These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
183 related articles for article (PubMed ID: 16696870)
21. 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]
22. Abnormal Cortical Thickness Is Associated With Deficits in Social Cognition in Patients With Myotonic Dystrophy Type 1. Serra L; Bianchi G; Bruschini M; Giulietti G; Domenico CD; Bonarota S; Petrucci A; Silvestri G; Perna A; Meola G; Caltagirone C; Bozzali M Front Neurol; 2020; 11():113. PubMed ID: 32180756 [No Abstract] [Full Text] [Related]
23. Facial emotion recognition in myotonic dystrophy type 1 correlates with CTG repeat expansion. Winblad S; Hellström P; Lindberg C; Hansen S J Neurol Neurosurg Psychiatry; 2006 Feb; 77(2):219-23. PubMed ID: 16421126 [TBL] [Abstract][Full Text] [Related]
24. Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1). Jean S; Richer L; Laberge L; Mathieu J Orphanet J Rare Dis; 2014 Nov; 9():186. PubMed ID: 25424323 [TBL] [Abstract][Full Text] [Related]
25. The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1. Ballester-Lopez A; Linares-Pardo I; Koehorst E; Núñez-Manchón J; Pintos-Morell G; Coll-Cantí J; Almendrote M; Lucente G; Arbex A; Magaña JJ; Murillo-Melo NM; Lucia A; Monckton DG; Cumming SA; Ramos-Fransi A; Martínez-Piñeiro A; Nogales-Gadea G Genes (Basel); 2020 Jul; 11(7):. PubMed ID: 32645888 [TBL] [Abstract][Full Text] [Related]
26. Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms. Ekström AB; Hakenäs-Plate L; Samuelsson L; Tulinius M; Wentz E Am J Med Genet B Neuropsychiatr Genet; 2008 Sep; 147B(6):918-26. PubMed ID: 18228241 [TBL] [Abstract][Full Text] [Related]
27. Instability in the transmission of the myotonic dystrophy CTG repeat in human oocytes and preimplantation embryos. Dean NL; Tan SL; Ao A Fertil Steril; 2006 Jul; 86(1):98-105. PubMed ID: 16716318 [TBL] [Abstract][Full Text] [Related]
28. Parental repeat length instability in myotonic dystrophy type 1 pre- and protomutations. Joosten IBT; Hellebrekers DMEI; de Greef BTA; Smeets HJM; de Die-Smulders CEM; Faber CG; Gerrits MM Eur J Hum Genet; 2020 Jul; 28(7):956-962. PubMed ID: 32203199 [TBL] [Abstract][Full Text] [Related]
29. Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins. van den Broek WJ; Nelen MR; Wansink DG; Coerwinkel MM; te Riele H; Groenen PJ; Wieringa B Hum Mol Genet; 2002 Jan; 11(2):191-8. PubMed ID: 11809728 [TBL] [Abstract][Full Text] [Related]
30. IgG deficiency and expansion of CTG repeats in myotonic dystrophy. Kaminsky P; Lesesve JF; Jonveaux P; Pruna L Clin Neurol Neurosurg; 2011 Jul; 113(6):464-8. PubMed ID: 21371814 [TBL] [Abstract][Full Text] [Related]
31. Myotonic dystrophies. Huang CC; Kuo HC Chang Gung Med J; 2005 Aug; 28(8):517-26. PubMed ID: 16265841 [TBL] [Abstract][Full Text] [Related]
32. Cognitive profile in childhood myotonic dystrophy type 1: is there a global impairment? Angeard N; Gargiulo M; Jacquette A; Radvanyi H; Eymard B; Héron D Neuromuscul Disord; 2007 Jun; 17(6):451-8. PubMed ID: 17433680 [TBL] [Abstract][Full Text] [Related]
33. Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry. Chong-Nguyen C; Wahbi K; Algalarrondo V; Bécane HM; Radvanyi-Hoffman H; Arnaud P; Furling D; Lazarus A; Bassez G; Béhin A; Fayssoil A; Laforêt P; Stojkovic T; Eymard B; Duboc D Circ Cardiovasc Genet; 2017 Jun; 10(3):. PubMed ID: 28611030 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1. Pan H; Lin HM; Ku WY; Li TC; Li SY; Lin CC; Hsiao KM Eur J Hum Genet; 2001 Aug; 9(8):638-41. PubMed ID: 11528511 [TBL] [Abstract][Full Text] [Related]
36. Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes. Overend G; Légaré C; Mathieu J; Bouchard L; Gagnon C; Monckton DG Hum Mol Genet; 2019 Jul; 28(13):2245-2254. PubMed ID: 31220271 [TBL] [Abstract][Full Text] [Related]
37. Application of a reliable and rapid polymerase chain reaction based method in the diagnosis of myotonic dystrophy type 1 (DM1) in India. Kumar A; Agarwal S; Phadke SR; Pradhan S Meta Gene; 2014 Dec; 2():106-13. PubMed ID: 25606394 [TBL] [Abstract][Full Text] [Related]
38. Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy. Mootha VV; Hansen B; Rong Z; Mammen PP; Zhou Z; Xing C; Gong X Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4579-4585. PubMed ID: 28886202 [TBL] [Abstract][Full Text] [Related]
39. Mutagenic stress modulates the dynamics of CTG repeat instability associated with myotonic dystrophy type 1. Piñeiro E; Fernàndez-López L; Gamez J; Marcos R; Surrallés J; Velázquez A Nucleic Acids Res; 2003 Dec; 31(23):6733-40. PubMed ID: 14627806 [TBL] [Abstract][Full Text] [Related]
40. The correlation of CTG repeat length with material and social deprivation in myotonic dystrophy. Laberge L; Veillette S; Mathieu J; Auclair J; Perron M Clin Genet; 2007 Jan; 71(1):59-66. PubMed ID: 17204048 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]