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 |