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                             13 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A novel nonsense PIEZO2 mutation in a family with scoliosis and proprioceptive defect Masingue, Marion

29 1 p. 75-79
artikel
2 Autophagic vacuolar myopathy caused by a CLN3 mutation. A case report Moro, Francesca

29 1 p. 67-69
artikel
3 Commentary from the Editor Dubowitz, Victor

29 1 p. 1-4
artikel
4 Editorial Board
29 1 p. IFC
artikel
5 Electromyography and muscle biopsy in paediatric neuromuscular disorders – Evaluation of current practice and literature review Hafner, Patricia

29 1 p. 14-20
artikel
6 Fractures and bone health monitoring in boys with Duchenne muscular dystrophy managed within the Scottish Muscle Network Joseph, Shuko

29 1 p. 59-66
artikel
7 Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire study van Ruitenbeek, E.

29 1 p. 30-38
artikel
8 Idiopathic inflammatory myopathies with anti-mitochondrial antibodies: Clinical features and treatment outcomes in a Chinese cohort Hou, Ying

29 1 p. 5-13
artikel
9 Immunoglobulin (Ig)G-4 related myositis – A new entity? Casteleyn, Vincent

29 1 p. 70-74
artikel
10 Late onset distal myopathy: A new telethoninopathy Blanco-Palmero, Víctor Antonio

29 1 p. 80-83
artikel
11 Mental wellbeing in non-ambulant youth with neuromuscular disorders: What makes the difference? Travlos, Vivienne

29 1 p. 48-58
artikel
12 Myopathies featuring non-caseating granulomas: Sarcoidosis, inclusion body myositis and an unfolding overlap Alhammad, Reem M.

29 1 p. 39-47
artikel
13 The oral splicing modifier RG7800 increases full length survival of motor neuron 2 mRNA and survival of motor neuron protein: Results from trials in healthy adults and patients with spinal muscular atrophy Kletzl, Heidemarie

29 1 p. 21-29
artikel
                             13 gevonden resultaten
 
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