Showing results (401-410 of 831) with videos related to

Sort By:
Pageof 84
Veterinary Parasitology|September 16, 2011
The value of a bulk-tank milk ELISA and individual serological and faecal examination for diagnosing (sub)clinical Dictyocaulus viviparus infection in dairy cowsH W Ploeger, P C Verbeek, C W H Dekkers, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 20, 2005
Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-IJ S Kalkman, M L Schillings, S P van der Werf, et al.
Mitochondrion|June 29, 2010
Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophyMike Gerards, Bianca van den Bosch, Chantal Calis, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Neuromuscular Disorders : NMD|April 26, 2023
Assessment of the burden of outpatient clinic and MRI-guided needle muscle biopsies as reported by patients with facioscapulohumeral muscular dystrophyJoost Kools, Willem Aerts, Erik H Niks, et al.
Journal of Neuromuscular Diseases|March 4, 2025
The participants' perspective on facioscapulohumeral muscular dystrophy trials in The Netherlands - A qualitative studyLizan Stinissen, Joost Kools, Sietse Bouma, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 11, 2008
Identifying deficits in balance control following vestibular or proprioceptive loss using posturographic analysis of stance tasksC G C Horlings, U M Küng, B R Bloem, et al.
Disability and Rehabilitation. Assistive Technology|March 6, 2009
Ambulatory disabilities and the use of walking aids in patients with hereditary motor and sensory neuropathy type I (HMSN I)Marleen H van der Linden, Joke S Kalkman, Henk T Hendricks, et al.
Neuromuscular Disorders : NMD|July 8, 2008
Gastrointestinal involvement is frequent in Myotonic Dystrophy type 2Alide A Tieleman, Judith van Vliet, Jan B M J Jansen, et al.
Familial Cancer|April 3, 2021
Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphomaN van Engelen, F van Dijk, E Waanders, et al.
Pageof 84