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Updates on progress in cancer screening for children with hereditary cancer predisposition syndromes

Current opinion in pediatrics, 2019-02, Vol.31 (1), p.41-47

Rednam, Surya P

2019

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Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Clinical cancer research, 2017-06, Vol.23 (12), p.e68-e75

2017

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PTEN, DICER1, FH , and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Clinical cancer research, 2017-06, Vol.23 (12), p.e76-e82

2017

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Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma

Clinical cancer research, 2017-07, Vol.23 (13), p.e115-e122

2017

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Germ-line and somatic DICER1 mutations in pineoblastoma

Acta neuropathologica, 2014-10, Vol.128 (4), p.583-595

2014

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Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Clinical cancer research, 2017-07, Vol.23 (13), p.e123-e132

2017

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Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population‐based assessment in seven million children

Cancer, 2024-02, Vol.130 (3), p.467-475

2024

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Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors

Clinical cancer research, 2024-06, Vol.30 (11), p.2342-OF9

2024

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Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith–Wiedemann Syndrome and Other Predisposition Syndromes

Clinical cancer research, 2024-09, p.OF1-OF10

2024

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Impact of vascular anomalies on the PTEN phenotype in children and young adults

Pediatric blood & cancer, 2020-06, Vol.67 (6), p.e28258-n/a

2020

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Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features

American journal of human genetics, 2017-10, Vol.101 (4), p.503-515

2017

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Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition

Cancer prevention research (Philadelphia, Pa.), 2022-10, Vol.15 (10), p.645-652

2022

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Gadolinium is not necessary for surveillance MR imaging in children with chiasmatic‐hypothalamic low‐grade glioma

Pediatric blood & cancer, 2021-10, Vol.68 (10), p.e29178-n/a

2021

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Sa2085 Ten Year Experience With Large Polyp Removal in Pediatric Patients

Gastrointestinal endoscopy, 2017-05, Vol.85 (5), p.AB289-AB290

2017

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P059: Reanalysis of intronic variants reveals novel likely pathogenic DICER1 splice variant in pleuropulmonary blastoma proband

Genetics in Medicine Open, 2023, Vol.1 (1), p.100078, Article 100078

2023

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Pilot study of DNA methylation-derived neutrophil-to-lymphocyte ratio and survival in pediatric medulloblastoma

Cancer epidemiology, 2019-04, Vol.59, p.71-74

2019

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DNA methylation of a novel PAK4 locus influences ototoxicity susceptibility following cisplatin and radiation therapy for pediatric embryonal tumors

Neuro-oncology (Charlottesville, Va.), 2017-10, Vol.19 (10), p.1372-1379

2017

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Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency

Cold Spring Harbor molecular case studies, 2019-10, Vol.5 (5), p.a004499

2019

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Considerations for total thyroidectomy in an adolescent with PTEN mutation

Therapeutic advances in endocrinology and metabolism, 2018-09, Vol.9 (9), p.299-301

2018

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Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients

Cancer epidemiology, 2016-10, Vol.44, p.161-166

2016

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Combined bioinformatic and splicing analysis of likely benign intronic and synonymous variants reveals evidence for pathogenicity

Genetics in Medicine Open, 2024, Vol.2, p.101850, Article 101850

2024

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Mo1991 INCREASED ENDOSCOPIC AND SURGICAL INTERVENTION IN EARLY PRESENTATION OF PEUTZ-JEGHERS SYNDROME: A SINGLE CENTER STUDY

Gastrointestinal endoscopy, 2020-06, Vol.91 (6), p.AB502-AB503

2020

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Guidelines for surveillance of patients with von Hippel‐Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance

Cancer, 2023-10, Vol.129 (19), p.2927-2940

2023

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Glutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma

Pediatric blood & cancer, 2013-04, Vol.60 (4), p.593-598

2013

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Updates on progress in cancer screening for children with hereditary cancer predisposition syndromes

Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

PTEN, DICER1, FH , and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma

Germ-line and somatic DICER1 mutations in pineoblastoma

Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population‐based assessment in seven million children

Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors

Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith–Wiedemann Syndrome and Other Predisposition Syndromes

Impact of vascular anomalies on the PTEN phenotype in children and young adults

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis

Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features

Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition

Gadolinium is not necessary for surveillance MR imaging in children with chiasmatic‐hypothalamic low‐grade glioma

Sa2085 Ten Year Experience With Large Polyp Removal in Pediatric Patients

P059: Reanalysis of intronic variants reveals novel likely pathogenic DICER1 splice variant in pleuropulmonary blastoma proband

Pilot study of DNA methylation-derived neutrophil-to-lymphocyte ratio and survival in pediatric medulloblastoma

DNA methylation of a novel PAK4 locus influences ototoxicity susceptibility following cisplatin and radiation therapy for pediatric embryonal tumors

Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency

Considerations for total thyroidectomy in an adolescent with PTEN mutation

Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients

Combined bioinformatic and splicing analysis of likely benign intronic and synonymous variants reveals evidence for pathogenicity

Mo1991 INCREASED ENDOSCOPIC AND SURGICAL INTERVENTION IN EARLY PRESENTATION OF PEUTZ-JEGHERS SYNDROME: A SINGLE CENTER STUDY

Guidelines for surveillance of patients with von Hippel‐Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance

Glutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma

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