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                             11 results found
no title author magazine year volume issue page(s) type
1 A novel mitochondrial m.4414T>C MT-TM gene variant causing progressive external ophthalmoplegia and myopathy Hellebrekers, Debby M.E.I.
2019
29 9 p. 693-697
article
2 Assessment of muscle involvement in patients with Duchenne muscular dystrophy via segmental multifrequency bioelectrical analysis Kuru, Satoshi
2019
29 9 p. 671-677
article
3 Autosomal recessive Bethlem myopathy: A clinical, genetic and functional study Caria, Filomena
2019
29 9 p. 657-663
article
4 Chronic inflammatory demyelinating polyneuropathy: Plasmapheresis or cyclosporine can be good treatment options in refractory cases Kim, WooJoong
2019
29 9 p. 684-692
article
5 Editorial Board 2019
29 9 p. IFC
article
6 Heterogeneity and shifts in distribution of muscle weakness in myasthenia gravis de Meel, Robert H.P.
2019
29 9 p. 664-670
article
7 243rd ENMC international workshop: Developing guidelines for management of reproductive options for families with maternally inherited mtDNA disease, Amsterdam, the Netherlands, 22–24 March 2019 Poulton, Joanna
2019
29 9 p. 725-733
article
8 241st ENMC international workshop: Towards a European unifying lab for Kennedy's disease. 15–17th February, 2019 Hoofddorp, The Netherlands Greensmith, L.
2019
29 9 p. 716-724
article
9 240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25–27 January 2019, Hoofddorp, The Netherlands Morgan, Jennifer
2019
29 9 p. 704-715
article
10 Women in the history of neuromuscular medicine Thomas, Eleanor
2019
29 9 p. 698-703
article
11 X-linked Emery–Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures Brisset, Marion
2019
29 9 p. 678-683
article
                             11 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands