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Barbara Pasini

Showing results (21-30 of 96) with videos related to

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Diseases (Basel, Switzerland)|June 25, 2025
Germline Non-CDKN2A Variants in Melanoma and Associated Hereditary Cancer SyndromesChiara Anna Fiasconaro, Alice Carbone, Silvia Giordano, et al.
Tumori|July 5, 2003
Breast MRI screening in patients with increased familial and/or genetic risk for breast cancer: a preliminary experienceGiovanna Trecate, Daniele Vergnaghi, Silvana Bergonzi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 11, 2002
Lack of SYT-SSX fusion transcripts in malignant peripheral nerve sheath tumors on RT-PCR analysis of 34 archival casesElena Tamborini, Viviana Agus, Federica Perrone, et al.
Journal of Clinical Medicine|July 9, 2022
Gynecological Cancers in Lynch Syndrome: A Comparison of the Histological Features with Sporadic Cases of the General PopulationValentina Elisabetta Bounous, Elisabetta Robba, Stefania Perotto, et al.
Surgery|April 28, 2005
The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A caseAntonella Aiello, Katia Cioni, Morena Gobbo, et al.
Hypertension (Dallas, Tex. : 1979)|September 4, 2024
Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension UnitMartina Tetti, Jacopo Burrello, Marguerite Hureaux, et al.
Hypertension (Dallas, Tex. : 1979)|March 3, 2020
Prevalence of Hypokalemia and Primary Aldosteronism in 5100 Patients Referred to a Tertiary Hypertension UnitJacopo Burrello, Silvia Monticone, Isabel Losano, et al.
Medicina (Kaunas, Lithuania)|July 10, 2019
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in PiebaldismLaura Cristina Gironi, Enrico Colombo, Alfredo Brusco, et al.
European Journal of Human Genetics : EJHG|July 12, 2012
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian originIolanda Borelli, Marco A Barberis, Francesca Spina, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|July 13, 2017
[Hyperuricemia and gene mutations: a case report]Fabio Tattoli, Daniela Falconi, Ornella De Prisco, et al.
Pageof 10

Showing results (21-30 of 96) with videos related to

Sort By:
Pageof 10
Diseases (Basel, Switzerland)|June 25, 2025
Germline Non-CDKN2A Variants in Melanoma and Associated Hereditary Cancer SyndromesChiara Anna Fiasconaro, Alice Carbone, Silvia Giordano, et al.
Tumori|July 5, 2003
Breast MRI screening in patients with increased familial and/or genetic risk for breast cancer: a preliminary experienceGiovanna Trecate, Daniele Vergnaghi, Silvana Bergonzi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 11, 2002
Lack of SYT-SSX fusion transcripts in malignant peripheral nerve sheath tumors on RT-PCR analysis of 34 archival casesElena Tamborini, Viviana Agus, Federica Perrone, et al.
Journal of Clinical Medicine|July 9, 2022
Gynecological Cancers in Lynch Syndrome: A Comparison of the Histological Features with Sporadic Cases of the General PopulationValentina Elisabetta Bounous, Elisabetta Robba, Stefania Perotto, et al.
Surgery|April 28, 2005
The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A caseAntonella Aiello, Katia Cioni, Morena Gobbo, et al.
Hypertension (Dallas, Tex. : 1979)|September 4, 2024
Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension UnitMartina Tetti, Jacopo Burrello, Marguerite Hureaux, et al.
Hypertension (Dallas, Tex. : 1979)|March 3, 2020
Prevalence of Hypokalemia and Primary Aldosteronism in 5100 Patients Referred to a Tertiary Hypertension UnitJacopo Burrello, Silvia Monticone, Isabel Losano, et al.
Medicina (Kaunas, Lithuania)|July 10, 2019
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in PiebaldismLaura Cristina Gironi, Enrico Colombo, Alfredo Brusco, et al.
European Journal of Human Genetics : EJHG|July 12, 2012
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian originIolanda Borelli, Marco A Barberis, Francesca Spina, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|July 13, 2017
[Hyperuricemia and gene mutations: a case report]Fabio Tattoli, Daniela Falconi, Ornella De Prisco, et al.
Pageof 10