Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups

New concepts and outcomes for children with hepatoblastoma based on the experience of a tertiary center over the last 21 years

(2015) AC Tannuri et al.   Clinics

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome

(2015) Alessandro Mussa et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations of the ImprintedCDKN1CGene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization

(2015) Frederic Brioude et al.   HUMAN MUTATION

Screening Hepatoblastoma in Beckwith-Wiedemann Syndrome

(2015) Alessandro Mussa et al.   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY

Neuroblastoma

(2015) Meredith S. Irwin et al.   PEDIATRIC CLINICS OF NORTH AMERICA

Hepatoblastoma in Children With Beckwith-Wiedemann Syndrome

(2014) Angela D. Trobaugh-Lotrario et al.   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY

Relapse surveillance in AFP-positive hepatoblastoma: re-evaluating the role of imaging

(2014) Yesenia Rojas et al.   PEDIATRIC RADIOLOGY

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

(2014) Abdulla Ibrahim et al.   Clinical Epigenetics

Molecular Findings in Beckwith-Wiedemann Syndrome

(2013) SANAA CHOUFANI et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Clinical utility gene card for: Beckwith–Wiedemann Syndrome

(2013) Thomas Eggermann et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance

(2013) F. Brioude et al.   Hormone Research in Paediatrics

Beckwith–Wiedemann and Russell–Silver Syndromes

(2013) Salah Azzi et al.   Current Opinion in Endocrinology Diabetes and Obesity

Relapses in hepatoblastoma patients: Clinical characteristics and outcome – Experience of the International Childhood Liver Tumour Strategy Group (SIOPEL)

(2012) M. Semeraro et al.   EUROPEAN JOURNAL OF CANCER

Pediatric Malignancies

(2012) Katherine P. Davenport et al.   SURGICAL CLINICS OF NORTH AMERICA

 -Fetoprotein

(2011) M. J. Murray et al.   Archives of Disease in Childhood-Education and Practice Edition

Educational paper

(2011) Alexis Teplick et al.   EUROPEAN JOURNAL OF PEDIATRICS

Nephrological findings and genotype–phenotype correlation in Beckwith–Wiedemann syndrome

(2011) Alessandro Mussa et al.   PEDIATRIC NEPHROLOGY

Beckwith-Wiedemann syndrome

(2010) Sanaa Choufani et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Surveillance CT scans are a source of anxiety and fear of recurrence in long-term lymphoma survivors

(2010) C. A. Thompson et al.   ANNALS OF ONCOLOGY

Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases

(2010) Margaret Elliott et al.   CLINICAL GENETICS

Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol

(2009) Yuri A. Zarate et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Beckwith–Wiedemann syndrome

(2009) Rosanna Weksberg et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Risque tumoral et syndrome de Wiedemann-Beckwith : quelle surveillance proposer ?

(2008) J. Santiago et al.   ARCHIVES DE PEDIATRIE

Genetic testing and tumor surveillance for children with cancer predisposition syndromes

(2008) Aarati Rao et al.   CURRENT OPINION IN PEDIATRICS

Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis

(2008) Marielle Alders et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The International Neuroblastoma Risk Group (INRG) Staging System: An INRG Task Force Report

(2008) Tom Monclair et al.   JOURNAL OF CLINICAL ONCOLOGY

Effectiveness of screening for neuroblastoma at 6 months of age: a retrospective population-based cohort study

(2008) Eiso Hiyama et al.   LANCET