Piero Pignataro
Naples, Italy
Last Updated: 09/26/2026
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Found 18 publications
Peculiar footprints in a child with agenesis of corpus callosum.
Journal: Journal of paediatrics and child health
Published: June 02, 2020
The Pro12Ala polymorphism of PPARγ2 modulates beta cell function and failure to oral glucose-lowering drugs in patients with type 2 diabetes.
Journal: Diabetes/metabolism research and reviews
Published: May 08, 2020
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability.
Journal: Clinical genetics
Published: February 17, 2020
Two cases of 16q12.1q21 deletions and refinement of the critical region.
Journal: European journal of medical genetics
Published: July 16, 2019
Incidence of fatigue and low-dose corticosteroid use in prostate cancer patients receiving systemic treatment: a meta-analysis of randomized controlled trials.
Journal: World journal of urology
Published: October 27, 2018
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency.
Journal: Medical sciences (Basel, Switzerland)
Published: October 01, 2018
Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor.
Journal: International journal of cancer
Published: March 15, 2018
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
Journal: American journal of hematology
Published: January 29, 2018
Erratum to: Association Study between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
Journal: Journal of cardiovascular translational research
Published: July 14, 2017
Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
Journal: Journal of cardiovascular translational research
Published: April 03, 2017
Last Updated: 09/26/2026