Lista de obras -

A metastasis of an adenocarcinoma in a BRCA1 mutation carrier, a diagnostic problem not solved by morphology alone

artículo científico publicado en 2004

A mononucleotide repeat in PRRT2 is an important, frequent target of mismatch repair deficiency in cancer.

artículo científico publicado en 2016

A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory

artículo científico publicado en 2009

A subset of head and neck squamous cell carcinomas exhibits integration of HPV 16/18 DNA and overexpression of p16INK4A and p53 in the absence of mutations in p53 exons 5–8 ⬇️

artículo científico publicado el 10 de noviembre de 2003

Adjuvant procarbazine, lomustine, and vincristine chemotherapy in newly diagnosed anaplastic oligodendroglioma: long-term follow-up of EORTC brain tumor group study 26951.

artículo científico publicado en 2012

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

Anisometric Cell and Dysplastic Lipomas in a Retinoblastoma Patient

scientific article published on 04 May 2020

Array-comparative genomic hybridization in sporadic benign pheochromocytomas

scientific article published on 19 January 2009

Barrett's oesophageal adenocarcinoma encompasses tumour-initiating cells that do not express common cancer stem cell markers

artículo científico publicado en 2010

Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma

artículo científico publicado en 2007

Chemotherapy followed by surgery versus surgery alone in patients with resectable oesophageal squamous cell carcinoma: Long-term results of a randomized controlled trial ⬇️

artículo científico publicado el 19 de mayo de 2011

Chromosomal anomalies in oligodendroglial tumors are correlated with clinical features.

artículo científico publicado en 2003

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

artículo científico publicado en 2017

Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.

artículo científico publicado en 2005

Clinical importance of molecular determinations in gynecologic patients with multiple tumors

scientific article published on 01 April 2003

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

artículo científico publicado en 2015

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

artículo científico publicado en 2009

Construction and application of a full-coverage, high-resolution, human chromosome 8q genomic microarray for comparative genomic hybridization

artículo científico

Correction: Functional Ex Vivo Assay Reveals Homologous Recombination Deficiency in Breast Cancer Beyond BRCA Gene Defects

scientific article published on 01 May 2019

Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations

artículo científico publicado en 2010

Detection of spontaneous tumorigenic transformation during culture expansion of human mesenchymal stromal cells.

artículo científico publicado en 2013

Determination of the molecular relationship between multiple tumors within one patient is of clinical importance

artículo científico publicado en 2002

Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment

artículo científico publicado en 2016

EGFR and KRAS quality assurance schemes in pathology: generating normative data for molecular predictive marker analysis in targeted therapy.

artículo científico publicado en 2011

Early onset esophageal adenocarcinoma: a distinct molecular entity?

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Expression of the bile acid receptor FXR in Barrett's esophagus and enhancement of apoptosis by guggulsterone in vitro.

artículo científico publicado en 2006

First-line temozolomide chemotherapy in progressive low-grade astrocytomas after radiotherapy: molecular characteristics in relation to response

artículo científico publicado en 2010

Frequent genetic changes in childhood pheochromocytomas

artículo científico publicado en 2006

Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.

artículo científico publicado en 2002

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

artículo científico publicado en 2008

Functional Assay Reveals Homologous Recombination Deficiency in Breast Cancer Beyond BRCA Gene Defects

article

Functional Polymorphisms Associated with Disease-Free Survival in Resected Carcinoma of the Esophagus ⬇️

artículo científico publicado el 5 de octubre de 2010

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

Hereditary Factors in Esophageal Adenocarcinoma

artículo científico

IDH1 and IDH2 mutations are prognostic but not predictive for outcome in anaplastic oligodendroglial tumors: a report of the European Organization for Research and Treatment of Cancer Brain Tumor Group

artículo científico publicado en 2010

IL-7 Receptor Mutations and Steroid Resistance in Pediatric T cell Acute Lymphoblastic Leukemia: A Genome Sequencing Study

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Identification of a 7.1-mega base pairs minimal deletion at 14q31.1-32.11 in adenocarcinomas of the gastroesophageal junction

artículo científico publicado en 2006

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 Y-Chromosome during Male Breast Carcinogenesis

artículo científico publicado en 2020

MGMT promoter hypermethylation is a frequent, early, and consistent event in astrocytoma progression, and not correlated with TP53 mutation.

