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Silverio Perrotta

Showing results (31-40 of 200) with videos related to

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Orphanet Journal of Rare Diseases|October 22, 2013
Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhoodRaffaella Colombatti, Silverio Perrotta, Piera Samperi, et al.
Haematologica|November 4, 2005
Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantationSilverio Perrotta, Maria Luisa Conte, Angela La Manna, et al.
Annales De Genetique|October 17, 2002
Non-allelic heterogeneity in familial unilateral renal adysplasiaSalvatore Li Volti, Antonio Faiella, Silverio Perrotta, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 4, 2007
Renal hypoplasia without optic coloboma associated with PAX2 gene deletionElisa Benetti, Lina Artifoni, Leonardo Salviati, et al.
Cells|March 6, 2021
Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting ObesityGirolamo Di Maio, Nicola Alessio, Ibrahim Halil Demirsoy, et al.
Children (Basel, Switzerland)|February 25, 2023
Neuropsychiatric Manifestations, Reduced Self-Esteem and Poor Quality of Life in Children and Adolescents with Neurofibromatosis Type 1 (NF1): The Impact of Symptom Visibility and Bullying BehaviorNicola Davide Cavallo, Gianpaolo Maggi, Francesco Ferraiuolo, et al.
International Journal of Molecular Sciences|April 21, 2019
The Endocannabinoid/Endovanilloid System in Bone: From Osteoporosis to OsteosarcomaFrancesca Rossi, Chiara Tortora, Francesca Punzo, et al.
Platelets|January 28, 2009
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown originAnna Savoia, Patrizia Noris, Silverio Perrotta, et al.
British Journal of Haematology|October 31, 2002
Successful umbilical cord blood transplantation in a child with dyskeratosis congenita after a fludarabine-based reduced-intensity conditioning regimenBruno Nobili, Gabriele Rossi, Piero De Stefano, et al.
Children (Basel, Switzerland)|August 29, 2024
Quality of Life in Children with Neurofibromatosis Type 1: Agreement between Parents and Patients, and the Role of Disease Severity and VisibilityNicola Davide Cavallo, Paola Maietta, Silverio Perrotta, et al.
Pageof 20

Showing results (31-40 of 200) with videos related to

Sort By:
Pageof 20
Orphanet Journal of Rare Diseases|October 22, 2013
Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhoodRaffaella Colombatti, Silverio Perrotta, Piera Samperi, et al.
Haematologica|November 4, 2005
Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantationSilverio Perrotta, Maria Luisa Conte, Angela La Manna, et al.
Annales De Genetique|October 17, 2002
Non-allelic heterogeneity in familial unilateral renal adysplasiaSalvatore Li Volti, Antonio Faiella, Silverio Perrotta, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 4, 2007
Renal hypoplasia without optic coloboma associated with PAX2 gene deletionElisa Benetti, Lina Artifoni, Leonardo Salviati, et al.
Cells|March 6, 2021
Evaluation of Browning Agents on the White Adipogenesis of Bone Marrow Mesenchymal Stromal Cells: A Contribution to Fighting ObesityGirolamo Di Maio, Nicola Alessio, Ibrahim Halil Demirsoy, et al.
Children (Basel, Switzerland)|February 25, 2023
Neuropsychiatric Manifestations, Reduced Self-Esteem and Poor Quality of Life in Children and Adolescents with Neurofibromatosis Type 1 (NF1): The Impact of Symptom Visibility and Bullying BehaviorNicola Davide Cavallo, Gianpaolo Maggi, Francesco Ferraiuolo, et al.
International Journal of Molecular Sciences|April 21, 2019
The Endocannabinoid/Endovanilloid System in Bone: From Osteoporosis to OsteosarcomaFrancesca Rossi, Chiara Tortora, Francesca Punzo, et al.
Platelets|January 28, 2009
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown originAnna Savoia, Patrizia Noris, Silverio Perrotta, et al.
British Journal of Haematology|October 31, 2002
Successful umbilical cord blood transplantation in a child with dyskeratosis congenita after a fludarabine-based reduced-intensity conditioning regimenBruno Nobili, Gabriele Rossi, Piero De Stefano, et al.
Children (Basel, Switzerland)|August 29, 2024
Quality of Life in Children with Neurofibromatosis Type 1: Agreement between Parents and Patients, and the Role of Disease Severity and VisibilityNicola Davide Cavallo, Paola Maietta, Silverio Perrotta, et al.
Pageof 20