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Francesca Menni

Showing results (11-20 of 44) with videos related to

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Journal of Child Neurology|September 26, 2013
Think about it: FMR1 gene mosaicismFrancesca Andrea Bonarrigo, Silvia Russo, Paola Vizziello, et al.
Italian Journal of Pediatrics|August 20, 2022
CHARGE syndrome presenting with persistent hypoglycemia: case report and overview of the main genetic syndromes associated with neonatal hypoglycemiaAlessandra Consales, Beatrice Letizia Crippa, Lorenzo Colombo, et al.
Human Genetics|August 5, 2017
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowthLuca Ferrari, Giulietta Scuvera, Arianna Tucci, et al.
Vaccine|September 10, 2013
Preliminary data on immunogenicity, safety and tolerability of trivalent inactivated influenza vaccine in children with inborn errors of metabolism at risk of decompensationSusanna Esposito, Filippo Salvini, Francesca Menni, et al.
American Journal of Medical Genetics. Part A|October 31, 2009
Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndromeGiovanna Olioso, Alice Passarini, Francesca Atzeri, et al.
Case Reports in Pediatrics|August 25, 2017
Late Onset Cobalamin Disorder and Hemolytic Uremic Syndrome: A Rare Cause of Nephrotic SyndromeGianluigi Ardissino, Michela Perrone, Francesca Tel, et al.
Human Vaccines|April 22, 2011
Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndromeSusanna Esposito, Angelo Selicorni, Cristina Daleno, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|April 26, 2007
Combined liver-kidney transplantation in glycogen storage disease Ia: a case beyond the guidelinesMirco Belingheri, Luciana Ghio, Ambra Sala, et al.
Journal of Child Neurology|January 10, 2008
High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemiaMassimo Mastrangelo, Laura Canafoglia, Silvana Franceschetti, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Healthcare transition in patients with rare genetic disorders with and without developmental disability: neurofibromatosis 1 and Williams-Beuren syndromeAndrea Van Lierde, Francesca Menni, Maria Francesca Bedeschi, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Journal of Child Neurology|September 26, 2013
Think about it: FMR1 gene mosaicismFrancesca Andrea Bonarrigo, Silvia Russo, Paola Vizziello, et al.
Italian Journal of Pediatrics|August 20, 2022
CHARGE syndrome presenting with persistent hypoglycemia: case report and overview of the main genetic syndromes associated with neonatal hypoglycemiaAlessandra Consales, Beatrice Letizia Crippa, Lorenzo Colombo, et al.
Human Genetics|August 5, 2017
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowthLuca Ferrari, Giulietta Scuvera, Arianna Tucci, et al.
Vaccine|September 10, 2013
Preliminary data on immunogenicity, safety and tolerability of trivalent inactivated influenza vaccine in children with inborn errors of metabolism at risk of decompensationSusanna Esposito, Filippo Salvini, Francesca Menni, et al.
American Journal of Medical Genetics. Part A|October 31, 2009
Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndromeGiovanna Olioso, Alice Passarini, Francesca Atzeri, et al.
Case Reports in Pediatrics|August 25, 2017
Late Onset Cobalamin Disorder and Hemolytic Uremic Syndrome: A Rare Cause of Nephrotic SyndromeGianluigi Ardissino, Michela Perrone, Francesca Tel, et al.
Human Vaccines|April 22, 2011
Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndromeSusanna Esposito, Angelo Selicorni, Cristina Daleno, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|April 26, 2007
Combined liver-kidney transplantation in glycogen storage disease Ia: a case beyond the guidelinesMirco Belingheri, Luciana Ghio, Ambra Sala, et al.
Journal of Child Neurology|January 10, 2008
High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemiaMassimo Mastrangelo, Laura Canafoglia, Silvana Franceschetti, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Healthcare transition in patients with rare genetic disorders with and without developmental disability: neurofibromatosis 1 and Williams-Beuren syndromeAndrea Van Lierde, Francesca Menni, Maria Francesca Bedeschi, et al.
Pageof 5