Clinical, genetic, and prognostic features of adrenocortical tumors inchildren. A 10-year single-center experience

Autor: Maria Debora De Pasquale, Rita Alaggio, Maria Giuseppina Cefalo, Aurora Castellano, Annalisa Serra, Alessandro Crocoli, Angela Di Giannatale, Evelina Miele, Raffaele Cozza, Antonella Cacchione

Publikováno v: Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology

Background and Aims: Pediatric adrenocortical tumors (ACTs) are very rare endocrine neoplasms in childhood. In this study, we performed a retrospective analysis of children with ACT treated at our institution by examining clinical and genetic disease

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d4ca4072c7763a4238ff25c4ff8802d
http://hdl.handle.net/11573/1626261

El tumor de Wilms. Un paradigma de heterogeneidad genética: a paradigm of genetic heterogeneity Wilm's toumor

Autor: Rolando A Hernández Fernández

Publikováno v: Revista Habanera de Ciencias Médicas, Vol 10, Iss 2, p 0 (2011)

El Tumor de Wilms constituye el más frecuente de los cánceres renales pediátricos, aparece antes de los 5 años de edad y con igual frecuencia en ambos sexos. El gen causante de la enfermedad está localizado en 11p13, se extiende unas 50 kb con 1

Externí odkaz: https://doaj.org/article/99e4594a974846119028cf70105117ea

Relaxation of Insulin-like Growth Factor 2 Imprinting and Discordant Methylation at KvDMR1 in Two First Cousins Affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber Syndromes

Autor: Paola Ungaro, Paolo V. Pedone, Flavia Cerrato, Andrea Riccio, Stefano Casola, Maria Vernucci, Carmelo B. Bruni, Gianfranco Sebastio, Maria Pia Sperandeo, Maria Vittoria Cubellis, Generoso Andria, Lucia Perone

Publikováno v: American journal of human genetics (Online) (2000).
info:cnr-pdr/source/autori:Sperandeo MP, Ungaro P, Vernucci M, Pedone PV, Cerrato F, Perone L, Casola S, Cubellis MV, Bruni CB, Andria G, Sebastio G, Riccio A./titolo:Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes./doi:/rivista:American journal of human genetics (Online)/anno:2000/pagina_da:/pagina_a:/intervallo_pagine:/volume

Beckwith-Wiedeman syndrome (BWS) and Klippel-Trenaunay-Weber syndrome (KTWS) are different human disorders characterized, among other features, by tissue overgrowth. Deregulation of one or more imprinted genes located at chromosome 11p15.5, of which

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa74193fdfaec98cea3ae08b9ed9841
http://hdl.handle.net/11588/515524

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