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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy Di Blasi, Claudia
2010
20 5 p. 326-329
4 p.
artikel
2 Editorial Board 2010
20 5 p. IFC-
1 p.
artikel
3 Episodic myoglobinuria in a primary gamma-sarcoglycanopathy Pena, Loren
2010
20 5 p. 337-339
3 p.
artikel
4 Friedreich ataxia presenting as sudden cardiac death in childhood: Clinical, genetic and pathological correlation, with implications for genetic testing and counselling Quercia, Nada
2010
20 5 p. 340-342
3 p.
artikel
5 Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian family Stober, Andrea
2010
20 5 p. 335-336
2 p.
artikel
6 Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN) Cordelli, D.M.
2010
20 5 p. 343-345
3 p.
artikel
7 Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin–proteasome pathway Vignaud, Alban
2010
20 5 p. 319-325
7 p.
artikel
8 Rasch-built myotonic dystrophy type 1 activity and participation scale (DM1-Activ) Hermans, Mieke C.E.
2010
20 5 p. 310-318
9 p.
artikel
9 Reverse protein arrays as novel approach for protein quantification in muscular dystrophies Escher, Claudia
2010
20 5 p. 302-309
8 p.
artikel
10 Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: Implication for clinical trials Arechavala-Gomeza, Virginia
2010
20 5 p. 295-301
7 p.
artikel
11 The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: Report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009 Muntoni, F.
2010
20 5 p. 355-362
8 p.
artikel
12 166th ENMC International Workshop on Collagen type VI-related Myopathies, 22–24 May 2009, Naarden, The Netherlands Allamand, Valérie
2010
20 5 p. 346-354
9 p.
artikel
13 Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings Kumar, Kishore R.
2010
20 5 p. 330-334
5 p.
artikel
14 WMS 2010 2010
20 5 p. I-
1 p.
artikel
15 WMS News 2010
20 5 p. III-IV
nvt p.
artikel
16 WMS online application form 2010
20 5 p. II-
1 p.
artikel
                             16 gevonden resultaten
 
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