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European Journal of Neurology|July 25, 2015
The EGR2 gene is involved in axonal Charcot-Marie-Tooth diseaseT Sevilla, R Sivera, D Martínez-Rubio, et al.Journal of Neurology|October 11, 2011
Autoimmunity as a prognostic factor in sporadic adult onset cerebellar ataxiaR Sivera, N Martín, I Boscá, et al.Neurologia (Barcelona, Spain)|November 1, 1995
[Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure]A Pou Serradell, J M Espadaler, J M Aragonés, et al.Clinical Genetics|March 15, 2011
Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patientsN Muelas, P Hackman, H Luque, et al.Neurologia|September 4, 2024
The cross-sectional area of the median nerve: An independent prognostic biomarker in amyotrophic lateral sclerosisJ J Martínez-Payá, J Ríos-Díaz, M E Del Baño-Aledo, et al.Neurologia|August 8, 2022
Validation of Neuromyotype: a smart keyboard for the evaluation of spinal muscular atrophy patientsP Lizandra Cortés, D Poveda Verdú, A Albert Férriz, et al.Human Genetics|June 1, 1997
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsiesS Bort, E Nelis, V Timmerman, et al.Waste Management (New York, N.Y.)|December 16, 2011
Pollution profiles and physicochemical parameters in old uncontrolled landfillsM Regadío, A I Ruiz, I S de Soto, et al.Neurology|August 25, 2010
MYH7 gene tail mutation causing myopathic profiles beyond Laing distal myopathyN Muelas, P Hackman, H Luque, et al.European Journal of Neurology|February 15, 2020
Clinical spectrum of BICD2 mutationsM Frasquet, A Camacho, R Vílchez, et al.Pageof 5