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Marco Spada

Showing results (121-130 of 243) with videos related to

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Children (Basel, Switzerland)|April 23, 2022
Association between EEG Paroxysmal Abnormalities and Levels of Plasma Amino Acids and Urinary Organic Acids in Children with Autism Spectrum DisorderDaniele Marcotulli, Chiara Davico, Alessandra Somà, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|July 30, 2011
Impact of recipients' socio-economic status on patient and graft survival after liver transplantation: the IsMeTT experienceSalvatore Gruttadauria, Giuseppe Grosso, Antonio Mistretta, et al.
Frontiers in Nutrition|July 11, 2022
Case Report: Morphologic and Functional Characteristics of Intestinal Mucosa in a Child With Short Bowel Syndrome After Treatment With Teduglutide: Evidence in Favor of GLP-2 Analog SafetyEnrico Costantino Falco, Antonella Lezo, Pierluigi Calvo, et al.
Orphanet Journal of Rare Diseases|November 17, 2021
Italian national consensus statement on management and pharmacological treatment of phenylketonuriaAlberto Burlina, Giacomo Biasucci, Maria Teresa Carbone, et al.
Cell Transplantation|June 18, 2013
Isolation and characterization of multipotent cells from human fetal dermisCinzia Maria Chinnici, Giandomenico Amico, Marcello Monti, et al.
Biochimica Et Biophysica Acta|February 24, 2006
Identification of nine new IDS alleles in mucopolysaccharidosis II. Quantitative evaluation by real-time RT-PCR of mRNAs sensitive to nonsense-mediated and nonstop decay mechanismsSusanna Lualdi, Maja Di Rocco, Fabio Corsolini, et al.
Orphanet Journal of Rare Diseases|February 3, 2022
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialistsSilvia Kalantari, Brigida Brezzi, Valeria Bracciamà, et al.
Pediatric Transplantation|October 2, 2009
Combined split liver and kidney transplantation in a three-year-old child with primary hyperoxaluria type 1 and complete thrombosis of the inferior vena cavaZahida Khan, Marco Sciveres, Paola Salis, et al.
Italian Journal of Pediatrics|May 28, 2013
A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiencyFrancesca Santarelli, Michela Cassanello, Ausilia Enea, et al.
Frontiers in Surgery|March 18, 2024
Biliary atresia in preterm infants: a single center experience and review of literatureFederico Beati, Antonella Mosca, Andrea Pietrobattista, et al.
Pageof 25

Showing results (121-130 of 243) with videos related to

Sort By:
Pageof 25
Children (Basel, Switzerland)|April 23, 2022
Association between EEG Paroxysmal Abnormalities and Levels of Plasma Amino Acids and Urinary Organic Acids in Children with Autism Spectrum DisorderDaniele Marcotulli, Chiara Davico, Alessandra Somà, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|July 30, 2011
Impact of recipients' socio-economic status on patient and graft survival after liver transplantation: the IsMeTT experienceSalvatore Gruttadauria, Giuseppe Grosso, Antonio Mistretta, et al.
Frontiers in Nutrition|July 11, 2022
Case Report: Morphologic and Functional Characteristics of Intestinal Mucosa in a Child With Short Bowel Syndrome After Treatment With Teduglutide: Evidence in Favor of GLP-2 Analog SafetyEnrico Costantino Falco, Antonella Lezo, Pierluigi Calvo, et al.
Orphanet Journal of Rare Diseases|November 17, 2021
Italian national consensus statement on management and pharmacological treatment of phenylketonuriaAlberto Burlina, Giacomo Biasucci, Maria Teresa Carbone, et al.
Cell Transplantation|June 18, 2013
Isolation and characterization of multipotent cells from human fetal dermisCinzia Maria Chinnici, Giandomenico Amico, Marcello Monti, et al.
Biochimica Et Biophysica Acta|February 24, 2006
Identification of nine new IDS alleles in mucopolysaccharidosis II. Quantitative evaluation by real-time RT-PCR of mRNAs sensitive to nonsense-mediated and nonstop decay mechanismsSusanna Lualdi, Maja Di Rocco, Fabio Corsolini, et al.
Orphanet Journal of Rare Diseases|February 3, 2022
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialistsSilvia Kalantari, Brigida Brezzi, Valeria Bracciamà, et al.
Pediatric Transplantation|October 2, 2009
Combined split liver and kidney transplantation in a three-year-old child with primary hyperoxaluria type 1 and complete thrombosis of the inferior vena cavaZahida Khan, Marco Sciveres, Paola Salis, et al.
Italian Journal of Pediatrics|May 28, 2013
A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiencyFrancesca Santarelli, Michela Cassanello, Ausilia Enea, et al.
Frontiers in Surgery|March 18, 2024
Biliary atresia in preterm infants: a single center experience and review of literatureFederico Beati, Antonella Mosca, Andrea Pietrobattista, et al.
Pageof 25