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Silvia Bianchi

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Neuropsychiatric Disease and Treatment|August 9, 2011
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli familyRadi Shahien, Silvia Bianchi, Abdalla Bowirrat
Vaccine|January 18, 2003
Primary prevention of hepatitis C virus infectionAlessandro R Zanetti, Luisa Romanò, Silvia Bianchi
Journal of Cellular Physiology|November 5, 2005
Physiology and pathology of notch signalling systemSilvia Bianchi, Maria Teresa Dotti, Antonio Federico
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 21, 2010
Congenital primary hydrothorax: effect of thoracoamniotic shunting on neonatal clinical outcomeSilvia Bianchi, Gianluca Lista, Francesca Castoldi, et al.
Acta Bio-Medica : Atenei Parmensis|October 4, 2012
Surfactant and mechanical ventilationGianluca Lista, Francesca Castoldi, Silvia Bianchi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 24, 2022
Primary familial brain calcification with mild phenotype due to a new PDGFB mutationSara Locci, Silvia Bianchi, Nicola De Stefano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 25, 2016
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular geneticsCarmen Stabile, Ilaria Taglia, Carla Battisti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 26, 2012
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long courseLuisa Sambati, Raffaele Agati, Antonella Bacci, et al.
Clinical Drug Investigation|December 14, 2006
Bronchoalveolar lavage with diluted porcine surfactant in mechanically ventilated term infants with meconium aspiration syndromeGianluca Lista, Silvia Bianchi, Francesca Castoldi, et al.
Clinical Neurology and Neurosurgery|June 22, 2021
Gordon Holmes syndrome caused by two novel mutations in the PNPLA6 geneSara Locci, Silvia Bianchi, Alessandra Tessa, et al.
Pageof 12

Showing results (1-10 of 118) with videos related to

Sort By:
Pageof 12
Neuropsychiatric Disease and Treatment|August 9, 2011
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli familyRadi Shahien, Silvia Bianchi, Abdalla Bowirrat
Vaccine|January 18, 2003
Primary prevention of hepatitis C virus infectionAlessandro R Zanetti, Luisa Romanò, Silvia Bianchi
Journal of Cellular Physiology|November 5, 2005
Physiology and pathology of notch signalling systemSilvia Bianchi, Maria Teresa Dotti, Antonio Federico
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 21, 2010
Congenital primary hydrothorax: effect of thoracoamniotic shunting on neonatal clinical outcomeSilvia Bianchi, Gianluca Lista, Francesca Castoldi, et al.
Acta Bio-Medica : Atenei Parmensis|October 4, 2012
Surfactant and mechanical ventilationGianluca Lista, Francesca Castoldi, Silvia Bianchi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 24, 2022
Primary familial brain calcification with mild phenotype due to a new PDGFB mutationSara Locci, Silvia Bianchi, Nicola De Stefano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 25, 2016
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular geneticsCarmen Stabile, Ilaria Taglia, Carla Battisti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 26, 2012
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long courseLuisa Sambati, Raffaele Agati, Antonella Bacci, et al.
Clinical Drug Investigation|December 14, 2006
Bronchoalveolar lavage with diluted porcine surfactant in mechanically ventilated term infants with meconium aspiration syndromeGianluca Lista, Silvia Bianchi, Francesca Castoldi, et al.
Clinical Neurology and Neurosurgery|June 22, 2021
Gordon Holmes syndrome caused by two novel mutations in the PNPLA6 geneSara Locci, Silvia Bianchi, Alessandra Tessa, et al.
Pageof 12