Lista de obras -

A pathologic link between Wilms tumor suppressor gene, WT1, and IFI16.

artículo científico publicado en 2008

A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain

scientific article published on 04 July 2019

Adolescent and Young Adult Perspectives on Challenges and Improvements to Cancer Survivorship Care: How Are We Doing?

scientific article published on 15 September 2020

Amplification and overexpression of CACNA1E correlates with relapse in favorable histology Wilms' tumors

artículo científico publicado en 2006

B7-h1 as a biomarker for therapy failure in patients with favorable histology Wilms tumor.

artículo científico publicado en 2012

BRIDGING THE GAP – BENEFITS OF NEUROSURGICAL TISSUE FOR PRE-CLINICAL RESEARCH

Barriers to the enrollment of children in the Children's Oncology Group study of very low risk Wilms tumor: a report from the Children's Oncology Group

artículo científico publicado en 2011

Blastemal expression of type I insulin-like growth factor receptor in Wilms' tumors is driven by increased copy number and correlates with relapse.

artículo científico publicado en 2006

CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors

artículo científico publicado en 2004

Canadian cancer statistics at a glance: cancer in children

artículo científico publicado en 2009

Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor

artículo científico publicado en 2005

Clinical Outcome and Biological Predictors of Relapse After Nephrectomy Only for Very Low-risk Wilms Tumor: A Report From Children's Oncology Group AREN0532.

artículo científico publicado en 2016

Clinical significance of pulmonary nodules detected by CT and Not CXR in patients treated for favorable histology Wilms tumor on national Wilms tumor studies-4 and -5: a report from the Children's Oncology Group

artículo científico publicado en 2012

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study

artículo científico publicado en 2012

Clinicopathologic findings predictive of relapse in children with stage III favorable-histology Wilms tumor

artículo científico publicado en 2013

Cytotoxicity of 2-chlorodeoxyadenosine and arabinosylcytosine in leukaemic lymphoblasts from paediatric patients: significance of cellular nucleoside transporter content

artículo científico publicado en 2002

Decrease in LDL receptor-related protein expression and function correlates with advanced stages of Wilms tumors.

artículo científico publicado en 2006

Decreased E-cadherin expression correlates with higher stage of Wilms' tumors.

artículo científico publicado en 2005

Delineation of a 1Mb breakpoint region at 1p13 in Wilms tumors by fine-tiling oligonucleotide array CGH

scientific article published on 01 June 2007

Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidney

artículo científico publicado en 2004

Early discontinuation of intravenous antimicrobial therapy in pediatric oncology patients with febrile neutropenia

artículo científico publicado en 2005

Effect of duration of treatment on treatment outcome for patients with clear-cell sarcoma of the kidney: a report from the National Wilms' Tumor Study Group

artículo científico publicado en 2004

Fine mapping of Wilms' tumors with 16q loss of heterozygosity localizes the putative tumor suppressor gene to a region of 6.7 megabases

scientific article published on 01 March 2003

Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour.

artículo científico publicado en 2011

Hepatic metastasis at diagnosis in patients with Wilms tumor is not an independent adverse prognostic factor for stage IV Wilms tumor: a report from the Children's Oncology Group/National Wilms Tumor Study Group

artículo científico publicado en 2009

Impact of Surveillance Imaging Modality on Survival After Recurrence in Patients With Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group

artículo científico publicado en 2018

Increased microvascular density predicts relapse in Wilms' tumor

scientific article published on 01 March 2003

Long-term outcomes for infants with very low risk Wilms tumor treated with surgery alone in National Wilms Tumor Study-5.

artículo científico publicado en 2010

Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group

artículo científico publicado en 2005

Minimising length of stay following brain tumour surgery: benefits to patients, providers and the NHS

Outcome and Prognostic Factors in Stage III Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group Study AREN0532.

artículo científico publicado en 2017

Outcome of patients with Stage II/favorable histology Wilms tumor with and without local tumor spill: a report from the National Wilms Tumor Study Group

artículo científico publicado en 2013

Outcomes of children with favorable histology wilms tumor and peritoneal implants treated in National Wilms Tumor Studies-4 and -5.

artículo científico publicado en 2010

Outcomes of patients with revised stage I clear cell sarcoma of kidney treated in National Wilms Tumor Studies 1-5.

artículo científico publicado en 2012

PATIENT SATISFACTION WITH DAY-CASE BRAIN BIOPSY

Predicting relapse in favorable histology Wilms tumor using gene expression analysis: a report from the Renal Tumor Committee of the Children's Oncology Group

artículo científico publicado en 2009

Primary nephrectomy and intraoperative tumor spill: report from the Children's Oncology Group (COG) renal tumors committee

artículo científico publicado en 2013

Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour

artículo científico publicado en 2014

Results of the First Prospective Multi-institutional Treatment Study in Children With Bilateral Wilms Tumor (AREN0534): A Report From the Children's Oncology Group

artículo científico

SHARED DECISION MAKING, THE BRIDGE BETWEEN PATERNALISM AND AUTONOMY

Second malignant neoplasms after childhood non-central nervous system embryonal tumours in North America: A population-based study.

artículo científico publicado en 2017

THE SURVIVAL OF GLIOBLASTOMA MULTIFORME PATIENTS AFTER BURR HOLE BIOPSY BASED ON THEIR POST BIOPSY TREATMENT WITH OR WITHOUT CHEMOTHERAPY AND OR RADIOTHERAPY

article published in 2018

Treatment of Stage IV Favorable Histology Wilms Tumor With Lung Metastases: A Report From the Children's Oncology Group AREN0533 Study.

