| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family
|
Dankwa, Lois
|
|
2019
|
29 |
2 |
p. 134-137
|
artikel
|
| 2 |
Autologous hematopoietic stem cell transplantation in a patient with refractory seropositive myasthenia gravis: A case report
|
Sossa Melo, Claudia Lucía
|
|
2019
|
29 |
2 |
p. 142-145
|
artikel
|
| 3 |
Clinical spectrum of neuromuscular complications after immune checkpoint inhibition
|
Puwanant, Araya
|
|
2019
|
29 |
2 |
p. 127-133
|
artikel
|
| 4 |
Colonic distension treatment in Duchenne muscular dystrophy
|
Fiorentino, Giuseppe
|
|
2019
|
29 |
2 |
p. 157-158
|
artikel
|
| 5 |
Colonic distension treatment in Duchenne muscular dystrophy - response
|
Vianello, Andrea
|
|
2019
|
29 |
2 |
p. 159
|
artikel
|
| 6 |
Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene
|
Kiiski, Kirsi J.
|
|
2019
|
29 |
2 |
p. 97-107
|
artikel
|
| 7 |
Dropped head syndrome as a manifestation of Charcot–Marie–Tooth disease type 4C
|
de Oliveira, Camila Maria
|
|
2019
|
29 |
2 |
p. 138-141
|
artikel
|
| 8 |
Editorial Board
|
|
|
2019
|
29 |
2 |
p. IFC
|
artikel
|
| 9 |
Long-term follow-up and characteristic pathological findings in severe nemaline myopathy due to LMOD3 mutations
|
Michael, Eva
|
|
2019
|
29 |
2 |
p. 108-113
|
artikel
|
| 10 |
Muscle hypertrophy in amyloid myopathy
|
Tasca, Giorgio
|
|
2019
|
29 |
2 |
p. 150-151
|
artikel
|
| 11 |
Neuromuscular disorders in Anatolia – A personal review
|
Topaloğlu, Haluk
|
|
2019
|
29 |
2 |
p. 152-156
|
artikel
|
| 12 |
[No title]
|
Damian, Heidelinde
|
|
2019
|
29 |
2 |
p. 164
|
artikel
|
| 13 |
[No title]
|
McEntagart, Meriel
|
|
2019
|
29 |
2 |
p. 163
|
artikel
|
| 14 |
Professor Frank Lehmann-Horn, M.D. (1948–2018)
|
Rüdel, Reinhardt
|
|
2019
|
29 |
2 |
p. 165-166
|
artikel
|
| 15 |
Replication studies of MIR149 association in Charcot–Marie–Tooth disease type 1A in a European population
|
Tao, Feifei
|
|
2019
|
29 |
2 |
p. 160-162
|
artikel
|
| 16 |
Replication studies of MIR149 association in Charcot–Marie–Tooth disease type 1A in a European population - response
|
Choi, Byung-Ok
|
|
2019
|
29 |
2 |
p. 160-162
|
artikel
|
| 17 |
Spinal muscular atrophy with respiratory distress type 1: A multicenter retrospective study
|
Viguier, Agnès
|
|
2019
|
29 |
2 |
p. 114-126
|
artikel
|
| 18 |
Targeted gene approach with biochemical assay confirms ABCD1 mutation of X-linked adrenoleukodystrophy in a 62-year-old man with gait imbalance
|
Mauermann, Michelle L.
|
|
2019
|
29 |
2 |
p. 146-149
|
artikel
|
| 19 |
The clinical management of neuromuscular disorders in intensive care
|
Damian, Maxwell S.
|
|
2019
|
29 |
2 |
p. 85-96
|
artikel
|
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