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Maria Guarnaccia
Maria Guarnaccia
Afiliació desconeguda
Correu electrònic verificat a irib.cnr.it
Títol
Citada per
Citada per
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Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway
AR Fetoni, V Zorzi, F Paciello, G Ziraldo, C Peres, M Raspa, F Scavizzi, ...
Redox biology 19, 301-317, 2018
742018
Dysregulated miRNAs as biomarkers and therapeutical targets in neurodegenerative diseases
G Gentile, G Morello, V La Cognata, M Guarnaccia, FL Conforti, ...
Journal of Personalized Medicine 12 (5), 770, 2022
432022
Integrative multi-omic analysis identifies new drivers and pathways in molecularly distinct subtypes of ALS
G Morello, M Guarnaccia, AG Spampinato, S Salomone, V D’Agata, ...
Scientific reports 9 (1), 9968, 2019
422019
Is this the real time for genomics?
M Guarnaccia, G Gentile, E Alessi, C Schneider, S Petralia, S Cavallaro
Genomics 103 (2-3), 177-182, 2014
422014
A neurocutaneous phenotype with paired hypo-and hyperpigmented macules, microcephaly and stunted growth as prominent features
P Pavone, AD Praticò, G Gentile, R Falsaperla, R Iemmolo, M Guarnaccia, ...
European Journal of Medical Genetics 59 (5), 283-289, 2016
412016
A systems biology approach for personalized medicine in refractory epilepsy
GD Naimo, M Guarnaccia, T Sprovieri, C Ungaro, FL Conforti, S Andò, ...
International Journal of Molecular Sciences 20 (15), 3717, 2019
402019
Copy number variations in amyotrophic lateral sclerosis: piecing the mosaic tiles together through a systems biology approach
G Morello, M Guarnaccia, AG Spampinato, V La Cognata, V D’Agata, ...
Molecular neurobiology 55, 1299-1322, 2018
352018
Deletion of Voltage-Dependent Anion Channel 1 knocks mitochondria down triggering metabolic rewiring in yeast
A Magrì, MC Di Rosa, I Orlandi, F Guarino, S Reina, M Guarnaccia, ...
Cellular and Molecular Life Sciences 77, 3195-3213, 2020
322020
Endoscopic assisted cochlear implants in ear malformations
D Marchioni, D Soloperto, MC Guarnaccia, E Genovese, ...
European Archives of Oto-Rhino-Laryngology 272, 2643-2652, 2015
282015
Highlights on genomics applications for lysosomal storage diseases
V La Cognata, M Guarnaccia, A Polizzi, M Ruggieri, S Cavallaro
Cells 9 (8), 1902, 2020
252020
Endoscopic approach for cochlear implantation in advanced otosclerosis: a case report
D Marchioni, D Soloperto, L Bianconi, MC Guarnaccia, E Genovese, ...
Auris Nasus Larynx 43 (5), 584-590, 2016
232016
Miniaturized Real-Time PCR on a Q3 System for Rapid KRAS Genotyping
M Guarnaccia, R Iemmolo, S Petralia, S Conoci, S Cavallaro
Sensors 17 (4), 831, 2017
192017
Design and validation of a custom NGS panel targeting a set of lysosomal storage diseases candidate for NBS applications
V La Cognata, M Guarnaccia, G Morello, M Ruggieri, A Polizzi, ...
International Journal of Molecular Sciences 22 (18), 10064, 2021
132021
Genotyping of KRAS mutational status by the in-check lab-on-chip platform
M Guarnaccia, R Iemmolo, F San Biagio, E Alessi, S Cavallaro
Sensors 18 (1), 131, 2018
92018
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse Stria Vascularis
G Gentile, F Paciello, V Zorzi, AG Spampinato, M Guarnaccia, G Crispino, ...
Frontiers in Cell and Developmental Biology 8, 616878, 2021
82021
Genomic portrait of a sporadic amyotrophic lateral sclerosis case in a large spinocerebellar ataxia type 1 family
G Morello, G Gentile, R Spataro, AG Spampinato, M Guarnaccia, ...
Journal of Personalized Medicine 10 (4), 262, 2020
72020
Endoscopic approaches to middle ear cholesteatoma: classification and indications for surgery
D Marchioni, A Grammatica, E Genovese, MC Guarnaccia, D Villari, ...
Endoscopic ear surgery: principles, indications, and techniques. Stuttgart …, 2015
72015
CXCR2 is deregulated in ALS spinal cord and its activation triggers apoptosis in motor neuron-like cells overexpressing hSOD1-G93A
V La Cognata, AG D’Amico, G Maugeri, G Morello, M Guarnaccia, B Magrì, ...
Cells 12 (14), 1813, 2023
62023
New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation
I Stanghellini, E Genovese, S Palma, A Ravani, C Falcinelli, ...
Genetic Testing and Molecular Biomarkers 18 (12), 839-844, 2014
62014
A targeted next-generation sequencing panel to genotype gliomas
M Guarnaccia, L Guarnaccia, V La Cognata, SE Navone, R Campanella, ...
Life 12 (7), 956, 2022
52022
En aquests moments el sistema no pot dur a terme l'operació. Torneu-ho a provar més tard.
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