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P Balestri

Showing results (31-40 of 64) with videos related to

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Clinical Genetics|June 13, 2009
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsiesA Orrico, L Galli, S Grosso, et al.
The Neuroradiology Journal|October 24, 2013
L-2 Hydroxyglutaric Aciduria: Magnetization Transfer Contrast and Diffusion Weighted Magnetic Resonance Imaging Findings. A case ReportP Galluzzi, S Grosso, A Cerase, et al.
European Journal of Pediatrics|May 1, 1988
Trichothiodystrophy without photosensitivity. Biochemical, ultrastructural and DNA repair studiesA Fois, P Balestri, S Calvieri, et al.
European Journal of Neurology|July 19, 2008
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart reviewS Grosso, D Maria Cordelli, G Coppola, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|November 1, 1988
[The hair in a case of biotinidase deficiency]S Calvieri, S Giustini, V Giannelli, et al.
American Journal of Medical Genetics|September 5, 2002
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?S Grosso, M A Farnetani, R Berardi, et al.
Journal of Neurology|July 5, 2001
Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging studyN De Stefano, P Balestri, M T Dotti, et al.
Acta Neurologica Scandinavica|February 1, 2014
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndromeS Grosso, G Coppola, R Cusmai, et al.
Minerva Medica|November 1, 1996
[Coagulation in hemodialysis]M Camici, L Evangelisti, P Balestri, et al.
Lancet (London, England)|October 31, 1992
Epilepsy, progressive cerebral calcifications, and coeliac diseaseA Fois, P Balestri, M Vascotto, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Clinical Genetics|June 13, 2009
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsiesA Orrico, L Galli, S Grosso, et al.
The Neuroradiology Journal|October 24, 2013
L-2 Hydroxyglutaric Aciduria: Magnetization Transfer Contrast and Diffusion Weighted Magnetic Resonance Imaging Findings. A case ReportP Galluzzi, S Grosso, A Cerase, et al.
European Journal of Pediatrics|May 1, 1988
Trichothiodystrophy without photosensitivity. Biochemical, ultrastructural and DNA repair studiesA Fois, P Balestri, S Calvieri, et al.
European Journal of Neurology|July 19, 2008
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart reviewS Grosso, D Maria Cordelli, G Coppola, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|November 1, 1988
[The hair in a case of biotinidase deficiency]S Calvieri, S Giustini, V Giannelli, et al.
American Journal of Medical Genetics|September 5, 2002
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?S Grosso, M A Farnetani, R Berardi, et al.
Journal of Neurology|July 5, 2001
Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging studyN De Stefano, P Balestri, M T Dotti, et al.
Acta Neurologica Scandinavica|February 1, 2014
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndromeS Grosso, G Coppola, R Cusmai, et al.
Minerva Medica|November 1, 1996
[Coagulation in hemodialysis]M Camici, L Evangelisti, P Balestri, et al.
Lancet (London, England)|October 31, 1992
Epilepsy, progressive cerebral calcifications, and coeliac diseaseA Fois, P Balestri, M Vascotto, et al.
Pageof 7