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Barbara Pasini

Showing results (1-10 of 96) with videos related to

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Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary paragangliomasMargarita Raygada, Barbara Pasini, Constantine A Stratakis
The New England Journal of Medicine|September 7, 2007
Familial gastrointestinal stromal tumors and germ-line mutationsSarah R McWhinney, Barbara Pasini, Constantine A Stratakis, et al.
European Journal of Endocrinology|January 20, 2018
GENETICS IN ENDOCRINOLOGY: The expanding genetic horizon of primary aldosteronismSilvia Monticone, Fabrizio Buffolo, Martina Tetti, et al.
The American Journal of Surgical Pathology|September 27, 2006
Incidental carcinomas in prophylactic specimens in BRCA1 and BRCA2 germ-line mutation carriers, with emphasis on fallopian tube lesions: report of 6 cases and review of the literatureMaria L Carcangiu, Bernard Peissel, Barbara Pasini, et al.
Retinal Cases & Brief Reports|February 27, 2024
MULTIMODAL IMAGING OF A NOVEL MFSD8/CLN7 MUTATION ASSOCIATED WITH NONSYNDROMIC SYMMETRIC ADULT-ONSET MACULAR DYSTROPHYFrancesco Gelormini, Veronica Vallino, Mark P Breazzano, et al.
Journal of Cutaneous Medicine and Surgery|June 21, 2012
Gastric leiomyoma and hyperplastic polyposis coli in a patient with multiple cutaneous and uterine leiomyomatosisDavid Serra, Pedro Amaro, Margarida Gonçalo, et al.
Frontiers in Genetics|October 4, 2023
Phenotype reversion as "natural gene therapy" in Fanconi anemia by a gene conversion eventIlaria Persico, Ilaria Fiscarelli, Alessandra Pelle, et al.
International Journal of Dermatology|September 19, 2015
Germline CDKN2A mutations in childhood melanoma: a case of melanoma-pancreatic cancer syndromeLaura Cristina Gironi, Enrico Colombo, Pamela Farinelli, et al.
Urologia|March 4, 2017
Treatment of multiple synchronous misdiagnosed renal cell cancers in a young patient affected by a "de novo" Von Hippel-Lindau syndromeMarco Allasia, Antonino Battaglia, Barbara Pasini, et al.
International Journal of Molecular Sciences|March 15, 2018
Liddle Syndrome: Review of the Literature and Description of a New CaseMartina Tetti, Silvia Monticone, Jacopo Burrello, et al.
Pageof 10

Showing results (1-10 of 96) with videos related to

Sort By:
Pageof 10
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary paragangliomasMargarita Raygada, Barbara Pasini, Constantine A Stratakis
The New England Journal of Medicine|September 7, 2007
Familial gastrointestinal stromal tumors and germ-line mutationsSarah R McWhinney, Barbara Pasini, Constantine A Stratakis, et al.
European Journal of Endocrinology|January 20, 2018
GENETICS IN ENDOCRINOLOGY: The expanding genetic horizon of primary aldosteronismSilvia Monticone, Fabrizio Buffolo, Martina Tetti, et al.
The American Journal of Surgical Pathology|September 27, 2006
Incidental carcinomas in prophylactic specimens in BRCA1 and BRCA2 germ-line mutation carriers, with emphasis on fallopian tube lesions: report of 6 cases and review of the literatureMaria L Carcangiu, Bernard Peissel, Barbara Pasini, et al.
Retinal Cases & Brief Reports|February 27, 2024
MULTIMODAL IMAGING OF A NOVEL MFSD8/CLN7 MUTATION ASSOCIATED WITH NONSYNDROMIC SYMMETRIC ADULT-ONSET MACULAR DYSTROPHYFrancesco Gelormini, Veronica Vallino, Mark P Breazzano, et al.
Journal of Cutaneous Medicine and Surgery|June 21, 2012
Gastric leiomyoma and hyperplastic polyposis coli in a patient with multiple cutaneous and uterine leiomyomatosisDavid Serra, Pedro Amaro, Margarida Gonçalo, et al.
Frontiers in Genetics|October 4, 2023
Phenotype reversion as "natural gene therapy" in Fanconi anemia by a gene conversion eventIlaria Persico, Ilaria Fiscarelli, Alessandra Pelle, et al.
International Journal of Dermatology|September 19, 2015
Germline CDKN2A mutations in childhood melanoma: a case of melanoma-pancreatic cancer syndromeLaura Cristina Gironi, Enrico Colombo, Pamela Farinelli, et al.
Urologia|March 4, 2017
Treatment of multiple synchronous misdiagnosed renal cell cancers in a young patient affected by a "de novo" Von Hippel-Lindau syndromeMarco Allasia, Antonino Battaglia, Barbara Pasini, et al.
International Journal of Molecular Sciences|March 15, 2018
Liddle Syndrome: Review of the Literature and Description of a New CaseMartina Tetti, Silvia Monticone, Jacopo Burrello, et al.
Pageof 10