Showing results (611-620 of 831) with videos related to
Sort By:
Pageof 84
European Journal of Radiology|September 1, 2023
Pneumonia pattern recognition on ultra-low-dose CT does not allow for a reliable differentiation between viral and bacterial pneumonia: A multicentre observer studyInge A H van den Berk, Maadrika M N P Kanglie, Tjitske S R van Engelen, et al.BMC Neurology|October 15, 2013
Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocolSaskia Lassche, Coen A C Ottenheijm, Nicol C Voermans, et al.Clinical Genetics|September 14, 2018
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1Karlien Mul, Nicol C Voermans, Richard J L F Lemmers, et al.Journal of the Peripheral Nervous System : JPNS|June 23, 2011
The phenotype of the Gly94fsX222 PMP22 insertionSara D J de Vries, Camiel Verhamme, Fred van Ruissen, et al.Annals of Human Genetics|January 30, 2004
Molecular analysis of myophosphorylase deficiency in Dutch patients with McArdle's diseaseM A Martín, J C Rubio, R A Wevers, et al.Neurology|December 17, 2024
Longitudinal Insights Into Childhood Onset Facioscapulohumeral Dystrophy: A 5-Year Natural History StudyJildou N Dijkstra, Helena T M Boon, Anne Koekkoek, et al.Neuromuscular Disorders : NMD|December 31, 2023
Bone quality in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a one-year prospective natural history studyKarlijn Bouman, Anne T M Dittrich, Jan T Groothuis, et al.Neurology|October 15, 2017
Adding quantitative muscle MRI to the FSHD clinical trial toolboxKarlien Mul, Sanne C C Vincenten, Nicol C Voermans, et al.Brain : a Journal of Neurology|June 1, 1997
Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological studyL L Teunissen, N C Notermans, H Franssen, et al.Brain : a Journal of Neurology|June 14, 2003
A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesionsI M P Gommans, M Davis, K Saar, et al.Pageof 84