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Foot & Ankle International|July 11, 2015
Hind- and Midfoot Motion After Ankle ArthrodesisLaurens W van der Plaat, Susanne J P M van Engelen, Quirine E Wajer, et al.Analytical Chemistry|January 18, 2006
Urine testing for designer steroids by liquid chromatography with androgen bioassay detection and electrospray quadrupole time-of-flight mass spectrometry identificationMichel W F Nielen, Toine F H Bovee, Marcel C van Engelen, et al.Brain Communications|September 21, 2020
Ophthalmological findings in facioscapulohumeral dystrophyRianne J M Goselink, Vivian Schreur, Caroline R van Kernebeek, et al.Disability and Rehabilitation|September 16, 2021
Experiences of patients with facioscapulohumeral dystrophy with facial weakness: a qualitative studySümeyye Sezer, Edith H C Cup, Lieve M Roets-Merken, et al.Archives of Physical Medicine and Rehabilitation|October 30, 2007
Exercise therapy and other types of physical therapy for patients with neuromuscular diseases: a systematic reviewEdith H Cup, Allan J Pieterse, Jessica M Ten Broek-Pastoor, et al.Brain Communications|March 2, 2022
Visuomotor processing is altered after peripheral nerve damage in neuralgic amyotrophyRenee Lustenhouwer, Ian G M Cameron, Elze Wolfs, et al.Journal of Neurology|February 11, 2022
Long-term follow-up of respiratory function in facioscapulohumeral muscular dystrophySjan Teeselink, Sanne C C Vincenten, Nicol C Voermans, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|November 5, 2020
Electrocardiographic predictors of infrahissian conduction disturbances in myotonic dystrophy type 1Isis B T Joosten, Romy van Lohuizen, Dennis W den Uijl, et al.Journal of Neuromuscular Diseases|October 31, 2022
Bone Quality in Patients with a Congenital Myopathy: A Scoping ReviewKarlijn Bouman, Anne T M Dittrich, Jan T Groothuis, et al.Clinical Genetics|September 2, 2016
Recognizing the tenascin-X deficient type of Ehlers-Danlos syndrome: a cross-sectional study in 17 patientsS Demirdas, E Dulfer, L Robert, et al.Pageof 84