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Beckwith–Wiedemann syndrome

International journal of oral and maxillofacial surgery, 2019-12, Vol.48 (12), p.1606-1607

Schendel, S.A.

2019

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Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

Trends in genetics, 2008-04, Vol.24 (4), p.195-204

2008

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Surgical treatment of macroglossia in patients with Beckwith–Wiedemann syndrome: a 20-year experience and review of the literature

International journal of oral and maxillofacial surgery, 2012-03, Vol.41 (3), p.300-308

2012

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Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

The Journal of pediatrics, 2016-09, Vol.176, p.142-149.e1

2016

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Tongue reduction in Beckwith–Wiedemann syndrome: outcome and treatment algorithm

International journal of oral and maxillofacial surgery, 2019-01, Vol.48 (1), p.9-16

2019

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CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Placenta (Eastbourne), 2009-06, Vol.30 (6), p.551-554

2009

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Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome

Journal of cranio-maxillo-facial surgery, 2023-09, Vol.51 (9), p.568-573

2023

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Pancreatic surgery in infants with Beckwith–Wiedemann Syndrome and Hyperinsulinism

Journal of pediatric surgery, 2013-12, Vol.48 (12), p.2511-2516

2013

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Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

Trends in Genetics, 1997-08, Vol.13 (8), p.330-334

1997

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Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome

Molecular genetics and metabolism, 2016-09, Vol.119 (1-2), p.8-13

2016

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CDKN1C mutations: two sides of the same coin

Trends in molecular medicine, 2014-11, Vol.20 (11), p.614-622

2014

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Long-term longitudinal evalutation of mandibular growth in patients with Beckwith-Wiedemann Syndrome treated and not treated with glossectomy

Journal of cranio-maxillo-facial surgery, 2020-12, Vol.48 (12), p.1126-1131

2020

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Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome

Journal of cranio-maxillo-facial surgery, 2016-06, Vol.44 (6), p.659-663

2016

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The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome

Current problems in pediatric and adolescent health care, 2015-04, Vol.45 (4), p.112-117

Pappas, John G., MD

2015

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Response to the Letter to the Editor in response to the publication “Tongue reduction in Beckwith–Wiedemann syndrome: outcome and treatment algorithm”

International journal of oral and maxillofacial surgery, 2019-12, Vol.48 (12), p.1607-1608

2019

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Management of macroglossia in Beckwith–Wiedemann syndrome

British journal of oral & maxillofacial surgery, 2013-01, Vol.51 (1), p.e6-e8

2013

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Insulin-like growth factor system on adrenocortical tumorigenesis

Molecular and cellular endocrinology, 2012-03, Vol.351 (1), p.96-100

2012

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Mitotic recombination and uniparental disomy in Beckwith–Wiedemann syndrome

Genomics (San Diego, Calif.), 2007-05, Vol.89 (5), p.613-617

2007

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Development of the Serum α-Fetoprotein Reference Range in Patients with Beckwith-Wiedemann Spectrum

The Journal of pediatrics, 2019-09, Vol.212, p.195-200.e2

2019

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Placental Mesenchymal Dysplasia with Beckwith–Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines

Placenta (Eastbourne), 2008-05, Vol.29 (5), p.454-460

2008

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Prevalence of Beckwith Wiedemann Syndrome and Risk of Embryonal Tumors in Children Born with Omphalocele

Journal of pediatric surgery, 2023-11, Vol.58 (11), p.2114-2118

2023

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Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia

The Journal of pediatrics, 2003-08, Vol.143 (2), p.270-272

2003

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The 11p15.5 chromosomal region: When did the instability occur?

Medical hypotheses, 2018-12, Vol.121, p.21-25

2018

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The spectrum of nephrocutaneous diseases and associations: Genetic causes of nephrocutaneous disease

Journal of the American Academy of Dermatology, 2016-02, Vol.74 (2), p.231-44; quiz 245-6

2016

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Long-term impact of tongue reduction on speech intelligibility, articulation and oromyofunctional behaviour in a child with Beckwith–Wiedemann syndrome

International journal of pediatric otorhinolaryngology, 2010-03, Vol.74 (3), p.309-318

2010

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Beckwith–Wiedemann syndrome

Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

Surgical treatment of macroglossia in patients with Beckwith–Wiedemann syndrome: a 20-year experience and review of the literature

Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

Tongue reduction in Beckwith–Wiedemann syndrome: outcome and treatment algorithm

CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome

Pancreatic surgery in infants with Beckwith–Wiedemann Syndrome and Hyperinsulinism

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome

CDKN1C mutations: two sides of the same coin

Long-term longitudinal evalutation of mandibular growth in patients with Beckwith-Wiedemann Syndrome treated and not treated with glossectomy

Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome

The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome

Response to the Letter to the Editor in response to the publication “Tongue reduction in Beckwith–Wiedemann syndrome: outcome and treatment algorithm”

Management of macroglossia in Beckwith–Wiedemann syndrome

Insulin-like growth factor system on adrenocortical tumorigenesis

Mitotic recombination and uniparental disomy in Beckwith–Wiedemann syndrome

Development of the Serum α-Fetoprotein Reference Range in Patients with Beckwith-Wiedemann Spectrum

Placental Mesenchymal Dysplasia with Beckwith–Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines

Prevalence of Beckwith Wiedemann Syndrome and Risk of Embryonal Tumors in Children Born with Omphalocele

Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia

The 11p15.5 chromosomal region: When did the instability occur?

The spectrum of nephrocutaneous diseases and associations: Genetic causes of nephrocutaneous disease

Long-term impact of tongue reduction on speech intelligibility, articulation and oromyofunctional behaviour in a child with Beckwith–Wiedemann syndrome

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