Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 51

1.

Gene therapy for inherited muscle diseases: where genetics meets rehabilitation medicine.

Braun R, Wang Z, Mack DL, Childers MK.

Am J Phys Med Rehabil. 2014 Nov;93(11 Suppl 3):S97-107. doi: 10.1097/PHM.0000000000000138. Review.

PMID:
25313664
[PubMed - indexed for MEDLINE]
2.

Respiratory assessment in centronuclear myopathies.

Smith BK, Goddard M, Childers MK.

Muscle Nerve. 2014 Sep;50(3):315-26. doi: 10.1002/mus.24249. Epub 2014 Aug 5. Review.

PMID:
24668768
[PubMed - indexed for MEDLINE]
3.

Amphiphysin 2 (BIN1) in physiology and diseases.

Prokic I, Cowling BS, Laporte J.

J Mol Med (Berl). 2014 May;92(5):453-63. doi: 10.1007/s00109-014-1138-1. Epub 2014 Mar 5. Review.

PMID:
24590001
[PubMed - indexed for MEDLINE]
4.

[Structural congenital myopathies].

Erazo-Torricelli R.

Rev Neurol. 2013 Sep 6;57 Suppl 1:S53-64. Review. Spanish.

PMID:
23897157
[PubMed - indexed for MEDLINE]
Free Article
5.

New horizons for congenital myasthenic syndromes.

Engel AG, Shen XM, Selcen D, Sine S.

Ann N Y Acad Sci. 2012 Dec;1275:54-62. doi: 10.1111/j.1749-6632.2012.06803.x. Review. Erratum in: Ann N Y Acad Sci. 2013 Apr;1283:103.

PMID:
23278578
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms.

Nowak KJ, Ravenscroft G, Laing NG.

Acta Neuropathol. 2013 Jan;125(1):19-32. doi: 10.1007/s00401-012-1019-z. Epub 2012 Jul 24. Review.

PMID:
22825594
[PubMed - indexed for MEDLINE]
7.

Myopathies associated with β-tropomyosin mutations.

Tajsharghi H, Ohlsson M, Palm L, Oldfors A.

Neuromuscul Disord. 2012 Nov;22(11):923-33. doi: 10.1016/j.nmd.2012.05.018. Epub 2012 Jun 29. Review.

PMID:
22749895
[PubMed - indexed for MEDLINE]
8.

Defective membrane remodeling in neuromuscular diseases: insights from animal models.

Cowling BS, Toussaint A, Muller J, Laporte J.

PLoS Genet. 2012;8(4):e1002595. doi: 10.1371/journal.pgen.1002595. Epub 2012 Apr 5. Review.

PMID:
22496665
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Congenital myopathies: an update.

Nance JR, Dowling JJ, Gibbs EM, Bönnemann CG.

Curr Neurol Neurosci Rep. 2012 Apr;12(2):165-74. doi: 10.1007/s11910-012-0255-x. Review.

PMID:
22392505
[PubMed - indexed for MEDLINE]
10.

Congenital fiber-type disproportion.

Clarke NF.

Semin Pediatr Neurol. 2011 Dec;18(4):264-71. doi: 10.1016/j.spen.2011.10.008. Review.

PMID:
22172422
[PubMed - indexed for MEDLINE]
11.

Nemaline myopathies.

Wallgren-Pettersson C, Sewry CA, Nowak KJ, Laing NG.

Semin Pediatr Neurol. 2011 Dec;18(4):230-8. doi: 10.1016/j.spen.2011.10.004. Review.

PMID:
22172418
[PubMed - indexed for MEDLINE]
12.
13.

Dominant and recessive RYR1 mutations in adults with core lesions and mild muscle symptoms.

Duarte ST, Oliveira J, Santos R, Pereira P, Barroso C, Conceição I, Evangelista T.

Muscle Nerve. 2011 Jul;44(1):102-8. doi: 10.1002/mus.22009. Review.

PMID:
21674524
[PubMed - indexed for MEDLINE]
14.

Neuromuscular pathology unknown.

Kraker JB, Abdel-Hamid H, Lacomis D.

J Clin Neuromuscul Dis. 2010 Sep;12(1):22-5. doi: 10.1097/CND.0b013e3181dc34d8. Review. No abstract available.

PMID:
20808160
[PubMed - indexed for MEDLINE]
15.

Inborn errors of energy metabolism associated with myopathies.

Das AM, Steuerwald U, Illsinger S.

J Biomed Biotechnol. 2010;2010:340849. doi: 10.1155/2010/340849. Epub 2010 May 26. Review.

PMID:
20589068
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias.

Platt D, Griggs R.

Curr Opin Neurol. 2009 Oct;22(5):524-31. doi: 10.1097/WCO.0b013e32832efa8f. Review.

PMID:
19571750
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

[Adult-onset nemaline myopathy with distal muscle atrophy--case report].

Niwa F, Shiga K, Kimura M, Yamaguchi T, Kondo M, Nakagawa M.

Brain Nerve. 2009 Jun;61(6):695-9. Review. Japanese.

PMID:
19526838
[PubMed - indexed for MEDLINE]
18.

Myotubular/centronuclear myopathy and central core disease.

Fujimura-Kiyono C, Racz GZ, Nishino I.

Neurol India. 2008 Jul-Sep;56(3):325-32. Review.

PMID:
18974559
[PubMed - indexed for MEDLINE]
Free Article
19.

Congenital myopathies.

D'Amico A, Bertini E.

Curr Neurol Neurosci Rep. 2008 Jan;8(1):73-9. Review.

PMID:
18367042
[PubMed - indexed for MEDLINE]
20.

Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm.

Treves S, Jungbluth H, Muntoni F, Zorzato F.

Curr Opin Pharmacol. 2008 Jun;8(3):319-26. doi: 10.1016/j.coph.2008.01.005. Epub 2008 Mar 4. Review.

PMID:
18313359
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk