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Patrizia Dello Russo

Showing results (1-10 of 8) with videos related to

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Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 27, 2014
Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control studyPatrizia Dello Russo, Giuseppe Damante, Samantha Pasca, et al.
Thrombosis Research|October 31, 2009
WITHDRAWN: Retinal vein occlusion: Risk factors evaluation, treatment and prophylaxisGiovanni Barillari, Samantha Pasca, Patrizia Dello Russo, et al.
Molecular and Cellular Probes|July 15, 2019
Quantitative PCR evaluation of deletions/duplications identified by array CGHFederica Baldan, Nadia Passon, Silvia Burra, et al.
Molecular Syndromology|June 15, 2017
Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with EpilepsyChiara Gnan, Alessandra Franzoni, Federica Baldan, et al.
Journal of Thrombosis and Thrombolysis|August 12, 2009
Retinal vein occlusion: evaluation of "classic" and "emerging" risk factors and treatmentMarina Turello, Samantha Pasca, Roberto Daminato, et al.
Molecular and Cellular Probes|December 7, 2016
A CGH array procedure to detect PAX6 gene structural defectsAlessandra Franzoni, Patrizia Dello Russo, Federica Baldan, et al.
Cytogenetic and Genome Research|May 11, 2016
Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical FindingsPatrizia Dello Russo, Eliana Demori, Annalisa Sechi, et al.
BMC Medical Genetics|October 15, 2015
A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosisPatrizia Dello Russo, Alessandra Franzoni, Federica Baldan, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 27, 2014
Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control studyPatrizia Dello Russo, Giuseppe Damante, Samantha Pasca, et al.
Thrombosis Research|October 31, 2009
WITHDRAWN: Retinal vein occlusion: Risk factors evaluation, treatment and prophylaxisGiovanni Barillari, Samantha Pasca, Patrizia Dello Russo, et al.
Molecular and Cellular Probes|July 15, 2019
Quantitative PCR evaluation of deletions/duplications identified by array CGHFederica Baldan, Nadia Passon, Silvia Burra, et al.
Molecular Syndromology|June 15, 2017
Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with EpilepsyChiara Gnan, Alessandra Franzoni, Federica Baldan, et al.
Journal of Thrombosis and Thrombolysis|August 12, 2009
Retinal vein occlusion: evaluation of "classic" and "emerging" risk factors and treatmentMarina Turello, Samantha Pasca, Roberto Daminato, et al.
Molecular and Cellular Probes|December 7, 2016
A CGH array procedure to detect PAX6 gene structural defectsAlessandra Franzoni, Patrizia Dello Russo, Federica Baldan, et al.
Cytogenetic and Genome Research|May 11, 2016
Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical FindingsPatrizia Dello Russo, Eliana Demori, Annalisa Sechi, et al.
BMC Medical Genetics|October 15, 2015
A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosisPatrizia Dello Russo, Alessandra Franzoni, Federica Baldan, et al.
Pageof 1