Lista de obras -

Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome

artículo científico publicado en 2014

An International Ki67 Reproducibility Study in Adrenal Cortical Carcinoma.

artículo científico publicado en 2015

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

artículo científico publicado en 2009

Array-comparative genomic hybridization in sporadic benign pheochromocytomas

scientific article published on 19 January 2009

Assessment of VAV2 Expression Refines Prognostic Prediction in Adrenocortical Carcinoma.

artículo científico publicado en 2017

Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma

artículo científico publicado en 2007

Catecholamine-Synthesizing Enzymes Are Expressed in Parasympathetic Head and Neck Paraganglioma Tissue.

artículo científico publicado en 2015

Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis

artículo científico publicado en 2015

Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

artículo científico

Comprehensive Characterization of Cancer Driver Genes and Mutations

article

Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

artículo científico publicado en 2017

Conditional Pten knock-out mice: a model for metastatic phaeochromocytoma

artículo científico publicado en 2009

Cytogenetic and p53 profiles in congenital cystic adenomatoid malformation: insights into its relationship with pleuropulmonary blastoma

artículo científico publicado en 2006

DNA Methylation Is an Independent Prognostic Marker of Survival in Adrenocortical Cancer.

artículo científico publicado en 2016

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

artículo científico publicado en 2015

Expression of Contactin 4 Is Associated With Malignant Behavior in Pheochromocytomas and Paragangliomas

artículo científico publicado en 2017

Expression of GAD67 and novel GAD67 splice variants during human fetal pancreas development: GAD67 expression in the fetal pancreas

artículo científico publicado en 2007

Frequent genetic changes in childhood pheochromocytomas

artículo científico publicado en 2006

Frequent loss of 17p, but no p53 mutations or protein overexpression in benign and malignant pheochromocytomas.

artículo científico publicado en 2008

Gain-of-function mutations in DNMT3A in patients with paraganglioma

artículo científico publicado en 2018

H-RAS mutations are restricted to sporadic pheochromocytomas lacking specific clinical or pathological features: data from a multi-institutional series.

artículo científico publicado en 2014

Identification of Mutations in Cell-Free Circulating Tumor DNA in Adrenocortical Carcinoma: A Case Series

artículo científico publicado en 2017

Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors.

artículo científico

Intra-tumoral molecular heterogeneity in benign and malignant pheochromocytomas and extra-adrenal sympathetic paragangliomas

artículo científico publicado en 2010

Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas.

artículo científico publicado en 2009

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas

artículo científico publicado en 2017

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

scientific article published on 27 March 2012

Murine models and cell lines for the investigation of pheochromocytoma: applications for future therapies?

artículo científico publicado en 2012

Mutation of SDHB is a cause of hypoxia-related high-altitude paraganglioma

artículo científico publicado en 2010

New developments in the detection of the clinical behavior of pheochromocytomas and paragangliomas

artículo científico publicado en 2006

Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC-PGL syndromes: a clinicopathological and molecular analysis.

artículo científico publicado en 2013

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations

artículo científico publicado en 2014

Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.

artículo científico publicado en 2009

PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics

artículo científico publicado en 2017

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

artículo científico publicado en 2015

SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

artículo científico publicado en 2011

SDHA mutations in adult and pediatric wild-type gastrointestinal stromal tumors ⬇️

artículo científico publicado el 23 de noviembre de 2012

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

artículo científico publicado en 2010

SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors

artículo científico publicado en 2010

SDHB loss predicts malignancy in pheochromocytomas/sympathethic paragangliomas, but not through hypoxia signalling

artículo científico publicado en 2010

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T).

artículo científico publicado en 2015

Sarcomatoid adrenocortical carcinoma: a comprehensive pathological, immunohistochemical, and targeted next-generation sequencing analysis.

artículo científico publicado en 2016

Somatic RET mutation in a patient with pigmented adrenal pheochromocytoma

artículo científico publicado en 2016

Somatic SDHB mutation in an extraadrenal pheochromocytoma

artículo científico publicado en 2007

Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.

