| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A boy with neck weakness
|
Yiş, Uluç
|
|
2018
|
28 |
3 |
p. 236-237
|
artikel
|
| 2 |
A database for screening and registering late onset Pompe disease in Turkey
|
Gokyigit, Munevver Celik
|
|
2018
|
28 |
3 |
p. 262-267
|
artikel
|
| 3 |
Book review
|
Tedesco, Francesco Saverio
|
|
2018
|
28 |
3 |
p. 299
|
artikel
|
| 4 |
Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?
|
Angeard, N.
|
|
2018
|
28 |
3 |
p. 216-221
|
artikel
|
| 5 |
Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases
|
Calucho, Maite
|
|
2018
|
28 |
3 |
p. 208-215
|
artikel
|
| 6 |
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics
|
Finkel, Richard S.
|
|
2018
|
28 |
3 |
p. 197-207
|
artikel
|
| 7 |
DOK7 myasthenic syndrome with subacute adult onset during pregnancy and partial response to fluoxetine
|
Santos, Mariana
|
|
2018
|
28 |
3 |
p. 278-282
|
artikel
|
| 8 |
Editorial Board
|
|
|
2018
|
28 |
3 |
p. CO2
|
artikel
|
| 9 |
Falls and resulting fractures in Myotonic Dystrophy: Results from a multinational retrospective survey
|
Jiménez-Moreno, A.C.
|
|
2018
|
28 |
3 |
p. 229-235
|
artikel
|
| 10 |
Genotype and other determinants of respiratory function in myotonic dystrophy type 1
|
Boussaïd, Ghilas
|
|
2018
|
28 |
3 |
p. 222-228
|
artikel
|
| 11 |
Giovanni Nigro 1931–2017
|
Politano, Luisa
|
|
2018
|
28 |
3 |
p. 300-301
|
artikel
|
| 12 |
Hereditary myopathy with early respiratory failure (HMERF): Still rare, but common enough
|
Tasca, Giorgio
|
|
2018
|
28 |
3 |
p. 268-276
|
artikel
|
| 13 |
Imaging of respiratory muscles in neuromuscular disease: A review
|
Harlaar, L.
|
|
2018
|
28 |
3 |
p. 246-256
|
artikel
|
| 14 |
Mitophagy in three cases of immune-mediated necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: ultrastructural and immunohistochemical studies
|
Matsubara, Shiro
|
|
2018
|
28 |
3 |
p. 283-288
|
artikel
|
| 15 |
Ophthalmoplegia due to concurrent thyrotoxicosis and myasthenia gravis
|
Ray, Sucharita
|
|
2018
|
28 |
3 |
p. 277
|
artikel
|
| 16 |
Prevalence of adult Pompe disease in patients with proximal myopathic syndrome and undiagnosed muscle biopsy
|
Golsari, Amir
|
|
2018
|
28 |
3 |
p. 257-261
|
artikel
|
| 17 |
Specific muscle strength is reduced in facioscapulohumeral dystrophy: An MRI based musculoskeletal analysis
|
Marra, Marco A.
|
|
2018
|
28 |
3 |
p. 238-245
|
artikel
|
| 18 |
228th ENMC International Workshop:
|
Toussaint, Michel
|
|
2018
|
28 |
3 |
p. 289-298
|
artikel
|
| 19 |
Update in NMD Announcement
|
|
|
2018
|
28 |
3 |
p. IV
|
artikel
|
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