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2017 2
2018 2
2019 3
2020 3
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Page 1
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
Pediatric heart failure therapy: why β1-receptor blocker, tissue ACE-I and mineralocorticoid-receptor-blocker?
Recla S, Schmidt D, Logeswaran T, Esmaeili A, Schranz D. Recla S, et al. Among authors: logeswaran t. Transl Pediatr. 2019 Apr;8(2):127-132. doi: 10.21037/tp.2019.04.08. Transl Pediatr. 2019. PMID: 31161079 Free PMC article. Review.
Neurodevelopmental outcome in hypoplastic left heart syndrome after hybrid procedure.
Reich B, Heye KN, Wetterling K, Logeswaran T, Hahn A, Akintürk H, Jux C, Schranz D. Reich B, et al. Among authors: logeswaran t. Transl Pediatr. 2019 Apr;8(2):94-106. doi: 10.21037/tp.2019.04.05. Transl Pediatr. 2019. PMID: 31161076 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
A novel SPEG mutation causes non-compaction cardiomyopathy and neuropathy in a floppy infant with centronuclear myopathy.
Wang H, Schänzer A, Kampschulte B, Daimagüler HS, Logeswaran T, Schlierbach H, Petzinger J, Ehrhardt H, Hahn A, Cirak S. Wang H, et al. Among authors: logeswaran t. Acta Neuropathol Commun. 2018 Aug 29;6(1):83. doi: 10.1186/s40478-018-0589-y. Acta Neuropathol Commun. 2018. PMID: 30157964 Free PMC article. No abstract available.
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 Apr;173(4):959-965. doi: 10.1002/ajmg.a.38102. Am J Med Genet A. 2017. PMID: 28328125
Symptom-orientated oral hygiene for children after heart transplantation: Effectiveness of a standardized prophylactic program.
Schulz-Weidner N, Bulski JC, Siahi-Benlarbi R, Bauer J, Logeswaran T, Jux C, Wetzel WE, Krämer N. Schulz-Weidner N, et al. Among authors: logeswaran t. Pediatr Transplant. 2020 Nov;24(7):e13845. doi: 10.1111/petr.13845. Epub 2020 Sep 30. Pediatr Transplant. 2020. PMID: 32997421
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.
Parental Awareness of Oral Health and Nutritional Behavior in Children with Congenital Heart Diseases Compared to Healthy Children.
Schulz-Weidner N, Logeswaran T, Schlenz MA, Krämer N, Bulski JC. Schulz-Weidner N, et al. Among authors: logeswaran t. Int J Environ Res Public Health. 2020 Sep 27;17(19):7057. doi: 10.3390/ijerph17197057. Int J Environ Res Public Health. 2020. PMID: 32992501 Free PMC article.
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