Lista de obras - Daniela Perotti - Dominio Público Uruguay

A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor

artículo científico publicado en 2008

A novelWT1mutation in familial wilms tumor

artículo científico publicado en 2013

Adult Wilms' tumor: A monoinstitutional experience and a review of the literature

artículo científico publicado en 2004

Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11

article

Analysis of the mutational status of SIX1/2 and microRNA processing genes in paired primary and relapsed Wilms tumors and association with relapse

artículo científico publicado en 2020

Bilateral preaxial polydactyly in a WAGR syndrome patient.

artículo científico publicado en 2005

Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences

artículo científico publicado en 2016

Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complex

artículo científico publicado en 2011

Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

artículo científico publicado en 2015

Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies

artículo científico publicado en 2010

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour

scientific article published on 01 February 2008

Disseminated Burkitt's Lymphoma After Kidney Transplantation: A Case Report in a Boy with Drash Syndrome

artículo científico publicado en 1997

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

artículo científico publicado en 2008

Factors possibly affecting prognosis in children with Wilms' tumor diagnosed before 24 months of age: A report from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) Wilms Tumor Working Group.

artículo científico publicado en 2017

First Evidence of Vertical Paternal Transmission of Osteopatia Striata With Cranial Sclerosis

artículo científico publicado en 2013

Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors

artículo científico publicado en 2008

Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse

artículo científico publicado en 2012

Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14.

artículo científico publicado en 2004

Is WTX a suitable target for cancer therapy?

artículo científico publicado en 2010

Is Wilms tumor a candidate neoplasia for treatment with WNT/β-catenin pathway modulators?--A report from the renal tumors biology-driven drug development workshop

artículo científico publicado en 2013

Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor.

artículo científico publicado en 2013

Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors

artículo científico publicado en 1996

Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome

scientific article published on 01 September 2008

Molecular insight into multiple Wilms tumors arising in germline WT1-mutated/11p13-deleted patients

scientific article published on 17 July 2018

No evidence of WT1 involvement in a Burkitt's lymphoma in a patient with Denys-Drash syndrome

artículo científico publicado en 1998

Non-chromosome 11-p syndromes in Wilms tumor patients: Clinical and cytogenetic report of two Down syndrome cases and one Turner syndrome case

artículo científico publicado en 2007

Possible role of pandemic AH1N1 swine flu virus in a childhood leukemia cluster

artículo científico publicado en 2017

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

artículo científico publicado en 2013

Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours

artículo científico publicado en 2001

Response Re: Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor

artículo científico publicado en 2014

Results of the Third AIEOP Cooperative Protocol on Wilms Tumor (TW2003) and Related Considerations

artículo científico publicado en 2017

Retina-derived POU domain factor 1 coordinates expression of genes relevant to renal and neuronal development

artículo científico publicado en 2016

Severe polyuria and polydipsia in hyponatremic-hypertensive syndrome associated with Wilms tumor.

artículo científico publicado en 2010

Telomere maintenance in Wilms tumors: first evidence for the presence of alternative lengthening of telomeres mechanism.

artículo científico publicado en 2011

The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol

scholarly article by Gordan M. Vujanić published in October 2018

The clinical phenotype of YWHAE-NUTM2B/E positive pediatric clear cell sarcoma of the kidney.

artículo científico publicado en 2015

Treatment of high-risk relapsed Wilms tumor with dose-intensive chemotherapy, marrow-ablative chemotherapy, and autologous hematopoietic stem cell support: Experience by the Italian association of pediatric hematology and oncology

article

WARNING: G-401 and SK-NEP-1 cell lines are not Wilms tumor cell lines

scientific article published on 29 March 2019

WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features.

artículo científico publicado en 2012

Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney

artículo científico publicado en 2015

Wilms tumor in monozygous twins: clinical, pathological, cytogenetic and molecular case report

artículo científico publicado en 2005

Lista de obras de Daniela Perotti

A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor

A novelWT1mutation in familial wilms tumor

Adult Wilms' tumor: A monoinstitutional experience and a review of the literature

Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11

Analysis of the mutational status of SIX1/2 and microRNA processing genes in paired primary and relapsed Wilms tumors and association with relapse

Bilateral preaxial polydactyly in a WAGR syndrome patient.

Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences

Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complex

Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour

Disseminated Burkitt's Lymphoma After Kidney Transplantation: A Case Report in a Boy with Drash Syndrome

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

Factors possibly affecting prognosis in children with Wilms' tumor diagnosed before 24 months of age: A report from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) Wilms Tumor Working Group.

First Evidence of Vertical Paternal Transmission of Osteopatia Striata With Cranial Sclerosis

Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors

Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse

Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14.

Is WTX a suitable target for cancer therapy?

Is Wilms tumor a candidate neoplasia for treatment with WNT/β-catenin pathway modulators?--A report from the renal tumors biology-driven drug development workshop

Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor.

Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors

Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome

Molecular insight into multiple Wilms tumors arising in germline WT1-mutated/11p13-deleted patients

No evidence of WT1 involvement in a Burkitt's lymphoma in a patient with Denys-Drash syndrome

Non-chromosome 11-p syndromes in Wilms tumor patients: Clinical and cytogenetic report of two Down syndrome cases and one Turner syndrome case

Possible role of pandemic AH1N1 swine flu virus in a childhood leukemia cluster

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours

Response Re: Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor

Results of the Third AIEOP Cooperative Protocol on Wilms Tumor (TW2003) and Related Considerations

Retina-derived POU domain factor 1 coordinates expression of genes relevant to renal and neuronal development

Severe polyuria and polydipsia in hyponatremic-hypertensive syndrome associated with Wilms tumor.

Telomere maintenance in Wilms tumors: first evidence for the presence of alternative lengthening of telomeres mechanism.

The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol

The clinical phenotype of YWHAE-NUTM2B/E positive pediatric clear cell sarcoma of the kidney.

Treatment of high-risk relapsed Wilms tumor with dose-intensive chemotherapy, marrow-ablative chemotherapy, and autologous hematopoietic stem cell support: Experience by the Italian association of pediatric hematology and oncology

WARNING: G-401 and SK-NEP-1 cell lines are not Wilms tumor cell lines

WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features.

Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney

Wilms tumor in monozygous twins: clinical, pathological, cytogenetic and molecular case report