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Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy.
Götz A, Tyynismaa H, Euro L, Ellonen P, Hyötyläinen T, Ojala T, Hämäläinen RH, Tommiska J, Raivio T, Oresic M, Karikoski R, Tammela O, Simola KO, Paetau A, Tyni T, Suomalainen A. Götz A, et al. Among authors: ojala t. Am J Hum Genet. 2011 May 13;88(5):635-42. doi: 10.1016/j.ajhg.2011.04.006. Epub 2011 May 5. Am J Hum Genet. 2011. PMID: 21549344 Free PMC article.
Genetic Basis of Severe Childhood-Onset Cardiomyopathies.
Vasilescu C, Ojala TH, Brilhante V, Ojanen S, Hinterding HM, Palin E, Alastalo TP, Koskenvuo J, Hiippala A, Jokinen E, Jahnukainen T, Lohi J, Pihkala J, Tyni TA, Carroll CJ, Suomalainen A. Vasilescu C, et al. Among authors: ojala th. J Am Coll Cardiol. 2018 Nov 6;72(19):2324-2338. doi: 10.1016/j.jacc.2018.08.2171. J Am Coll Cardiol. 2018. PMID: 30384889 Free article.
Perinatal and perioperative factors associated with mortality and an increased need for hospital care in infants with transposition of the great arteries: A nationwide 11-year population-based cohort.
Hautala J, Gissler M, Ritvanen A, Helle E, Pihkala J, Mattila IP, Pätilä T, Salminen J, Puntila J, Jokinen E, Räsänen J, Vahlberg T, Ojala T. Hautala J, et al. Among authors: ojala t. Acta Obstet Gynecol Scand. 2020 Dec;99(12):1728-1735. doi: 10.1111/aogs.13953. Epub 2020 Jul 23. Acta Obstet Gynecol Scand. 2020. PMID: 32640036 Free article.
The implementation of a nationwide anomaly screening programme improves prenatal detection of major cardiac defects: an 11-year national population-based cohort study.
Hautala J, Gissler M, Ritvanen A, Tekay A, Pitkänen-Argillander O, Stefanovic V, Sarkola T, Helle E, Pihkala J, Pätilä T, Mattila IP, Jokinen E, Räsänen J, Ojala T. Hautala J, et al. Among authors: ojala t. BJOG. 2019 Jun;126(7):864-873. doi: 10.1111/1471-0528.15589. Epub 2019 Jan 25. BJOG. 2019. PMID: 30576052
130 results