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Psychiatric symptoms in a Spanish sample with hereditary cancer risk

Journal of community genetics, 2022-06, Vol.13 (3), p.339-346

2022

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MicroRNA signatures in hereditary breast cancer

Breast cancer research and treatment, 2013-11, Vol.142 (1), p.19-30

2013

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Cancer worry at higher-risk sample of hereditary cancer in Spain

European journal of cancer prevention, 2024-07, Vol.33 (4), p.293-298

2024

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Comparison of psychological distress for breast, ovarian and colorectal cancer predisposition in a Spanish sample at high risk of hereditary cancer

European journal of cancer prevention, 2022-09, Vol.31 (5), p.482-486

2022

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CXCR4: From Signaling to Clinical Applications in Neuroendocrine Neoplasms

Cancers, 2024-05, Vol.16 (10), p.1799

2024

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Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence

Familial cancer, 2010-09, Vol.9 (3), p.291-295

2010

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CASP8 D302H polymorphism delays the age of onset of breast cancer in BRCA1 and BRCA2 carriers

Breast cancer research and treatment, 2010, Vol.119 (1), p.87-93

2010

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Broad BRCA1 and BRCA2 mutational spectrum and high incidence of recurrent and novel mutations in the eastern Spain population

Breast cancer research and treatment, 2010-05, Vol.121 (1), p.257-260

2010

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Mutaciones de BRCA1 y BRCA2 en familias estudiadas en el Programa de Consejo Genético en el Cáncer de la Comunidad Valenciana

Medicina clínica, 2008-02, Vol.130 (4), p.121-126

2008

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Pleuropulmonary and Lymph Node Progression after Docetaxel - Benefits from Treatment with Cabazitaxel in Metastatic Prostate Cancer

Case reports in oncology, 2013-07, Vol.6 (2), p.391-396

2013

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Impact of Event Scale (IES): Psychometric properties in a Spanish sample with hereditary cancer risk

Revista de psicopatología y psicología clínica, 2022-04, Vol.27 (1), p.25-34

2022

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Problemática asistencial del tratamiento combinado en los pacientes con tumores de cabeza y cuello localmente avanzados (réplica)

Clinical & translational oncology, 2005-09, Vol.7 (8), p.370-371

2005

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Safety and efficacy of sorafenib in the treatment of advanced hepatocellular carcinoma: a single center experience

Medical oncology (Northwood, London, England), 2014-05, Vol.31 (5), p.948-948, Article 948

2014

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Manejo farmacológico del dolor crónico oncológico. Una aproximación actual

Clinical & translational oncology, 2004-06, Vol.6 (5), p.272-282

2004

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Low penetrance alleles as risk modifiers in familial and sporadic breast cancer

Familial cancer, 2012-12, Vol.11 (4), p.629-636

2012

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Identification of a novel BRCA1 large genomic rearrangement in a Spanish breast/ovarian cancer family

Breast cancer research and treatment, 2008-11, Vol.112 (1), p.63-67

2008

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High risk Ewing's sarcomas. Effectiveness and toxicity of a regimen designed for children and used in adults

Clinical & translational oncology, 2004-04, Vol.6 (3), p.165-169

2004

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Toxic epidermal necrolysis associated with interleukin-2

The Annals of pharmacotherapy, 2002-07, Vol.36 (7-8), p.1171-1174

2002

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Pseudomixoma peritoneal tipo adenomucinosis peritoneal diseminada con imágenes radiológicas atípicas

Clinical & translational oncology, 2004-04, Vol.6 (3), p.173-175

2004

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Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families of Eastern Spain

Breast cancer research and treatment, 2008-11, Vol.112 (1), p.69-73

2008

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Hipereosinofilia mantenida que precede al diagnóstico de una leucemia linfoblástica aguda

Medicina clínica, 2001, Vol.116 (1), p.38-39

2001

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

Journal of medical genetics, 2015-10, Vol.52 (10), p.647-656

2015

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Actualidad de los cuidados paliativos: revisión de una situación poco estandarizada

Pediatría Atención Primaria, 2015-09, Vol.17 (67), p.e215-e222

2015

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Psychiatric symptoms in a Spanish sample with hereditary cancer risk

MicroRNA signatures in hereditary breast cancer

Cancer worry at higher-risk sample of hereditary cancer in Spain

Comparison of psychological distress for breast, ovarian and colorectal cancer predisposition in a Spanish sample at high risk of hereditary cancer

CXCR4: From Signaling to Clinical Applications in Neuroendocrine Neoplasms

Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence

Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer

Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence

CASP8 D302H polymorphism delays the age of onset of breast cancer in BRCA1 and BRCA2 carriers

Broad BRCA1 and BRCA2 mutational spectrum and high incidence of recurrent and novel mutations in the eastern Spain population

Mutaciones de BRCA1 y BRCA2 en familias estudiadas en el Programa de Consejo Genético en el Cáncer de la Comunidad Valenciana

Pleuropulmonary and Lymph Node Progression after Docetaxel - Benefits from Treatment with Cabazitaxel in Metastatic Prostate Cancer

Impact of Event Scale (IES): Psychometric properties in a Spanish sample with hereditary cancer risk

Problemática asistencial del tratamiento combinado en los pacientes con tumores de cabeza y cuello localmente avanzados (réplica)

Safety and efficacy of sorafenib in the treatment of advanced hepatocellular carcinoma: a single center experience

Manejo farmacológico del dolor crónico oncológico. Una aproximación actual

Low penetrance alleles as risk modifiers in familial and sporadic breast cancer

Identification of a novel BRCA1 large genomic rearrangement in a Spanish breast/ovarian cancer family

High risk Ewing's sarcomas. Effectiveness and toxicity of a regimen designed for children and used in adults

Toxic epidermal necrolysis associated with interleukin-2

Pseudomixoma peritoneal tipo adenomucinosis peritoneal diseminada con imágenes radiológicas atípicas

Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families of Eastern Spain

Hipereosinofilia mantenida que precede al diagnóstico de una leucemia linfoblástica aguda

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

Actualidad de los cuidados paliativos: revisión de una situación poco estandarizada

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