Clarice Patrono
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Found 39 results
Filters: Author is Clarice Patrono
Editorial: Developing novel materials and new techniques of biological and physical retrospective dosimetry for affected individuals in radiological and nuclear emergencies,
, Frontiers in Public Health, Volume 10, (2023)
RENEB Inter-Laboratory Comparison 2021: Inter-Assay Comparison of Eight Dosimetry Assays ,
, Radiation Research, Jan-06-2023, Volume 199, Issue 6, (2023)
RENEB Inter-Laboratory Comparison 2021: The Cytokinesis-Block Micronucleus Assay,
, Radiation Research, Jan-06-2023, Volume 199, Issue 6, (2023)
RENEB Inter-Laboratory Comparison 2021: The Dicentric Chromosome Assay,
, Radiation Research, Jan-06-2023, Volume 199, Issue 6, (2023)
Background Level of Unstable Chromosome Aberrations in the Kazakhstan Population: A Human Biomonitoring Study,
, International journal of environmental research and public health, Volume 19, Number 14, (2022)
The role of dosimetry and biological effects in metastatic castration–resistant prostate cancer (mCRPC) patients treated with 223Ra: first in human study,
, Journal of Experimental and Clinical Cancer Research, Volume 40, Number 1, (2021)
NATO Science for Peace and Security (SPS) project “BioPhyMeTRE”: “Novel biological and physical methods for triage in radiological and nuclear (R/N) emergencies”,
, Nuovo Cimento della Societa Italiana di Fisica C, Volume 43, Number 6, (2020)
Analysis of Radiation-Induced Chromosomal Aberrations on a Cell-by-Cell Basis after Alpha-Particle Microbeam Irradiation: Experimental Data and Simulations,
, Radiation Research, Volume 189, Number 6, p.597-604, (2018)
Exposing primary rat retina cell cultures to γ-rays: An in vitro model for evaluating radiation responses,
, Experimental Eye Research, Volume 166, p.21-28, (2018)
Protein oxidative damage and redox imbalance induced by ionising radiation in CHO cells,
, Free Radical Research, Volume 52, Number 4, p.465-479, (2018)
INTEGRATED APPROACH TO DEVELOP INNOVATIVE TECHNOLOGY AND TRAINING OF OPERATORS-Biomedicine & Prevention (2017)-vol. 4-CBRNe safety,
, Special issue (PART 2)-(133)-DOI, Volume 10, p.000000085, (2017)
Integration of new biological and physical retrospective dosimetry methods into EU emergency response plans–joint RENEB and EURADOS inter-laboratory comparisons,
, International Journal of Radiation Biology, Volume 93, Number 1, p.99-109, (2017)
RENEB accident simulation exercise,
, International Journal of Radiation Biology, Volume 93, Number 1, p.75-80, (2017)
RENEB–Running the European Network of biological dosimetry and physical retrospective dosimetry,
, International Journal of Radiation Biology, Volume 93, Number 1, p.2-14, (2017)
'BioQuaRT' project: Design of a novel In Situ protocol for the simultaneous visualisation of chromosomal aberrations and micronuclei after irradiation at microbeam facilities,
, Radiation Protection Dosimetry, Volume 166, Number 1-4, p.197-199, (2015)
Polymorphisms in base excision repair genes: Breast cancer risk and individual radiosensitivity,
, World Journal of Clinical Oncology, Volume 5, Number 5, p.874-882, (2014)
Epidemiological, clinical, and molecular study of a cohort of Italian Parkinson disease patients: Association with glutathione-s-transferase and DNA repair gene polymorphisms,
, Cellular and Molecular Neurobiology, Volume 33, Number 5, p.673-680, (2013)
Single-nucleotide polymorphisms in BER and HRR genes, XRCC1 haplotypes and breast cancer risk in Caucasian women,
, Journal of Cancer Research and Clinical Oncology, Volume 136, Number 4, p.631-636, (2010)
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis,
, Brain, Volume 133, Number 2, p.591-598, (2010)
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity,
, European Journal of Neurology, Volume 16, Number 1, p.121-126, (2009)
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4,
, Neurology, Volume 70, Number 21, p.1959-1966, (2008)
Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.,
, Human mutation, Volume 25, Number 5, p.506, (2005)
Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNALys gene,
, Biochemical Journal, Volume 387, Number 3, p.773-778, (2005)
Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy.,
, Human mutation., Volume 25, Number 2, p.222, (2005)
Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cysts,
, Neurology, Volume 61, Number 4, p.534-537, (2003)