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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.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|April 20, 2005
[Visual assessment of functional lungs parenchyma on HRCT and (3)He-MRI in patients after single lung transplantation: comparison with quantitative volumetric results]J Zaporozhan, S Ley, K K Gast, et al.Human Mutation|July 5, 2001
Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian familiesM L Mostacciuolo, E Righetti, M Zortea, et al.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|June 18, 2003
[Reformation as proposed solution for the problem of sectioning different levels with 3He-MRT and HR-CT of the chest]K K Gast, J Zaporozhan, S Ley, et al.Developmental Biology|October 17, 2009
Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in miceC L Fisher, I Lee, S Bloyer, et al.Neurology|September 11, 2009
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortN Ticozzi, V Silani, A L LeClerc, et al.Mucosal Immunology|May 8, 2009
Balancing inflammation and tolerance in vivo through dendritic cells by the commensal Candida albicansP Bonifazi, T Zelante, C D'Angelo, et al.Mucosal Immunology|November 20, 2009
Intranasally delivered siRNA targeting PI3K/Akt/mTOR inflammatory pathways protects from aspergillosisP Bonifazi, C D'Angelo, S Zagarella, et al.Pageof 18