artículo científico publicado en 2010

MGMT promoter methylation is prognostic but not predictive for outcome to adjuvant PCV chemotherapy in anaplastic oligodendroglial tumors: a report from EORTC Brain Tumor Group Study 26951.

artículo científico publicado en 2009

Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts

artículo científico publicado en 2011

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p

artículo científico publicado en 2006

Microsatellite instability of germ cell tumors is associated with resistance to systemic treatment.

artículo científico publicado en 2002

Mismatch repair and treatment resistance in ovarian cancer

artículo científico publicado en 2006

Mistaken identity of widely used esophageal adenocarcinoma cell line TE-7.

artículo científico publicado en 2007

Molecular biological challenges in he treatment of esophageal adenocarcinoma

artículo científico publicado en 2007

Molecular classification of anaplastic oligodendroglioma using next-generation sequencing: a report of the prospective randomized EORTC Brain Tumor Group 26951 phase III trial.

artículo científico publicado en 2015

Molecular clonality analysis of esophageal adenocarcinoma by multiregion sequencing of tumor samples

artículo científico publicado en 2017

Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas

artículo científico publicado en 2003

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

Next generation diagnostic molecular pathology: critical appraisal of quality assurance in Europe.

artículo científico

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

PIK3CA mutations in ductal carcinoma in situ and adjacent invasive breast cancer

artículo científico publicado en 2019

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

Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas

artículo científico publicado en 2012

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/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

Sarcoma classification by DNA methylation profiling

artículo científico publicado en 2021

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

artículo científico publicado en 2016

Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma

artículo científico publicado en 2015

Single-agent bevacizumab or lomustine versus a combination of bevacizumab plus lomustine in patients with recurrent glioblastoma (BELOB trial): a randomised controlled phase 2 trial.

artículo científico publicado en 2014

Somatic SDHB mutation in an extraadrenal pheochromocytoma

artículo científico publicado en 2007

Somatic aberrations of mismatch repair genes as a cause of microsatellite-unstable cancers

artículo científico publicado en 2014

Somatic mutations and copy number variations in breast cancers with heterogeneous HER2 amplification

scientific article published on 14 February 2020

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 Pathogenesis of Barrett’s Metaplasia and the Progression to Esophageal Adenocarcinoma ⬇️

artículo científico publicado el 1 de enero de 2010

The clonal relation of primary upper urinary tract urothelial carcinoma and paired urothelial carcinoma of the bladder

scientific article published on 02 October 2020

The molecular biology of esophageal adenocarcinoma.

artículo científico publicado en 2005

The occurrence of SDHB gene mutations in pheochromocytoma

artículo científico publicado en 2006

Three-Gene Immunohistochemical Panel Adds to Clinical Staging Algorithms to Predict Prognosis for Patients With Esophageal Adenocarcinoma ⬇️

artículo científico publicado el 18 de marzo de 2013

Tissue inhibitor of metalloproteinase-3 (TIMP3) expression decreases during melanoma progression and inhibits melanoma cell migration

artículo científico

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

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

artículo científico publicado en 2015

Verification and unmasking of widely used human esophageal adenocarcinoma cell lines.

artículo científico publicado en 2010

Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas

artículo científico publicado en 2003

p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas

artículo científico publicado en 2003

Lista de obras de

A metastasis of an adenocarcinoma in a BRCA1 mutation carrier, a diagnostic problem not solved by morphology alone

A mononucleotide repeat in PRRT2 is an important, frequent target of mismatch repair deficiency in cancer.

A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory

A subset of head and neck squamous cell carcinomas exhibits integration of HPV 16/18 DNA and overexpression of p16INK4A and p53 in the absence of mutations in p53 exons 5–8 ⬇️

Adjuvant procarbazine, lomustine, and vincristine chemotherapy in newly diagnosed anaplastic oligodendroglioma: long-term follow-up of EORTC brain tumor group study 26951.

