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CTG repeat length underlying cardiac events and sudden death in myotonic dystrophy type 1.
Itoh H, Hisamatsu T, Segawa K, Takahashi T, Sato T, Takada H, Kuru S, Wada C, Suzuki M, Tamura T, Suwazono S, Kimura K, Matsumura T, Takahashi MP. Itoh H, et al. Among authors: suzuki m. Eur Heart J Open. 2024 Sep 18;4(5):oeae078. doi: 10.1093/ehjopen/oeae078. eCollection 2024 Sep. Eur Heart J Open. 2024. PMID: 39391712 Free PMC article.
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1.
Itoh H, Hisamatsu T, Tamura T, Segawa K, Takahashi T, Takada H, Kuru S, Wada C, Suzuki M, Suwazono S, Sasaki S, Okumura K, Horie M, Takahashi MP, Matumura T. Itoh H, et al. Among authors: suzuki m. J Am Heart Assoc. 2020 Sep;9(17):e015709. doi: 10.1161/JAHA.119.015709. Epub 2020 Aug 19. J Am Heart Assoc. 2020. PMID: 32812471 Free PMC article.
Heart rate variability and hypercapnia in Duchenne muscular dystrophy.
Mochizuki H, Okahashi S, Ugawa Y, Tamura T, Suzuki M, Miyatake S, Shigeyama T, Ogata K, Kawai M. Mochizuki H, et al. Among authors: suzuki m. Intern Med. 2008;47(21):1893-7. doi: 10.2169/internalmedicine.47.1118. Epub 2008 Nov 4. Intern Med. 2008. PMID: 18981633 Free article.
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy.
Miyatake S, Mitsuhashi S, Hayashi YK, Purevjav E, Nishikawa A, Koshimizu E, Suzuki M, Yatabe K, Tanaka Y, Ogata K, Kuru S, Shiina M, Tsurusaki Y, Nakashima M, Mizuguchi T, Miyake N, Saitsu H, Ogata K, Kawai M, Towbin J, Nonaka I, Nishino I, Matsumoto N. Miyatake S, et al. Among authors: suzuki m. Am J Hum Genet. 2017 Jan 5;100(1):169-178. doi: 10.1016/j.ajhg.2016.11.017. Epub 2016 Dec 22. Am J Hum Genet. 2017. PMID: 28017374 Free PMC article.
15,436 results
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