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                             14 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An HTLV-1 carrier with sporadic late-onset nemaline myopathy accompanied by skin lesions indicating indolent adult T-cell leukemia/lymphoma and Sjögren’s syndrome: a case report and literature review Miyata, Ako

52 C p.
artikel
2 Distinguishing immune checkpoint inhibitor-induced hypothyroid myopathy from myositis: a case report and review Tawara, Nozomu

52 C p.
artikel
3 Editorial Board
52 C p.
artikel
4 ENMC Themed Workshops
52 C p.
artikel
5 Levels of exercise exposure among people living with neuromuscular disorders: lessons learned from real-world data Richardson, Mark

52 C p.
artikel
6 Like father, like son: RNA-sequencing from a 30-year-old muscle biopsy identifies a novel splice variant in ACTA1 as the cause of an attenuated nemaline myopathy phenotype Meyer, Alayne P.

52 C p.
artikel
7 Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathy Müller, Juliane S.

52 C p.
artikel
8 Myositis associated with antimitochondrial autoantibodies presenting with early respiratory failure Kawama, Kentaro

52 C p.
artikel
9 Prevalence and prognostic impact of cardiac resonance abnormalities in myotonic dystrophy patients Russo, Vincenzo

52 C p.
artikel
10 The recent clinical trial of losmapimod for the treatment of facioscapulohumeral muscular dystrophy Bloch, Robert J.

52 C p.
artikel
11 Two-year Risdiplam treatment in adults with spinal muscular atrophy: improvements in motor and respiratory function, quality of life and fatigue Iterbeke, Louise

52 C p.
artikel
12 WMS General Information
52 C p.
artikel
13 WMS 2025 Vienna announcement
52 C p.
artikel
14 WMS 2025 Vienna Congress Flyer
52 C p.
artikel
                             14 gevonden resultaten
 
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