Unbound MEDLINE

Neuromuscul Disord journal articles from PubMed MEDLINE database

Unbound MEDLINE results for:RSS FEEDBookmark this site
Neuromuscul Disord[TA]| Refine this search
1 - 10 of 1915 journal articles in the PubMed databaseEmail to a friend    
 
Bauer R, Blain A, Greally E, et al. 
Attenuation of adverse cardiac effects in prednisolone-treated delta-sarcoglycan-deficient mice by mineralocorticoid-receptor-antagonism. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Nov 11.
Abstract | Full Citation | Find Related Articles 
Halon M, Sielicka-Dudzin A, Wozniak M, et al. 
Up-regulation of ferritin ubiquitination in skeletal muscle of transgenic rats bearing the G93A hmSOD1 gene mutation. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Nov 10.
Abstract | Full Citation | Find Related Articles 
Marchini C, Marsala SZ, Bendini M, et al. 
Myelin protein zero Val102fs mutation manifesting with isolated spinal root hypertrophy. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Nov 9.
Abstract | Full Citation
Foley AR, Hu Y, Zou Y, et al. 
Autosomal recessive inheritance of classic Bethlem myopathy. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Oct 31.
Abstract | Full Citation | Find Related Articles 
Dinopoulos A, Papadopoulou A, Manta P, et al. 
Coinheritance of Noonan syndrome and Becker muscular dystrophy. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Oct 27.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Wein N, Krahn M, Courrier S, et al. 
Immunolabelling and flow cytometry as new tools to explore dysferlinopathies. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Oct 22.
Abstract | Full Citation
Wijk E, Messelink BJ, Heijnen L, et al. 
Prevalence and psychosocial impact of lower urinary tract symptoms in patients with Duchenne muscular dystrophy. [Journal Article]
Neuromuscul Disord 2009 Nov; 19(11):754-8.
Abstract | Full Citation
Massa R, Tessa A, Margollicci M, et al. 
Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Oct 21.
Abstract | Full Citation
Al-Dosary M, Whittaker RG, Haughton J, et al. 
Neuromuscular disease presentation with three genetic defects involving two genomes. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Oct 21.
Abstract | Full Citation
Bohlega S, Van Goethem G, Al Semari A, et al. 
Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failure. [JOURNAL ARTICLE]
Neuromuscul Disord 2009 Oct 21.
Abstract | Full Citation
New Search Next Results
  

Enter
www.unboundmedicine.com/medline
in your iPhone browser
or View our
Unbound MEDLINE
iPhone demo


Advertise on this site.