artículo científico publicado en 2015

Telomerase reverse transcriptase promoter mutations in tumors originating from the adrenal gland and extra-adrenal paraganglia

artículo científico publicado en 2014

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

article

The mTORC1 Complex Is Significantly Overactivated in SDHX-Mutated Paragangliomas

artículo científico publicado en 2017

The occurrence of SDHB gene mutations in pheochromocytoma

artículo científico publicado en 2006

Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations.

artículo científico publicado en 2014

Trp53 inactivation leads to earlier phaeochromocytoma formation in pten knockout mice

artículo científico publicado en 2012

Value of Molecular Classification for Prognostic Assessment of Adrenocortical Carcinoma

scientific article published on 11 July 2019

Vascular pattern analysis for the prediction of clinical behaviour in pheochromocytomas and paragangliomas

artículo científico publicado en 2015

Lista de obras de

Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome

An International Ki67 Reproducibility Study in Adrenal Cortical Carcinoma.

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

Array-comparative genomic hybridization in sporadic benign pheochromocytomas

Assessment of VAV2 Expression Refines Prognostic Prediction in Adrenocortical Carcinoma.

Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma

Catecholamine-Synthesizing Enzymes Are Expressed in Parasympathetic Head and Neck Paraganglioma Tissue.

Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis

Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

Comprehensive Characterization of Cancer Driver Genes and Mutations

Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

Conditional Pten knock-out mice: a model for metastatic phaeochromocytoma

Cytogenetic and p53 profiles in congenital cystic adenomatoid malformation: insights into its relationship with pleuropulmonary blastoma

DNA Methylation Is an Independent Prognostic Marker of Survival in Adrenocortical Cancer.

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

Expression of Contactin 4 Is Associated With Malignant Behavior in Pheochromocytomas and Paragangliomas

Expression of GAD67 and novel GAD67 splice variants during human fetal pancreas development: GAD67 expression in the fetal pancreas

Frequent genetic changes in childhood pheochromocytomas

Frequent loss of 17p, but no p53 mutations or protein overexpression in benign and malignant pheochromocytomas.

Gain-of-function mutations in DNMT3A in patients with paraganglioma

H-RAS mutations are restricted to sporadic pheochromocytomas lacking specific clinical or pathological features: data from a multi-institutional series.

Identification of Mutations in Cell-Free Circulating Tumor DNA in Adrenocortical Carcinoma: A Case Series

Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors.

Intra-tumoral molecular heterogeneity in benign and malignant pheochromocytomas and extra-adrenal sympathetic paragangliomas

Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas.

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Murine models and cell lines for the investigation of pheochromocytoma: applications for future therapies?

Mutation of SDHB is a cause of hypoxia-related high-altitude paraganglioma

New developments in the detection of the clinical behavior of pheochromocytomas and paragangliomas

Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC-PGL syndromes: a clinicopathological and molecular analysis.

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations

Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.

PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

SDHA mutations in adult and pediatric wild-type gastrointestinal stromal tumors ⬇️

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors

SDHB loss predicts malignancy in pheochromocytomas/sympathethic paragangliomas, but not through hypoxia signalling

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T).

Sarcomatoid adrenocortical carcinoma: a comprehensive pathological, immunohistochemical, and targeted next-generation sequencing analysis.

Somatic RET mutation in a patient with pigmented adrenal pheochromocytoma

Somatic SDHB mutation in an extraadrenal pheochromocytoma

Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.

Telomerase reverse transcriptase promoter mutations in tumors originating from the adrenal gland and extra-adrenal paraganglia

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

The mTORC1 Complex Is Significantly Overactivated in SDHX-Mutated Paragangliomas

The occurrence of SDHB gene mutations in pheochromocytoma

Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations.

Trp53 inactivation leads to earlier phaeochromocytoma formation in pten knockout mice

Value of Molecular Classification for Prognostic Assessment of Adrenocortical Carcinoma

Vascular pattern analysis for the prediction of clinical behaviour in pheochromocytomas and paragangliomas