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2017 2
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Page 1
Risk Factors for Perioperative Brain Lesions in Infants With Congenital Heart Disease: A European Collaboration.
Bonthrone AF, Stegeman R, Feldmann M, Claessens NHP, Nijman M, Jansen NJG, Nijman J, Groenendaal F, de Vries LS, Benders MJNL, Haas F, Bekker MN, Logeswaran T, Reich B, Kottke R, Hagmann C, Latal B, Dave H, Simpson J, Pushparajah K, Austin C, Kelly CJ, Arulkumaran S, Rutherford MA, Counsell SJ, Knirsch W, Breur JMPJ. Bonthrone AF, et al. Among authors: logeswaran t. Stroke. 2022 Dec;53(12):3652-3661. doi: 10.1161/STROKEAHA.122.039492. Epub 2022 Oct 27. Stroke. 2022. PMID: 36300371 Free PMC article.
Genetic basis of hypertrophic cardiomyopathy in children.
Rupp S, Felimban M, Schänzer A, Schranz D, Marschall C, Zenker M, Logeswaran T, Neuhäuser C, Thul J, Jux C, Hahn A. Rupp S, et al. Among authors: logeswaran t. Clin Res Cardiol. 2019 Mar;108(3):282-289. doi: 10.1007/s00392-018-1354-8. Epub 2018 Aug 13. Clin Res Cardiol. 2019. PMID: 30105547
Perioperative Brain Injury in Relation to Early Neurodevelopment Among Children with Severe Congenital Heart Disease: Results from a European Collaboration.
Neukomm A, Claessens NHP, Bonthrone AF, Stegeman R, Feldmann M, Nijman M, Jansen NJG, Nijman J, Groenendaal F, de Vries LS, Benders MJNL, Breur JMPJ, Haas F, Bekker MN, Logeswaran T, Reich B, Kottke R, Dave H, Simpson J, Pushparajah K, Kelly CJ, Arulkumaran S, Rutherford MA, Counsell SJ, Chew A, Knirsch W, Sprong MCA, van Schooneveld MM, Hagmann C, Latal B; European Association Brain in Congenital Heart Disease (EU-ABC) consortium. Neukomm A, et al. Among authors: logeswaran t. J Pediatr. 2024 Mar;266:113838. doi: 10.1016/j.jpeds.2023.113838. Epub 2023 Nov 22. J Pediatr. 2024. PMID: 37995930 Free article.
Neuromonitoring, neuroimaging, and neurodevelopmental follow-up practices in neonatal congenital heart disease: a European survey.
Feldmann M, Hagmann C, de Vries L, Disselhoff V, Pushparajah K, Logeswaran T, Jansen NJG, Breur JMPJ, Knirsch W, Benders M, Counsell S, Reich B, Latal B. Feldmann M, et al. Among authors: logeswaran t. Pediatr Res. 2023 Jan;93(1):168-175. doi: 10.1038/s41390-022-02063-2. Epub 2022 Apr 12. Pediatr Res. 2023. PMID: 35414671 Free PMC article.
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy.
Motta M, Sagi-Dain L, Krumbach OHF, Hahn A, Peleg A, German A, Lissewski C, Coppola S, Pantaleoni F, Kocherscheid L, Altmüller F, Schanze D, Logeswaran T, Chahrokh-Zadeh S, Munzig A, Nakhaei-Rad S, Cavé H, Ahmadian MR, Tartaglia M, Zenker M. Motta M, et al. Among authors: logeswaran t. Hum Mol Genet. 2020 Jul 21;29(11):1772-1783. doi: 10.1093/hmg/ddz108. Hum Mol Genet. 2020. PMID: 31108500
14 results