[HTML][HTML] Epigenetic regulation in premature ovarian failure: A literature review
J Wang, X Sun, Z Yang, S Li, Y Wang, R Ren… - Frontiers in …, 2023 - frontiersin.org
Premature ovarian failure (POF), or premature ovarian insufficiency (POI), is a multifactorial
and heterogeneous disease characterized by amenorrhea, decreased estrogen levels and …
and heterogeneous disease characterized by amenorrhea, decreased estrogen levels and …
[HTML][HTML] Maxillo-facial morphology in Beckwith-Wiedemann syndrome: A preliminary study on (epi) genotype-phenotype association in caucasians
P Defabianis, A Mussa, R Ninivaggi, D Carli… - International Journal of …, 2022 - mdpi.com
Beckwith–Wiedemann syndrome (BWS) is a congenital overgrowth disorder caused by
various (epi) genetic alterations affecting the expression of genes on chromosome 11p15 …
various (epi) genetic alterations affecting the expression of genes on chromosome 11p15 …
[HTML][HTML] Oral health-related quality of life among children and adolescents with Beckwith–Wiedemann syndrome in northern Italy
P Defabianis, R Ninivaggi, F Romano - Journal of Clinical Medicine, 2022 - mdpi.com
Due to associated maxillofacial growth anomalies and the impairment of oral functions,
macroglossia may negatively impact the oral health-related quality of life (OHRQoL) of …
macroglossia may negatively impact the oral health-related quality of life (OHRQoL) of …
[HTML][HTML] Investigation of 11p15. 5 Methylation Defects Associated with Beckwith-Wiedemann Spectrum and Embryonic Tumor Risk in Lateralized Overgrowth Patients
B Tüysüz, S Bozlak, D Uludağ Alkaya, S Ocak, B Kasap… - Cancers, 2023 - mdpi.com
Simple Summary Lateralized overgrowth may be isolated or accompany syndromes.
Recently, international BWS consensus proposed that the patients with isolated lateralized …
Recently, international BWS consensus proposed that the patients with isolated lateralized …
[HTML][HTML] Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines
S Pileggi, EA Colombo, S Ancona, R Quadri… - International Journal of …, 2024 - mdpi.com
Beckwith–Wiedemann Syndrome (BWS) is an imprinting disorder characterized by
overgrowth, stemming from various genetic and epigenetic changes. This study delves into …
overgrowth, stemming from various genetic and epigenetic changes. This study delves into …
[PDF][PDF] 罕见病Beckwith-Wiedemann 综合征1 例病例报告
李登峰， 陈名武， 方涛， 程舒鹏 - 中国循证儿科杂志, 2023 - cjebp.net
罕见病Beckwith⁃Wiedemann综合征1例病例报告 Page 1 基金项目中国科学技术大学附属第一
医院(安徽省立医院)创新项目:MAI2022C008;安徽省自然科学基金面上项目:1608085MH196 …
医院(安徽省立医院)创新项目:MAI2022C008;安徽省自然科学基金面上项目:1608085MH196 …
Alterações epigenéticas raras do Espectro de Beckwith-Wiedemann: Relato de caso
KC Lopes, HL Borges, FBC Ramos, LR Mikami… - …, 2022 - bioscience.org.br
INTRODUÇÃO: A Síndrome de Beckwith-Wiedemann é uma condição genética rara,
caracterizada por hipercrescimento congênito decorrente de uma alteração em 11p15. 5 …
caracterizada por hipercrescimento congênito decorrente de uma alteração em 11p15. 5 …