Laura Peeters

The trunk in spinal musclar atrophy | 109 5 REFERENCES 1. Arnold WD, Kassar D, Kissel JT. Spinal muscular atrophy: diagnosis and management in a new therapeutic era. Muscle & Nerve 2015;51:157-167. 2. Rouault F, Christie-Brown V, Broekgaarden R, et al. Disease impact on general well- being and therapeutic expectations of European Type II and Type III spinal muscular atrophy patients. Neuromuscular Disorders 2017;27:428-438. 3. Bergsma A, Janssen M, Geurts ACH, Cup EHC, de Groot IJM. Different profiles of upper limb function in four types of neuromuscular disorders. Neuromuscular Disorders 2017;27:1115-1122. 4. Carter GT, Abresch RT, Fowler WM, Jr., Johnson ER, Kilmer DD, McDonald CM. Profiles of neuromuscular diseases. Spinal muscular atrophy. American Journal of Physical Medicine & Rehabilitation / Association of Academic Physiatrists 1995;74:S150-159. 5. Vuillerot C, Payan C, Iwaz J, Ecochard R, Berard C, Group MFMSMAS. Responsiveness of the motor function measure in patients with spinal muscular atrophy. Archives of Physical Medicine and Rehabilitation 2013;94:1555-1561. 6. Mercuri E, Darras BT, Chiriboga CA, et al. Nusinersen versus Sham Control in Later- Onset Spinal Muscular Atrophy. New England Journal of Medicine 2018;378:625-635. 7. Bouisset S, DoMC. Posture, dynamic stability, and voluntary movement. Neurophysiol Clin 2008;38:345-362. 8. Flatters I, Mushtaq F, Hill LJ, et al. Children’s head movements and postural stability as a function of task. Experimental Brain Research Experimentelle Hirnforschung Experimentation Cerebrale 2014;232:1953-1970. 9. Peeters LHC, Kingma I, Faber GS, van Dieen JH, de Groot IJM. Trunk, head and pelvis interactions in healthy children when performing seated daily arm tasks. Experimental Brain Research Experimentelle Hirnforschung Experimentation Cerebrale 2018;236:2023-2036. 10. Robertson JV, Roby-Brami A. The trunk as a part of the kinematic chain for reaching movements in healthy subjects and hemiparetic patients. Brain Research 2011;1382:137-146. 11. Wadman RI, Wijngaarde CA, Stam M, et al. Muscle strength and motor function throughout life in a cross-sectional cohort of 180 patients with spinal muscular atrophy types 1c-4. European Journal of Neurology 2018;25:512-518. 12. Schneiberg S, Sveistrup H, McFadyen B, McKinley P, Levin MF. The development of coordination for reach-to-grasp movements in children. Experimental Brain Research Experimentelle Hirnforschung Experimentation Cerebrale 2002;146:142-154. 13. Peeters LHC, Kingma I, van Dieen JH, de Groot IJM. Don’t forget the trunk in Duchenne muscular dystrophy patients: more muscle weakness and compensation than expected. Journal of Neuroengineering and Rehabilitation 2019;16:44. 14. Vignos PJ, Jr., Archibald KC. Maintenance of ambulation in childhood muscular dystrophy. Journal of Chronic Diseases 1960;12:273-290.