 |
|
Genotype-phenotype correlations in pediatric patients with myotonic dystrophy type 1
Hyeong Jung Kim (Kim HJ), Ji-Hoon Na (Na JH), Young-Mock Lee (Lee YM)
Clin Exp Pediatr. 2019;62(2):55-61. Published online 2018 Sep 23 DOI: https://doi.org/10.3345/kjp.2018.06919
|
|
Citations to this article as recorded by
 The characteristics of dysphagia and the incidence of pneumonia in Myotonic dystrophy type 1 patients especially concerning swallowing function evaluated by endoscopy
Tomonori Kambayashi, Ai Hirano-Kawamoto, Toshiaki Takahashi, Sayaka Taniguchi, Masaru Yoshioka, Hiroyasu Tanaka, Hideki Oizumi, Tomoko Totsune, Saki Oshiro, Toru Baba, Atsushi Takeda, Takuma Hisaoka, Jun Ohta, Ryoukichi Ikeda, Jun Suzuki, Kengo Kato, Yuki
Auris Nasus Larynx.2022; 49(6): 1003. CrossRef Impact of prematurity and the CTG repeat length on outcomes in congenital myotonic dystrophy
Yu Saito, Kenta Matsumura, Misao Kageyama, Yuichi Kato, Eiji Ohta, Kiyoaki Sumi, Takeshi Futatani, Taketoshi Yoshida
BMC Research Notes.2020;[Epub] CrossRef Preliminary Findings on CTG Expansion Determination in Different Tissues from Patients with Myotonic Dystrophy Type 1
Alfonsina Ballester-Lopez, Emma Koehorst, Ian Linares-Pardo, Judit Núñez-Manchón, Miriam Almendrote, Giuseppe Lucente, Andrea Arbex, Carles Puente Puente, Alejandro Lucia, Darren G. Monckton, Sarah A. Cumming, Guillem Pintos-Morell, Jaume Coll-Cantí, Alb
Genes.2020; 11(11): 1321. CrossRef
|