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Silverio Perrotta

Showing results (81-90 of 200) with videos related to

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American Journal of Hematology|October 14, 2010
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B geneRoberta Russo, Maria Rosaria Esposito, Roberta Asci, et al.
Journal of Pediatric Hematology/Oncology|August 11, 2018
Childhood Head and Neck Lymphadenopathy: A Report by a Single Institution (2003-2017)Paolo Indolfi, Silverio Perrotta, Francesca Rossi, et al.
Haematologica|August 11, 2011
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpuraFrancesca Rossi, Silvia Mancusi, Giulia Bellini, et al.
Blood|March 6, 2002
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibitionSilverio Perrotta, Bruno Nobili, Francesca Rossi, et al.
Italian Journal of Pediatrics|March 24, 2018
Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?Claudia Santoro, Pia Bernardo, Antonietta Coppola, et al.
Journal of Crohn'S & Colitis|January 7, 2016
Serum Hepcidin and Iron Absorption in Paediatric Inflammatory Bowel DiseaseMassimo Martinelli, Caterina Strisciuglio, Annalisa Alessandrella, et al.
Archives of Disease in Childhood. Education and Practice Edition|April 29, 2018
A 23-month-old girl with chronic 'seborrhoeic' dermatitis, dehydration and failure to thrivePierluigi Marzuillo, Anna Grandone, Stefano Guarino, et al.
Haematologica|September 14, 2014
Iron overload causes osteoporosis in thalassemia major patients through interaction with transient receptor potential vanilloid type 1 (TRPV1) channelsFrancesca Rossi, Silverio Perrotta, Giulia Bellini, et al.
Plos One|July 13, 2018
Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1Claudia Santoro, Teresa Giugliano, Markus Kraemer, et al.
American Journal of Hematology|November 28, 2017
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overloadMaddalena Casale, Adriana Borriello, Saverio Scianguetta, et al.
Pageof 20

Showing results (81-90 of 200) with videos related to

Sort By:
Pageof 20
American Journal of Hematology|October 14, 2010
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B geneRoberta Russo, Maria Rosaria Esposito, Roberta Asci, et al.
Journal of Pediatric Hematology/Oncology|August 11, 2018
Childhood Head and Neck Lymphadenopathy: A Report by a Single Institution (2003-2017)Paolo Indolfi, Silverio Perrotta, Francesca Rossi, et al.
Haematologica|August 11, 2011
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpuraFrancesca Rossi, Silvia Mancusi, Giulia Bellini, et al.
Blood|March 6, 2002
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibitionSilverio Perrotta, Bruno Nobili, Francesca Rossi, et al.
Italian Journal of Pediatrics|March 24, 2018
Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?Claudia Santoro, Pia Bernardo, Antonietta Coppola, et al.
Journal of Crohn'S & Colitis|January 7, 2016
Serum Hepcidin and Iron Absorption in Paediatric Inflammatory Bowel DiseaseMassimo Martinelli, Caterina Strisciuglio, Annalisa Alessandrella, et al.
Archives of Disease in Childhood. Education and Practice Edition|April 29, 2018
A 23-month-old girl with chronic 'seborrhoeic' dermatitis, dehydration and failure to thrivePierluigi Marzuillo, Anna Grandone, Stefano Guarino, et al.
Haematologica|September 14, 2014
Iron overload causes osteoporosis in thalassemia major patients through interaction with transient receptor potential vanilloid type 1 (TRPV1) channelsFrancesca Rossi, Silverio Perrotta, Giulia Bellini, et al.
Plos One|July 13, 2018
Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1Claudia Santoro, Teresa Giugliano, Markus Kraemer, et al.
American Journal of Hematology|November 28, 2017
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overloadMaddalena Casale, Adriana Borriello, Saverio Scianguetta, et al.
Pageof 20