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

Year Number of Results
2004 3
2007 3
2008 2
2009 2
2010 2
2011 4
2012 7
2013 7
2014 9
2015 4
2016 7
2017 3
2018 6
2019 9
2020 4
2021 9
2022 4
2023 7
2024 3

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84 results

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Page 1
Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations.
Bourke J, Turner C, Bradlow W, Chikermane A, Coats C, Fenton M, Ilina M, Johnson A, Kapetanakis S, Kuhwald L, Morley-Davies A, Quinlivan R, Savvatis K, Schiava M, Yousef Z, Guglieri M. Bourke J, et al. Among authors: quinlivan r. Open Heart. 2022 Oct;9(2):e001977. doi: 10.1136/openhrt-2022-001977. Open Heart. 2022. PMID: 36252992 Free PMC article. Review.
Cardiac Outcomes in Adults With Mitochondrial Diseases.
Savvatis K, Vissing CR, Klouvi L, Florian A, Rahman M, Béhin A, Fayssoil A, Masingue M, Stojkovic T, Bécane HM, Berber N, Mochel F, Duboc D, Fontaine B, Krett B, Stalens C, Lejeune J, Pitceathly RDS, Lopes L, Saadi M, Gossios T, Procaccio V, Spinazzi M, Tard C, De Groote P, Dhaenens CM, Douillard C, Echaniz-Laguna A, Quinlivan R, Hanna MG, Yilmaz A, Vissing J, Laforêt P, Elliott P, Wahbi K. Savvatis K, et al. Among authors: quinlivan r. J Am Coll Cardiol. 2022 Oct 11;80(15):1421-1430. doi: 10.1016/j.jacc.2022.08.716. J Am Coll Cardiol. 2022. PMID: 36202532 Free article.
Rhabdomyolysis: a genetic perspective.
Scalco RS, Gardiner AR, Pitceathly RD, Zanoteli E, Becker J, Holton JL, Houlden H, Jungbluth H, Quinlivan R. Scalco RS, et al. Among authors: quinlivan r. Orphanet J Rare Dis. 2015 May 2;10:51. doi: 10.1186/s13023-015-0264-3. Orphanet J Rare Dis. 2015. PMID: 25929793 Free PMC article. Review.
Scoliosis in Duchenne muscular dystrophy (DMD).
Hsu JD, Quinlivan R. Hsu JD, et al. Among authors: quinlivan r. Neuromuscul Disord. 2013 Aug;23(8):611-7. doi: 10.1016/j.nmd.2013.05.003. Epub 2013 Jun 6. Neuromuscul Disord. 2013. PMID: 23746543 Review.
Skeletal muscle disorders of glycogenolysis and glycolysis.
Godfrey R, Quinlivan R. Godfrey R, et al. Among authors: quinlivan r. Nat Rev Neurol. 2016 Jul;12(7):393-402. doi: 10.1038/nrneurol.2016.75. Epub 2016 May 27. Nat Rev Neurol. 2016. PMID: 27231184 Review.
Myopathic causes of exercise intolerance with rhabdomyolysis.
Quinlivan R, Jungbluth H. Quinlivan R, et al. Dev Med Child Neurol. 2012 Oct;54(10):886-91. doi: 10.1111/j.1469-8749.2012.04320.x. Epub 2012 May 23. Dev Med Child Neurol. 2012. PMID: 22616958 Free article. Review.
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort.
de Bruyn A, Montagnese F, Holm-Yildiz S, Scharff Poulsen N, Stojkovic T, Behin A, Palmio J, Jokela M, De Bleecker JL, de Visser M, van der Kooi AJ, Ten Dam L, Domínguez González C, Maggi L, Gallone A, Kostera-Pruszczyk A, Macias A, Łusakowska A, Nedkova V, Olive M, Álvarez-Velasco R, Wanschitz J, Paradas C, Mavillard F, Querin G, Fernández-Eulate G, Quinlivan R, Walter MC, Depuydt CE, Udd B, Vissing J, Schoser B, Claeys KG. de Bruyn A, et al. Among authors: quinlivan r. Brain. 2023 Sep 1;146(9):3800-3815. doi: 10.1093/brain/awad088. Brain. 2023. PMID: 36913258
84 results