| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Between genetics and biology. Is ENMG useful in peripheral neuropathy diagnosis and management?
|
Stålberg, E.
|
|
2016
|
172 |
10 |
p. 627-631
5 p.
|
artikel
|
| 2 |
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC
|
Avila-Smirnow, D.
|
|
2016
|
172 |
10 |
p. 594-606
13 p.
|
artikel
|
| 3 |
Editorial Board
|
|
|
2016
|
172 |
10 |
p. i-
1 p.
|
artikel
|
| 4 |
Exercise training in metabolic myopathies
|
Vissing, J.
|
|
2016
|
172 |
10 |
p. 559-565
7 p.
|
artikel
|
| 5 |
Familial amyloid polyneuropathy: When does it stop to be asymptomatic and need a treatment?
|
Adams, D.
|
|
2016
|
172 |
10 |
p. 645-652
8 p.
|
artikel
|
| 6 |
Foreword
|
Eymard, B.
|
|
2016
|
172 |
10 |
p. 537-538
2 p.
|
artikel
|
| 7 |
Guillain-Barré syndrome: What have we learnt during one century? A personal historical perspective
|
Uncini, A.
|
|
2016
|
172 |
10 |
p. 632-644
13 p.
|
artikel
|
| 8 |
Intermediate filaments in peripheral nervous system: Their expression, dysfunction and diseases
|
Parlakian, A.
|
|
2016
|
172 |
10 |
p. 607-613
7 p.
|
artikel
|
| 9 |
Muscle MRI of facioscapulohumeral dystrophy (FSHD): A growing demand and a promising approach
|
Fatehi, F.
|
|
2016
|
172 |
10 |
p. 566-571
6 p.
|
artikel
|
| 10 |
Myofibrillar and distal myopathies
|
Palmio, J.
|
|
2016
|
172 |
10 |
p. 587-593
7 p.
|
artikel
|
| 11 |
Nemaline myopathies: State of the art
|
Malfatti, E.
|
|
2016
|
172 |
10 |
p. 614-619
6 p.
|
artikel
|
| 12 |
Regarding the past, what is the trial you have always been dreaming of in CIDP?
|
Hughes, R.A.C.
|
|
2016
|
172 |
10 |
p. 620-626
7 p.
|
artikel
|
| 13 |
RYR1-related rhabdomyolysis: A common but probably underdiagnosed manifestation of skeletal muscle ryanodine receptor dysfunction
|
Voermans, N.C.
|
|
2016
|
172 |
10 |
p. 546-558
13 p.
|
artikel
|
| 14 |
Sporadic inclusion-body myositis: Recent advances and the state of the art in 2016
|
Gallay, L.
|
|
2016
|
172 |
10 |
p. 581-586
6 p.
|
artikel
|
| 15 |
Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification
|
De Antonio, M.
|
|
2016
|
172 |
10 |
p. 572-580
9 p.
|
artikel
|
| 16 |
What have we learned about glycogenosis in recent years?
|
Laforêt, P.
|
|
2016
|
172 |
10 |
p. 541-545
5 p.
|
artikel
|
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