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Clinically Relevant Subsets Identified by Gene Expression Patterns Support a Revised Ontogenic Model of Wilms Tumor: A Children's Oncology Group Study

Neoplasia (New York, N.Y.), 2012-08, Vol.14 (8), p.742-IN21

2012

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Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

Pediatrics (Evanston), 2004-07, Vol.114 (1), p.234-238

2004

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Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2010-01, Vol.18 (1), p.8-14

2010

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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

Journal of clinical oncology, 2005-10, Vol.23 (29), p.7312-7321

2005

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Treatment of Anaplastic Histology Wilms' Tumor: Results From the Fifth National Wilms' Tumor Study

Journal of clinical oncology, 2006-05, Vol.24 (15), p.2352-2358

2006

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Rhabdoid Tumor of the Kidney in The National Wilms' Tumor Study: Age at Diagnosis As a Prognostic Factor

Journal of clinical oncology, 2005-10, Vol.23 (30), p.7641-7645

2005

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Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor

Pediatric blood & cancer, 2006-09, Vol.47 (3), p.260-267

2006

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Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical Features

Clinical cancer research, 2009-11, Vol.15 (22), p.6800-6809

2009

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Characteristics and Outcomes of Children With the Wilms Tumor-Aniridia Syndrome: A Report From the National Wilms Tumor Study Group

Journal of clinical oncology, 2003-12, Vol.21 (24), p.4579-4585

2003

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Intraoperative Spillage of Favorable Histology Wilms Tumor Cells: Influence of Irradiation and Chemotherapy Regimens on Abdominal Recurrence. A Report From the National Wilms Tumor Study Group

International journal of radiation oncology, biology, physics, 2010-01, Vol.76 (1), p.201-206

2010

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A case of macrosomia and macroglossia, likely Beckwith‐Wiedemann syndrome from 1628

American journal of medical genetics. Part C, Seminars in medical genetics, 2021-06, Vol.187 (2), p.173-175

2021

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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

Journal of clinical oncology, 2004-02, Vol.22 (3), p.468-473

2004

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Two extraordinarily severe cases of Treacher Collins syndrome

American journal of medical genetics. Part A, 2013-03, Vol.161A (3), p.445-452

2013

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Treasures in the Older Literature: General Pediatric Anatomy

Pediatric and developmental pathology, 2015-11, Vol.18 (6), p.477-480

Beckwith, J. Bruce

2015

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Congenital malformations: from superstition to understanding

Virchows Archiv : an international journal of pathology, 2012-12, Vol.461 (6), p.609-619

Beckwith, J. Bruce

2012

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Classification of malignant pediatric renal tumors by gene expression

Pediatric Blood & Cancer, 2006-06, Vol.46 (7), p.728-738

2006

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Management of incidentally encountered nephrogenic rests

Journal of pediatric hematology/oncology, 2007-06, Vol.29 (6), p.353-354

Beckwith, J Bruce

2007

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Detection of the ETV6-NTRK3 Chimeric RNA of Infantile Fibrosarcoma/Cellular Congenital Mesoblastic Nephroma in Paraffin-Embedded Tissue: Application to Challenging Pediatric Renal Stromal Tumors

Modern pathology, 2000-01, Vol.13 (1), p.29-36

2000

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Risk Factors for End Stage Renal Disease in Non- WT1 -Syndromic Wilms Tumor

The Journal of urology, 2011-08, Vol.186 (2), p.378-386

2011

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Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5

Annals of surgery, 2010-03, Vol.251 (3), p.555-558

2010

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

Pediatric blood & cancer, 2008-02, Vol.50 (2), p.236-241

2008

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Suggested change in definitional criteria for stage 1 Wilms tumor treated by surgery only

Pediatric blood & cancer, 2011-01, Vol.56 (1), p.168-168

Beckwith, J. Bruce

2011

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Renal medullary carcinoma: clinical, pathologic, immunohistochemical, and genetic analysis with pathogenetic implications

Urology (Ridgewood, N.J.), 2002-12, Vol.60 (6), p.1083-1089

2002

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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

Pediatric blood & cancer, 2014-01, Vol.61 (1), p.134-139

2014

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Treatment of Wilms' tumor. Results of the third national Wilms' tumor study

Cancer, 1989-07, Vol.64 (2), p.349-360

1989

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Clinically Relevant Subsets Identified by Gene Expression Patterns Support a Revised Ontogenic Model of Wilms Tumor: A Children's Oncology Group Study

Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

Beckwith-Wiedemann syndrome

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

Treatment of Anaplastic Histology Wilms' Tumor: Results From the Fifth National Wilms' Tumor Study

Rhabdoid Tumor of the Kidney in The National Wilms' Tumor Study: Age at Diagnosis As a Prognostic Factor

Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor

Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical Features

Characteristics and Outcomes of Children With the Wilms Tumor-Aniridia Syndrome: A Report From the National Wilms Tumor Study Group

Intraoperative Spillage of Favorable Histology Wilms Tumor Cells: Influence of Irradiation and Chemotherapy Regimens on Abdominal Recurrence. A Report From the National Wilms Tumor Study Group

A case of macrosomia and macroglossia, likely Beckwith‐Wiedemann syndrome from 1628

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

Two extraordinarily severe cases of Treacher Collins syndrome

Treasures in the Older Literature: General Pediatric Anatomy

Congenital malformations: from superstition to understanding

Classification of malignant pediatric renal tumors by gene expression

Management of incidentally encountered nephrogenic rests

Detection of the ETV6-NTRK3 Chimeric RNA of Infantile Fibrosarcoma/Cellular Congenital Mesoblastic Nephroma in Paraffin-Embedded Tissue: Application to Challenging Pediatric Renal Stromal Tumors

Risk Factors for End Stage Renal Disease in Non- WT1 -Syndromic Wilms Tumor

Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5

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

Suggested change in definitional criteria for stage 1 Wilms tumor treated by surgery only

Renal medullary carcinoma: clinical, pathologic, immunohistochemical, and genetic analysis with pathogenetic implications

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

Treatment of Wilms' tumor. Results of the third national Wilms' tumor study

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