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European Journal of Medical Genetics|November 3, 2009
Radicular dysfunction due to spinal deformities in Marfan syndrome at older age: three case reportsN C Voermans, A J Hosman, N van Alfen, et al.Physical Review Letters|September 7, 2019
Transverse Velocities with the Moving Lens EffectSelim C Hotinli, Joel Meyers, Neal Dalal, et al.Journal of Neuromuscular Diseases|August 15, 2018
MRI-Guided Biopsy as a Tool for Diagnosis and Research of Muscle DisordersSaskia Lassche, Barbara H Janssen, Ties IJzermans, et al.Journal of Neurology|March 16, 2007
Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophyE L van der Kooi, J S Kalkman, E Lindeman, et al.European Journal of Human Genetics : EJHG|November 16, 2006
The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-WhiteE Mariken Ruiter, Marloes H Siers, Christa van den Elzen, et al.Clinical Chemistry|December 16, 2006
Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N- and O-glycan biosynthesis defectsSuzan Wopereis, Stephanie Grünewald, Karin M L C Huijben, et al.Neurology|March 6, 2020
Muscle ultrasound is a responsive biomarker in facioscapulohumeral dystrophyRianne J M Goselink, Tim H A Schreuder, Karlien Mul, et al.Journal of Cachexia, Sarcopenia and Muscle|May 23, 2023
Five-year follow-up study on quantitative muscle magnetic resonance imaging in facioscapulohumeral muscular dystrophy: The link to clinical outcomeSanne C C Vincenten, Karlien Mul, Daniël van As, et al.Neuromuscular Disorders : NMD|December 4, 2001
A new phenotype of autosomal dominant nemaline myopathyI M P Gommans, B G M van Engelen, H J ter Laak, et al.American Journal of Medical Genetics. Part A|June 15, 2011
Adults with congenital heart disease: patients' knowledge and concerns about inheritanceKlaartje van Engelen, Marieke J H Baars, Lotte T van Rongen, et al.Pageof 84