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Barbara Pasini

Showing results (31-40 of 96) with videos related to

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Prenatal Diagnosis|September 27, 2021
Cell-free DNA screening for fetal aneuploidy using the rolling circle method: A step towards non invasive prenatal testing simplificationEnza Pavanello, Andrea Sciarrone, Varvara Guaraldo, et al.
NPJ Precision Oncology|March 9, 2022
Collision of germline POLE and PMS2 variants in a young patient treated with immune checkpoint inhibitorsEnrico Berrino, Roberto Filippi, Clara Visintin, et al.
Surgery|April 6, 2002
RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's diseaseBarbara Pasini, Roberta Rossi, Maria Rosaria Ambrosio, et al.
European Journal of Internal Medicine|April 11, 2016
Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian studyJacopo Azzollini, Giulietta Scuvera, Eleonora Bruno, et al.
Clinical Genitourinary Cancer|September 4, 2017
Radiofrequency Ablation for Renal Cancer in Von Hippel-Lindau Syndrome Patients: A Prospective Cohort AnalysisMarco Allasia, Francesco Soria, Antonino Battaglia, et al.
Archives of Dermatological Research|September 16, 2018
Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriersLaura Cristina Gironi, Enrico Colombo, Barbara Pasini, et al.
BMC Medical Genetics|June 3, 2014
A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanomaSimona Frigerio, Vittoria Disciglio, Siranoush Manoukian, et al.
Molecular Cytogenetics|January 25, 2014
Differences and homologies of chromosomal alterations within and between breast cancer cell lines: a clustering analysisMilena Rondón-Lagos, Ludovica Verdun Di Cantogno, Caterina Marchiò, et al.
Journal of Alzheimer'S Disease Reports|June 14, 2023
A Novel <i>PSEN1</i> Variant Leading to Posterior Cortical Atrophy: A Case ReportFausto Roveta, Andrea Marcinnò, Alberto Grassini, et al.
Journal of Human Genetics|September 11, 2019
Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcificationElisa Giorgio, Emanuela Garelli, Adriana Carando, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|September 27, 2021
Cell-free DNA screening for fetal aneuploidy using the rolling circle method: A step towards non invasive prenatal testing simplificationEnza Pavanello, Andrea Sciarrone, Varvara Guaraldo, et al.
NPJ Precision Oncology|March 9, 2022
Collision of germline POLE and PMS2 variants in a young patient treated with immune checkpoint inhibitorsEnrico Berrino, Roberto Filippi, Clara Visintin, et al.
Surgery|April 6, 2002
RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's diseaseBarbara Pasini, Roberta Rossi, Maria Rosaria Ambrosio, et al.
European Journal of Internal Medicine|April 11, 2016
Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian studyJacopo Azzollini, Giulietta Scuvera, Eleonora Bruno, et al.
Clinical Genitourinary Cancer|September 4, 2017
Radiofrequency Ablation for Renal Cancer in Von Hippel-Lindau Syndrome Patients: A Prospective Cohort AnalysisMarco Allasia, Francesco Soria, Antonino Battaglia, et al.
Archives of Dermatological Research|September 16, 2018
Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriersLaura Cristina Gironi, Enrico Colombo, Barbara Pasini, et al.
BMC Medical Genetics|June 3, 2014
A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanomaSimona Frigerio, Vittoria Disciglio, Siranoush Manoukian, et al.
Molecular Cytogenetics|January 25, 2014
Differences and homologies of chromosomal alterations within and between breast cancer cell lines: a clustering analysisMilena Rondón-Lagos, Ludovica Verdun Di Cantogno, Caterina Marchiò, et al.
Journal of Alzheimer'S Disease Reports|June 14, 2023
A Novel <i>PSEN1</i> Variant Leading to Posterior Cortical Atrophy: A Case ReportFausto Roveta, Andrea Marcinnò, Alberto Grassini, et al.
Journal of Human Genetics|September 11, 2019
Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcificationElisa Giorgio, Emanuela Garelli, Adriana Carando, et al.
Pageof 10