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Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer-Predisposing Mutations in Pheochromocytomas and Paragangliomas

Clinical cancer research, 2017-10, Vol.23 (20), p.6315-6324

2017

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The molecular pathology of hereditary breast cancer: genetic testing and therapeutic implications

Modern pathology, 2005-10, Vol.18 (10), p.1305-1320

2005

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The role of EZH2 in overall survival of colorectal cancer: a meta-analysis

Scientific reports, 2017-10, Vol.7 (1), p.13806-8, Article 13806

2017

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Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

Frontiers in endocrinology (Lausanne), 2023-01, Vol.13, p.1070074-1070074

2023

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Comprehensive characterization of the DNA amplification at 13q34 in human breast cancer reveals TFDP1 and CUL4A as likely candidate target genes

Breast cancer research : BCR, 2009-01, Vol.11 (6), p.R86-R86, Article R86

2009

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Relationship between Aldehyde Dehydrogenase, PD-L1 and Tumor-Infiltrating Lymphocytes with Pathologic Response and Survival in Breast Cancer

Cancers, 2022-09, Vol.14 (18), p.4418

2022

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A Predictor Based on the Somatic Genomic Changes of the BRCA1/BRCA2 Breast Cancer Tumors Identifies the Non-BRCA1/BRCA2 Tumors with BRCA1 Promoter Hypermethylation

Clinical cancer research, 2005-02, Vol.11 (3), p.1146-1153

2005

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Splenic Lesions and Other Findings in Kaposiform Lymphangiomatosis

The American journal of surgical pathology, 2023-05, Vol.47 (5), p.631-633

2023

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Peritoneal carcinomatosis from invasive lobular breast cancer in a 74 years old female patient 22 years after mastectomy

European journal of surgical oncology, 2024-02, Vol.50 (2), p.107869, Article 107869

2024

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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

American journal of human genetics, 2019-04, Vol.104 (4), p.651-664

2019

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Mesothelial hyperplasia: Presentation of a case of rectal adenocarcinoma with “diffuse peritoneal carcinomatosis”

European journal of surgical oncology, 2023-02, Vol.49 (2), p.e203-e204

2023

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Mesothelial hyperplasia: Presentation of a case of rectal adenocarcinoma with “diffuse peritoneal carcinomatosis”

European journal of surgical oncology, 2023-02, Vol.49 (2), p.e195-e195

2023

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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

American journal of human genetics, 2019-05, Vol.104 (5), p.1008-1010

2019

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Chronic lymphocytic leukemia and Richter transformation skin involvement recruited by herpesvirus infection

Journal of cutaneous pathology, 2021-05, Vol.48 (5), p.713-716

2021

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Perineurial cells in granular cell tumors and neoplasms with perineural invasion: an immunohistochemical study

The American journal of dermatopathology, 2012-12, Vol.34 (8), p.800-809

2012

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Metastatic clear cell renal cell carcinoma to the thyroid gland: A clinico-pathological and immunohistochemical study of 8 cases and review of the literature

Revista española de patología, 2019-04, Vol.52 (2), p.81-86

2019

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Intraneural hybrid granular cell tumor-perineurioma

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2013-07, Vol.121 (7), p.678-680

2013

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The pathology of hereditary breast cancer

Hereditary cancer in clinical practice, 2004-07, Vol.2 (3), p.131-138, Article 131

2004

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Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families

Modern pathology, 2007-12, Vol.20 (12), p.1298-1306

2007

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Carcinoma sarcomatoide en paciente diagnosticado de síndrome de Sjögren

Gastroenterología y hepatología, 2009-03, Vol.32 (3), p.150-154

2009

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Sarcomatoid carcinoma in a patient with Sjögren's syndrome

Gastroenterología y hepatología, 2009-03, Vol.32 (3), p.150-154

2009

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Re: Germline BRCA1 Mutations and a Basal Epithelial Phenotype in Breast Cancer

JNCI : Journal of the National Cancer Institute, 2004-05, Vol.96 (9), p.712-713

2004

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A novel candidate region linked to development of both pheochromocytoma and head/neck paraganglioma

Genes chromosomes & cancer, 2005-03, Vol.42 (3), p.260-268

2005

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Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer-Predisposing Mutations in Pheochromocytomas and Paragangliomas

The molecular pathology of hereditary breast cancer: genetic testing and therapeutic implications

The role of EZH2 in overall survival of colorectal cancer: a meta-analysis

Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

Comprehensive characterization of the DNA amplification at 13q34 in human breast cancer reveals TFDP1 and CUL4A as likely candidate target genes

Relationship between Aldehyde Dehydrogenase, PD-L1 and Tumor-Infiltrating Lymphocytes with Pathologic Response and Survival in Breast Cancer

A Predictor Based on the Somatic Genomic Changes of the BRCA1/BRCA2 Breast Cancer Tumors Identifies the Non-BRCA1/BRCA2 Tumors with BRCA1 Promoter Hypermethylation

Splenic Lesions and Other Findings in Kaposiform Lymphangiomatosis

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

Peritoneal carcinomatosis from invasive lobular breast cancer in a 74 years old female patient 22 years after mastectomy

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

Mesothelial hyperplasia: Presentation of a case of rectal adenocarcinoma with “diffuse peritoneal carcinomatosis”

Mesothelial hyperplasia: Presentation of a case of rectal adenocarcinoma with “diffuse peritoneal carcinomatosis”

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

Chronic lymphocytic leukemia and Richter transformation skin involvement recruited by herpesvirus infection

Perineurial cells in granular cell tumors and neoplasms with perineural invasion: an immunohistochemical study

Metastatic clear cell renal cell carcinoma to the thyroid gland: A clinico-pathological and immunohistochemical study of 8 cases and review of the literature

Intraneural hybrid granular cell tumor-perineurioma

DLST mutations in pheochromocytoma and paraganglioma cause proteome hyposuccinylation and metabolic remodeling

The pathology of hereditary breast cancer

Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families

Carcinoma sarcomatoide en paciente diagnosticado de síndrome de Sjögren

Sarcomatoid carcinoma in a patient with Sjögren's syndrome

Re: Germline BRCA1 Mutations and a Basal Epithelial Phenotype in Breast Cancer

A novel candidate region linked to development of both pheochromocytoma and head/neck paraganglioma

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