| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of inflammatory myopathy in graft vs host disease - A potential role for ibrutinib
|
Wilkinson, Michael
|
|
|
31 |
9 |
p. 865-869
|
artikel
|
| 2 |
Adult-type dermatomyositis with secondary lymphoid follicles harbouring reactive B-cells component
|
Maghrabi, Yazid
|
|
|
31 |
9 |
p. 881-885
|
artikel
|
| 3 |
A rare case of sporadic inclusion body myositis and rheumatoid arthritis exhibiting ectopic lymphoid follicle-like structures: a case report and literature review
|
Konomatsu, Kazutoshi
|
|
|
31 |
9 |
p. 870-876
|
artikel
|
| 4 |
A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophy
|
Matsumura, Tsuyoshi
|
|
|
31 |
9 |
p. 839-846
|
artikel
|
| 5 |
Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations
|
Sun, J.
|
|
|
31 |
9 |
p. 829-838
|
artikel
|
| 6 |
Editorial Board
|
|
|
|
31 |
9 |
p. IFC
|
artikel
|
| 7 |
Exploring the influence of smoking and alcohol consumption on clinical severity in patients with facioscapulohumeral muscular dystrophy
|
Vincenten, Sanne C.C.
|
|
|
31 |
9 |
p. 824-828
|
artikel
|
| 8 |
Fatal disseminated Anncaliia algerae myositis mimicking polymyositis in an immunocompromised patient
|
Ziad, Fouzia
|
|
|
31 |
9 |
p. 877-880
|
artikel
|
| 9 |
Leadless intracardiac transcatheter pacing system: 20 months follow up in adult Duchenne muscular dystrophy
|
Fayssoil, Abdallah
|
|
|
31 |
9 |
p. 896-898
|
artikel
|
| 10 |
Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation
|
Chandrasekharan, Soumya V.
|
|
|
31 |
9 |
p. 886-890
|
artikel
|
| 11 |
Reducing body myopathy – A new pathogenic FHL1 variant and literature review
|
Mota, Isabella Araujo
|
|
|
31 |
9 |
p. 847-853
|
artikel
|
| 12 |
Safety and clinical outcome of tamoxifen in Duchenne muscular dystrophy
|
Tsabari, Reuven
|
|
|
31 |
9 |
p. 803-813
|
artikel
|
| 13 |
1st FSHD European Trial Network workshop:Working towards trial readiness across Europe
|
Voermans, N.C.
|
|
|
31 |
9 |
p. 907-918
|
artikel
|
| 14 |
Tamoxifen in Duchenne muscular dystrophy – promising first results
|
Rüegg, Urs
|
|
|
31 |
9 |
p. 801-802
|
artikel
|
| 15 |
TREAT-NMD stakeholder meeting for natural history studies in limb girdle muscular dystrophy 18th June 2019, Amsterdam, The Netherlands
|
Guglieri, Michela
|
|
|
31 |
9 |
p. 899-906
|
artikel
|
| 16 |
Vasculitic peripheral neuropathy in deficiency of adenosine deaminase 2
|
Carneiro, Diogo Reis
|
|
|
31 |
9 |
p. 891-895
|
artikel
|
| 17 |
Whole-body muscle MRI characteristics of LAMA2-related congenital muscular dystrophy children: An emerging pattern
|
Sakr, Hossam M.
|
|
|
31 |
9 |
p. 814-823
|
artikel
|
| 18 |
Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletions
|
Guo, Le
|
|
|
31 |
9 |
p. 859-864
|
artikel
|
| 19 |
X-linked myopathy with excessive autophagy: First report of an Israeli family presenting with late onset lower limb girdle weakness
|
Alon, Tayir
|
|
|
31 |
9 |
p. 854-858
|
artikel
|
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