-
Sowmyanarayanan TV, Natarajan SK, Ramachandran A, Sarkar R, Moses PD, Simon A, Agarwal I, Christopher S, Kang G. Nitric oxide production in acute gastroenteritis in Indian children. Trans R Soc Trop Med Hyg. 2009 Aug;103(8):849-51. doi: 10.1016/j.trstmh.2009.05.003. Epub 2009 Jun 23. PMID: 19552932. Link
-
Babji S, Arumugam R, Priyahemavathy R, Sriraman A, Sarvanabhavan A, Manickavasagam P, Simon A, Aggarwal I, Moses PD, Arora R, Kang G. Genotype distribution of Group A rotavirus from southern India, 2005-2016. Vaccine. 2018 Dec 14;36(51):7816-7819. doi: 10.1016/j.vaccine.2017.08.035. Epub 2017 Aug 31. PMID: 28844408.
-
Groeneweg S, van Geest FS, Abacı A, Alcantud A, Ambegaonkar GP, Armour CM, Bakhtiani P, Barca D, Bertini ES, van Beynum IM, Brunetti-Pierri N, Bugiani M, Cappa M, Cappuccio G, Castellotti B, Castiglioni C, Chatterjee K, de Coo IFM, Coutant R, Craiu D, Crock P, DeGoede C, Demir K, Dica A, Dimitri P, Dolcetta-Capuzzo A, Dremmen MHG, Dubey R, Enderli A, Fairchild J, Gallichan J, George B, Gevers EF, Hackenberg A, Halász Z, Heinrich B, Huynh T, Kłosowska A, van der Knaap MS, van der Knoop MM, Konrad D, Koolen DA, Krude H, Lawson-Yuen A, Lebl J, Linder-Lucht M, Lorea CF, Lourenço CM, Lunsing RJ, Lyons G, Malikova J, Mancilla EE, McGowan A, Mericq V, Lora FM, Moran C, Müller KE, Oliver-Petit I, Paone L, Paul PG, Polak M, Porta F, Poswar FO, Reinauer C, Rozenkova K, Menevse TS, Simm P, Simon A, Singh Y, Spada M, van der Spek J, Stals MAM, Stoupa A, Subramanian GM, Tonduti D, Turan S, den Uil CA, Vanderniet J, van der Walt A, Wémeau JL, Wierzba J, de Wit MY, Wolf NI, Wurm M, Zibordi F, Zung A, Zwaveling-Soonawala N, Visser WE. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. Lancet Diabetes Endocrinol. 2020 Jul;8(7):594-605. doi: 10.1016/S2213-8587(20)30153-4. PMID: 32559475. Link
-
Menon VK, Sarkar R, Moses PD, Agarwal I, Simon A, Kang G. Norovirus genogroup II gastroenteritis in hospitalized children in South India. Am J Trop Med Hyg. 2013 Nov;89(5):1019-22. doi: 10.4269/ajtmh.13-0121. Epub 2013 Sep 23. PMID: 24062476; PMCID: PMC3820314.
-
Babji S, Arumugam R, Priyahemavathy R, Sriraman A, Sarvanabhavan A, Manickavasagam P, Simon A, Aggarwal I, Moses PD, Arora R, Kang G Genotype distribution of Group A rotavirus from southern India, 2005-2016. Vaccine. 2018 Dec 14;36(51):7816-7819. doi: 10.1016/j.vaccine.2017.08.035. Epub 2017 Aug 31. PMID: 28844408. Link
-
Babji S, Arumugam R, Priyahemavathy R, Sriraman A, Sarvanabhavan A, Manickavasagam P, Simon A, Aggarwal I, Moses PD, Arora R, Kang G. Genotype distribution of Group A rotavirus from southern India, 2005-2016. Vaccine. 2018 Dec 14;36(51):7816-7819. doi: 10.1016/j.vaccine.2017.08.035. Epub 2017 Aug 31. PMID: 28844408.
-
Babji S, Arumugam R, Sarvanabhavan A, Moses PD, Simon A, Aggarwal I, Mathew A, Sr Anita, Kang G. Multi-center surveillance of rotavirus diarrhea in hospitalized children <5 years of age in India, 2009-2012. Vaccine. 2014 Aug 11;32 Suppl 1:A10-2. doi: 10.1016/j.vaccine.2014.03.001. PMID: 25091661.
