WMS
@WorldMuscleSoc
We invite you to the 20th International Annual Congress of the World Muscle Society in 2015. This is the premier annual Congress on #neuromuscular disorders.
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@WorldMuscleSoc Highlights from#WMSCongress2015. A full report.#SearchingForACure#ImprovingLives http://www.actionduchenne.org/world-muscle-society-congress-highlights/ …1 retweet 1 favourite -
WMS Retweeted
Read about the highlights of
#WMSCongress2015 of@WorldMuscleSoc. http://bit.ly/1JSqUgw1 retweet 0 favourites -
WMS Retweeted
Katie Bushby Retweeted Muscular Dystrophy
Good luck! Great campaigning
@MDUK_News@MDUK_Robert https://twitter.com/mduk_news/status/651790853803896832 …Katie Bushby added,
Muscular Dystrophy @MDUK_NewsThanks to our supporters we're shortlisted for campaigns &@MD_Trailblazers action at#CharityTimesAwards tonight http://bit.ly/1VDkVrZ4 retweets 4 favourites -
WMS Retweeted
Great news re
#Translarna for#Duchenne#musculardystrophy in#Scotland now need access in rest of UK@NiceComms3 retweets 5 favourites -
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WMS followed Help4harry, Metabolomics Society, Roy Goodacre and Metabolomics
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@MetabolomicsSoc
The Twitter account of the international Metabolomics Society with the mission to promote and develop the field of metabolomics.
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A big thank you to everyone involved in
@WorldMuscleSoc#WMSCongress2015. Have a safe journey home and see you next year1 retweet 3 favourites -
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Elselvier prizes for outstanding young myologist B.Cowling,M.Van Putten,R.Bryson-Richardson,P.Mohassel,R.Foley
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mRNA regulation as efficient therapeutic strategy for FSHD dr.Dumonceaux
#WMSCongress20151 retweet 1 favourite -
A special thanks to all our sponsors and supporters
#WMSCongress2015 pic.twitter.com/8R8B19rtOi8:12 a.m. - 4 Oct 2015 · Details0 retweets 2 favourites -
RG7800 as splicing modifier of SMN2 splicing:first study in patients Dr.H.Kletzl
#WMScongress20152 retweets 1 favourite -
Dr.Mendell presenting exciting results on the SMA type1 clinical trial
#WMSCongress20153 retweets 1 favourite -
Dr.C.Weihl talking about OMICS approaches to identify genetic risks in inclusion body myositis
#WMSCongress20151 retweet 1 favourite -
SRPK3 mutations cause X-linked progressive congenital myopathy A.Topf and I.Zaharieva
@WorldMuscleSoc#WMScongress20150 retweets 1 favourite -
A new congenital myopathy associated with deficiency of kyphoscoliosis pepdidase C.Hedberg-Oldfors
#WMSCongress2015 pic.twitter.com/o0Mz8U2oQv7:06 a.m. - 4 Oct 2015 · Details2 retweets 0 favourites -
WMS Retweeted
Dr. Reghan Foley: GGPS1 mutations as a possible cause for some childhood-onset muscular dystrophy
#WMScongress2015 pic.twitter.com/hSTwN6Lqga6:58 a.m. - 4 Oct 2015 · Details1 retweet 2 favourites -
WMS Retweeted
Reghan Foley describing GGPS1 mutation in childhood-onset muscular dystrophy
@WorldMuscleSoc#WMSCongress2015 pic.twitter.com/kzzKCPd6Fa6:52 a.m. - 4 Oct 2015 · Details1 retweet 1 favourite -
Alessandra Ferlini presenting new form of autosomal LGMD linked to POPDC1 mutations
#WMSCongress2015 pic.twitter.com/PvSz75O8SN6:37 a.m. - 4 Oct 2015 · Details1 retweet 3 favourites
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