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Endocrine Connections
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October 24, 2018
Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging
Natalie 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 correlations
Sergio 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 1
Laura Gieldon, Jimmy Rusdian Masjkur, Susan Richter, et al.
Clinical Endocrinology
|
August 7, 2008
SDHC mutation in an elderly patient without familial antecedents
Elena 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 pheochromocytoma
Ines 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 paraganglioma
Alessa 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 Biomarkers
Marcel 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 analysis
Andrea Luchetti, Diana Walsh, Fay Rodger, et al.
European Journal of Endocrinology
|
November 6, 2014
Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma
Mariko 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 family
Alberto Cascón, Carlos Vázquez Huarte-Mendicoa, L Javier Leandro-García, et al.
Page
of 22
Search research articles
Search
Showing results (81-90 of 215) with videos related to
Sort By:
Page
of 22
Endocrine Connections
|
October 24, 2018
Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging
Natalie 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 correlations
Sergio 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 1
Laura Gieldon, Jimmy Rusdian Masjkur, Susan Richter, et al.
Clinical Endocrinology
|
August 7, 2008
SDHC mutation in an elderly patient without familial antecedents
Elena 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 pheochromocytoma
Ines 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 paraganglioma
Alessa 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 Biomarkers
Marcel 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 analysis
Andrea Luchetti, Diana Walsh, Fay Rodger, et al.
European Journal of Endocrinology
|
November 6, 2014
Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma
Mariko 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 family
Alberto Cascón, Carlos Vázquez Huarte-Mendicoa, L Javier Leandro-García, et al.
Page
of 22