Pio A. D'adamo

Trieste, Italy

Last Updated: 09/26/2026

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Found 24 publications

Identification of a different DNA methylation pattern for pain related genes in children with intellectual disability: a cross-sectional study.

Identification of a different DNA methylation pattern for pain related genes in children with intellectual disability: a cross-sectional study.

Journal: Italian journal of pediatrics

Published: January 24, 2025

Post-procedure sedation and apnea linked to ion channel variant: a case report on dexmedetomidine-propofol interaction.

Post-procedure sedation and apnea linked to ion channel variant: a case report on dexmedetomidine-propofol interaction.

Journal: Frontiers in pharmacology

Published: December 21, 2024

Identification of a New Mutation in RSK2, the Gene for Coffin-Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes.

Identification of a New Mutation in RSK2, the Gene for Coffin-Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes.

Journal: Brain sciences

Published: July 28, 2021

Impact of Methylmercury and Other Heavy Metals Exposure on Neurocognitive Function in Children Aged 7 Years: Study Protocol of the Follow-up.

Impact of Methylmercury and Other Heavy Metals Exposure on Neurocognitive Function in Children Aged 7 Years: Study Protocol of the Follow-up.

Journal: Journal of epidemiology

Published: April 07, 2020

Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?

Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?

Journal: European journal of medical genetics

Published: November 23, 2017

Opioid Resistance Associated with CYP3A4 Hyperactivity and COMT Polymorphism in an Oncological Patient.

Opioid Resistance Associated with CYP3A4 Hyperactivity and COMT Polymorphism in an Oncological Patient.

Journal: Pain medicine (Malden, Mass.)

Published: October 11, 2017

Carbamazepine-induced thrombocytopenic purpura in a child: Insights from a genomic analysis.

Carbamazepine-induced thrombocytopenic purpura in a child: Insights from a genomic analysis.

Journal: Blood cells, molecules & diseases

Published: March 25, 2016

Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion.

Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion.

Journal: Brain : a journal of neurology

Published: December 15, 2015

Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways.

Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways.

Journal: Cell death & disease

Published: September 11, 2015

Pharmacogenetics and induction/consolidation therapy toxicities in acute lymphoblastic leukemia patients treated with AIEOP-BFM ALL 2000 protocol.

Pharmacogenetics and induction/consolidation therapy toxicities in acute lymphoblastic leukemia patients treated with AIEOP-BFM ALL 2000 protocol.

Journal: The pharmacogenomics journal

Published: May 04, 2015

Brain-derived neurotrophic factor serum levels in genetically isolated populations: gender-specific association with anxiety disorder subtypes but not with anxiety levels or Val66Met polymorphism.

Brain-derived neurotrophic factor serum levels in genetically isolated populations: gender-specific association with anxiety disorder subtypes but not with anxiety levels or Val66Met polymorphism.

Journal: PeerJ

Published: April 29, 2015

A nonsense mutation of human XRCC4 is associated with adult-onset progressive encephalocardiomyopathy.

A nonsense mutation of human XRCC4 is associated with adult-onset progressive encephalocardiomyopathy.

Journal: EMBO molecular medicine

Published: April 16, 2015

Showing 1-12 of 24

Last Updated: 09/26/2026