Found: 25
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The Clinical Phenotype of YWHAE-NUTM2B/E Positive Pediatric Clear Cell Sarcoma of the Kidney.
- Published in:
- Genes, Chromosomes & Cancer, 2016, v. 55, n. 2, p. 143, doi. 10.1002/gcc.22320
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- Publication type:
- Article
Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse.
- Published in:
- Genes, Chromosomes & Cancer, 2012, v. 51, n. 7, p. 644, doi. 10.1002/gcc.21951
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- Publication type:
- Article
Telomere maintenance in wilms tumors: First evidence for the presence of alternative lengthening of telomeres mechanism.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 10, p. 823, doi. 10.1002/gcc.20903
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- Publication type:
- Article
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith–Wiedemann syndrome and Wilms' tumour.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 10, p. 1427, doi. 10.1093/hmg/ddn031
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- Publication type:
- Article
Molecular Signature of Biological Aggressiveness in Clear Cell Sarcoma of the Kidney (CCSK).
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3743, doi. 10.3390/ijms24043743
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- Publication type:
- Article
Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 42, doi. 10.1002/gcc.1116
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- Publication type:
- Article
A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor.
- Published in:
- 2009
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- Publication type:
- Report
Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer.
- Published in:
- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001849
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- Publication type:
- Article
The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromes.
- Published in:
- Pediatric Blood & Cancer, 2023, v. 70, n. 2, p. 1, doi. 10.1002/pbc.29984
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- Publication type:
- Article
Wilms tumour occurring in a patient with osteopathia striata with cranial sclerosis: A still unsolved biological question.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 9, p. 1, doi. 10.1002/pbc.29132
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- Publication type:
- Article
WARNING: G-401 and SK-NEP-1 cell lines are not Wilms tumor cell lines.
- Published in:
- 2019
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- Publication type:
- journal article
Molecular insight into multiple Wilms tumors arising in germline WT1-mutated/11p13-deleted patients.
- Published in:
- 2018
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- Publication type:
- journal article
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.
- Published in:
- 2017
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- Publication type:
- journal article
Response Re: Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor.
- Published in:
- Pediatric Blood & Cancer, 2014, v. 61, n. 9, p. 1714, doi. 10.1002/pbc.24986
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- Publication type:
- Article
Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor.
- Published in:
- Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1136, doi. 10.1002/pbc.24876
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- Publication type:
- Article
A novel WT1 mutation in familial wilms tumor.
- Published in:
- Pediatric Blood & Cancer, 2013, v. 60, n. 8, p. 1388, doi. 10.1002/pbc.24539
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- Publication type:
- Article
Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complex.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 6, p. 1419, doi. 10.1002/ajmg.a.34001
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- Publication type:
- Article
Is WTX a suitable target for cancer therapy?
- Published in:
- Pediatric Blood & Cancer, 2011, v. 56, n. 4, p. 682, doi. 10.1002/pbc.22947
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- Publication type:
- Article
Severe polyuria and polydipsia in hyponatremic-hypertensive syndrome associated with Wilms tumor.
- Published in:
- Pediatric Blood & Cancer, 2010, v. 55, n. 3, p. 566, doi. 10.1002/pbc.22610
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- Publication type:
- Article
Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome.
- Published in:
- Pediatric Blood & Cancer, 2008, v. 51, n. 3, p. 344, doi. 10.1002/pbc.21507
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- Publication type:
- Article
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.
- Published in:
- Pediatric Blood & Cancer, 2008, v. 51, n. 1, p. 23, doi. 10.1002/pbc.21524
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- Publication type:
- Article
Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14.
- Published in:
- Human Mutation, 2004, v. 24, n. 5, p. 400, doi. 10.1002/humu.20096
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- Publication type:
- Article
Prognostic Factors for Wilms Tumor Recurrence: A Review of the Literature.
- Published in:
- Cancers, 2021, v. 13, n. 13, p. 3142, doi. 10.3390/cancers13133142
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- Publication type:
- Article
First Evidence of Vertical Paternal Transmission of Osteopatia Striata With Cranial Sclerosis.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1173, doi. 10.1002/ajmg.a.35813
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- Publication type:
- Article
Adult Wilms' tumor: A monoinstitutional experience and a review of the literature.
- Published in:
- Cancer (0008543X), 2004, v. 101, n. 2, p. 289, doi. 10.1002/cncr.20387
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- Publication type:
- Article