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Results: 1 to 20 of 110

1.

Facioscapulohumeral muscular dystrophy.

Tawil R.

Neurotherapeutics. 2008 Oct;5(4):601-6. doi: 10.1016/j.nurt.2008.07.005. Review.

PMID:
19019312
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Richards M, Coppée F, Thomas N, Belayew A, Upadhyaya M.

Hum Genet. 2012 Mar;131(3):325-40. doi: 10.1007/s00439-011-1100-z. Epub 2011 Oct 9. Review.

PMID:
21984394
[PubMed - indexed for MEDLINE]
3.

Facioscapulohumeral dystrophy.

Pandya S, King WM, Tawil R.

Phys Ther. 2008 Jan;88(1):105-13. Epub 2007 Nov 6. Review.

PMID:
17986494
[PubMed - indexed for MEDLINE]
Free Article
4.

Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).

Zeng W, de Greef JC, Chen YY, Chien R, Kong X, Gregson HC, Winokur ST, Pyle A, Robertson KD, Schmiesing JA, Kimonis VE, Balog J, Frants RR, Ball AR Jr, Lock LF, Donovan PJ, van der Maarel SM, Yokomori K.

PLoS Genet. 2009 Jul;5(7):e1000559. doi: 10.1371/journal.pgen.1000559. Epub 2009 Jul 10.

PMID:
19593370
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Facioscapulohumeral muscular dystrophy.

Tawil R, Van Der Maarel SM.

Muscle Nerve. 2006 Jul;34(1):1-15. Review.

PMID:
16508966
[PubMed - indexed for MEDLINE]
6.

Facioscapulohumeral muscular dystrophy.

van der Maarel SM, Frants RR, Padberg GW.

Biochim Biophys Acta. 2007 Feb;1772(2):186-94. Epub 2006 Jun 6. Review.

PMID:
16837171
[PubMed - indexed for MEDLINE]
Free Article
7.

Molecular diagnosis of facioscapulohumeral muscular dystrophy.

Upadhyaya M, Cooper DN.

Expert Rev Mol Diagn. 2002 Mar;2(2):160-71. Review.

PMID:
11962336
[PubMed - indexed for MEDLINE]
8.

Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation.

Bodega B, Ramirez GD, Grasser F, Cheli S, Brunelli S, Mora M, Meneveri R, Marozzi A, Mueller S, Battaglioli E, Ginelli E.

BMC Biol. 2009 Jul 16;7:41. doi: 10.1186/1741-7007-7-41.

PMID:
19607661
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population.

Wang ZQ, Wang N, van der Maarel S, Murong SX, Wu ZY.

Eur J Hum Genet. 2011 Jan;19(1):64-9. doi: 10.1038/ejhg.2010.143. Epub 2010 Aug 25.

PMID:
20736973
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

[Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].

Jordan B, Müller-Reible C, Zierz S.

Nervenarzt. 2011 Jun;82(6):712-22. doi: 10.1007/s00115-010-2968-x. German.

PMID:
21567298
[PubMed - indexed for MEDLINE]
11.

Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011.

Attarian S, Salort-Campana E, Nguyen K, Behin A, Andoni Urtizberea J.

Rev Neurol (Paris). 2012 Dec;168(12):910-8. doi: 10.1016/j.neurol.2011.11.008. Epub 2012 Apr 30. Review.

PMID:
22551571
[PubMed - indexed for MEDLINE]
12.

Facioscapulohumeral muscular dystrophy: consequences of chromatin relaxation.

van der Maarel SM, Miller DG, Tawil R, Filippova GN, Tapscott SJ.

Curr Opin Neurol. 2012 Oct;25(5):614-20. doi: 10.1097/WCO.0b013e328357f22d. Review.

PMID:
22892954
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy].

Desnuelle C, Sacconi S, Marolleau JP, Larghero J, Vilquin JT.

Bull Acad Natl Med. 2005 Apr;189(4):697-713; discussion 713-4. French.

PMID:
16245686
[PubMed - indexed for MEDLINE]
14.

Clinical and genetic analysis of Korean patients with facioscapulohumeral muscular dystrophy.

Ki CS, Lee ST, Kim KS, Kim JW, Hong YH, Sung JJ, Park KS, Lee KW.

J Korean Med Sci. 2008 Dec;23(6):959-63. doi: 10.3346/jkms.2008.23.6.959. Epub 2008 Dec 23.

PMID:
19119436
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Therapeutic advances in muscular dystrophy.

Leung DG, Wagner KR.

Ann Neurol. 2013 Sep;74(3):404-11. doi: 10.1002/ana.23989. Review.

PMID:
23939629
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.

Goto K, Nishino I, Hayashi YK.

Neuromuscul Disord. 2006 Apr;16(4):256-61. Epub 2006 Mar 20.

PMID:
16545566
[PubMed - indexed for MEDLINE]
17.

The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.

Rossi M, Ricci E, Colantoni L, Galluzzi G, Frusciante R, Tonali PA, Felicetti L.

BMC Med Genet. 2007 Mar 2;8:8.

PMID:
17335567
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy.

Bortolanza S, Nonis A, Sanvito F, Maciotta S, Sitia G, Wei J, Torrente Y, Di Serio C, Chamberlain JR, Gabellini D.

Mol Ther. 2011 Nov;19(11):2055-64. doi: 10.1038/mt.2011.153. Epub 2011 Aug 9.

PMID:
21829175
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Molecular basis of facioscapulohumeral muscular dystrophy.

Tupler R, Gabellini D.

Cell Mol Life Sci. 2004 Mar;61(5):557-66. Review.

PMID:
15004695
[PubMed - indexed for MEDLINE]
20.

[Facioscapulohumeral muscular dystrophy type 2].

Sacconi S, Desnuelle C.

Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):564-72. doi: 10.1016/j.neurol.2013.02.004. Epub 2013 Aug 20. French.

PMID:
23969240
[PubMed - indexed for MEDLINE]

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