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45. Myotonic dystrophy and hyperthyroidism--a case report. Tjia TL; Yeow YK; Nei IP Singapore Med J; 1983 Oct; 24(5):309-11. PubMed ID: 6669997 [No Abstract] [Full Text] [Related]
46. Coincidence of myotonic dystrophy and Down's syndrome (trisomy 21). Ara JR; Tamparillas M; Montori M; Capablo JL; Oliveros A J Neurol Neurosurg Psychiatry; 1987 Jan; 50(1):110-1. PubMed ID: 2950207 [No Abstract] [Full Text] [Related]
47. "Shake hands"; diagnosing a floppy infant--myotonic dystrophy and the congenital subtype: a difficult perinatal diagnosis. Verrijn Stuart AA; Huisman M; van Straaten HL; Bakker JC; Arabin B J Perinat Med; 2000; 28(6):497-501. PubMed ID: 11155437 [TBL] [Abstract][Full Text] [Related]
48. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring. Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127 [TBL] [Abstract][Full Text] [Related]
49. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Harley HG; Brook JD; Rundle SA; Crow S; Reardon W; Buckler AJ; Harper PS; Housman DE; Shaw DJ Nature; 1992 Feb; 355(6360):545-6. PubMed ID: 1346923 [TBL] [Abstract][Full Text] [Related]
50. 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]
51. Myotonic dystrophy: from linkage with secretor status to mutation detection. Sutherland GR Clin Genet; 1993 Jun; 43(6):273-5. PubMed ID: 8370145 [No Abstract] [Full Text] [Related]
52. Myotonic dystrophy and the heart. Pelargonio G; Dello Russo A; Sanna T; De Martino G; Bellocci F Heart; 2002 Dec; 88(6):665-70. PubMed ID: 12433913 [No Abstract] [Full Text] [Related]
53. [Ocular findings in patients with Steinert myotonic dystrophy]. Markowska E; Zalewska R; Mariak Z; Wojnar M Przegl Lek; 2006; 63(8):662-3. PubMed ID: 17441379 [TBL] [Abstract][Full Text] [Related]
54. The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM). Greiner J; Spengler DH; Krüger J; Tariverdian G Hum Genet; 1988 Apr; 78(4):330-2. PubMed ID: 3162894 [TBL] [Abstract][Full Text] [Related]
55. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy. Johnson KJ; Jones PJ; Spurr N; Nimmo E; Davies J; Creed H; Weiss M; Williamson R Cytogenet Cell Genet; 1988; 48(1):13-5. PubMed ID: 2460293 [TBL] [Abstract][Full Text] [Related]
56. [Mutation analysis in the CTG-base multiplication in a family with myotonic dystrophy in three generations]. Molnár J; Kis A; Melegh B; Nádasi E; Varjas T; Kovács E; Kosztolanyi G Orv Hetil; 1998 May; 139(18):1083-5. PubMed ID: 9608771 [TBL] [Abstract][Full Text] [Related]
58. 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]
59. Early onset of myotonic dystrophy in infants. Zellweger H; Ionasescu V Am J Dis Child; 1973 Apr; 125(4):601-4. PubMed ID: 4121661 [No Abstract] [Full Text] [Related]
60. Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene. Sun C; Van Ghelue M; Tranebjærg L; Thyssen F; Nilssen Ø; Torbergsen T Clin Genet; 2011 Dec; 80(6):574-80. PubMed ID: 21204798 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]