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Elena Manara

Showing results (11-20 of 45) with videos related to

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Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Genetic analysis of intellectual disability and autismPietro Chiurazzi, Aysha Karim Kiani, Jan Miertus, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Sudden unexplained death due to cardiac arrestVincenza Precone, Giulia Guerri, Geraldo Krasi, et al.
Blood|January 28, 2012
Presence of high-ERG expression is an independent unfavorable prognostic marker in MLL-rearranged childhood myeloid leukemiaMartina Pigazzi, Riccardo Masetti, Francesco Martinolli, et al.
Blood|April 4, 2014
MLL-AF6 fusion oncogene sequesters AF6 into the nucleus to trigger RAS activation in myeloid leukemiaElena Manara, Emma Baron, Claudia Tregnago, et al.
International Angiology : a Journal of the International Union of Angiology|April 3, 2019
Vascular anomalies: molecular bases, genetic testing and therapeutic approachesStefano Paolacci, Alessandra Zulian, Alice Bruson, et al.
Blood|February 15, 2013
CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtypeRiccardo Masetti, Martina Pigazzi, Marco Togni, et al.
Blood|November 3, 2012
Screening of novel genetic aberrations in pediatric acute myeloid leukemia: a report from the AIEOP AML-2002 study groupMartina Pigazzi, Elena Manara, Valeria Bisio, et al.
Molecular Genetics & Genomic Medicine|May 6, 2020
Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatmentStefano Paolacci, Aysha Karim Kiani, Elena Manara, et al.
Global Medical Genetics|August 25, 2021
Psychomotor Delay in a Child with <i>FGFR3</i> G380R Pathogenic Mutation Causing AchondroplasiaMahmut C Ergoren, Erdal Eren, Elena Manara, et al.
Molecular Genetics & Genomic Medicine|March 16, 2021
Recessive multiple epiphyseal dysplasia and Stargardt disease in two sistersLeonardo Gatticchi, Dominika Vešelényiová, Jan Miertus, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Genetic analysis of intellectual disability and autismPietro Chiurazzi, Aysha Karim Kiani, Jan Miertus, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Sudden unexplained death due to cardiac arrestVincenza Precone, Giulia Guerri, Geraldo Krasi, et al.
Blood|January 28, 2012
Presence of high-ERG expression is an independent unfavorable prognostic marker in MLL-rearranged childhood myeloid leukemiaMartina Pigazzi, Riccardo Masetti, Francesco Martinolli, et al.
Blood|April 4, 2014
MLL-AF6 fusion oncogene sequesters AF6 into the nucleus to trigger RAS activation in myeloid leukemiaElena Manara, Emma Baron, Claudia Tregnago, et al.
International Angiology : a Journal of the International Union of Angiology|April 3, 2019
Vascular anomalies: molecular bases, genetic testing and therapeutic approachesStefano Paolacci, Alessandra Zulian, Alice Bruson, et al.
Blood|February 15, 2013
CBFA2T3-GLIS2 fusion transcript is a novel common feature in pediatric, cytogenetically normal AML, not restricted to FAB M7 subtypeRiccardo Masetti, Martina Pigazzi, Marco Togni, et al.
Blood|November 3, 2012
Screening of novel genetic aberrations in pediatric acute myeloid leukemia: a report from the AIEOP AML-2002 study groupMartina Pigazzi, Elena Manara, Valeria Bisio, et al.
Molecular Genetics & Genomic Medicine|May 6, 2020
Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatmentStefano Paolacci, Aysha Karim Kiani, Elena Manara, et al.
Global Medical Genetics|August 25, 2021
Psychomotor Delay in a Child with <i>FGFR3</i> G380R Pathogenic Mutation Causing AchondroplasiaMahmut C Ergoren, Erdal Eren, Elena Manara, et al.
Molecular Genetics & Genomic Medicine|March 16, 2021
Recessive multiple epiphyseal dysplasia and Stargardt disease in two sistersLeonardo Gatticchi, Dominika Vešelényiová, Jan Miertus, et al.
Pageof 5