María Teresa Vargas de los Monteros

Tipo Año Título Fuente
Artículo2020 ASXL1 mutation as a surrogate marker in acute myeloid leukemia with myelodysplasia-related changes and normal karyotype CANCER MEDICINE
Artículo2020 Eosinophils engulfing platelets and with ring-shaped nuclei in nivolumab-associated eosinophilia BRITISH JOURNAL OF HAEMATOLOGY
Editorial2018 Bone marrow erythrocyte and neutrophil phagocytosis and cannibalism by neuroendocrine carcinoma BRITISH JOURNAL OF HAEMATOLOGY
Artículo2018 Characterizing patients with multiple chromosomal aberrations detected by FISH in chronic lymphocytic leukemia LEUKEMIA & LYMPHOMA
Editorial2018 Eosinophil phagocytosis in advanced systemic mastocytosis with eosinophilia BRITISH JOURNAL OF HAEMATOLOGY
Letter2018 KIT D816V-chronic myelomonocytic leukemia progressing to KIT D816V+associated to mast cell leukemia responding to allogeneic hematopoietic cell transplantation ANNALS OF HEMATOLOGY
Artículo2018 MLL-rearranged acute myeloid leukemia: Influence of the genetic partner in allo-HSCT response and prognostic factor of MLL 3 ' region mRNA expression EUROPEAN JOURNAL OF HAEMATOLOGY
Editorial2018 Severe granulocytic dysplasia with vacuolar rosettes in a myelodysplastic syndrome with low-copy KMT2A gain BRITISH JOURNAL OF HAEMATOLOGY
Letter2017 Intravascular lymphoma: look through the small vessels ANNALS OF HEMATOLOGY
Nota2017 Platelet phagocytosis by granulopoietic precursors in a myelodysplastic syndrome overexpressing the P-selectin gene BRITISH JOURNAL OF HAEMATOLOGY
Artículo2017 RUNX1 amplification in AML with myelodysplasia-related changes and ring 21 chromosomes HEMATOLOGICAL ONCOLOGY
Letter2016 Erythrophagocytosis by peripheral monocytes and histiocytes in diffuse large B cell lymphoma ANNALS OF HEMATOLOGY
Editorial2016 Haemophagocytosis by neoplastic cells in aleukaemic variant of mast cell leukaemia BRITISH JOURNAL OF HAEMATOLOGY
Artículo2016 Karyotypic complexity rather than chromosome 8 abnormalities aggravates the outcome of chronic lymphocytic leukemia patients with TP53 aberrations ONCOTARGET
Artículo2016 Methionine synthase reductase deficiency (CblE): A report of two patients and a novel mutation Hematology
Artículo2016 MicroRNA deregulation in triple negative breast cancer reveals a role of miR-498 in regulating BRCA1 expression ONCOTARGET
Artículo2016 NUP98-HOXA9 bearing therapy-related myeloid neoplasm involves myeloid-committed cell and induces HOXA5, EVI1, FLT3, and MEIS1 expression INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
Letter2016 Unusual co-occurrence of Hodgkin lymphoma and hemophagocytic lymphohistiocytosis in a bone marrow aspirate ANNALS OF HEMATOLOGY
Letter2015 A new rearrangement giving rise to a very rare MLL-MLLT10 fusion mRNA in an infant acute myeloid leukemia CANCER GENETICS
Editorial2015 Bone marrow cellular cannibalism by medulloblastoma AMERICAN JOURNAL OF HEMATOLOGY
Artículo2015 Fluorescence in situ hybridization of TP53 for the detection of chromosome 17 abnormalities in myelodysplastic syndromes LEUKEMIA & LYMPHOMA
Artículo2015 Multiple Pseudo-Chediak-Higashi Inclusions Associated with MYC Deletion in a Patient with Acute Myeloid Leukemia ACTA HAEMATOLOGICA
Artículo2015 Tumor MicroRNA expression profiling identifies circulating MicroRNAs for early breast cancer detection CLINICAL CHEMISTRY
Artículo2014 Aportaciones de los estudios moleculares en el manejo de las neoplasias endocrinas múltiples en el niño Revista Española de Endocrinologia Pediátrica
Artículo2013 Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: Does-7/7q-detection by FISH have prognostic value? LEUKEMIA RESEARCH
