Lista de obras - Ana Carrió - Dominio Público Uruguay

12p13 rearrangements: 6 Mb deletion responsible for ID/MCA and reciprocal duplication without clinical responsibility

scientific article published on 09 April 2012

A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region.

artículo científico publicado en 2015

A new genetic abnormality leading to TP53 gene deletion in chronic lymphocytic leukaemia

article

Biallelic losses of 13q do not confer a poorer outcome in chronic lymphocytic leukaemia: analysis of 627 patients with isolated 13q deletion

article

Brachycephaly is ineffective for detection of Down syndrome in early midtrimester fetuses

scientific article published on 01 January 1997

CD49d (ITGA4) expression is a predictor of time to first treatment in patients with chronic lymphocytic leukaemia and mutatedIGHVstatus

artículo científico publicado en 2015

Chimeric BCR/ABL gene detected by fluorescence in situ hybridization in three new cases of Philadelphia chromosome-negative chronic myelocytic leukemia.

artículo científico publicado en 2003

Chorionic villus sampling by biopsy forceps. Results of 1580 procedures from a single centre

scientific article published on 01 June 1995

Chromosomal high-polysomies predict tumour progression in T1 transitional cell carcinoma of the bladder.

artículo científico publicado en 2004

Chronic lymphocytic leukaemia with 17p deletion: a retrospective analysis of prognostic factors and therapy results

artículo científico publicado en 2012

Chronic lymphocytic leukemia in the elderly: clinico-biological features, outcomes, and proposal of a prognostic model

artículo científico publicado en 2014

Clinical implications of ZAP-70 expressionin chronic lymphocytic leukemia

artículo científico publicado en 2006

Clonal evolution in chronic lymphocytic leukemia: analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance

artículo científico publicado en 2013

Comparative genomic hybridisation identifies two variants of smoldering multiple myeloma

artículo científico publicado en 2005

Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia.

artículo científico publicado en 2015

Different distribution of NOTCH1 mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations.

artículo científico publicado en 2012

Do we need to do fluorescence in situ hybridization analysis in myelodysplastic syndromes as often as we do?

article

Elastin mutation screening in a group of patients affected by vascular abnormalities

scientific article published on 01 November 2005

Fluorescence in situ hybridization analysis of matched primary tumour and lymph-node metastasis of D1 (pT2-3pN1M0) prostate cancer.

artículo científico publicado en 2004

Fluorescence in situ hybridization studies using BAC clones of the EVI1 locus in hematological malignancies with 3q rearrangements

artículo científico publicado en 2006

Gene expression profiling of acute myeloid leukemia with translocation t(8;16)(p11;p13) and MYST3-CREBBP rearrangement reveals a distinctive signature with a specific pattern of HOX gene expression.

artículo científico publicado en 2006

Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia

artículo científico publicado en 2004

Genomic complexity and IGHV mutational status are key predictors of outcome of chronic lymphocytic leukemia patients with TP53 disruption

artículo científico publicado en 2014

High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia

artículo científico publicado en 2003

High-grade prostate intraepithelial neoplasia shares cytogenetic alterations with invasive prostate cancer

artículo científico publicado en 2001

Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma.

artículo científico publicado en 2010

Integrating genomic alterations in diffuse large B-cell lymphoma identifies new relevant pathways and potential therapeutic targets.

artículo científico publicado en 2017

Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: Different genetic mechanisms but equivalent poorer clinical outcome

artículo científico publicado en 2014

LMO2-negative Expression Predicts the Presence of MYC Translocations in Aggressive B-Cell Lymphomas.

artículo científico publicado en 2017

Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genes.

artículo científico publicado en 2001

Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques

artículo científico publicado en 2008

NOTCH1 mutations in chronic lymphocytic leukemia with trisomy 12

New chromosomal alterations in a series of 23 splenic marginal zone lymphoma patients revealed by Spectral Karyotyping (SKY)

article by Cristina Baró et al published May 2008 in Leukemia Research

Non-coding recurrent mutations in chronic lymphocytic leukaemia

artículo científico publicado en 2015

Paraspinal extramedullary hematopoiesis in hereditary spherocytosis with a concurrent follicular lymphoma: case report and review of the literature

artículo científico publicado en 2015

Prenatal diagnosis of fragile X syndrome: (CGG)n expansion and methylation of chorionic villus samples.

artículo científico publicado en 1995

Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injection.

artículo científico publicado en 1998

Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes.

artículo científico publicado en 2015

Rapid Diagnosis of Acute Promyelocytic Leukemia by Analyzing the Immunocytochemical Pattern of the PML Protein With the Monoclonal Antibody PG-M3

artículo científico publicado en 2000

Rapid fetal karyotype from cystic hygroma and pleural effusions

artículo científico publicado en 1995

Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: review of 5,654 patients with an evaluable karyotype.

artículo científico

Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14′, 15, and 21 leading to balanced and unbalanced rearrangements in offspring

artículo científico publicado en 2005

Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours.

artículo científico publicado en 2014

Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes.

artículo científico publicado en 2015

Refining the diagnosis and prognostic categorization of acute myeloid leukemia patients with an integrated use of cytogenetic and molecular studies

artículo científico publicado en 2012

Response to lenalidomide in patients with myelodysplastic syndrome with deletion 5q: clinical and cytogenetic analysis of a single centre series

artículo científico publicado en 2010

Smoldering multiple myeloma: natural history and recognition of an evolving type

artículo científico publicado en 2003

Studies of complex Ph translocations in cases with chronic myelogenous leukemia and one with acute lymphoblastic leukemia