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

Anisometric Cell and Dysplastic Lipomas in a Retinoblastoma Patient

Array-comparative genomic hybridization in sporadic benign pheochromocytomas

Barrett's oesophageal adenocarcinoma encompasses tumour-initiating cells that do not express common cancer stem cell markers

Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma

Chemotherapy followed by surgery versus surgery alone in patients with resectable oesophageal squamous cell carcinoma: Long-term results of a randomized controlled trial ⬇️

Chromosomal anomalies in oligodendroglial tumors are correlated with clinical features.

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.

Clinical importance of molecular determinations in gynecologic patients with multiple tumors

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

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

Construction and application of a full-coverage, high-resolution, human chromosome 8q genomic microarray for comparative genomic hybridization

Correction: Functional Ex Vivo Assay Reveals Homologous Recombination Deficiency in Breast Cancer Beyond BRCA Gene Defects

Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations

Detection of spontaneous tumorigenic transformation during culture expansion of human mesenchymal stromal cells.

Determination of the molecular relationship between multiple tumors within one patient is of clinical importance

Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment

EGFR and KRAS quality assurance schemes in pathology: generating normative data for molecular predictive marker analysis in targeted therapy.

Early onset esophageal adenocarcinoma: a distinct molecular entity?

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

Expression of the bile acid receptor FXR in Barrett's esophagus and enhancement of apoptosis by guggulsterone in vitro.

First-line temozolomide chemotherapy in progressive low-grade astrocytomas after radiotherapy: molecular characteristics in relation to response

Frequent genetic changes in childhood pheochromocytomas

Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.

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

Functional Assay Reveals Homologous Recombination Deficiency in Breast Cancer Beyond BRCA Gene Defects

Functional Polymorphisms Associated with Disease-Free Survival in Resected Carcinoma of the Esophagus ⬇️

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

Hereditary Factors in Esophageal Adenocarcinoma

IDH1 and IDH2 mutations are prognostic but not predictive for outcome in anaplastic oligodendroglial tumors: a report of the European Organization for Research and Treatment of Cancer Brain Tumor Group

IL-7 Receptor Mutations and Steroid Resistance in Pediatric T cell Acute Lymphoblastic Leukemia: A Genome Sequencing Study

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

Identification of a 7.1-mega base pairs minimal deletion at 14q31.1-32.11 in adenocarcinomas of the gastroesophageal junction

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 Y-Chromosome during Male Breast Carcinogenesis

MGMT promoter hypermethylation is a frequent, early, and consistent event in astrocytoma progression, and not correlated with TP53 mutation.

MGMT promoter methylation is prognostic but not predictive for outcome to adjuvant PCV chemotherapy in anaplastic oligodendroglial tumors: a report from EORTC Brain Tumor Group Study 26951.

Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p

Microsatellite instability of germ cell tumors is associated with resistance to systemic treatment.

Mismatch repair and treatment resistance in ovarian cancer

Mistaken identity of widely used esophageal adenocarcinoma cell line TE-7.

Molecular biological challenges in he treatment of esophageal adenocarcinoma

Molecular classification of anaplastic oligodendroglioma using next-generation sequencing: a report of the prospective randomized EORTC Brain Tumor Group 26951 phase III trial.

Molecular clonality analysis of esophageal adenocarcinoma by multiregion sequencing of tumor samples

Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas

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

Next generation diagnostic molecular pathology: critical appraisal of quality assurance in Europe.

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

PIK3CA mutations in ductal carcinoma in situ and adjacent invasive breast cancer

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations

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

Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas

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/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).

Sarcoma classification by DNA methylation profiling

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

Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma

Single-agent bevacizumab or lomustine versus a combination of bevacizumab plus lomustine in patients with recurrent glioblastoma (BELOB trial): a randomised controlled phase 2 trial.

Somatic SDHB mutation in an extraadrenal pheochromocytoma

Somatic aberrations of mismatch repair genes as a cause of microsatellite-unstable cancers

Somatic mutations and copy number variations in breast cancers with heterogeneous HER2 amplification

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 Pathogenesis of Barrett’s Metaplasia and the Progression to Esophageal Adenocarcinoma ⬇️

The clonal relation of primary upper urinary tract urothelial carcinoma and paired urothelial carcinoma of the bladder