquid-Liquid Extraction and Solid Phase Extraction for Urinary Organic Acids: A Comparative Study from a Resource Constraint Setting.

Kumari C, Varughese B, Ramji S, Kapoor S. Kumari C, et al. Among authors: kapoor s. Indian J Clin Biochem. 2016 Oct;31(4):414-22. doi: 10.1007/s12291-016-0557-x. Epub 2016 Feb 11. Indian J Clin Biochem. 2016. PMID: 27605738 Free PMC article.

8

Mutation Analyses in Selected Exons of the MUT Gene in Indian Patients with Methylmalonic Acidemia.

Kumari C, Kapoor S, Varughese B, Pollipali SK, Ramji S. Kumari C, et al. Among authors: kapoor s. Indian J Clin Biochem. 2017 Jul;32(3):266-274. doi: 10.1007/s12291-016-0600-y. Epub 2016 Aug 4. Indian J Clin Biochem. 2017. PMID: 28811685 Free PMC article.

9

Frontotemporal Atrophy: Presenting Sign in Infantile Cobalamin Deficiency.

Vats P, Verma P, Varughese B, Kumar S, Kapoor S. Vats P, et al. Among authors: kapoor s. Indian J Pediatr. 2018 Jul;85(7):565-566. doi: 10.1007/s12098-017-2542-7. Epub 2017 Nov 23. Indian J Pediatr. 2018. PMID: 29170924 No abstract available.

10

Status of Newborn Screening and Inborn Errors of Metabolism in India.

Kapoor S, Thelma BK. Kapoor S, et al. Indian J Pediatr. 2018 Dec;85(12):1110-1117. doi: 10.1007/s12098-018-2681-5. Epub 2018 May 7. Indian J Pediatr. 2018. PMID: 29736696

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