F. Crippa

发表

Pleiotropic effects of spastin on neurite growth depending on expression levels

E. Rugarli, G. Siciliano, G. Mancuso, 2009, Journal of neurochemistry.

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

N. Bresolin, C. Zucca, G. Casari, 2004, Journal of Medical Genetics.

Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum

N. Bresolin, F. Boaretto, A. Martinuzzi, 2009, Journal of Medical Genetics.

TO JMG A novel mutation in the ATP 1 A 2 gene causes alternating hemiplegia of childhood

N. Bresolin, C. Zucca, G. Casari, 2004 .

A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia

N. Bresolin, G. Comi, G. Meola, 2008, Human mutation.

Checkpoint Kinase 1 Down-Regulation by an Inducible Small Interfering RNA Expression System Sensitized In vivo Tumors to Treatment with 5-Fluorouracil

M. Broggini, L. Carrassa, G. Damia, 2008, Clinical Cancer Research.

Checkpoint Kinase1Down-Regulation by an Inducible Small Interfering RNAExpression System Sensitized In vivo Tumors toTreatment with 5-Fluorouracil

M. Broggini, L. Carrassa, G. Damia, 2008 .

Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.

N. Bresolin, G. Comi, A. Trabacca, 2006, Archives of neurology.

A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia

N. Bresolin, G. Comi, G. Meola, 2008, Human mutation.