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Luisa Ronzoni

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Liver International : Official Journal of the International Association for the Study of the Liver|September 18, 2023
The genetics of portal hypertension: Recent developments and the road aheadSarah Shalaby, Luisa Ronzoni, Virginia Hernandez-Gea, et al.
BMC Medical Genetics|March 13, 2016
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz SyndromeArianna Tucci, Luisa Ronzoni, Carlo Arduino, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key geneLuisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
Blood Cells, Molecules & Diseases|September 25, 2007
Erythroid differentiation and maturation from peripheral CD34+ cells in liquid culture: cellular and molecular characterizationLuisa Ronzoni, Paola Bonara, Daniela Rusconi, et al.
American Journal of Medical Genetics. Part A|December 27, 2016
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 casesArianna Tucci, Lidia Pezzani, Giulietta Scuvera, et al.
British Journal of Haematology|March 11, 2014
Modulation of gamma globin genes expression by histone deacetylase inhibitors: an in vitro studyLuisa Ronzoni, Laura Sonzogni, Gianluca Fossati, et al.
European Journal of Medical Genetics|November 21, 2016
7p22.1 microduplication syndrome: Refinement of the critical regionLuisa Ronzoni, Francesca Sofia Grassi, Lidia Pezzani, et al.
Toxicology|August 7, 2010
Selective toxicity of dihydroartemisinin on human CD34+ erythroid cell differentiationSara Finaurini, Luisa Ronzoni, Alessandra Colancecco, et al.
Cytogenetic and Genome Research|December 5, 2016
2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal MalformationLuisa Ronzoni, Antonio Novelli, Giulia Brisighelli, et al.
American Journal of Medical Genetics. Part A|April 9, 2015
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysisLuisa Ronzoni, Angela Peron, Vera Bianchi, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Liver International : Official Journal of the International Association for the Study of the Liver|September 18, 2023
The genetics of portal hypertension: Recent developments and the road aheadSarah Shalaby, Luisa Ronzoni, Virginia Hernandez-Gea, et al.
BMC Medical Genetics|March 13, 2016
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz SyndromeArianna Tucci, Luisa Ronzoni, Carlo Arduino, et al.
American Journal of Medical Genetics. Part A|January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key geneLuisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
Blood Cells, Molecules & Diseases|September 25, 2007
Erythroid differentiation and maturation from peripheral CD34+ cells in liquid culture: cellular and molecular characterizationLuisa Ronzoni, Paola Bonara, Daniela Rusconi, et al.
American Journal of Medical Genetics. Part A|December 27, 2016
Is cutis verticis Gyrata-Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 casesArianna Tucci, Lidia Pezzani, Giulietta Scuvera, et al.
British Journal of Haematology|March 11, 2014
Modulation of gamma globin genes expression by histone deacetylase inhibitors: an in vitro studyLuisa Ronzoni, Laura Sonzogni, Gianluca Fossati, et al.
European Journal of Medical Genetics|November 21, 2016
7p22.1 microduplication syndrome: Refinement of the critical regionLuisa Ronzoni, Francesca Sofia Grassi, Lidia Pezzani, et al.
Toxicology|August 7, 2010
Selective toxicity of dihydroartemisinin on human CD34+ erythroid cell differentiationSara Finaurini, Luisa Ronzoni, Alessandra Colancecco, et al.
Cytogenetic and Genome Research|December 5, 2016
2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal MalformationLuisa Ronzoni, Antonio Novelli, Giulia Brisighelli, et al.
American Journal of Medical Genetics. Part A|April 9, 2015
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysisLuisa Ronzoni, Angela Peron, Vera Bianchi, et al.
Pageof 5