artículo científico publicado en 2018

Treatment of Wilms tumor relapsing after initial treatment with vincristine and actinomycin D: a report from the National Wilms Tumor Study Group

artículo científico publicado en 2007

Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group

artículo científico publicado en 2008

Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study

artículo científico publicado en 2006

Treatment of recurrent clear cell sarcoma of the kidney with brain metastasis

artículo científico publicado en 2008

Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificity

artículo científico publicado en 2002

WT1 mutation and 11P15 loss of heterozygosity predict relapse in very low-risk wilms tumors treated with surgery alone: a children's oncology group study

artículo científico publicado en 2010

What do adolescents and young adults perceive is the main challenge during the transition to survivorship?

artículo científico publicado en 2020

Lista de obras de

A pathologic link between Wilms tumor suppressor gene, WT1, and IFI16.

A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain

Adolescent and Young Adult Perspectives on Challenges and Improvements to Cancer Survivorship Care: How Are We Doing?

Amplification and overexpression of CACNA1E correlates with relapse in favorable histology Wilms' tumors

B7-h1 as a biomarker for therapy failure in patients with favorable histology Wilms tumor.

BRIDGING THE GAP – BENEFITS OF NEUROSURGICAL TISSUE FOR PRE-CLINICAL RESEARCH

Barriers to the enrollment of children in the Children's Oncology Group study of very low risk Wilms tumor: a report from the Children's Oncology Group

Blastemal expression of type I insulin-like growth factor receptor in Wilms' tumors is driven by increased copy number and correlates with relapse.

CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors

Canadian cancer statistics at a glance: cancer in children

Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor

Clinical Outcome and Biological Predictors of Relapse After Nephrectomy Only for Very Low-risk Wilms Tumor: A Report From Children's Oncology Group AREN0532.

Clinical significance of pulmonary nodules detected by CT and Not CXR in patients treated for favorable histology Wilms tumor on national Wilms tumor studies-4 and -5: a report from the Children's Oncology Group

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study

Clinicopathologic findings predictive of relapse in children with stage III favorable-histology Wilms tumor

Cytotoxicity of 2-chlorodeoxyadenosine and arabinosylcytosine in leukaemic lymphoblasts from paediatric patients: significance of cellular nucleoside transporter content

Decrease in LDL receptor-related protein expression and function correlates with advanced stages of Wilms tumors.

Decreased E-cadherin expression correlates with higher stage of Wilms' tumors.

Delineation of a 1Mb breakpoint region at 1p13 in Wilms tumors by fine-tiling oligonucleotide array CGH

Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidney

Early discontinuation of intravenous antimicrobial therapy in pediatric oncology patients with febrile neutropenia

Effect of duration of treatment on treatment outcome for patients with clear-cell sarcoma of the kidney: a report from the National Wilms' Tumor Study Group

Fine mapping of Wilms' tumors with 16q loss of heterozygosity localizes the putative tumor suppressor gene to a region of 6.7 megabases

Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour.

Hepatic metastasis at diagnosis in patients with Wilms tumor is not an independent adverse prognostic factor for stage IV Wilms tumor: a report from the Children's Oncology Group/National Wilms Tumor Study Group

Impact of Surveillance Imaging Modality on Survival After Recurrence in Patients With Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group

Increased microvascular density predicts relapse in Wilms' tumor

Long-term outcomes for infants with very low risk Wilms tumor treated with surgery alone in National Wilms Tumor Study-5.

Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group

Minimising length of stay following brain tumour surgery: benefits to patients, providers and the NHS

Outcome and Prognostic Factors in Stage III Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group Study AREN0532.

Outcome of patients with Stage II/favorable histology Wilms tumor with and without local tumor spill: a report from the National Wilms Tumor Study Group

Outcomes of children with favorable histology wilms tumor and peritoneal implants treated in National Wilms Tumor Studies-4 and -5.

Outcomes of patients with revised stage I clear cell sarcoma of kidney treated in National Wilms Tumor Studies 1-5.

PATIENT SATISFACTION WITH DAY-CASE BRAIN BIOPSY

Predicting relapse in favorable histology Wilms tumor using gene expression analysis: a report from the Renal Tumor Committee of the Children's Oncology Group

Primary nephrectomy and intraoperative tumor spill: report from the Children's Oncology Group (COG) renal tumors committee

Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour

Results of the First Prospective Multi-institutional Treatment Study in Children With Bilateral Wilms Tumor (AREN0534): A Report From the Children's Oncology Group

SHARED DECISION MAKING, THE BRIDGE BETWEEN PATERNALISM AND AUTONOMY

Second malignant neoplasms after childhood non-central nervous system embryonal tumours in North America: A population-based study.

THE SURVIVAL OF GLIOBLASTOMA MULTIFORME PATIENTS AFTER BURR HOLE BIOPSY BASED ON THEIR POST BIOPSY TREATMENT WITH OR WITHOUT CHEMOTHERAPY AND OR RADIOTHERAPY

Treatment of Stage IV Favorable Histology Wilms Tumor With Lung Metastases: A Report From the Children's Oncology Group AREN0533 Study.

Treatment of Wilms tumor relapsing after initial treatment with vincristine and actinomycin D: a report from the National Wilms Tumor Study Group

Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group

Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study

Treatment of recurrent clear cell sarcoma of the kidney with brain metastasis

Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificity

WT1 mutation and 11P15 loss of heterozygosity predict relapse in very low-risk wilms tumors treated with surgery alone: a children's oncology group study

What do adolescents and young adults perceive is the main challenge during the transition to survivorship?