| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A comparative study of care practices for young boys with Duchenne muscular dystrophy between Japan and European countries: Implications of early diagnosis
|
Takeuchi, Fumi
|
|
2017
|
27 |
10 |
p. 894-904
|
artikel
|
| 2 |
Acquired equine polyneuropathy of Nordic horses: A conspicuous inclusion body schwannopathy
|
Hanche-Olsen, S.
|
|
2017
|
27 |
10 |
p. 931-941
|
artikel
|
| 3 |
A novel mutation in FGD4 causes Charcot–Marie–Tooth disease type 4H with cranial nerve involvement
|
Kondo, Daisuke
|
|
2017
|
27 |
10 |
p. 959-961
|
artikel
|
| 4 |
Clinical spectra of neuromuscular manifestations in patients with lipodystrophy: A multicenter study
|
Akinci, Gulcin
|
|
2017
|
27 |
10 |
p. 923-930
|
artikel
|
| 5 |
Congenital myopathy due to myosin heavy chain 2 mutation presenting as chronic aspiration pneumonia in infancy
|
Tsabari, R.
|
|
2017
|
27 |
10 |
p. 947-950
|
artikel
|
| 6 |
Delayed onset of ambulation in boys with Duchenne muscular dystrophy: Potential use as an endpoint in clinical trials
|
Gissy, Jacob J.
|
|
2017
|
27 |
10 |
p. 905-910
|
artikel
|
| 7 |
Diagnosis of Duchenne muscular dystrophy in Italy in the last decade: Critical issues and areas for improvements
|
Haliloglu, Goknur
|
|
2017
|
27 |
10 |
p. 973
|
artikel
|
| 8 |
DMD and West syndrome
|
Cardas, Ruxandra
|
|
2017
|
27 |
10 |
p. 911-913
|
artikel
|
| 9 |
Double-seropositive myasthenia gravis with acetylcholine receptor and low-density lipoprotein receptor-related protein 4 antibodies associated with invasive thymoma
|
Ishikawa, Hidehiro
|
|
2017
|
27 |
10 |
p. 914-917
|
artikel
|
| 10 |
Editorial Board
|
|
|
2017
|
27 |
10 |
p. CO2
|
artikel
|
| 11 |
First clinical and genetic description of a family diagnosed with late-onset Pompe disease from Costa Rica
|
Torrealba-Acosta, Gabriel
|
|
2017
|
27 |
10 |
p. 951-955
|
artikel
|
| 12 |
Gluteus maximus hypertrophy: A diagnostic clue in four and a half LIM domain 1-mutated reducing body myopathy
|
Jokela, Manu
|
|
2017
|
27 |
10 |
p. 962-963
|
artikel
|
| 13 |
Longitudinal assessments in discordant twins with SMA
|
Pane, Marika
|
|
2017
|
27 |
10 |
p. 890-893
|
artikel
|
| 14 |
Memory B cell resurgence requires repeated rituximab in myasthenia gravis
|
Muto, Kohei
|
|
2017
|
27 |
10 |
p. 918-922
|
artikel
|
| 15 |
Monoclonal gammopathy with both nemaline myopathy and amyloid myopathy
|
Wang, Min
|
|
2017
|
27 |
10 |
p. 942-946
|
artikel
|
| 16 |
6MWT can identify type 3 SMA patients with neuromuscular junction dysfunction
|
Pera, Maria Carmela
|
|
2017
|
27 |
10 |
p. 879-882
|
artikel
|
| 17 |
Neuromuscular politics: The creation of RehabiliteringsCenter for Muskelsvind (The National Rehabilitation Centre for Neuromuscular Diseases)
|
Jeppesen, Jørgen
|
|
2017
|
27 |
10 |
p. 970-972
|
artikel
|
| 18 |
[No title]
|
Montes, Jacqueline
|
|
2017
|
27 |
10 |
p. 964-969
|
artikel
|
| 19 |
Spinal muscular atrophy: A changing phenotype beyond the clinical trials
|
Tizzano, Eduardo F.
|
|
2017
|
27 |
10 |
p. 883-889
|
artikel
|
| 20 |
Treatment with enzyme replacement therapy during pregnancy in a patient with Pompe disease
|
Holbeck-Brendel, Merete
|
|
2017
|
27 |
10 |
p. 956-958
|
artikel
|
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