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Mercedes Robledo

Showing results (161-170 of 215) with videos related to

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The American Journal of Pathology|December 4, 2012
Differential gene expression of medullary thyroid carcinoma reveals specific markers associated with genetic conditionsAgnieszka Maliszewska, Luis J Leandro-Garcia, Esmeralda Castelblanco, et al.
Frontiers in Endocrinology|February 10, 2023
Co-occurrence of mutations in <i>NF1</i> and other susceptibility genes in pheochromocytoma and paragangliomaSara Mellid, Eduardo Gil, Rocío Letón, et al.
Endocrinologia Y Nutricion : Organo De La Sociedad Espanola De Endocrinologia Y Nutricion|April 20, 2016
The Molecular Registry of Pituitary Adenomas (REMAH): A bet of Spanish Endocrinology for the future of individualized medicine and translational researchRaúl M Luque, Alejandro Ibáñez-Costa, Laura Sánchez-Tejada, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for adrenal and cardiovascular endocrinologyEystein S Husebye, Guillaume Assié, Nils Krone, et al.
American Journal of Human Genetics|May 4, 2019
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and ParagangliomasLaura Remacha, David Pirman, Christopher E Mahoney, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2018
Gain-of-function mutations in DNMT3A in patients with paragangliomaLaura Remacha, Maria Currás-Freixes, Raúl Torres-Ruiz, et al.
The Journal of Clinical Endocrinology and Metabolism|August 5, 2020
Sino-European Differences in the Genetic Landscape and Clinical Presentation of Pheochromocytoma and ParagangliomaJingjing Jiang, Jing Zhang, Yingxian Pang, et al.
American Journal of Human Genetics|April 2, 2019
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and ParagangliomasLaura Remacha, David Pirman, Christopher E Mahoney, et al.
Cancers|November 10, 2020
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic CharacterizationA Beatriz Sánchez-Heras, Adela Castillejo, Juan D García-Díaz, et al.
Molecular Endocrinology (Baltimore, Md.)|October 29, 2010
Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomasElena López-Jiménez, Gonzalo Gómez-López, L Javier Leandro-García, et al.
Pageof 22

Showing results (161-170 of 215) with videos related to

Sort By:
Pageof 22
The American Journal of Pathology|December 4, 2012
Differential gene expression of medullary thyroid carcinoma reveals specific markers associated with genetic conditionsAgnieszka Maliszewska, Luis J Leandro-Garcia, Esmeralda Castelblanco, et al.
Frontiers in Endocrinology|February 10, 2023
Co-occurrence of mutations in <i>NF1</i> and other susceptibility genes in pheochromocytoma and paragangliomaSara Mellid, Eduardo Gil, Rocío Letón, et al.
Endocrinologia Y Nutricion : Organo De La Sociedad Espanola De Endocrinologia Y Nutricion|April 20, 2016
The Molecular Registry of Pituitary Adenomas (REMAH): A bet of Spanish Endocrinology for the future of individualized medicine and translational researchRaúl M Luque, Alejandro Ibáñez-Costa, Laura Sánchez-Tejada, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for adrenal and cardiovascular endocrinologyEystein S Husebye, Guillaume Assié, Nils Krone, et al.
American Journal of Human Genetics|May 4, 2019
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and ParagangliomasLaura Remacha, David Pirman, Christopher E Mahoney, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2018
Gain-of-function mutations in DNMT3A in patients with paragangliomaLaura Remacha, Maria Currás-Freixes, Raúl Torres-Ruiz, et al.
The Journal of Clinical Endocrinology and Metabolism|August 5, 2020
Sino-European Differences in the Genetic Landscape and Clinical Presentation of Pheochromocytoma and ParagangliomaJingjing Jiang, Jing Zhang, Yingxian Pang, et al.
American Journal of Human Genetics|April 2, 2019
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and ParagangliomasLaura Remacha, David Pirman, Christopher E Mahoney, et al.
Cancers|November 10, 2020
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic CharacterizationA Beatriz Sánchez-Heras, Adela Castillejo, Juan D García-Díaz, et al.
Molecular Endocrinology (Baltimore, Md.)|October 29, 2010
Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomasElena López-Jiménez, Gonzalo Gómez-López, L Javier Leandro-García, et al.
Pageof 22