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Ilaria Meloni

Showing results (1-10 of 57) with videos related to

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Nature Genetics|December 30, 2004
Is Rett syndrome a loss-of-imprinting disorder?Chiara Pescucci, Ilaria Meloni, Alessandra Renieri
Journal of Molecular Medicine (Berlin, Germany)|May 17, 2003
Rett syndrome: the complex nature of a monogenic diseaseAlessandra Renieri, Ilaria Meloni, Ilaria Longo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2013
Huntington's disease gene expansion associates with early onset nonprogressive choreaLaura Dosa, Alessandro Malandrini, Ilaria Di Donato, et al.
Brain & Development|July 28, 2004
Lymphoblastoid cell lines of Rett syndrome patients exposed to oxidative-stress-induced apoptosisCarla Battisti, Patrizia Formichi, Sergio Antonio Tripodi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 23, 2003
Study of MECP2 gene in Rett syndrome variants and autistic girlsMichele Zappella, Ilaria Meloni, Ilaria Longo, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 25, 2002
Optic disc drusen, angioid streaks, and mottled fundus in various combinations in a Sicilian familySalvatore Li Volti, Teresio Avitabile, Giovanni Li Volti, et al.
Hematology/Oncology and Stem Cell Therapy|July 3, 2021
The Phenomenon of Multidrug Resistance in GlioblastomasAlexandr N Chernov, Diana A Alaverdian, Elvira S Galimova, et al.
Human Mutation|July 9, 2004
Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplicationFrancesca Ariani, Francesca Mari, Chiara Pescucci, et al.
European Journal of Medical Genetics|March 24, 2009
14q12 Microdeletion syndrome and congenital variant of Rett syndromeMaria Antonietta Mencarelli, Tjitske Kleefstra, Eleni Katzaki, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 26, 2007
RSK2 enzymatic assay as a second level diagnostic tool in Coffin-Lowry syndromeVanna Micheli, Sylvia Sestini, Veronica Parri, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Nature Genetics|December 30, 2004
Is Rett syndrome a loss-of-imprinting disorder?Chiara Pescucci, Ilaria Meloni, Alessandra Renieri
Journal of Molecular Medicine (Berlin, Germany)|May 17, 2003
Rett syndrome: the complex nature of a monogenic diseaseAlessandra Renieri, Ilaria Meloni, Ilaria Longo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2013
Huntington's disease gene expansion associates with early onset nonprogressive choreaLaura Dosa, Alessandro Malandrini, Ilaria Di Donato, et al.
Brain & Development|July 28, 2004
Lymphoblastoid cell lines of Rett syndrome patients exposed to oxidative-stress-induced apoptosisCarla Battisti, Patrizia Formichi, Sergio Antonio Tripodi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 23, 2003
Study of MECP2 gene in Rett syndrome variants and autistic girlsMichele Zappella, Ilaria Meloni, Ilaria Longo, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 25, 2002
Optic disc drusen, angioid streaks, and mottled fundus in various combinations in a Sicilian familySalvatore Li Volti, Teresio Avitabile, Giovanni Li Volti, et al.
Hematology/Oncology and Stem Cell Therapy|July 3, 2021
The Phenomenon of Multidrug Resistance in GlioblastomasAlexandr N Chernov, Diana A Alaverdian, Elvira S Galimova, et al.
Human Mutation|July 9, 2004
Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplicationFrancesca Ariani, Francesca Mari, Chiara Pescucci, et al.
European Journal of Medical Genetics|March 24, 2009
14q12 Microdeletion syndrome and congenital variant of Rett syndromeMaria Antonietta Mencarelli, Tjitske Kleefstra, Eleni Katzaki, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 26, 2007
RSK2 enzymatic assay as a second level diagnostic tool in Coffin-Lowry syndromeVanna Micheli, Sylvia Sestini, Veronica Parri, et al.
Pageof 6