Mathai S - Search Results

1

Upfront adjuvant irradiation versus postoperative surveillance following incomplete surgical resection of craniopharyngiomas in children and young adults.

Sarkar S, Korula S, Mathai S, Simon A, Balakrishnan R, Backianathan S, Chacko AG. Sarkar S, et al. Among authors: mathai s. Childs Nerv Syst. 2022 Oct;38(10):1877-1883. doi: 10.1007/s00381-022-05635-z. Epub 2022 Aug 9. Childs Nerv Syst. 2022. PMID: 35945339

2

Eating disorders among adolescents in a tertiary care centre in India.

Basker MM, Mathai S, Korula S, Mammen PM. Basker MM, et al. Among authors: mathai s. Indian J Pediatr. 2013 Mar;80(3):211-4. doi: 10.1007/s12098-012-0819-4. Epub 2012 Jul 14. Indian J Pediatr. 2013. PMID: 22798272

3

Sirolimus therapy for congenital hyperinsulinism in an infant with a novel homozygous KCNJ11 mutation.

Korula S, Chapla A, Priyambada L, Mathai S, Simon A. Korula S, et al. Among authors: mathai s. J Pediatr Endocrinol Metab. 2018 Jan 26;31(1):87-89. doi: 10.1515/jpem-2017-0238. J Pediatr Endocrinol Metab. 2018. PMID: 29176012

4

Smartphone App as Motivational Intervention to Improve Glycemic Control in Adolescents with Type 1 Diabetes.

Pramanik BK, Angelin JJ, Mathai VJ, Mathai S, Korula S, Simon A. Pramanik BK, et al. Among authors: mathai vj, mathai s. Indian J Pediatr. 2019 Dec;86(12):1118-1123. doi: 10.1007/s12098-019-03035-x. Epub 2019 Jul 29. Indian J Pediatr. 2019. PMID: 31353430

5

Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India.

Mohan S, Danda S, Mathai S, Simon A. Mohan S, et al. Among authors: mathai s. Natl Med J India. 2019 May-Jun;32(3):141-143. doi: 10.4103/0970-258X.278692. Natl Med J India. 2019. PMID: 32129306 Free article.

6

Hepatic Glycogenoses Among Children-Clinical and Biochemical Characterization: Single-Center Study.

Korula S, Danda S, Paul PG, Mathai S, Simon A. Korula S, et al. Among authors: mathai s. J Clin Exp Hepatol. 2020 May-Jun;10(3):222-227. doi: 10.1016/j.jceh.2019.07.007. Epub 2019 Jul 25. J Clin Exp Hepatol. 2020. PMID: 32405178 Free PMC article.

7

Long-term outcomes following maximal safe resection in a contemporary series of childhood craniopharyngiomas.

Sarkar S, Chacko SR, Korula S, Simon A, Mathai S, Chacko G, Chacko AG. Sarkar S, et al. Among authors: mathai s. Acta Neurochir (Wien). 2021 Feb;163(2):499-509. doi: 10.1007/s00701-020-04591-4. Epub 2020 Oct 19. Acta Neurochir (Wien). 2021. PMID: 33078364

8

Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study.

Barney AM, Danda S, Abraham A, Fouzia NA, Gowdra A, Abraham SSC, Sony M, Das S, Korula S, Mathai S, Simon A, Kumar S. Barney AM, et al. Among authors: mathai s. Public Health Genomics. 2021;24(3-4):139-148. doi: 10.1159/000514507. Epub 2021 Apr 6. Public Health Genomics. 2021. PMID: 33823526 Free article.

9

Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent.

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Abraham SSC, et al. Among authors: mathai s. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. Eur J Med Genet. 2021. PMID: 34303877

10

Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India.

Ravichandran L, Korula S, Asha HS, Varghese D, Parthiban R, Johnson J, Ishwarya J, Shetty S, Cherian KE, Jebasingh F, Kapoor N, Pachat D, Mathai S, Simon A, Rajaratnam S, Paul TV, Thomas N, Chapla A. Ravichandran L, et al. Among authors: mathai s. Eur J Med Genet. 2021 Dec;64(12):104369. doi: 10.1016/j.ejmg.2021.104369. Epub 2021 Oct 27. Eur J Med Genet. 2021. PMID: 34718183

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