-
Korula S, Danda S, Paul PG, Mathai S, Simon A. Hepatic Glycogenoses Among Children-Clinical and Biochemical Characterization: Single-Center Study. J Clin Exp Hepatol. 2020 May-Jun;10(3):222-227. doi: 10.1016/j.jceh.2019.07.007. Epub 2019 Jul 25. PMID: 32405178; PMCID: PMC7212290.
-
Giri S, Nair NP, Mathew A, Manohar B, Simon A, Singh T, Suresh Kumar S, Mathew MA, Babji S, Arora R, Girish Kumar CP, Venkatasubramanian S, Mehendale S, Gupte MD, Kang G. Rotavirus gastroenteritis in Indian children < 5 years hospitalized for diarrhoea, 2012 to 2016. BMC Public Health. 2019 Jan 15;19(1):69. doi: 10.1186/s12889-019-6406-0. PMID: 30646867; PMCID: PMC6334384.
-
Jacob J, Joseph TK, Srinivasan R, Kompithra RZ, Simon A, Kang G. Direct and Indirect Costs of Pediatric Gastroenteritis in Vellore, India. Indian Pediatr. 2016 Jul 8;53(7):642-4. doi: 10.1007/s13312-016-0903-3. PMID: 27508545.
-
Barney AM, Danda S, Abraham A, Fouzia NA, Gowdra A, Abraham SSC, Sony M, Das S, Korula S, Mathai S, Simon A, Kumar S. Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study. Public Health Genomics. 2021;24(3-4):139-148. doi: 10.1159/000514507. Epub 2021 Apr 6. PMID: 33823526.
-
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. Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India. Eur J Med Genet. 2021 Dec;64(12):104369. doi: 10.1016/j.ejmg.2021.104369. Epub 2021 Oct 27. PMID: 34718183. Link
-
Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. PMID: 34303877.
-
Paul PG, Rebekah G, Korula S, Kumar M, Bondu JD, Palany R, Simon A, Mathai S. Optimizing Cord Blood Thyroid Stimulating Hormone Cutoff for Screening of Congenital Hypothyroidism-Experience from Screening 164,000 Newborns in a Tertiary Hospital in India. Indian J Endocrinol Metab. 2021 Jul-Aug;25(4):348-353. doi: 10.4103/ijem.ijem_220_21. Epub 2021 Dec 15. PMID: 35136744; PMCID: PMC8793950.
-
Ramachandran J, Chandramohan A, Gangadharan SK, Unnikrishnan LS, Priyambada L, Simon A. Visceral larva migrans presenting as multiple liver abscesses. Trop Doct. 2013 Oct;43(4):154-7. doi: 10.1177/0049475513507254. Epub 2013 Oct 7. PMID: 24100348.
-
Korula S, Ravichandran L, Paul PG, Johnson J, Chapla A, Santhanam S, Simon A, Mathai S. Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India. Indian J Endocrinol Metab. 2022 Jan-Feb;26(1):79-86. doi: 10.4103/ijem.ijem_429_21. Epub 2022 Apr 27. PMID: 35662751; PMCID: PMC9162257.
-
Mohan S, Danda S, Mathai S, Simon A. 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. Natl Med J India. 2019 May-Jun;32(3):141-143. doi: 10.4103/0970-258X.278692. PMID: 32129306.
-
van Geest FS, Groeneweg S, van den Akker ELT, Bacos I, Barca D, van den Berg SAA, Bertini E, Brunner D, Brunetti-Pierri N, Cappa M, Cappuccio G, Chatterjee K, Chesover AD, Christian P, Coutant R, Craiu D, Crock P, Dewey C, Dica A, Dimitri P, Dubey R, Enderli A, Fairchild J, Gallichan J, Garibaldi LR, George B, Hackenberg A, Heinrich B, Huynh T, Kłosowska A, Lawson-Yuen A, Linder-Lucht M, Lyons G, Monti Lora F, Moran C, Müller KE, Paone L, Paul PG, Polak M, Porta F, Reinauer C, de Rijke YB, Seckold R, Menevşe TS, Simm P, Simon A, Spada M, Stoupa A, Szeifert L, Tonduti D, van Toor H, Turan S, Vanderniet J, de Waart M, van der Wal R, van der Walt A, van Wermeskerken AM, Wierzba J, Zibordi F, Zung A, Peeters RP, Visser WE. Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study. J Clin Endocrinol Metab. 2022 Feb 17;107(3):e1136-e1147. doi: 10.1210/clinem/dgab750. PMID: 34679181; PMCID: PMC8852204.