Artículo2012 Application of fluorescence in situ hybridization as a diagnostic tool in melanocytic lesions, using paraffin wax-embedded tissues and imprint-cytology specimens CLINICAL AND EXPERIMENTAL DERMATOLOGY
Artículo2011 Molecular findings of nasopharyngeal carcinoma in a European population ANALYTICAL AND QUANTITATIVE CYTOLOGY AND HISTOLOGY
Artículo2010 Hypertensive urgency and stunding. What is the diagnosis? NEFROLOGIA
Artículo2009 Cytogenetic study of a pulmonary sclerosing hemangioma CANCER GENETICS AND CYTOGENETICS
Artículo2009 Cytogenetic, fluorescence in situ hybridization, and immunohistochemistry studies in a malignant pleural solitary fibrous tumor CANCER GENETICS AND CYTOGENETICS
Artículo2009 Cytogenetic, fluorescence in situ hybridization, and molecular characterization of chronic myeloid leukemia in chronic phase with four BCR/ABL1 fusion signals: a case report CANCER GENETICS AND CYTOGENETICS
Letter2006 Extra BCR/ABL fusion mosaicism in 18p in a CML Ph-positive patient with erythroblastic transformation CANCER GENETICS AND CYTOGENETICS
Artículo2006 Liposarcomas. Aspectos clínico-patológicos y moleculares Patología
Letter2006 Partial tetrasomy chromosome 14. A new prenatal diagnosis case Prenatal Diagnosis                          
Letter2002 Chronic myeloid leukemia with chromosome 8 trisomy and negative ABL/BCR translocation Revista Médica de Chile
Artículo2001 Balanced reciprocal translocation mosaicism: clinical implications. Two new cases Genetic Counseling
Artículo2001 Dos hermanos con síndrome de Prader-Willy por deleción clásica. ¿Es la excepción que confirma la regla? REVISTA DE NEUROLOGIA
Artículo2000 A genetic study of 64 patients clinically suspected of having Angelman's syndrome REVISTA DE NEUROLOGIA
Artículo2000 Neonatal hypotonia in the Prader-Willi syndrome due to t(15;16) REVISTA DE NEUROLOGIA
Letter1999 Chronic myeloid leukemia in chronic phase with a partial trisomy 9 mosaicism [2] HAEMATOLOGICA
Artículo1999 Consejo genético. Diagnóstico de las enfermedades monogénicas y cromosómicas Vox Paediatrica
Artículo1999 Prevención y diagnóstico prenatal de las enfermedades genéticas Vox Paediatrica
Letter1999 Síndrome mielodisplásico ABL / BCR+. A propósito de una nueva observación SANGRE
Letter1996 Detección de la traslocación Mbcr/abl por FISH en muestras de medula ósea de pacientes diagnosticados de LMC y LLA SANGRE
Artículo1991 Pericentric inversion of chromosome 13: familial study and review of the literature Genetic Counseling
Artículo1991 Trisomía parcial del cromosoma 9. Aportación de un nuevo caso Revista Española de Pediatría Clínica e Investigación
Artículo1990 Inversión pericéntrica del cromosoma 9. Resumen de nuestros resultados ANALES DE PEDIATRIA
Artículo1990 Trisomía 9 completa con inversión pericéntrica del cromosoma 9 Revista Española de Pediatría Clínica e Investigación
Artículo1989 Traslocacion 8:11. Estudio familiar ANALES DE PEDIATRIA

Proyectos de Investigación

Fecha de inicio Fecha de fin Rol Denominación Agencia financiadora
13/01/2009 13/01/2012 Investigador/a Estudio del Papel Regulador de los Péptidos Orexigénicos y Anorexigénicos Producidos por las Células C a Nivel del Tiroides sobre la Síntesis de Hormonas Tiroideas (P08-CVI-03598) Junta de Andalucía - Consejería de Innovación, Ciencia y Empresas (Autonómico)
01/01/2011 31/12/2013 Investigador/a Terapias dirigidas para el tratamiento del cáncer de tiroides mediante nanopartículas (PI-0280-2010) Consejería de Salud y Bienestar Social (Fundación Progreso y Salud) (Autonómico)