| scholarly article | Q13442814 |
| P2093 | author name string | Ashajyothi M Siddappa | |
| Kunal Gupta | |||
| Marie R Kennelly | |||
| P2860 | cites work | Congenital and childhood myotonic dystrophy: Current aspects of disease and future directions | Q26777206 |
| Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene | Q28285882 | ||
| Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy? | Q28353993 | ||
| Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome | Q34232976 | ||
| Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland | Q34627289 | ||
| Respiratory involvement in inherited primary muscle conditions | Q36596271 | ||
| Congenital myotonic dystrophy: prenatal ultrasound findings and pregnancy outcome | Q36713141 | ||
| Congenital and infantile myotonic dystrophy | Q38102248 | ||
| Myotonic dystrophy and Brugada syndrome: A common pathophysiologic pathway? | Q39227217 | ||
| Congenital myotonic dystrophy; a report on thirteen cases and a review of the literature | Q40744732 | ||
| Congenital myotonic dystrophy: Canadian population-based surveillance study. | Q45975792 | ||
| Swallowing in myotonic muscular dystrophy: a videofluoroscopic study | Q46453569 | ||
| Brain magnetic resonance image changes in a family with congenital and classic myotonic dystrophy | Q48908614 | ||
| Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms | Q50310770 | ||
| Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation. | Q51143455 | ||
| Myotonic dystrophy type I in childhood Long-term evolution in patients surviving the neonatal period. | Q51899032 | ||
| Course, prognosis and complications of childhood-onset myotonic dystrophy | Q52092992 | ||
| Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1. | Q54401968 | ||
| Gastroparesis in neonatal myotonic dystrophy | Q70804108 | ||
| Pharyngo-esophageal motility disturbances in patients with myotonic dystrophy | Q73085985 | ||
| [Epidemiological study of Steinert's congenital myotonic dystrophy: dysmorphological characteristics] | Q73482662 | ||
| Congenital myotonic dystrophy with cardiac conduction defect and eventration of the diaphragm | Q82915081 | ||
| Myotonic dystrophy | Q87411199 | ||
| Myotonic dystrophy type 1: clinical manifestations in children and adolescents | Q89000100 | ||
| Update on Brugada Syndrome 2019 | Q90114237 | ||
| P921 | main subject | Brugada syndrome | Q599683 |
| myotonic dystrophy | Q1860507 | ||
| P304 | page(s) | e919867 | |
| P577 | publication date | 2020-01-09 | |
| P1433 | published in | The American journal of case reports | Q27722384 |
| P1476 | title | Congenital Myotonic Dystrophy and Brugada Syndrome: A Report of Two Cases | |
| P478 | volume | 21 |
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