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Alberto Cascón

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Biochimica Et Biophysica Acta. Reviews on Cancer|June 22, 2024
Clinical and molecular markers guide the genetics of pheochromocytoma and paragangliomaAlberto Cascón, Mercedes Robledo
Biochimica Et Biophysica Acta. Reviews on Cancer|April 13, 2025
Corrigendum to "Clinical and molecular markers guide the genetics of pheochromocytoma and paraganglioma" [Biochimica et Biophysica Acta (BBA) - Reviews on Cancer Volume 1879, Issue 5, September 2024]Alberto Cascón, Mercedes Robledo
Medicina Clinica|March 7, 2013
[Hereditary pheochromocytoma and paraganglioma: the disease with ten faces]Alberto Cascón, Mercedes Robledo
Cancer Research|June 19, 2012
MAX and MYC: a heritable breakupAlberto Cascón, Mercedes Robledo
Endocrine Pathology|February 11, 2012
From transcriptional profiling to tumor biology in pheochromocytoma and paragangliomaAlberto Cascón, Daniel A Tennant
Pediatric Blood & Cancer|November 24, 2005
Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutationsJaume Mora, Alberto Cascón, Mercedes Robledo, et al.
Cancers|May 19, 2019
Pheochromocytomas and Paragangliomas: Bypassing Cellular RespirationAlberto Cascón, Laura Remacha, Bruna Calsina, et al.
Genes, Chromosomes & Cancer|April 16, 2003
G12S and H50R variations are polymorphisms in the SDHD geneAlberto Cascón, Sergio Ruiz-Llorente, Arancha Cebrián, et al.
Endocrine Pathology|October 8, 2013
Usefulness of negative and weak-diffuse pattern of SDHB immunostaining in assessment of SDH mutations in paragangliomas and pheochromocytomasEsmeralda Castelblanco, Maria Santacana, Joan Valls, et al.
Journal of Human Genetics|August 9, 2002
A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresisCebrián Arancha, Sergio Ruíz-Llorente, Alberto Cascón, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Biochimica Et Biophysica Acta. Reviews on Cancer|June 22, 2024
Clinical and molecular markers guide the genetics of pheochromocytoma and paragangliomaAlberto Cascón, Mercedes Robledo
Biochimica Et Biophysica Acta. Reviews on Cancer|April 13, 2025
Corrigendum to "Clinical and molecular markers guide the genetics of pheochromocytoma and paraganglioma" [Biochimica et Biophysica Acta (BBA) - Reviews on Cancer Volume 1879, Issue 5, September 2024]Alberto Cascón, Mercedes Robledo
Medicina Clinica|March 7, 2013
[Hereditary pheochromocytoma and paraganglioma: the disease with ten faces]Alberto Cascón, Mercedes Robledo
Cancer Research|June 19, 2012
MAX and MYC: a heritable breakupAlberto Cascón, Mercedes Robledo
Endocrine Pathology|February 11, 2012
From transcriptional profiling to tumor biology in pheochromocytoma and paragangliomaAlberto Cascón, Daniel A Tennant
Pediatric Blood & Cancer|November 24, 2005
Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutationsJaume Mora, Alberto Cascón, Mercedes Robledo, et al.
Cancers|May 19, 2019
Pheochromocytomas and Paragangliomas: Bypassing Cellular RespirationAlberto Cascón, Laura Remacha, Bruna Calsina, et al.
Genes, Chromosomes & Cancer|April 16, 2003
G12S and H50R variations are polymorphisms in the SDHD geneAlberto Cascón, Sergio Ruiz-Llorente, Arancha Cebrián, et al.
Endocrine Pathology|October 8, 2013
Usefulness of negative and weak-diffuse pattern of SDHB immunostaining in assessment of SDH mutations in paragangliomas and pheochromocytomasEsmeralda Castelblanco, Maria Santacana, Joan Valls, et al.
Journal of Human Genetics|August 9, 2002
A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresisCebrián Arancha, Sergio Ruíz-Llorente, Alberto Cascón, et al.
Pageof 8