787 related articles for article (PubMed ID: 19070492)
1. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
Park YE; Hayashi YK; Goto K; Komaki H; Hayashi Y; Inuzuka T; Noguchi S; Nonaka I; Nishino I
Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?
Gnocchi VF; Ellis JA; Zammit PS
Biochem Soc Trans; 2008 Dec; 36(Pt 6):1344-9. PubMed ID: 19021553
[TBL] [Abstract][Full Text] [Related]
4. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.
Cenni V; Sabatelli P; Mattioli E; Marmiroli S; Capanni C; Ognibene A; Squarzoni S; Maraldi NM; Bonne G; Columbaro M; Merlini L; Lattanzi G
J Med Genet; 2005 Mar; 42(3):214-20. PubMed ID: 15744034
[TBL] [Abstract][Full Text] [Related]
7. A novel LMNA gene mutation Leu162Pro and the associated clinical characteristics in a family with autosomal-dominant emery-dreifuss muscular dystrophy.
Kim HY; Ki CS; Kang SJ; Khang SK; Koh SH; Kim DW; Kim SH; Sung IH
Muscle Nerve; 2008 Oct; 38(4):1336-9. PubMed ID: 18816602
[TBL] [Abstract][Full Text] [Related]
8. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
Hong JS; Ki CS; Kim JW; Suh YL; Kim JS; Baek KK; Kim BJ; Ahn KJ; Kim DK
J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [The laminopathy saga].
Bonne G
Rev Neurol; 2003 Oct 16-31; 37(8):772-4. PubMed ID: 14593639
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
Scharner J; Brown CA; Bower M; Iannaccone ST; Khatri IA; Escolar D; Gordon E; Felice K; Crowe CA; Grosmann C; Meriggioli MN; Asamoah A; Gordon O; Gnocchi VF; Ellis JA; Mendell JR; Zammit PS
Hum Mutat; 2011 Feb; 32(2):152-67. PubMed ID: 20848652
[TBL] [Abstract][Full Text] [Related]
13. Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.
Walter MC; Witt TN; Weigel BS; Reilich P; Richard P; Pongratz D; Bonne G; Wehnert MS; Lochmüller H
Neuromuscul Disord; 2005 Jan; 15(1):40-4. PubMed ID: 15639119
[TBL] [Abstract][Full Text] [Related]
14. Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy.
Menezes MP; Waddell LB; Evesson FJ; Cooper S; Webster R; Jones K; Mowat D; Kiernan MC; Johnston HM; Corbett A; Harbord M; North KN; Clarke NF
Neurology; 2012 Apr; 78(16):1258-63. PubMed ID: 22491857
[TBL] [Abstract][Full Text] [Related]
15. TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
Liang WC; Mitsuhashi H; Keduka E; Nonaka I; Noguchi S; Nishino I; Hayashi YK
Ann Neurol; 2011 Jun; 69(6):1005-13. PubMed ID: 21391237
[TBL] [Abstract][Full Text] [Related]
16. Pathological changes of the myonuclear fibrous lamina and internal nuclear membrane in two cases of autosomal dominant limb-girdle muscular dystrophy with atrioventricular conduction disturbance (LGMD1B).
Matsubara S; Kitaguchi T
Acta Neuropathol; 2004 Feb; 107(2):111-8. PubMed ID: 14673599
[TBL] [Abstract][Full Text] [Related]
17. Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene.
Kandert S; Wehnert M; Müller CR; Buendia B; Dabauvalle MC
Eur J Cell Biol; 2009 Oct; 88(10):593-608. PubMed ID: 19589617
[TBL] [Abstract][Full Text] [Related]
18. Myofiber degeneration in autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) (LGMD1B).
Mittelbronn M; Hanisch F; Gleichmann M; Stötter M; Korinthenberg R; Wehnert M; Bonne G; Rudnik-Schöneborn S; Bornemann A
Brain Pathol; 2006 Oct; 16(4):266-72. PubMed ID: 17107595
[TBL] [Abstract][Full Text] [Related]
19. Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations.
Carboni N; Mura M; Marrosu G; Cocco E; Marini S; Solla E; Mateddu A; Maioli MA; Piras R; Mallarini G; Mercuro G; Porcu M; Marrosu MG
Muscle Nerve; 2010 Apr; 41(4):458-63. PubMed ID: 19882644
[TBL] [Abstract][Full Text] [Related]
20. [Autosomal recessive limb-girdle muscular dystrophy].
Hernández-Caballero ME; Miranda-Duarte A; Escobar-Cedillo RE; Villegas-Castrejon H
Rev Neurol; 2010 Oct; 51(8):489-96. PubMed ID: 20925031
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]