-
Pramanik BK, Angelin JJ, Mathai VJ, Mathai S, Korula S, Simon A. Smartphone App as Motivational Intervention to Improve Glycemic Control in Adolescents with Type 1 Diabetes. Indian J Pediatr. 2019 Dec;86(12):1118-1123 .doi: 10.1007/s12098-019-03035-x. Epub 2019 Jul 29. PMID: 31353430.
-
Jacob J, Joseph TK, Srinivasan R, Kompithra RZ, Simon A, Kang G. Direct and Indirect Costs of Pediatric Gastroenteritis in Vellore, India. Indian Pediatr. 2016 Jul 8;53(7):642-4. doi: 10.1007/s13312-016-0903-3. PMID: 27508545.
-
Sarkar S, Chacko SR, Korula S, Hesarghatta A, Balakrishnan R, Mathai S, Simon A, Chacko G, Prabhu K, Chacko AG. A Comparison of Long-Term Treatment Outcomes Between Giant and Nongiant Craniopharyngiomas. World Neurosurg. 2022 Mar 20:S1878-8750(22)00363-1. doi: 10.1016/j.wneu.2022.03.073. Epub ahead of print. PMID: 35321841.
-
Korula S, Ravichandran L, Paul PG, Johnson J, Chapla A, Santhanam S, Simon A, Mathai S. Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India. Indian J Endocrinol Metab. 2022 Jan-Feb;26(1):79-86. doi: 10.4103/ijem.ijem_429_21. Epub 2022 Apr 27. PMID: 35662751; PMCID: PMC9162257.
-
Sarkar S, Chacko SR, Korula S, Simon A, Mathai S, Chacko G, Chacko AG. Long-term outcomes following maximal safe resection in a contemporary series of childhood craniopharyngiomas. Acta Neurochir (Wien). 2021 Feb;163(2):499-509. doi: 10.1007/s00701-020-04591-4. Epub 2020 Oct 19. PMID: 33078364.
-
Anna Simon.Detection Of Rhinoviruses Causing Acute Respiratory Infection Among Children At A Tertiary Care Center In South India Indian Journal of Medical Microbiology 2021 39(Sup1):S1–S133
-
Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. PMID: 34303877.
-
Sarkar S, Korula S, Mathai S, Simon A, Balakrishnan R, Backianathan S, Chacko AG. Upfront adjuvant irradiation versus postoperative surveillance following incomplete surgical resection of craniopharyngiomas in children and young adults. Childs Nerv Syst. 2022 Oct;38(10):1877-1883. doi: 10.1007/s00381-022-05635-z. Epub 2022 Aug 9. PMID: 35945339.
-
Tergestina M, Rebekah G, Job V, Simon A, Thomas N. A randomized double-blind controlled trial comparing two regimens of vitamin D supplementation in preterm neonates. J Perinatol. 2016 Sep;36(9):763-7. doi: 10.1038/jp.2016.70. Epub 2016 May 5. PMID: 27149055. Link
-
Ramprasad C, Zachariah R, Steinhoff M, Simon A. Parental attitudes towards influenza vaccination for children in South India. World J Pediatr. 2017 Feb;13(1):84-90. doi: 10.1007/s12519-016-0053-7. Epub 2016 Aug 15. PMID: 27577192.
-
Ravichandran L, Paul S, A R, Hs A, Mathai S, Simon A, Danda S, Thomas N, Chapla A. High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia. Endocrine. 2024 Mar 5. doi: 10.1007/s12020-024-03747-x. Epub ahead of print. PMID: 38441846. Link