| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Editorial Board
|
|
|
|
32 |
2 |
p. IFC
|
artikel
|
| 2 |
Erratum to ``Clinical practice guidelines for glycogen storage disease V & VII (McArdle disease and Tarui disease) from an international study group'' [Neuromuscular Disorders 31 (2021) 1296–1310]
|
Lucia, Alejandro
|
|
|
32 |
2 |
p. e3
|
artikel
|
| 3 |
Hypotonic infant with PURA syndrome-related channelopathy successfully treated with pyridostigmine
|
Wyrebek, Rita
|
|
|
32 |
2 |
p. 166-169
|
artikel
|
| 4 |
Idiopathic eosinophilic myositis: a systematic literature review
|
Fermon, Cécile
|
|
|
32 |
2 |
p. 116-124
|
artikel
|
| 5 |
Influence of β2 adrenergic receptor genotype on longitudinal measures of forced vital capacity in patients with Duchenne muscular dystrophy
|
Kelley, Eli F
|
|
|
32 |
2 |
p. 150-158
|
artikel
|
| 6 |
Muscle “islands”: An MRI signature distinguishing neurogenic from myopathic causes of early onset distal weakness
|
Astrea, Guja
|
|
|
32 |
2 |
p. 142-149
|
artikel
|
| 7 |
Natural history of 10-meter walk/run test performance in spinal muscular atrophy: A longitudinal analysis
|
Krosschell, Kristin J.
|
|
|
32 |
2 |
p. 125-134
|
artikel
|
| 8 |
Newborn screening for spinal muscular atrophy: The Wisconsin first year experience
|
Baker, Mei W.
|
|
|
32 |
2 |
p. 135-141
|
artikel
|
| 9 |
Outcome measures frequently used to assess muscle strength in patients with myotonic dystrophy type 1: a systematic review
|
Mateus, Tiago
|
|
|
32 |
2 |
p. 99-115
|
artikel
|
| 10 |
Psychosocial adjustment in adults with Duchenne muscular dystrophy: A pilot study on a shortened parent-report questionnaire
|
Weerkamp, Pien M.M.
|
|
|
32 |
2 |
p. 159-165
|
artikel
|
| 11 |
TNNT1 myopathy with novel compound heterozygous mutations
|
Lee, Seungbok
|
|
|
32 |
2 |
p. 176-184
|
artikel
|
| 12 |
Unusual cases of Anti-SRP necrotizing myopathy with predominant distal leg weakness and atrophy
|
Moshe-Lilie, Orly
|
|
|
32 |
2 |
p. 170-175
|
artikel
|
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