Transfusion intensity, not the cumulative red blood cell transfusion burden, determines the prognosis of patients with myelodysplastic syndrome on chronic transfusion support.

artículo científico publicado en 2011

Transient donor cell-derived myelodysplastic syndrome with monosomy 7 after unrelated cord blood transplantation

artículo científico publicado en 2006

Type I MOZ/CBP (MYST3/CREBBP) is the most common chimeric transcript in acute myeloid leukemia with t(8;16)(p11;p13) translocation

artículo científico publicado en 2004

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid

artículo científico publicado en 1993

Lista de obras de Ana Carrió

12p13 rearrangements: 6 Mb deletion responsible for ID/MCA and reciprocal duplication without clinical responsibility

A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region.

A new genetic abnormality leading to TP53 gene deletion in chronic lymphocytic leukaemia

Biallelic losses of 13q do not confer a poorer outcome in chronic lymphocytic leukaemia: analysis of 627 patients with isolated 13q deletion

Brachycephaly is ineffective for detection of Down syndrome in early midtrimester fetuses

CD49d (ITGA4) expression is a predictor of time to first treatment in patients with chronic lymphocytic leukaemia and mutatedIGHVstatus

Chimeric BCR/ABL gene detected by fluorescence in situ hybridization in three new cases of Philadelphia chromosome-negative chronic myelocytic leukemia.

Chorionic villus sampling by biopsy forceps. Results of 1580 procedures from a single centre

Chromosomal high-polysomies predict tumour progression in T1 transitional cell carcinoma of the bladder.

Chronic lymphocytic leukaemia with 17p deletion: a retrospective analysis of prognostic factors and therapy results

Chronic lymphocytic leukemia in the elderly: clinico-biological features, outcomes, and proposal of a prognostic model

Clinical implications of ZAP-70 expressionin chronic lymphocytic leukemia

Clonal evolution in chronic lymphocytic leukemia: analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance

Comparative genomic hybridisation identifies two variants of smoldering multiple myeloma

Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia.

Different distribution of NOTCH1 mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations.

Do we need to do fluorescence in situ hybridization analysis in myelodysplastic syndromes as often as we do?

Elastin mutation screening in a group of patients affected by vascular abnormalities

Fluorescence in situ hybridization analysis of matched primary tumour and lymph-node metastasis of D1 (pT2-3pN1M0) prostate cancer.

Fluorescence in situ hybridization studies using BAC clones of the EVI1 locus in hematological malignancies with 3q rearrangements

Gene expression profiling of acute myeloid leukemia with translocation t(8;16)(p11;p13) and MYST3-CREBBP rearrangement reveals a distinctive signature with a specific pattern of HOX gene expression.

Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia

Genomic complexity and IGHV mutational status are key predictors of outcome of chronic lymphocytic leukemia patients with TP53 disruption

High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia

High-grade prostate intraepithelial neoplasia shares cytogenetic alterations with invasive prostate cancer

Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma.

Integrating genomic alterations in diffuse large B-cell lymphoma identifies new relevant pathways and potential therapeutic targets.

Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: Different genetic mechanisms but equivalent poorer clinical outcome

LMO2-negative Expression Predicts the Presence of MYC Translocations in Aggressive B-Cell Lymphomas.

Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genes.

Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques

NOTCH1 mutations in chronic lymphocytic leukemia with trisomy 12

New chromosomal alterations in a series of 23 splenic marginal zone lymphoma patients revealed by Spectral Karyotyping (SKY)

Non-coding recurrent mutations in chronic lymphocytic leukaemia

Paraspinal extramedullary hematopoiesis in hereditary spherocytosis with a concurrent follicular lymphoma: case report and review of the literature

Prenatal diagnosis of fragile X syndrome: (CGG)n expansion and methylation of chorionic villus samples.

Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injection.

Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes.

Rapid Diagnosis of Acute Promyelocytic Leukemia by Analyzing the Immunocytochemical Pattern of the PML Protein With the Monoclonal Antibody PG-M3

Rapid fetal karyotype from cystic hygroma and pleural effusions

Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: review of 5,654 patients with an evaluable karyotype.

Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14′, 15, and 21 leading to balanced and unbalanced rearrangements in offspring

Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours.

Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes.

Refining the diagnosis and prognostic categorization of acute myeloid leukemia patients with an integrated use of cytogenetic and molecular studies

Response to lenalidomide in patients with myelodysplastic syndrome with deletion 5q: clinical and cytogenetic analysis of a single centre series

Smoldering multiple myeloma: natural history and recognition of an evolving type

Studies of complex Ph translocations in cases with chronic myelogenous leukemia and one with acute lymphoblastic leukemia

Transfusion intensity, not the cumulative red blood cell transfusion burden, determines the prognosis of patients with myelodysplastic syndrome on chronic transfusion support.

Transient donor cell-derived myelodysplastic syndrome with monosomy 7 after unrelated cord blood transplantation

Type I MOZ/CBP (MYST3/CREBBP) is the most common chimeric transcript in acute myeloid leukemia with t(8;16)(p11;p13) translocation

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid