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Pediatric Neurology|March 10, 1998
Walker-Warburg syndrome: neurologic features and muscle membrane structureR J Kanoff, R G Curless, C Petito, et al.Neuromuscular Disorders : NMD|September 25, 2025
282nd ENMC international workshop - standards of diagnosis and care for the sarcoglycanopathies. 8-10 November 2024, Amsterdam, NetherlandsM A Iammarino, J Alonso-Pérez, T Stojkovic, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2006
The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophyD M Bonifati, S F Witchel, M Ermani, et al.Human Molecular Genetics|April 1, 1995
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutationJ Wang, E Pegoraro, E Menegazzo, et al.Neurological Research|January 23, 2010
Quality of life and motor impairment in ALS: Italian validation of ALSAQA Palmieri, G Sorarù, L Lombardi, et al.American Journal of Medical Genetics|February 2, 1996
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.Neurology|April 11, 2001
A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivationF F Wu, M P Takahashi, E Pegoraro, et al.European Journal of Neurology|May 29, 2009
Epidemiology of ALS in Padova district, Italy, from 1992 to 2005V Cima, G Logroscino, C D'Ascenzo, et al.Journal of Neurology|February 5, 2011
Cognitive profile and MRI findings in limb-girdle muscular dystrophy 2IA Palmieri, R Manara, L Bello, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 16, 2010
Retrospective study on PET-SPECT imaging in a large cohort of myotonic dystrophy type 1 patientsVincenzo Romeo, E Pegoraro, F Squarzanti, et al.Pageof 8