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Tobias Else

Showing results (41-50 of 135) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 29, 2022
Quality of Life and its Determinants in Patients With Adrenal Insufficiency: A Survey Study at 3 Centers in the United StatesDingfeng Li, Sarah Brand, Oksana Hamidi, et al.
Journal of the Endocrine Society|April 15, 2024
3-[<sup>18</sup>F]Fluoro-<i>para</i>-hydroxyphenethylguanidine (3-[<sup>18</sup>F]pHPG) PET-A Novel Imaging Modality for ParagangliomaTobias Else, Ka Kit Wong, Kirk A Frey, et al.
European Journal of Nuclear Medicine and Molecular Imaging|January 28, 2022
PET imaging of metastatic paraganglioma using novel 3-[<sup>18</sup>F]fluoro-para-hydroxyphenethylguanidine (3-[<sup>18</sup>F]pHPG) radiotracerKa Kit Wong, Tobias Else, Benjamin L Viglianti, et al.
Journal of Pediatric Surgery|May 21, 2021
Laparoscopic adrenal-sparing approach for children with bilateral pheochromocytoma in Von Hippel-Lindau diseaseNathan S Rubalcava, R Elliott Overman, Tanvi T Kartal, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 2012
Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinomaVictoria M Raymond, Tobias Else, Jessica N Everett, et al.
JAAD Case Reports|June 9, 2020
An adolescent with uveal melanoma and <i>BAP1</i> tumor predisposition syndromeKelly Z Young, Sara L Fossum, Lori Lowe, et al.
European Journal of Endocrinology|May 12, 2016
Double adrenocortical adenomas harboring independent KCNJ5 and PRKACA somatic mutationsKazutaka Nanba, Kei Omata, Scott A Tomlins, et al.
JCO Precision Oncology|August 25, 2020
DICER1 Mutations in the Era of Expanding Integrative Clinical Sequencing in Pediatric OncologyKelly M Bailey, Michelle F Jacobs, Bailey Anderson, et al.
Hormones & Cancer|August 8, 2020
Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated HypercalcemiaShafaq Khairi, Jenae Osborne, Michelle F Jacobs, et al.
Familial Cancer|September 24, 2014
Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individualsShanna L Gustafson, Victoria M Raymond, Monica L Marvin, et al.
Pageof 14

Showing results (41-50 of 135) with videos related to

Sort By:
Pageof 14
The Journal of Clinical Endocrinology and Metabolism|March 29, 2022
Quality of Life and its Determinants in Patients With Adrenal Insufficiency: A Survey Study at 3 Centers in the United StatesDingfeng Li, Sarah Brand, Oksana Hamidi, et al.
Journal of the Endocrine Society|April 15, 2024
3-[<sup>18</sup>F]Fluoro-<i>para</i>-hydroxyphenethylguanidine (3-[<sup>18</sup>F]pHPG) PET-A Novel Imaging Modality for ParagangliomaTobias Else, Ka Kit Wong, Kirk A Frey, et al.
European Journal of Nuclear Medicine and Molecular Imaging|January 28, 2022
PET imaging of metastatic paraganglioma using novel 3-[<sup>18</sup>F]fluoro-para-hydroxyphenethylguanidine (3-[<sup>18</sup>F]pHPG) radiotracerKa Kit Wong, Tobias Else, Benjamin L Viglianti, et al.
Journal of Pediatric Surgery|May 21, 2021
Laparoscopic adrenal-sparing approach for children with bilateral pheochromocytoma in Von Hippel-Lindau diseaseNathan S Rubalcava, R Elliott Overman, Tanvi T Kartal, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 2012
Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinomaVictoria M Raymond, Tobias Else, Jessica N Everett, et al.
JAAD Case Reports|June 9, 2020
An adolescent with uveal melanoma and <i>BAP1</i> tumor predisposition syndromeKelly Z Young, Sara L Fossum, Lori Lowe, et al.
European Journal of Endocrinology|May 12, 2016
Double adrenocortical adenomas harboring independent KCNJ5 and PRKACA somatic mutationsKazutaka Nanba, Kei Omata, Scott A Tomlins, et al.
JCO Precision Oncology|August 25, 2020
DICER1 Mutations in the Era of Expanding Integrative Clinical Sequencing in Pediatric OncologyKelly M Bailey, Michelle F Jacobs, Bailey Anderson, et al.
Hormones & Cancer|August 8, 2020
Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated HypercalcemiaShafaq Khairi, Jenae Osborne, Michelle F Jacobs, et al.
Familial Cancer|September 24, 2014
Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individualsShanna L Gustafson, Victoria M Raymond, Monica L Marvin, et al.
Pageof 14