Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2015 1
2017 2
2018 2
2019 3
2020 3
2021 2
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

12 results
Results by year
Filters applied: . Clear all
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
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 Uniform Description of Perioperative Brain MRI Findings in Infants with Severe Congenital Heart Disease: Results of a European Collaboration.
Stegeman R, Feldmann M, Claessens NHP, Jansen NJG, Breur JMPJ, de Vries LS, Logeswaran T, Reich B, Knirsch W, Kottke R, Hagmann C, Latal B, Simpson J, Pushparajah K, Bonthrone AF, Kelly CJ, Arulkumaran S, Rutherford MA, Counsell SJ, Benders MJNL; European Association Brain in Congenital Heart Disease Consortium. Stegeman R, et al. Among authors: logeswaran t. AJNR Am J Neuroradiol. 2021 Nov;42(11):2034-2039. doi: 10.3174/ajnr.A7328. Epub 2021 Oct 21. AJNR Am J Neuroradiol. 2021. PMID: 34674999
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.
12 results