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A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome

International journal of surgery case reports, 2024-06, Vol.119, p.109777, Article 109777

2024

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40 years since genomic imprinting was discovered

Nature (London), 2024-05, Vol.629 (8013), p.763-765

2024

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A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome

International journal of surgery case reports, 2024, Vol.119, p.109777-109777

2024

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Expanded phenotype and cancer risk in patients with Beckwith-Wiedemann spectrum caused by CDKN1C variants

American journal of medical genetics. Part A, 2024-06, p.e63777-e63777

2024

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Imprinting disorders in children conceived with assisted reproductive technology in Sweden

Fertility and sterility, 2024-05

2024

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Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum

Autopsy & case reports, 2024, Vol.14, p.e2024486-e2024486

2024

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A case of pancreatoblastoma in a child with Simpson-Golabi-Behmel syndrome: Highlighting the importance of alpha fetoprotein monitoring

Pediatric blood & cancer, 2024-05, p.e31097-e31097

2024

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Pancreatic Lesions

iClinical Pediatric Surgery: A Case-Based Interactive Approach, 2020, p.565-574

Emil, Sherif

1, 2020

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Adrenocortical Neoplasms

iClinical Pediatric Surgery: A Case-Based Interactive Approach, 2020, p.558-564

Emil, Sherif

1, 2020

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Establishing a Standardized DNA Extraction Method Using NaCl from Oral Mucosa Cells for Its Application in Imprinting Diseases Such as Prader-Willi and Angelman Syndromes: A Preliminary Investigation

Genes, 2024-05, Vol.15 (5), p.641

2024

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Anatomic parameters of omphaloceles and their association with anatomic, genetic, or syndromic malformations: a retrospective study

Pediatric surgery international, 2024-05, Vol.40 (1), p.136-136

2024

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The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know

Children (Basel), 2024-05, Vol.11 (5), p.578

2024

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Congenital Heart Disease, Genetic Syndromes, and Childhood Cancer

Kampitsi, Christina-Evmorfia

2024

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ProQuest

Prune Belly Syndrome

The Kelalis-King-Belman, 2019, p.1108-1134

6, 2019

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Macrocephaly and Finger Changes: A Narrative Review

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5567

2024

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Epigenetic Features, Allelic Expression aand Transcriptional Regulatory Elements at the Peg13, Trappc9, Ago2 Imprinted Gene Cluster in Brain and Neural Cells

Claxton, Michael

2023

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ProQuest

Surgical Approaches for Pediatric and Adolescent Renal Tumors

The Kelalis-King-Belman, 2019, p.548-561

6, 2019

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Adrenal Tumors and Functional Consequences

The Kelalis-King-Belman, 2019, p.303-311

6, 2019

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Imprinted Grb10, encoding growth factor receptor bound protein 10, regulates fetal growth independently of the insulin-like growth factor type 1 receptor genes

BMC biology, 2024-05, Vol.22 (1)

2024

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Microcephaly Gene IMcph1/I Deficiency Induces p19ARF-Dependent Cell Cycle Arrest and Senescence

International journal of molecular sciences, 2024-05, Vol.25 (9)

2024

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Analysis of VEGF, IGF1/2 and the Long Noncoding RNA (lncRNA) H19 Expression in Polish Women with Endometriosis

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5271

2024

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Wilms' Tumor

The Kelalis-King-Belman, 2019, p.525-547

6, 2019

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Wilms Tumor

iClinical Pediatric Surgery: A Case-Based Interactive Approach, 2020, p.523-535

Emil, Sherif

1, 2020

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Anesthesia and Pain Management for the Pediatric Urology Patient

The Kelalis-King-Belman, 2019, p.234-247

6, 2019

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Pivotal functions and impact of long con-coding RNAs on cellular processes and genome integrity

Journal of biomedical science, 2024-05, Vol.31 (1), p.52-52

2024

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A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome

40 years since genomic imprinting was discovered

A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome

Expanded phenotype and cancer risk in patients with Beckwith-Wiedemann spectrum caused by CDKN1C variants

Imprinting disorders in children conceived with assisted reproductive technology in Sweden

Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum

A case of pancreatoblastoma in a child with Simpson-Golabi-Behmel syndrome: Highlighting the importance of alpha fetoprotein monitoring

Pancreatic Lesions

Adrenocortical Neoplasms

Establishing a Standardized DNA Extraction Method Using NaCl from Oral Mucosa Cells for Its Application in Imprinting Diseases Such as Prader-Willi and Angelman Syndromes: A Preliminary Investigation

Anatomic parameters of omphaloceles and their association with anatomic, genetic, or syndromic malformations: a retrospective study

The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know

Congenital Heart Disease, Genetic Syndromes, and Childhood Cancer

Prune Belly Syndrome

Macrocephaly and Finger Changes: A Narrative Review

Epigenetic Features, Allelic Expression aand Transcriptional Regulatory Elements at the Peg13, Trappc9, Ago2 Imprinted Gene Cluster in Brain and Neural Cells

Surgical Approaches for Pediatric and Adolescent Renal Tumors

Adrenal Tumors and Functional Consequences

Imprinted Grb10, encoding growth factor receptor bound protein 10, regulates fetal growth independently of the insulin-like growth factor type 1 receptor genes

Microcephaly Gene IMcph1/I Deficiency Induces p19ARF-Dependent Cell Cycle Arrest and Senescence

Analysis of VEGF, IGF1/2 and the Long Noncoding RNA (lncRNA) H19 Expression in Polish Women with Endometriosis

Wilms' Tumor

Wilms Tumor

Anesthesia and Pain Management for the Pediatric Urology Patient

Pivotal functions and impact of long con-coding RNAs on cellular processes and genome integrity

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