| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An analysis of the sensitivity and specificity of MHC-I and MHC-II immunohistochemical staining in muscle biopsies for the diagnosis of inflammatory myopathies
|
Rodríguez Cruz, Pedro M.
|
|
2014
|
24 |
12 |
p. 1025-1035
11 p.
|
artikel
|
| 2 |
Announcement
|
|
|
2014
|
24 |
12 |
p. IV-
1 p.
|
artikel
|
| 3 |
Atypical presentation of GNE myopathy with asymmetric hand weakness
|
de Dios, John Karl L.
|
|
2014
|
24 |
12 |
p. 1063-1067
5 p.
|
artikel
|
| 4 |
Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies
|
ten Dam, Leroy
|
|
2014
|
24 |
12 |
p. 1097-1102
6 p.
|
artikel
|
| 5 |
Congenital myopathies with secondary neuromuscular transmission defects; A case report and review of the literature
|
Rodríguez Cruz, Pedro M.
|
|
2014
|
24 |
12 |
p. 1103-1110
8 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2014
|
24 |
12 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Extraocular muscle function in adult-onset Pompe disease tested by saccadic eye movements
|
Anagnostou, E.
|
|
2014
|
24 |
12 |
p. 1073-1078
6 p.
|
artikel
|
| 8 |
Global T2 versus water T2 in NMR imaging of fatty infiltrated muscles: Different methodology, different information, and different implications
|
Willcocks, Rebecca
|
|
2014
|
24 |
12 |
p. 1120-1121
2 p.
|
artikel
|
| 9 |
GNE myopathy associated with congenital thrombocytopenia: A report of two siblings
|
Izumi, Rumiko
|
|
2014
|
24 |
12 |
p. 1068-1072
5 p.
|
artikel
|
| 10 |
Isolated semitendinosus involvement in the initial stages of limb-girdle muscular dystrophy 2L
|
Tasca, Giorgio
|
|
2014
|
24 |
12 |
p. 1118-1119
2 p.
|
artikel
|
| 11 |
Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies
|
Sewry, Caroline A.
|
|
2014
|
24 |
12 |
p. 1122-
1 p.
|
artikel
|
| 12 |
Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2
|
Cardani, Rosanna
|
|
2014
|
24 |
12 |
p. 1042-1053
12 p.
|
artikel
|
| 13 |
PYGM expression analysis in white blood cells: A complementary tool for diagnosing McArdle disease?
|
de Luna, Noemí
|
|
2014
|
24 |
12 |
p. 1079-1086
8 p.
|
artikel
|
| 14 |
Response (to Sewry and Goebel)
|
Kayman-Kurekci, G.
|
|
2014
|
24 |
12 |
p. 1122-
1 p.
|
artikel
|
| 15 |
Skeletal muscle imaging in facioscapulohumeral muscular dystrophy, pattern and asymmetry of individual muscle involvement
|
Rijken, N.H.M.
|
|
2014
|
24 |
12 |
p. 1087-1096
10 p.
|
artikel
|
| 16 |
Sleep disordered breathing and subclinical impairment of respiratory function are common in sporadic inclusion body myositis
|
Rodríguez Cruz, Pedro M.
|
|
2014
|
24 |
12 |
p. 1036-1041
6 p.
|
artikel
|
| 17 |
Swallowing assessment in myotonic dystrophy type 1 using fiberoptic endoscopic evaluation of swallowing (FEES)
|
Pilz, Walmari
|
|
2014
|
24 |
12 |
p. 1054-1062
9 p.
|
artikel
|
| 18 |
The 2015 version of the gene table of monogenic neuromuscular disorders (nuclear genome)
|
Kaplan, Jean-Claude
|
|
2014
|
24 |
12 |
p. 1123-1153
31 p.
|
artikel
|
| 19 |
When a mid-intronic variation of DMD gene creates an ESE site
|
Trabelsi, Madiha
|
|
2014
|
24 |
12 |
p. 1111-1117
7 p.
|
artikel
|
Tijdschrift beschrijving