Raffaella Stallone

Foggia, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

miRNA deregulation and relationship with metabolic parameters after Mediterranean dietary intervention in BRCA-mutated women.

miRNA deregulation and relationship with metabolic parameters after Mediterranean dietary intervention in BRCA-mutated women.

Journal: Frontiers in oncology

Published: January 18, 2023

Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines via the mTOR/GSK-3β Axis.

Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines via the mTOR/GSK-3β Axis.

Journal: Frontiers in immunology

Published: January 04, 2021

Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders.

Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders.

Journal: European journal of medical genetics

Published: October 25, 2017

Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome.

Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome.

Journal: American journal of medical genetics. Part A

Published: June 30, 2017

Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.

Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.

Journal: Molecular and cellular probes

Published: December 06, 2016

PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature.

PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature.

Journal: Molecular syndromology

Published: July 20, 2016

Clinical and molecular characterization of a de novo 19p13.3 microdeletion.

Clinical and molecular characterization of a de novo 19p13.3 microdeletion.

Journal: Molecular cytogenetics

Published: April 18, 2016

Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancer.

Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancer.

Journal: Nucleic acids research

Published: September 17, 2014

Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay.

Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay.

Journal: American journal of medical genetics. Part A

Published: September 12, 2014

Microdeletion of 12q24.31: report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms.

Microdeletion of 12q24.31: report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms.

Journal: American journal of medical genetics. Part A

Published: February 28, 2014

Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlation.

Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlation.

Journal: European journal of medical genetics

Published: May 11, 2012

An emerging phenotype of interstitial 15q25.2 microdeletions: clinical report and review.

An emerging phenotype of interstitial 15q25.2 microdeletions: clinical report and review.

Journal: American journal of medical genetics. Part A

Published: April 10, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026