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                             15 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy Riisager, M.
2013
23 7 p. 562-567
6 p.
artikel
2 A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement Park, Jin-Mo
2013
23 7 p. 580-586
7 p.
artikel
3 A Portuguese case of Fukuyama congenital muscular dystrophy caused by a multi-exonic duplication in the fukutin gene Costa, C.
2013
23 7 p. 557-561
5 p.
artikel
4 Assessment of a symptomatic Duchenne muscular dystrophy carrier 20years after myoblast transplantation from her asymptomatic identical twin sister Hogrel, Jean-Yves
2013
23 7 p. 575-579
5 p.
artikel
5 Double seronegative myasthenia gravis with anti-LRP 4 antibodies Zouvelou, Vasiliki
2013
23 7 p. 568-570
3 p.
artikel
6 Editorial Board 2013
23 7 p. IFC-
1 p.
artikel
7 Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network Connolly, Anne M.
2013
23 7 p. 529-539
11 p.
artikel
8 Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation Türk, Matthias
2013
23 7 p. 587-590
4 p.
artikel
9 Muscular dystrophy with large mitochondria associated with mutations in the CHKB gene in three British patients: Extending the clinical and pathological phenotype Quinlivan, Ros
2013
23 7 p. 549-556
8 p.
artikel
10 Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis Dlamini, N.
2013
23 7 p. 540-548
9 p.
artikel
11 Myocardial infarction after rituximab infusion Renard, Dimitri
2013
23 7 p. 599-601
3 p.
artikel
12 Quinine sulfate as a therapeutic option in a patient with slow channel congenital myasthenic syndrome Peyer, Anne-Kathrin
2013
23 7 p. 571-574
4 p.
artikel
13 Steroids in Duchenne dystrophy Dubowitz, V.
2013
23 7 p. 527-528
2 p.
artikel
14 190th ENMC international workshop: Spinal muscular atrophy with respiratory distress/distal spinal muscular atrophy type 1 van der Pol, W. Ludo
2013
23 7 p. 602-609
8 p.
artikel
15 Uninterrupted CCTG tracts in the myotonic dystrophy type 2 associated locus Radvanszky, Jan
2013
23 7 p. 591-598
8 p.
artikel
                             15 gevonden resultaten
 
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