Publications by authors named "Clarice Patrono"

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RENEB/EURADOS field exercise 2019: robust dose estimation under outdoor conditions based on the dicentric chromosome assay.
David Endesfelder, Ursula Oestreicher, Ulrike Kulka, Elizabeth A Ainsbury, Jayne Moquet, Clarice Patrono

Int J Radiat Biol· July 2024

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Editorial: Developing novel materials and new techniques of biological and physical retrospective dosimetry for affected individuals in radiological and nuclear emergencies.
Nadica Maltar-Strmečki, Emanuela Bortolin, Laura Kenzhina, Clarice Patrono, Antonella Testa

Front Public Health· January 2023

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Background Level of Unstable Chromosome Aberrations in the Kazakhstan Population: A Human Biomonitoring Study.
Laura B Kenzhina, Aigul N Mamyrbayeva, Sergey N Lukashenko, Zhanat A Baigazinov, Dina B Biyakhmetova, Clarice Patrono

Int J Environ Res Public Health· July 2022

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The role of dosimetry and biological effects in metastatic castration-resistant prostate cancer (mCRPC) patients treated with Ra: first in human study.
Rosa Sciuto, Sandra Rea, Sara Ungania, Antonella Testa, Valentina Dini, Clarice Patrono

J Exp Clin Cancer Res· September 2021

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Dicentric Chromosome Assay (DCA) and Cytokinesis-Block Micronucleus (CBMN) Assay in the Field of Biological Dosimetry.
Antonella Testa, Valentina Palma, Clarice Patrono

Methods Mol Biol· April 2020

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Analysis of Radiation-Induced Chromosomal Aberrations on a Cell-by-Cell Basis after Alpha-Particle Microbeam Irradiation: Experimental Data and Simulations.
Antonella Testa, Francesca Ballarini, Ulrich Giesen, Octávia Monteiro Gil, Mario P Carante, Clarice Patrono

Radiat Res· June 2018

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Protein oxidative damage and redox imbalance induced by ionising radiation in CHO cells.
Donatella Pietraforte, Eleonora Paulicelli, Clarice Patrono, Lucrezia Gambardella, Giuseppe Scorza

Free Radic Res· April 2018

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Exposing primary rat retina cell cultures to γ-rays: An in vitro model for evaluating radiation responses.
Lucia Gaddini, Maria Balduzzi, Alessandro Campa, Giuseppe Esposito, Fiorella Malchiodi-Albedi, Clarice Patrono

Exp Eye Res· January 2018

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Integration of new biological and physical retrospective dosimetry methods into EU emergency response plans - joint RENEB and EURADOS inter-laboratory comparisons.
Elizabeth Ainsbury, Christophe Badie, Stephen Barnard, Grainne Manning, Jayne Moquet, Clarice Patrono

Int J Radiat Biol· January 2017

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RENEB accident simulation exercise.
Beata Brzozowska, Elizabeth Ainsbury, Annelot Baert, Lindsay Beaton-Green, Leonardo Barrios, Clarice Patrono

Int J Radiat Biol· January 2017

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RENEB - Running the European Network of biological dosimetry and physical retrospective dosimetry.
Ulrike Kulka, Michael Abend, Elizabeth Ainsbury, Christophe Badie, Joan Francesc Barquinero, Clarice Patrono

Int J Radiat Biol· January 2017

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Polymorphisms in base excision repair genes: Breast cancer risk and individual radiosensitivity.
Clarice Patrono, Silvia Sterpone, Antonella Testa, Renata Cozzi

World J Clin Oncol· December 2014

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Epidemiological, clinical, and molecular study of a cohort of Italian Parkinson disease patients: association with glutathione-S-transferase and DNA repair gene polymorphisms.
Tommaso Cornetta, Clarice Patrono, Irene Terrenato, Francesca De Nigris, Anna Rita Bentivoglio

Cell Mol Neurobiol· July 2013

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Single-nucleotide polymorphisms in BER and HRR genes, XRCC1 haplotypes and breast cancer risk in Caucasian women.
Silvia Sterpone, Valeria Mastellone, Luca Padua, Flavia Novelli, Clarice Patrono

J Cancer Res Clin Oncol· April 2010

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SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis.
Antonio Orlacchio, Carla Babalini, Antonella Borreca, Clarice Patrono, Roberto Massa

Brain· February 2010

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Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.
Belén Bornstein, José Antonio Mas, Clarice Patrono, Miguel Angel Fernández-Moreno, Emiliano González-Vioque

Biochem J· May 2005

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Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.
Clarice Patrono, Valentina Scarano, Federica Cricchi, Mariarosa A B Melone, Maria Chiriaco

Hum Mutat· May 2005

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Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy.
Giorgia Montagna, Antonella Di Biase, Marco Cappa, Mariarosa A B Melone, Carlo Piantadosi, Clarice Patrono

Hum Mutat· February 2005

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The relationship between anaerobic lactate threshold and plasma catecholamines during incremental exercise in hereditary spastic paraplegia.
Gabriele Siciliano, Livia Pasquali, Maria Laura Manca, Alberto Del Corona, Alessandra Tessa, Clarice Patrono

Funct Neurol· October 2003

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Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34.
Enza Maria Valente, Francesco Brancati, Viviana Caputo, Enrico Bertini, Clarice Patrono

Ann Neurol· June 2002

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Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegia.
Clarice Patrono, Carlo Casali, Alessandra Tessa, Federica Cricchi, Daniela Fortini

J Neurol· February 2002

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