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Diagnosis of Beckwith–Wiedemann syndrome in children presenting with Wilms tumor

Pediatric blood & cancer, 2018-10, Vol.65 (10), p.e27296-n/a

2018

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Management of adrenal masses in patients with Beckwith–Wiedemann syndrome

Pediatric blood & cancer, 2017-08, Vol.64 (8), p.n/a

2017

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Defining an optimal time window to screen for hepatoblastoma in children with Beckwith‐Wiedemann syndrome

Pediatric blood & cancer, 2019-01, Vol.66 (1), p.e27492-n/a

2019

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Adrenocortical carcinoma in atypical Beckwith‐Wiedemann syndrome due to loss of methylation at imprinting control region 2

Pediatric blood & cancer, 2020-01, Vol.67 (1), p.e28042-n/a

2020

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Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith-Wiedemann Syndrome or Isolated Hemihypertrophy?

Pediatric blood & cancer, 2016-09, Vol.63 (9), p.1571-1577

2016

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The epidemiology of hepatoblastoma

Pediatric blood & cancer, 2012-11, Vol.59 (5), p.776-779

2012

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Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith–Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis

Pediatric blood & cancer, 2017-03, Vol.64 (3), p.np-n/a

2017

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Acute megakaryocytic leukemia (AMKL,FAB;M7) with Beckwith-wiedemann syndrome

Pediatric blood & cancer, 2010-10, Vol.55 (4), p.733-735

2010

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Comment on: Juvenile granulosa cell ovarian tumor in a child with Beckwith‐Wiedemann syndrome

Pediatric blood & cancer, 2017-08, Vol.64 (8), p.n/a

2017

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Primitive neuroectodermal tumor in 3-year-old boy with Beckwith-Wiedemann syndrome

Pediatric blood & cancer, 2007-07, Vol.49 (1), p.107-107

2007

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Successful treatment of doxorubicin and cisplatin resistant hepatoblastoma in a child with Beckwith-Wiedemann syndrome with high dose acetaminophen and N-acetylcysteine rescue

Pediatric blood & cancer, 2005-08, Vol.45 (2), p.222-225

2005

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Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome

Pediatric Blood & Cancer, 2008-11, Vol.51 (5), p.695-698

2008

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Multiple tumors due to mosaic genome‐wide paternal uniparental disomy

Pediatric blood & cancer, 2019-06, Vol.66 (6), p.e27715-n/a

2019

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KCNQ1OT1 hypomethylation: A Novel disguised genetic predisposition in sporadic pediatric adrenocortical tumors?

Pediatric Blood & Cancer, 2012-09, Vol.59 (3), p.565-566

2012

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Juvenile Granulosa Cell Ovarian Tumor in a Child With Beckwith-Wiedmann Syndrome

Pediatric blood & cancer, 2016-04, Vol.63 (4), p.750-751

2016

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Successful treatment of doxorubicin and cisplatin resistant hepatoblastoma in a child with Beckwith-Wiedemann syndrome with high dose acetaminophen and N -acetylcysteine rescue: High Dose Acetaminophen for Hepatoblastoma

Pediatric blood & cancer, 2005-08, Vol.45 (2), p.222-225

2005

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Maintenance chemotherapy to reduce the risk of a metachronous Wilms tumor in children with bilateral nephroblastomatosis

Pediatric blood & cancer, 2019-01, Vol.66 (1), p.e27500-n/a

2019

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Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Pediatric blood & cancer, 2006-11, Vol.47 (6), p.811-818

2006

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Hepatoblastoma in a child with neurofibromatosis type I

Pediatric blood & cancer, 2007-09, Vol.49 (3), p.357-359

2007

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Retrospective evaluation of a decision‐support algorithm (MIPOGG) for genetic referrals for children with neuroblastic tumors

Pediatric blood & cancer, 2018-12, Vol.65 (12), p.e27390-n/a

2018

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The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromes

Pediatric blood & cancer, 2023-05, Vol.70 (S2), p.e29984-n/a

2023

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Sonographic screening for Wilms tumor in children with CLOVES syndrome

Pediatric blood & cancer, 2017-12, Vol.64 (12), p.n/a

2017

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Consequences of diagnosing a tumor predisposition syndrome in children with cancer: A literature review

Pediatric blood & cancer, 2018-01, Vol.65 (1), p.n/a

2018

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Congenital malformation syndromes associated with peripheral neuroblastic tumors: A systematic review

Pediatric blood & cancer, 2019-10, Vol.66 (10), p.e27901-n/a

2019

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Malformations, genetic abnormalities, and wilms tumor

Pediatric blood & cancer, 2014-01, Vol.61 (1), p.140-144

2014

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Diagnosis of Beckwith–Wiedemann syndrome in children presenting with Wilms tumor

Management of adrenal masses in patients with Beckwith–Wiedemann syndrome

Defining an optimal time window to screen for hepatoblastoma in children with Beckwith‐Wiedemann syndrome

Adrenocortical carcinoma in atypical Beckwith‐Wiedemann syndrome due to loss of methylation at imprinting control region 2

Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith-Wiedemann Syndrome or Isolated Hemihypertrophy?

The epidemiology of hepatoblastoma

Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith–Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis

Acute megakaryocytic leukemia (AMKL,FAB;M7) with Beckwith-wiedemann syndrome

Comment on: Juvenile granulosa cell ovarian tumor in a child with Beckwith‐Wiedemann syndrome

Primitive neuroectodermal tumor in 3-year-old boy with Beckwith-Wiedemann syndrome

Successful treatment of doxorubicin and cisplatin resistant hepatoblastoma in a child with Beckwith-Wiedemann syndrome with high dose acetaminophen and N-acetylcysteine rescue

Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome

Multiple tumors due to mosaic genome‐wide paternal uniparental disomy

KCNQ1OT1 hypomethylation: A Novel disguised genetic predisposition in sporadic pediatric adrenocortical tumors?

Juvenile Granulosa Cell Ovarian Tumor in a Child With Beckwith-Wiedmann Syndrome

Successful treatment of doxorubicin and cisplatin resistant hepatoblastoma in a child with Beckwith-Wiedemann syndrome with high dose acetaminophen and N -acetylcysteine rescue: High Dose Acetaminophen for Hepatoblastoma

Maintenance chemotherapy to reduce the risk of a metachronous Wilms tumor in children with bilateral nephroblastomatosis

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Hepatoblastoma in a child with neurofibromatosis type I

Retrospective evaluation of a decision‐support algorithm (MIPOGG) for genetic referrals for children with neuroblastic tumors

The pathophysiology of bilateral and multifocal Wilms tumors: What we can learn from the study of predisposition syndromes

Sonographic screening for Wilms tumor in children with CLOVES syndrome

Consequences of diagnosing a tumor predisposition syndrome in children with cancer: A literature review

Congenital malformation syndromes associated with peripheral neuroblastic tumors: A systematic review

Malformations, genetic abnormalities, and wilms tumor

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