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Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.Health Policy (Amsterdam, Netherlands)|February 8, 1991
Hospital comparisons using a Euro Health Data Base for resource management and strategic planningF H France, A Alban, B Barber, et al.Hepatology (Baltimore, Md.)|September 1, 1987
A population study on the prevalence of gallstone disease: the Sirmione StudyL Barbara, C Sama, A M Morselli Labate, et al.Neurology|June 11, 2003
A neuropathological, stereo-EEG, and MRI study of subcortical band heterotopiaR Mai, L Tassi, M Cossu, et al.Neuromuscular Disorders : NMD|June 28, 2016
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1bL Corrado, S Magri, A Bagarotti, et al.Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.Journal of Pediatric Urology|July 10, 2019
Voiding cystourethrography and 99MTC-MAG3 renal scintigraphy in pediatric vesicoureteral reflux: what is the role of indirect cystography?V Capone, F Taroni, M A Pavesi, et al.Human Mutation|February 19, 2009
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosisLucia Corrado, A Ratti, C Gellera, et al.European Neurology|July 1, 2010
Predictive genetic tests in neurodegenerative disorders: a methodological approach integrating psychological counseling for at-risk individuals and referring cliniciansC Mariotti, A Ferruta, C Gellera, et al.Neurology|January 12, 2005
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxiaA Brussino, C Gellera, A Saluto, et al.Pageof 16