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Journal of Rehabilitation Medicine|April 23, 2010
Measurement of muscle strength with a handheld dynamometer in patients with chronic spinal muscular atrophyAnna Febrer, Natalia Rodriguez, Laura Alias, et al.Journal of Neuropathology and Experimental Neurology|May 9, 2014
Abnormalities in early markers of muscle involvement support a delay in myogenesis in spinal muscular atrophyRebeca Martínez-Hernández, Sara Bernal, Laura Alias, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2006
Two independent mutations of the SMN1 gene in the same spinal muscular atrophy family branch: lessons for carrier diagnosisMaría Jesús Barceló, Laura Alias, Lídia Caselles, et al.Neurology. Genetics|December 16, 2020
Practical guidelines to manage discordant situations of SMN2 copy number in patients with spinal muscular atrophyIvon Cuscó, Sara Bernal, Laura Blasco-Pérez, et al.Neuromuscular Disorders : NMD|April 22, 2004
A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemiaLaura Alias, Pía Gallano, Dolores Moreno, et al.European Journal of Human Genetics : EJHG|July 13, 2007
Evidence of a segregation ratio distortion of SMN1 alleles in spinal muscular atrophyLaura Alias, Maria J Barceló, Ignasi Gich, et al.Human Mutation|March 19, 2021
Beyond copy number: A new, rapid, and versatile method for sequencing the entire SMN2 gene in SMA patientsLaura Blasco-Pérez, Ida Paramonov, Jordi Leno, et al.Journal of Neuropathology and Experimental Neurology|June 16, 2009
The developmental pattern of myotubes in spinal muscular atrophy indicates prenatal delay of muscle maturationRebeca Martínez-Hernández, Carolina Soler-Botija, Eva Also, et al.Clinical Neurology and Neurosurgery|September 14, 2007
Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patientsJosep Gamez, Eva Also, Laura Alias, et al.International Journal of Molecular Sciences|September 28, 2021
High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced TherapiesSara Bernal, Irene Pelaez, Laura Alias, et al.Pageof 2