Publications by authors named "Roberta Gallo"

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Hormone replacement therapy in gynecological cancer survivors and BRCA mutation carriers: a MITO group survey.
Innocenza Palaia, Giuseppe Caruso, Violante Di Donato, Camilla Turetta, Antonella Savarese, Roberta Gallo

J Gynecol Oncol· May 2024

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Vulvar Paget's Disease: A Systematic Review of the MITO Rare Cancer Group.
Giuseppe Caruso, Amelia Barcellini, Roberta Mazzeo, Roberta Gallo, Maria Giuseppa Vitale

Cancers (Basel)· March 2023

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Chemo-surgical approach in vulvar leiomyosarcoma: A case report.
Giuseppe Capalbo, Alessandra Logoteta, Roberta Gallo, Ilaria Cuccu, Gabriella Gentile

Tumori· December 2022

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Artificial neural networks reveal sex differences in gene methylation, and connections between maternal risk factors and symptom severity in autism spectrum disorder.
Andrea Stoccoro, Roberta Gallo, Sara Calderoni, Romina Cagiano, Filippo Muratori

Epigenomics· October 2022

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Correlation among maternal risk factors, gene methylation and disease severity in females with autism spectrum disorder.
Roberta Gallo, Andrea Stoccoro, Romina Cagiano, Vanessa Nicolì, Rosanna Ricciardi

Epigenomics· February 2022

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Radical Surgery After Neoadjuvant Chemotherapy for Locally Advanced Neuroendocrine Cancer of the Cervix.
Giuseppe Caruso, Innocenza Palaia, Violante DI Donato, Angelina Pernazza, Roberta Gallo

Anticancer Res· September 2021

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Physical and mental health in the oldest-old: a mixed-methods study on a southern Italy sample.
Rosa Angela Fabio, Roberta Gallo, Barbara Colombo

Aging Clin Exp Res· June 2021

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Investigation of GHSR methylation levels in thymomas from patients with Myasthenia Gravis.
Fabio Coppedè, Andrea Stoccoro, Vanessa Nicolì, Roberta Gallo, Anna De Rosa

Gene· August 2020

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Association of Polymorphisms in Genes Involved in One-Carbon Metabolism with Methylation Levels.
Fabio Coppedè, Andrea Stoccoro, Pierpaola Tannorella, Roberta Gallo, Vanessa Nicolì

Int J Mol Sci· July 2019

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Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations.
Fabio Coppedè, Andrea Stoccoro, Lorena Mosca, Roberta Gallo, Claudia Tarlarini

Amyotroph Lateral Scler Frontotemporal Degener· February 2018

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