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Maria Bonanni

Showing results (1-10 of 6) with videos related to

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Journal of the Society for Cardiovascular Angiography & Interventions|December 1, 2025
A Blueprint for Building a Renal Denervation ProgramTayyab Shah, Catherine Vanchiere, Maria Bonanni, et al.
Cancers|April 27, 2024
Head and Neck Paragangliomas: Overview of Institutional ExperienceSwar N Vimawala, Alex Z Graboyes, Bonita Bennett, et al.
NPJ Precision Oncology|January 31, 2026
Metastatic progression of pheochromocytoma and paraganglioma occurs via parallel evolutionAndrew M Pregnall, Bradley Wubbenhorst, Kurt D'Andrea, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma-pheochromocytoma syndromeSamantha E Greenberg, Michelle F Jacobs, Heather Wachtel, et al.
Medrxiv : the Preprint Server for Health Sciences|August 23, 2023
A genotype-first approach identifies high incidence of <i>NF1</i> pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Nature Communications|April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of the Society for Cardiovascular Angiography & Interventions|December 1, 2025
A Blueprint for Building a Renal Denervation ProgramTayyab Shah, Catherine Vanchiere, Maria Bonanni, et al.
Cancers|April 27, 2024
Head and Neck Paragangliomas: Overview of Institutional ExperienceSwar N Vimawala, Alex Z Graboyes, Bonita Bennett, et al.
NPJ Precision Oncology|January 31, 2026
Metastatic progression of pheochromocytoma and paraganglioma occurs via parallel evolutionAndrew M Pregnall, Bradley Wubbenhorst, Kurt D'Andrea, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma-pheochromocytoma syndromeSamantha E Greenberg, Michelle F Jacobs, Heather Wachtel, et al.
Medrxiv : the Preprint Server for Health Sciences|August 23, 2023
A genotype-first approach identifies high incidence of <i>NF1</i> pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Nature Communications|April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associationsAnton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
Pageof 1