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V Silani

Showing results (71-80 of 96) with videos related to

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Biochemical and Molecular Medicine|June 1, 1997
Expression study of survival motor neuron gene in human fetal tissuesG Novelli, L Calzà, P Amicucci, et al.
Bollettino Dell'Istituto Sieroterapico Milanese|January 1, 1990
Human neuronal cells in culture: from concepts to basic methodologyV Silani, A Pizzuti, M F Donato, et al.
Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.
Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, 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.
Neurology|August 26, 1998
A placebo-controlled trial of insulin-like growth factor-I in amyotrophic lateral sclerosis. European ALS/IGF-I Study GroupG D Borasio, W Robberecht, P N Leigh, et al.
Scientific Reports|June 25, 2020
Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral SclerosisC Carlomagno, P I Banfi, A Gualerzi, et al.
Acta Neurologica Scandinavica|May 15, 2013
Dysphagia in amyotrophic lateral sclerosis: prevalence and clinical findingsG Ruoppolo, I Schettino, V Frasca, et al.
Neurology|August 22, 2007
Phase II/III randomized trial of TCH346 in patients with ALSR Miller, W Bradley, M Cudkowicz, et al.
The Neuroradiology Journal|September 25, 2013
Cerebral amyloid angiopathy-related inflammation: an emerging diseaseM Savoiardo, A Erbetta, J C Di Francesco, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Biochemical and Molecular Medicine|June 1, 1997
Expression study of survival motor neuron gene in human fetal tissuesG Novelli, L Calzà, P Amicucci, et al.
Bollettino Dell'Istituto Sieroterapico Milanese|January 1, 1990
Human neuronal cells in culture: from concepts to basic methodologyV Silani, A Pizzuti, M F Donato, et al.
Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.
Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, 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.
Neurology|August 26, 1998
A placebo-controlled trial of insulin-like growth factor-I in amyotrophic lateral sclerosis. European ALS/IGF-I Study GroupG D Borasio, W Robberecht, P N Leigh, et al.
Scientific Reports|June 25, 2020
Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral SclerosisC Carlomagno, P I Banfi, A Gualerzi, et al.
Acta Neurologica Scandinavica|May 15, 2013
Dysphagia in amyotrophic lateral sclerosis: prevalence and clinical findingsG Ruoppolo, I Schettino, V Frasca, et al.
Neurology|August 22, 2007
Phase II/III randomized trial of TCH346 in patients with ALSR Miller, W Bradley, M Cudkowicz, et al.
The Neuroradiology Journal|September 25, 2013
Cerebral amyloid angiopathy-related inflammation: an emerging diseaseM Savoiardo, A Erbetta, J C Di Francesco, et al.
Pageof 10