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International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology|March 10, 2018
No meditation-related changes in the auditory N1 during first-time meditationL J Barnes, G M McArthur, B A Biedermann, 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.International Journal of Radiation Oncology, Biology, Physics|January 1, 1992
Characterization of a CHO cell line resistant to killing by the hypoxic cell cytotoxin SR 4233A J Giaccia, K A Biedermann, L M Tosto, 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.Neuroscience|May 1, 1995
Mesopontine neurons in schizophreniaE Garcia-Rill, J A Biedermann, T Chambers, et al.Cancer Research|December 15, 1993
Complementation of the radiosensitive phenotype in severe combined immunodeficient mice by human chromosome 8C U Kirchgessner, L M Tosto, K A Biedermann, 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 17