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Teresa Sprovieri

Showing results (1-10 of 21) with videos related to

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Analytical Biochemistry|March 30, 2010
Quantification of thymosin beta(4) in human cerebrospinal fluid using matrix-assisted laser desorption/ionization time-of-flight mass spectrometryElena Urso, Maria Le Pera, Sabrina Bossio, et al.
Expert Review of Proteomics|December 15, 2010
Proteomic profiling of cerebrospinal fluid in Creutzfeldt-Jakob diseaseAntonio Qualtieri, Elena Urso, Maria Le Pera, et al.
International Journal of Molecular Sciences|August 2, 2019
A Systems Biology Approach for Personalized Medicine in Refractory EpilepsyGiuseppina Daniela Naimo, Maria Guarnaccia, Teresa Sprovieri, et al.
Cellular and Molecular Neurobiology|August 7, 2019
Alternative Splicing of ALS Genes: Misregulation and Potential TherapiesBenedetta Perrone, Valentina La Cognata, Teresa Sprovieri, et al.
Journal of Child Neurology|May 23, 2003
A simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatographyRosalucia Mazzei, Francesca Luisa Conforti, Maria Muglia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 6, 2019
A novel S379A TARDBP mutation associated to late-onset sporadic ALSTeresa Sprovieri, Carmine Ungaro, Benedetta Perrone, et al.
Neuroscience Letters|March 21, 2007
Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathyCarmine Ungaro, Teresa Sprovieri, Francesca L Conforti, et al.
Acta Neurologica Belgica|October 15, 2018
ALS and CHARGE syndrome: a clinical and genetic studyCarmine Ungaro, Luigi Citrigno, Francesca Trojsi, et al.
Archives of Neurology|March 21, 2012
Contribution of cerebrospinal fluid thymosin β4 levels to the clinical differentiation of Creutzfeldt-Jakob diseaseMaria Le Pera, Elena Urso, Teresa Sprovieri, et al.
BMC Medical Genetics|March 15, 2019
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case reportTeresa Sprovieri, Carmine Ungaro, Serena Sivo, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Analytical Biochemistry|March 30, 2010
Quantification of thymosin beta(4) in human cerebrospinal fluid using matrix-assisted laser desorption/ionization time-of-flight mass spectrometryElena Urso, Maria Le Pera, Sabrina Bossio, et al.
Expert Review of Proteomics|December 15, 2010
Proteomic profiling of cerebrospinal fluid in Creutzfeldt-Jakob diseaseAntonio Qualtieri, Elena Urso, Maria Le Pera, et al.
International Journal of Molecular Sciences|August 2, 2019
A Systems Biology Approach for Personalized Medicine in Refractory EpilepsyGiuseppina Daniela Naimo, Maria Guarnaccia, Teresa Sprovieri, et al.
Cellular and Molecular Neurobiology|August 7, 2019
Alternative Splicing of ALS Genes: Misregulation and Potential TherapiesBenedetta Perrone, Valentina La Cognata, Teresa Sprovieri, et al.
Journal of Child Neurology|May 23, 2003
A simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatographyRosalucia Mazzei, Francesca Luisa Conforti, Maria Muglia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 6, 2019
A novel S379A TARDBP mutation associated to late-onset sporadic ALSTeresa Sprovieri, Carmine Ungaro, Benedetta Perrone, et al.
Neuroscience Letters|March 21, 2007
Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathyCarmine Ungaro, Teresa Sprovieri, Francesca L Conforti, et al.
Acta Neurologica Belgica|October 15, 2018
ALS and CHARGE syndrome: a clinical and genetic studyCarmine Ungaro, Luigi Citrigno, Francesca Trojsi, et al.
Archives of Neurology|March 21, 2012
Contribution of cerebrospinal fluid thymosin β4 levels to the clinical differentiation of Creutzfeldt-Jakob diseaseMaria Le Pera, Elena Urso, Teresa Sprovieri, et al.
BMC Medical Genetics|March 15, 2019
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case reportTeresa Sprovieri, Carmine Ungaro, Serena Sivo, et al.
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