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8. Parkinsonism may aggravate dysphagia in myotonic dystrophy type 1: two case reports. Stano S; Barp A; Bacchin R; Zuccarino R Acta Myol; 2023; 42(1):31-34. PubMed ID: 37091528 [TBL] [Abstract][Full Text] [Related]
9. Diastolic heart dysfunction is correlated with CTG repeat length in myotonic dystrophy type 1. Park JS; Kim N; Park D Neurol Sci; 2018 Nov; 39(11):1935-1943. PubMed ID: 30094526 [TBL] [Abstract][Full Text] [Related]
10. Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1. Winkler NS; Milone M; Martinez-Thompson JM; Raja H; Aleff RA; Patel SV; Fautsch MP; Wieben ED; Baratz KH Invest Ophthalmol Vis Sci; 2018 Jun; 59(7):3053-3057. PubMed ID: 30025114 [TBL] [Abstract][Full Text] [Related]
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12. Myotonic dystrophy (DM1) and dysphagia: the need for dysphagia management guidelines and an assessment tool. LaDonna KA; Koopman WJ; Venance SL Can J Neurosci Nurs; 2011; 33(1):42-6. PubMed ID: 21560885 [TBL] [Abstract][Full Text] [Related]
13. Reduced renal function in patients with Myotonic Dystrophy type 1 and the association to CTG expansion and other potential risk factors for chronic kidney disease. Aldenbratt A; Lindberg C; Svensson MK Neuromuscul Disord; 2017 Nov; 27(11):1038-1042. PubMed ID: 29029879 [TBL] [Abstract][Full Text] [Related]
14. Neuromyelitis Optica in a Patient from Family with both Myotonic Dystrophy Type 1 and 2. Rakocevic-Stojanovic V; Peric S; Dujmovic I; Drulovic J; Pesovic J; Savic-Pavicevic D J Neuromuscul Dis; 2017; 4(1):89-92. PubMed ID: 28106565 [TBL] [Abstract][Full Text] [Related]
15. How genetics affects the brain to produce higher-level dysfunctions in myotonic dystrophy type 1. Serra L; Petrucci A; Spanò B; Torso M; Olivito G; Lispi L; Costanzi-Porrini S; Giulietti G; Koch G; Giacanelli M; Caltagirone C; Cercignani M; Bozzali M Funct Neurol; 2015; 30(1):21-31. PubMed ID: 26214024 [TBL] [Abstract][Full Text] [Related]
16. Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA). DiPaolo G; Jimenez-Moreno C; Nikolenko N; Atalaia A; Monckton DG; Guglieri M; Lochmüller H J Neurol; 2017 Apr; 264(4):701-708. PubMed ID: 28168524 [TBL] [Abstract][Full Text] [Related]
17. Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism. Tomé S; Dandelot E; Dogan C; Bertrand A; Geneviève D; Péréon Y; ; Simon M; Bonnefont JP; Bassez G; Gourdon G Hum Mutat; 2018 Jul; 39(7):970-982. PubMed ID: 29664219 [TBL] [Abstract][Full Text] [Related]
18. Stapedial reflex in myotonic dystrophy type 1 and CTG repeat expansion. Osanai R; Kinoshita M; Hirose K J Neurol; 2001 Dec; 248(12):1056-61. PubMed ID: 12013582 [TBL] [Abstract][Full Text] [Related]
19. Oral motor movements and swallowing in patients with myotonic dystrophy type 1. Ercolin B; Sassi FC; Mangilli LD; Mendonça LI; Limongi SC; de Andrade CR Dysphagia; 2013 Sep; 28(3):446-54. PubMed ID: 23460343 [TBL] [Abstract][Full Text] [Related]
20. The characteristics of dysphagia and the incidence of pneumonia in Myotonic dystrophy type 1 patients especially concerning swallowing function evaluated by endoscopy. Kambayashi T; Hirano-Kawamoto A; Takahashi T; Taniguchi S; Yoshioka M; Tanaka H; Oizumi H; Totsune T; Oshiro S; Baba T; Takeda A; Hisaoka T; Ohta J; Ikeda R; Suzuki J; Kato K; Katori Y Auris Nasus Larynx; 2022 Dec; 49(6):1003-1008. PubMed ID: 35428520 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]