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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 10, 2004
Multifocal intrafollicular granulosa cell tumor of the ovary associated with an unusual germline p53 mutation
Francisco F Nogales, Maria L Musto, Ana I Sáez, et al.
Leukemia Research
|
April 19, 2003
Coincidental LOH regions in mouse and humans: evidence for novel tumor suppressor loci at 9q22-q34 in non-Hodgkin's lymphomas
Bárbara Meléndez, Marta Cuadros, Mercedes Robledo, et al.
Journal of Molecular Endocrinology
|
December 15, 2022
Genetic bases of pheochromocytoma and paraganglioma
Alberto Cascón, Bruna Calsina, María Monteagudo, et al.
European Journal of Endocrinology
|
December 2, 2011
Functional characterization of a rare germline mutation in the gene encoding the cyclin-dependent kinase inhibitor p27Kip1 (CDKN1B) in a Spanish patient with multiple endocrine neoplasia-like phenotype
Donatella Malanga, Silvia De Gisi, Miriam Riccardi, et al.
European Urology
|
May 13, 2026
Expanding Bevacizumab-Erlotinib Therapy Through Fumarate Hydratase Deficiency Screening and Drug Target Pathway Analysis in Papillary Morphology Metastatic Renal Cell Carcinoma
Javier de Nicolás-Hernández, Carlos Valdivia, Alicia Arenas, 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 pheochromocytomas
Esmeralda Castelblanco, Maria Santacana, Joan Valls, et al.
Endocrine Reviews
|
February 20, 2024
The Immune Landscape of Pheochromocytoma and Paraganglioma: Current Advances and Perspectives
Ondrej Uher, Katerina Hadrava Vanova, David Taïeb, et al.
Histopathology
|
August 19, 2014
Simultaneous KIT mutation and succinate dehydrogenase (SDH) deficiency in a patient with a gastrointestinal stromal tumour and Carney-Stratakis syndrome: a case report
Maria Jové, Jaume Mora, Xavier Sanjuan, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 15, 2004
The RET IVS1-126G>T variant is strongly associated with the development of sporadic medullary thyroid cancer
R M Fernandez, Mercedes Robledo, Guillermo Antinolo, 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 electrophoresis
Cebrián Arancha, Sergio Ruíz-Llorente, Alberto Cascón, et al.
Page
of 22
Search research articles
Search
Showing results (21-30 of 215) with videos related to
Sort By:
Page
of 22
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 10, 2004
Multifocal intrafollicular granulosa cell tumor of the ovary associated with an unusual germline p53 mutation
Francisco F Nogales, Maria L Musto, Ana I Sáez, et al.
Leukemia Research
|
April 19, 2003
Coincidental LOH regions in mouse and humans: evidence for novel tumor suppressor loci at 9q22-q34 in non-Hodgkin's lymphomas
Bárbara Meléndez, Marta Cuadros, Mercedes Robledo, et al.
Journal of Molecular Endocrinology
|
December 15, 2022
Genetic bases of pheochromocytoma and paraganglioma
Alberto Cascón, Bruna Calsina, María Monteagudo, et al.
European Journal of Endocrinology
|
December 2, 2011
Functional characterization of a rare germline mutation in the gene encoding the cyclin-dependent kinase inhibitor p27Kip1 (CDKN1B) in a Spanish patient with multiple endocrine neoplasia-like phenotype
Donatella Malanga, Silvia De Gisi, Miriam Riccardi, et al.
European Urology
|
May 13, 2026
Expanding Bevacizumab-Erlotinib Therapy Through Fumarate Hydratase Deficiency Screening and Drug Target Pathway Analysis in Papillary Morphology Metastatic Renal Cell Carcinoma
Javier de Nicolás-Hernández, Carlos Valdivia, Alicia Arenas, 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 pheochromocytomas
Esmeralda Castelblanco, Maria Santacana, Joan Valls, et al.
Endocrine Reviews
|
February 20, 2024
The Immune Landscape of Pheochromocytoma and Paraganglioma: Current Advances and Perspectives
Ondrej Uher, Katerina Hadrava Vanova, David Taïeb, et al.
Histopathology
|
August 19, 2014
Simultaneous KIT mutation and succinate dehydrogenase (SDH) deficiency in a patient with a gastrointestinal stromal tumour and Carney-Stratakis syndrome: a case report
Maria Jové, Jaume Mora, Xavier Sanjuan, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 15, 2004
The RET IVS1-126G>T variant is strongly associated with the development of sporadic medullary thyroid cancer
R M Fernandez, Mercedes Robledo, Guillermo Antinolo, 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 electrophoresis
Cebrián Arancha, Sergio Ruíz-Llorente, Alberto Cascón, et al.
Page
of 22