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Patrizia Accorsi

Showing results (21-30 of 107) with videos related to

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Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|February 7, 2018
Disposal of the residual autologous HSC units: Results of a survey carried out two years after the publication of a national policy in ItalyPaolo Perseghin, Daniele Laszlò, Francesca Bonifazi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 24, 2012
Clinical features of Sturge-Weber syndrome without facial nevus: five novel casesLaura Siri, Lucio Giordano, Patrizia Accorsi, et al.
Blood Transfusion = Trasfusione Del Sangue|May 27, 2020
Position paper on the preparation of immune plasma to be used in the treatment of patients with COVID-19Patrizia Accorsi, Pierluigi Berti, Vincenzo de Angelis, et al.
Pediatric Dermatology|November 11, 2010
Congenital systematized basaloid follicular hamartoma with microphthalmia and hemimegalencephalyValeria Boccaletti, Patrizia Accorsi, Lorenzo Pinelli, et al.
Anticancer Research|February 13, 2010
Prolonged disease control after myeloablative chemotherapy, autologous transplantation and immunotherapy in high-risk early breast cancerFrancesco Recchia, Giampiero Candeloro, Stefano Necozione, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2010
Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?Nune S Yeghiazaryan, Pasquale Striano, Patrizia Accorsi, et al.
Clinical Neurology and Neurosurgery|September 30, 2023
Frequency of SCN2A-related disorder in the regional epilepsy centre of brescia between 2002 and 2021Corinna Filippi, Giuseppe Milito, Patrizia Accorsi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 23, 2018
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literatureAnnalisa Agostini, Daniela Marchetti, Claudia Izzi, et al.
Seizure|January 8, 2015
Do pure absence seizures occur in myoclonic epilepsy of infancy? A case seriesVincenzo Belcastro, Lucio Giordano, Dario Pruna, et al.
Minerva Pediatrics|May 5, 2022
Repetitive and stereotyped behaviors in neurodevelopmental disorders: an observational analysis of four diagnostic groupsSara Brunetti, Andrea Rossi, Jessica Galli, et al.
Pageof 11

Showing results (21-30 of 107) with videos related to

Sort By:
Pageof 11
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|February 7, 2018
Disposal of the residual autologous HSC units: Results of a survey carried out two years after the publication of a national policy in ItalyPaolo Perseghin, Daniele Laszlò, Francesca Bonifazi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 24, 2012
Clinical features of Sturge-Weber syndrome without facial nevus: five novel casesLaura Siri, Lucio Giordano, Patrizia Accorsi, et al.
Blood Transfusion = Trasfusione Del Sangue|May 27, 2020
Position paper on the preparation of immune plasma to be used in the treatment of patients with COVID-19Patrizia Accorsi, Pierluigi Berti, Vincenzo de Angelis, et al.
Pediatric Dermatology|November 11, 2010
Congenital systematized basaloid follicular hamartoma with microphthalmia and hemimegalencephalyValeria Boccaletti, Patrizia Accorsi, Lorenzo Pinelli, et al.
Anticancer Research|February 13, 2010
Prolonged disease control after myeloablative chemotherapy, autologous transplantation and immunotherapy in high-risk early breast cancerFrancesco Recchia, Giampiero Candeloro, Stefano Necozione, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2010
Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?Nune S Yeghiazaryan, Pasquale Striano, Patrizia Accorsi, et al.
Clinical Neurology and Neurosurgery|September 30, 2023
Frequency of SCN2A-related disorder in the regional epilepsy centre of brescia between 2002 and 2021Corinna Filippi, Giuseppe Milito, Patrizia Accorsi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 23, 2018
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literatureAnnalisa Agostini, Daniela Marchetti, Claudia Izzi, et al.
Seizure|January 8, 2015
Do pure absence seizures occur in myoclonic epilepsy of infancy? A case seriesVincenzo Belcastro, Lucio Giordano, Dario Pruna, et al.
Minerva Pediatrics|May 5, 2022
Repetitive and stereotyped behaviors in neurodevelopmental disorders: an observational analysis of four diagnostic groupsSara Brunetti, Andrea Rossi, Jessica Galli, et al.
Pageof 11