| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy
|
Meinke, Peter
|
|
2015
|
25 |
2 |
p. 127-136
10 p.
|
artikel
|
| 2 |
Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy
|
Morris, Glenn E.
|
|
2015
|
25 |
2 |
p. 137-
1 p.
|
artikel
|
| 3 |
A case report comparing clinical, imaging and neuropsychological assessment findings in twins discordant for the VCP p.R155C mutation
|
Surampalli, Abhilasha
|
|
2015
|
25 |
2 |
p. 177-183
7 p.
|
artikel
|
| 4 |
A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish family
|
Lefter, Stela
|
|
2015
|
25 |
2 |
p. 155-160
6 p.
|
artikel
|
| 5 |
Clinical and electrophysiological features in a French family presenting with seipinopathy
|
Ollivier, Yolaine
|
|
2015
|
25 |
2 |
p. 161-164
4 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2015
|
25 |
2 |
p. CO2-
1 p.
|
artikel
|
| 7 |
Eosinophilic myositis as first manifestation in a patient with type 2 myotonic dystrophy CCTG expansion mutation and rheumatoid arthritis
|
Meyer, Alain
|
|
2015
|
25 |
2 |
p. 149-152
4 p.
|
artikel
|
| 8 |
Growing up with spinal muscular atrophy with respiratory distress (SMARD1)
|
Hamilton, Mark James
|
|
2015
|
25 |
2 |
p. 169-171
3 p.
|
artikel
|
| 9 |
Investigating sodium valproate as a treatment for McArdle disease in sheep
|
Howell, J.McC.
|
|
2015
|
25 |
2 |
p. 111-119
9 p.
|
artikel
|
| 10 |
Isolated laryngeal myasthenia gravis for 26 years
|
Renard, Dimitri
|
|
2015
|
25 |
2 |
p. 153-154
2 p.
|
artikel
|
| 11 |
Left ventricular non-compaction cardiomyopathy associated with epidermolysis bullosa simplex with muscular dystrophy and PLEC1 mutation
|
Villa, Chet R.
|
|
2015
|
25 |
2 |
p. 165-168
4 p.
|
artikel
|
| 12 |
Muscle force, balance and falls in muscular impaired individuals with myotonic dystrophy type 1: A five-year prospective cohort study
|
Hammarén, Elisabet
|
|
2015
|
25 |
2 |
p. 141-148
8 p.
|
artikel
|
| 13 |
Muscle ultrasound in classic infantile and adult Pompe disease: A useful screening tool in adults but not in infants
|
Vill, K.
|
|
2015
|
25 |
2 |
p. 120-126
7 p.
|
artikel
|
| 14 |
New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failure
|
Yue, Dongyue
|
|
2015
|
25 |
2 |
p. 172-176
5 p.
|
artikel
|
| 15 |
RYR1-related malignant hyperthermia with marked cerebellar involvement – A paradigm of heat-induced CNS injury?
|
Forrest, Katharine M.L.
|
|
2015
|
25 |
2 |
p. 138-140
3 p.
|
artikel
|
| 16 |
204th ENMC International Workshop on Biomarkers in Duchenne Muscular Dystrophy 24–26 January 2014, Naarden, The Netherlands
|
Ferlini, Alessandra
|
|
2015
|
25 |
2 |
p. 184-198
15 p.
|
artikel
|
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