Professor in Pathology, Northwestern University Medical School
Pathology
Dr. Elizabeth J. Perlman, MD
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Elizabeth Perlman practices Pathology. She attended Johns Hopkins University School of Medicine. Johns Hopkins University School of Medicine is one of the top medical schools in the US. Johns Hopkins University School of Medicine is ranked 3/29 in Research/PrimaryCare. She over the years received 1 awards: "Super Doctor". Elizabeth J. Perlman, MD is a published physician. She published 57 publications, including: 'BCOR Internal Tandem Duplications in Clear Cell Sarcoma of the Kidney.'
Publications
- Expanding the Spectrum of Renal Tumors in Children: Primary Renal Myoepithelial Carcinomas With a Novel EWSR1-KLF15 Fusion.
- Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations.
- BCOR Internal Tandem Duplications in Clear Cell Sarcoma of the Kidney.
- Comparison of diagnostic performance of CT and MRI for abdominal staging of pediatric renal tumors: a report from the Children's Oncology Group.
- Recurrent DGCR8, DROSHA, and SIX homeodomain mutations in favorable histology Wilms tumors.
- CD84 is Markedly Upregulated in Kawasaki Disease Arteriopathy.
- DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma.
- Validation of a prognostic multi-gene signature in high-risk neuroblastoma using the high throughput digital NanoString nCounter⢠system.
- Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: A report from the children's oncology group.
- 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.
- Is adrenalectomy necessary during unilateral nephrectomy for Wilms Tumor? A report from the Children's Oncology Group.
- Integrins ?4 and ?M, collagen1A1, and matrix metalloproteinase 7 are upregulated in acute Kawasaki disease vasculopathy.
- Clinicopathologic Findings Predictive of Relapse in Children With Stage III Favorable-Histology Wilms Tumor.
- Detection of Preoperative Wilms Tumor Rupture with CT: A Report from the Children's Oncology Group.
- Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study.
- Outcomes of patients with revised stage I clear cell sarcoma of kidney treated in National Wilms Tumor Studies 1-5.
- ?-Catenin and K-RAS Synergize to Form Primitive Renal Epithelial Tumors with Features of Epithelial Wilms' Tumors.
- Molecular profiling reveals frequent gain of MYCN and anaplasia-specific loss of 4q and 14q in wilms tumor.
- Insights on neoplastic stem cells from gel-based proteomics of childhood germ cell tumors.
- Ultrastructural, immunofluorescence, and RNA evidence support the hypothesis of a "new" virus associated with Kawasaki disease.
- 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.
- Pediatric Renal Cell Carcinoma.
- Long-term outcomes for infants with very low risk Wilms tumor treated with surgery alone in National Wilms Tumor Study-5.
- 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 Onc...
- Predicting relapse in favorable histology Wilms tumor using gene expression analysis: a report from the Renal Tumor Committee of the Children's Oncology Group.
- Synchronous bilateral Wilm's tumor with complete radiographic response managed without surgical resection: a report from the National Wilm's Tumor Study 4.
- Treatment of metastatic Ewing sarcoma/primitive neuroectodermal tumor of bone: evaluation of increasing the dose intensity of chemotherapy--a report from the Children'...
- Anaplastic sarcoma of the kidney: a clinicopathologic study of 20 cases of a new entity with polyphenotypic features.
- RANBP2 and CLTC are involved in ALK rearrangements in inflammatory myofibroblastic tumors.
- Desmoplastic small round cell tumor of the kidney in childhood.
- Therapy-related myelodysplasia and acute myeloid leukemia after Ewing sarcoma and primitive neuroectodermal tumor of bone: A report from the Children's Oncology Group.
- Bilateral Wilms' tumor with anaplasia: lessons from the National Wilms' Tumor Study.
- Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor.
- Molecular genetic analysis of central nervous system germ cell tumors with comparative genomic hybridization.
- Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study.
- Bilateral Wilms' tumors with progressive or nonresponsive disease.
- Activation of Wnt/beta-catenin signaling in distinct histologic subtypes of human germ cell tumors.
- High telomerase RNA expression level is an adverse prognostic factor for favorable-histology Wilms' tumor.
- IGF2/H19 imprinting analysis of human germ cell tumors (GCTs) using the methylation-sensitive single-nucleotide primer extension method reflects the origin of GCTs in ...
- Renal medullary carcinoma and ABL gene amplification.
- Pediatric renal tumors: practical updates for the pathologist.
- Immunohistochemical analysis of hSNF5/INI1 distinguishes renal and extra-renal malignant rhabdoid tumors from other pediatric soft tissue tumors.
- Expression of WT-1, Bcl-2, and CD34 by primary renal spindle cell tumors in children.
- Treatment of metastatic Ewing's sarcoma or primitive neuroectodermal tumor of bone: evaluation of combination ifosfamide and etoposide--a Children's Cancer Group and P...
- Methylation-associated silencing of the heat shock protein 47 gene in human neuroblastoma.
- Ewing sarcoma/primitive neuroectodermal tumor of the chest wall: impact of initial versus delayed resection on tumor margins, survival, and use of radiation therapy.
- Genetic and genetic expression analyses of clear cell sarcoma of the kidney.
- hTERT gene amplification and increased mRNA expression in central nervous system embryonal tumors.
- POU5F1 (OCT3/4) identifies cells with pluripotent potential in human germ cell tumors.
- Addition of ifosfamide and etoposide to standard chemotherapy for Ewing's sarcoma and primitive neuroectodermal tumor of bone.
- Performance characteristics of a reverse transcriptase-polymerase chain reaction assay for the detection of tumor-specific fusion transcripts from archival tissue.
- Functional genomic comparison of lineage-related human bladder cancer cell lines with differing tumorigenic and metastatic potentials by spectral karyotyping, comparat...
- Renal medullary carcinoma: clinical, pathologic, immunohistochemical, and genetic analysis with pathogenetic implications.
- Primary synovial sarcoma of the kidney diagnosed by molecular detection of SYT-SSX fusion transcripts.
- Genetic analysis of mediastinal nonseminomatous germ cell tumors in children and adolescents.
- Risk stratification for wilms tumor: current approach and future directions.
Schools
Johns Hopkins University School Of Medicine
Johns Hopkins Hospital
Doctors Specialties
- Pediatric Pathology
- Pathology
Accepted Insurances
Awards
- Super Doctor
Education
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Johns Hopkins University -
Johns Hopkins University School of Medicine
Hospital
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Lurie Children's Hospital of Chicago -
Northwestern Memorial Hospital -
Ann & Robert H. Lurie Children?
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