347 related articles for article (PubMed ID: 15691357)
1. Cardiac involvement in Emery-Dreifuss muscular dystrophy.
Wessely R; Seidl S; Schömig A
Clin Genet; 2005 Mar; 67(3):220-3. PubMed ID: 15691357
[TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
[TBL] [Abstract][Full Text] [Related]
3. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
Onishi Y; Higuchi J; Ogawa T; Namekawa A; Hayashi H; Odakura H; Goto K; Hayashi YK
Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964
[TBL] [Abstract][Full Text] [Related]
4. [Cardiac involvement in Emery-Dreifuss muscular dystrophy: a case report].
Chabrak S; Ammar S; Ammar N; Ouali S; Mghaieth F; Larbi N; Kafsi N; Hentati F; Mechmeche R
Tunis Med; 2006 Jun; 84(6):361-4. PubMed ID: 17042210
[TBL] [Abstract][Full Text] [Related]
5. Hereditary muscular dystrophies and the heart.
Hermans MC; Pinto YM; Merkies IS; de Die-Smulders CE; Crijns HJ; Faber CG
Neuromuscul Disord; 2010 Aug; 20(8):479-92. PubMed ID: 20627570
[TBL] [Abstract][Full Text] [Related]
6. Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations.
Sanna T; Dello Russo A; Toniolo D; Vytopil M; Pelargonio G; De Martino G; Ricci E; Silvestri G; Giglio V; Messano L; Zachara E; Bellocci F
Eur Heart J; 2003 Dec; 24(24):2227-36. PubMed ID: 14659775
[TBL] [Abstract][Full Text] [Related]
7. Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy.
Zhang L; Shen H; Zhao Z; Bing Q; Hu J
Mol Med Rep; 2015 Oct; 12(4):5065-71. PubMed ID: 26165385
[TBL] [Abstract][Full Text] [Related]
8. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
Jakobs PM; Hanson EL; Crispell KA; Toy W; Keegan H; Schilling K; Icenogle TB; Litt M; Hershberger RE
J Card Fail; 2001 Sep; 7(3):249-56. PubMed ID: 11561226
[TBL] [Abstract][Full Text] [Related]
9. Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation.
Carboni N; Mura M; Marrosu G; Cocco E; Ahmad M; Solla E; Mateddu A; Maioli MA; Marini S; Nissardi V; Frau J; Mallarini G; Mercuro G; Marrosu MG
Neuromuscul Disord; 2008 Apr; 18(4):291-8. PubMed ID: 18337098
[TBL] [Abstract][Full Text] [Related]
10. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
Bakay M; Wang Z; Melcon G; Schiltz L; Xuan J; Zhao P; Sartorelli V; Seo J; Pegoraro E; Angelini C; Shneiderman B; Escolar D; Chen YW; Winokur ST; Pachman LM; Fan C; Mandler R; Nevo Y; Gordon E; Zhu Y; Dong Y; Wang Y; Hoffman EP
Brain; 2006 Apr; 129(Pt 4):996-1013. PubMed ID: 16478798
[TBL] [Abstract][Full Text] [Related]
11. Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant.
Mercuri E; Poppe M; Quinlivan R; Messina S; Kinali M; Demay L; Bourke J; Richard P; Sewry C; Pike M; Bonne G; Muntoni F; Bushby K
Arch Neurol; 2004 May; 61(5):690-4. PubMed ID: 15148145
[TBL] [Abstract][Full Text] [Related]
12. Orthopedic deformities in Emery-Dreifuss muscular dystrophy.
Shapiro F; Specht L
J Pediatr Orthop; 1991; 11(3):336-40. PubMed ID: 2056082
[TBL] [Abstract][Full Text] [Related]
13. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
van Tintelen JP; Hofstra RM; Katerberg H; Rossenbacker T; Wiesfeld AC; du Marchie Sarvaas GJ; Wilde AA; van Langen IM; Nannenberg EA; van der Kooi AJ; Kraak M; van Gelder IC; van Veldhuisen DJ; Vos Y; van den Berg MP;
Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
[TBL] [Abstract][Full Text] [Related]
14. High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene.
Sakata K; Shimizu M; Ino H; Yamaguchi M; Terai H; Fujino N; Hayashi K; Kaneda T; Inoue M; Oda Y; Fujita T; Kaku B; Kanaya H; Mabuchi H
Circulation; 2005 Jun; 111(25):3352-8. PubMed ID: 15967842
[TBL] [Abstract][Full Text] [Related]
15. Cardiac involvement in Emery Dreifuss muscular dystrophy: a case series.
Buckley AE; Dean J; Mahy IR
Heart; 1999 Jul; 82(1):105-8. PubMed ID: 10377322
[TBL] [Abstract][Full Text] [Related]
16. Heart involvement in lamin A/C related diseases.
Ben Yaou R; Gueneau L; Demay L; Stora S; Chikhaoui K; Richard P; Bonne G
Arch Mal Coeur Vaiss; 2006 Sep; 99(9):848-55. PubMed ID: 17067107
[TBL] [Abstract][Full Text] [Related]
17. [Emery-Dreifuss muscular dystrophy--reported a family with 5 cases].
Luo D
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1991 Dec; 24(6):330-1, 382. PubMed ID: 1800056
[TBL] [Abstract][Full Text] [Related]
18. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
Arimura T; Helbling-Leclerc A; Massart C; Varnous S; Niel F; Lacène E; Fromes Y; Toussaint M; Mura AM; Keller DI; Amthor H; Isnard R; Malissen M; Schwartz K; Bonne G
Hum Mol Genet; 2005 Jan; 14(1):155-69. PubMed ID: 15548545
[TBL] [Abstract][Full Text] [Related]
19. Molecular signatures of Emery-Dreifuss muscular dystrophy.
Wheeler MA; Ellis JA
Biochem Soc Trans; 2008 Dec; 36(Pt 6):1354-8. PubMed ID: 19021555
[TBL] [Abstract][Full Text] [Related]
20. Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity.
Zhang Q; Bethmann C; Worth NF; Davies JD; Wasner C; Feuer A; Ragnauth CD; Yi Q; Mellad JA; Warren DT; Wheeler MA; Ellis JA; Skepper JN; Vorgerd M; Schlotter-Weigel B; Weissberg PL; Roberts RG; Wehnert M; Shanahan CM
Hum Mol Genet; 2007 Dec; 16(23):2816-33. PubMed ID: 17761684
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
