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Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome.
Logeswaran T, Friedburg C, Hofmann K, Akintuerk H, Biskup S, Graef M, Rad A, Weber A, Neubauer BA, Schranz D, Bouvagnet P, Lorenz B, Hahn A. Logeswaran T, et al. Am J Med Genet A. 2017 Sep;173(9):2566. doi: 10.1002/ajmg.a.38329. Epub 2017 Jun 23. Am J Med Genet A. 2017. PMID: 28816420 No abstract available.
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
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.
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.
16 results