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Mercedes Robledo

Showing results (81-90 of 215) with videos related to

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Endocrine Connections|October 24, 2018
Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imagingNatalie Rogowski-Lehmann, Aikaterini Geroula, Aleksander Prejbisz, et al.
Human Mutation|January 15, 2004
Genetic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlationsSergio Ruiz-Llorente, Jerónimo Bravo, Arancha Cebrián, et al.
European Journal of Endocrinology|November 22, 2017
Next-generation panel sequencing identifies <i>NF1</i> germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1Laura Gieldon, Jimmy Rusdian Masjkur, Susan Richter, et al.
Clinical Endocrinology|August 7, 2008
SDHC mutation in an elderly patient without familial antecedentsElena López-Jiménez, José M de Campos, Elena M Kusak, et al.
Oncotarget|September 5, 2015
Oncogenic features of the bone morphogenic protein 7 (BMP7) in pheochromocytomaInes Leinhäuser, Andrea Richter, Misu Lee, et al.
European Journal of Nuclear Medicine and Molecular Imaging|April 27, 2026
[<sup>68</sup>Ga]Ga-DOTATATE uptake in pheochromocytoma/paraganglioma predicts SSTR2 expression by immunohistochemistry: Strongest uptake in head and neck paragangliomaAlessa Fischer, Umberto Maccio, Junko Inoue Inukai, et al.
Journal of the Endocrine Society|August 15, 2024
Identification of Succinate Dehydrogenase Gene Variant Carriers by Blood BiomarkersMarcel Gebhardt, Carola Kunath, Dennis Fröbel, et al.
International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.
European Journal of Endocrinology|November 6, 2014
Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytomaMariko Sue, Victoria Martucci, Florina Frey, et al.
Genes, Chromosomes & Cancer|August 13, 2011
Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome familyAlberto Cascón, Carlos Vázquez Huarte-Mendicoa, L Javier Leandro-García, et al.
Pageof 22

Showing results (81-90 of 215) with videos related to

Sort By:
Pageof 22
Endocrine Connections|October 24, 2018
Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imagingNatalie Rogowski-Lehmann, Aikaterini Geroula, Aleksander Prejbisz, et al.
Human Mutation|January 15, 2004
Genetic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlationsSergio Ruiz-Llorente, Jerónimo Bravo, Arancha Cebrián, et al.
European Journal of Endocrinology|November 22, 2017
Next-generation panel sequencing identifies <i>NF1</i> germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1Laura Gieldon, Jimmy Rusdian Masjkur, Susan Richter, et al.
Clinical Endocrinology|August 7, 2008
SDHC mutation in an elderly patient without familial antecedentsElena López-Jiménez, José M de Campos, Elena M Kusak, et al.
Oncotarget|September 5, 2015
Oncogenic features of the bone morphogenic protein 7 (BMP7) in pheochromocytomaInes Leinhäuser, Andrea Richter, Misu Lee, et al.
European Journal of Nuclear Medicine and Molecular Imaging|April 27, 2026
[<sup>68</sup>Ga]Ga-DOTATATE uptake in pheochromocytoma/paraganglioma predicts SSTR2 expression by immunohistochemistry: Strongest uptake in head and neck paragangliomaAlessa Fischer, Umberto Maccio, Junko Inoue Inukai, et al.
Journal of the Endocrine Society|August 15, 2024
Identification of Succinate Dehydrogenase Gene Variant Carriers by Blood BiomarkersMarcel Gebhardt, Carola Kunath, Dennis Fröbel, et al.
International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.
European Journal of Endocrinology|November 6, 2014
Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytomaMariko Sue, Victoria Martucci, Florina Frey, et al.
Genes, Chromosomes & Cancer|August 13, 2011
Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome familyAlberto Cascón, Carlos Vázquez Huarte-Mendicoa, L Javier Leandro-García, et al.
Pageof 22