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Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines

International journal of molecular sciences, 2024-04, Vol.25 (7), p.3586

2024

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A supervised learning method for classifying methylation disorders

BMC bioinformatics, 2024-02, Vol.25 (1), p.66-66

2024

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Depression and Anxiety in Pediatric Patients with Beckwith-Wiedemann Syndrome: A Pilot Study

Children (Basel), 2024-03, Vol.11 (3), p.342

2024

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Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Plastic and reconstructive surgery. Global open, 2024-03, Vol.12 (3), p.e5635

2024

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Beckwith–Wiedemann syndrome with juvenile fibrous nodules and lobular breast tumors: a case report and review of the literature

Surgical case reports, 2024-03, Vol.10 (1), p.69-69

2024

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Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

Archives of endocrinology and metabolism, 2024-02, Vol.68, p.e220395

2024

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Evaluation of keyhole-pattern reduction glossoplasty for macroglossia in beckwith-wiedemann syndrome: A multidimensional analysis of postoperative course and outcomes

Journal of cranio-maxillo-facial surgery, 2024-02

2024

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Beckwith–Wiedemann Syndrome Diagnosed in the Early Second Trimester in Two Fetuses with Isolated Omphalocele

Journal of medical ultrasound, 2024-02

2024

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Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias

Fetal and pediatric pathology, 2024-04, p.1-9

2024

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Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith–Wiedemann Syndrome

Annals of laboratory medicine, 2022-11, p.668-677

2022

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Tongue Reduction Surgery Improves Mandibular Prognathism in Beckwith-Wiedemann Syndrome Without Compromising Tongue Function

Clinical and experimental otorhinolaryngology, 2023-02, p.67-74

2023

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P369: Acute lymphocytic leukemia in a child with Beckwith Wiedemann syndrome: Coincidence or related to loss of CDKN1C function?

Genetics in Medicine Open, 2024, Vol.2, p.101263

2024

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Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome

Journal of pathology and translational medicine, 2019-03, p.129-135

2019

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Beckwith–Wiedemann Syndrome

Handbook of Tumor Syndromes, 2020, p.683-697

1, 2020

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Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome

Genes & genomics, 2013-04, p.141-147

2013

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Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature

Frontiers in pediatrics, 2024-03, Vol.12, p.1334544

2024

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Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Plastic and reconstructive surgery. Global open, 2024, Vol.12 (3), p.e5635-e5635

2024

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Surgical approach to a rare case of Beckwith Wiedemann syndrome with left thigh hyperplasia

JPRAS open, 2024, Vol.39, p.303-306

2024

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Polyhydramnios associated with rare genetic syndromes: two case reports

Journal of medical case reports, 2024-02, Vol.18 (1), p.97-97

2024

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Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

Prenatal diagnosis, 2024-04

2024

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A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

Genes & development, 2024-03, Vol.38 (3-4), p.131

2024

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Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemia

Histology and histopathology, 2024-01, p.18709-18709

2024

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Locus-Specific and Stable DNA Demethylation at the IH19/I/IIGF2/I ICR1 by Epigenome Editing Using a dCas9-SunTag System and the Catalytic Domain of TET1

Genes, 2024-01, Vol.15 (1)

2024

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Familial Wilms Tumor and Related Syndromes

Handbook of Tumor Syndromes, 2020, p.253-258

Liu, Dongyou

1, 2020

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Simpson–Golabi–Behmel Syndrome

Handbook of Tumor Syndromes, 2020, p.769-773

Liu, Dongyou

1, 2020

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Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines

A supervised learning method for classifying methylation disorders

Depression and Anxiety in Pediatric Patients with Beckwith-Wiedemann Syndrome: A Pilot Study

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Beckwith–Wiedemann syndrome with juvenile fibrous nodules and lobular breast tumors: a case report and review of the literature

Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

Evaluation of keyhole-pattern reduction glossoplasty for macroglossia in beckwith-wiedemann syndrome: A multidimensional analysis of postoperative course and outcomes

Beckwith–Wiedemann Syndrome Diagnosed in the Early Second Trimester in Two Fetuses with Isolated Omphalocele

Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias

Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith–Wiedemann Syndrome

Tongue Reduction Surgery Improves Mandibular Prognathism in Beckwith-Wiedemann Syndrome Without Compromising Tongue Function

P369: Acute lymphocytic leukemia in a child with Beckwith Wiedemann syndrome: Coincidence or related to loss of CDKN1C function?

Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome

Beckwith–Wiedemann Syndrome

Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome

Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Surgical approach to a rare case of Beckwith Wiedemann syndrome with left thigh hyperplasia

Polyhydramnios associated with rare genetic syndromes: two case reports

Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemia

Locus-Specific and Stable DNA Demethylation at the IH19/I/IIGF2/I ICR1 by Epigenome Editing Using a dCas9-SunTag System and the Catalytic Domain of TET1

Familial Wilms Tumor and Related Syndromes

Simpson–Golabi–Behmel Syndrome

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