320 related articles for article (PubMed ID: 15967842)
1. 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]
2. [Emery-Dreifuss muscular dystrophy].
Kubo S; Tsukahara T; Arahata K
Nihon Rinsho; 1997 Dec; 55(12):3186-9. PubMed ID: 9436433
[TBL] [Abstract][Full Text] [Related]
3. Emery-Dreifuss muscular dystrophy.
Zacharias AS; Wagener ME; Warren ST; Hopkins LC
Semin Neurol; 1999; 19(1):67-79. PubMed ID: 10711990
[TBL] [Abstract][Full Text] [Related]
4. Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy.
Canki-Klain N; Récan D; Milicić D; Llense S; Leturcq F; Deburgrave N; Kaplan JC; Debevec M; Zurak N
Croat Med J; 2000 Dec; 41(4):389-95. PubMed ID: 11063761
[TBL] [Abstract][Full Text] [Related]
5. [A novel splice-site mutation in the STA gene in a Japanese patient with Emery-Dreifuss muscular dystrophy].
Hasegawa T; Kobayashi K; Arahata K; Itoyama Y
Rinsho Shinkeigaku; 1999 Nov; 39(11):1138-43. PubMed ID: 10689937
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. A Japanese family carrying a novel mutation in the Emery-Dreifuss muscular dystrophy gene.
Ichikawa Y; Watanabe M; Kowa H; Murayama S; Mizuno T; Komuro I; Ishiki R; Goto J; Kanazawa I
Ann Neurol; 1997 Mar; 41(3):399-402. PubMed ID: 9066362
[TBL] [Abstract][Full Text] [Related]
8. X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization.
Paradas C; Márquez C; Gallardo E; De Luna N; Chinchón I; Recan D; Jiménez MD; Illa I
Muscle Nerve; 2005 Jul; 32(1):61-5. PubMed ID: 15880484
[TBL] [Abstract][Full Text] [Related]
9. Emery dreifuss muscular dystrophy: a clinico-pathological study.
Gayathri N; Taly AB; Sinha S; Suresh TG; Gorai D
Neurol India; 2006 Jun; 54(2):197-9. PubMed ID: 16804269
[TBL] [Abstract][Full Text] [Related]
10. Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.
Muntoni F; Bonne G; Goldfarb LG; Mercuri E; Piercy RJ; Burke M; Yaou RB; Richard P; Récan D; Shatunov A; Sewry CA; Brown SC
Brain; 2006 May; 129(Pt 5):1260-8. PubMed ID: 16585054
[TBL] [Abstract][Full Text] [Related]
11. [Cardiologic evaluation in a family with Emery-Dreifuss muscular dystrophy].
Pinelli G; Dominici P; Merlini L; Di Pasquale G; Granata C; Bonfiglioli S
G Ital Cardiol; 1987 Jul; 17(7):589-93. PubMed ID: 3678709
[TBL] [Abstract][Full Text] [Related]
12. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
Mercuri E; Counsell S; Allsop J; Jungbluth H; Kinali M; Bonne G; Schwartz K; Bydder G; Dubowitz V; Muntoni F
Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
[TBL] [Abstract][Full Text] [Related]
13. Emery-Dreifuss muscular dystrophy.
Helbling-Leclerc A; Bonne G; Schwartz K
Eur J Hum Genet; 2002 Mar; 10(3):157-61. PubMed ID: 11973618
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations in the emerin gene in Israeli families.
Nevo Y; Ahituv S; Yaron Y; Kedmi M; Shomrat R; Legum C; Orr-Urtreger A
Hum Mutat; 2001 Jun; 17(6):522. PubMed ID: 11385714
[TBL] [Abstract][Full Text] [Related]
15. Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion.
Fujimoto S; Ishikawa T; Saito M; Wada Y; Wada I; Arahata K; Nonaka I
Neuropediatrics; 1999 Jun; 30(3):161-3. PubMed ID: 10480214
[TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype.
Yates JR; Bagshaw J; Aksmanovic VM; Coomber E; McMahon R; Whittaker JL; Morrison PJ; Kendrick-Jones J; Ellis JA
Neuromuscul Disord; 1999 May; 9(3):159-65. PubMed ID: 10382909
[TBL] [Abstract][Full Text] [Related]
17. Dilated, arrhythmogenic cardiomyopathy in emery-dreifuss muscular dystrophy due to the emerin splice-site mutation c.449 + 1G>A.
Finsterer J; Stöllberger C; Sehnal E; Rehder H; Laccone F
Cardiology; 2015; 130(1):48-51. PubMed ID: 25502304
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Limb-girdle muscular dystrophy due to emerin gene mutations.
Ura S; Hayashi YK; Goto K; Astejada MN; Murakami T; Nagato M; Ohta S; Daimon Y; Takekawa H; Hirata K; Nonaka I; Noguchi S; Nishino I
Arch Neurol; 2007 Jul; 64(7):1038-41. PubMed ID: 17620497
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
