Search Results - "RENGO, C."

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    Cytotoxicity effects and differentiation potential of ormocer-based and nanohybrid composite resins on human dental pulp stem cells by Del Giudice, C., Rengo, C., Maglitto, M., Armogida, N.G., Iaculli, F., Rengo, S., Menale, C., Spagnuolo, G.

    Published in Dental materials (01-06-2024)
    “…to compare conventional nanohybrid (Ceram.x Spectra) and ormocer-based (Admira fusion) dental composite resins effects on human dental pulp stem cells (hDPSCs)…”
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    Journal Article
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    Effect of autoclaving on the surfaces of TiN-coated and conventional nickel-titanium rotary instruments by Spagnuolo, G., Ametrano, G., D'Antò, V., Rengo, C., Simeone, M., Riccitiello, F., Amato, M.

    Published in International endodontic journal (01-12-2012)
    “…Aim To evaluate the effects of repeated autoclave sterilization cycles on surface topography of conventional nickel–titanium ( NiTi ) and titanium nitride (…”
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    Journal Article
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    Marginal Leakage of Class V Composite Restorations Assessed Using Microcomputed Tomography and Scanning Electron Microscope by Rengo, C, Goracci, C, Ametrano, G, Chieffi, N, Spagnuolo, G, Rengo, S, Ferrari, M

    Published in Operative dentistry (01-07-2015)
    “…The aim of the study was to compare in Class V composite restorations marginal leakage measurements obtained with microcomputed tomography (micro-CT) and…”
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    Journal Article
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    Influence of phosphoric acid etching on microleakage of a self-etch adhesive and a self-adhering composite by Rengo, C, Goracci, C, Juloski, J, Chieffi, N, Giovannetti, A, Vichi, A, Ferrari, M

    Published in Australian dental journal (01-06-2012)
    “…Background:  The aim of this study was to evaluate the influence of preliminary phosphoric acid etching on the microleakage of a self‐adhering flowable…”
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    Journal Article
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    Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs by Di Lorenzo, C, Pierelli, F, Coppola, G, Grieco, G S, Rengo, C, Ciccolella, M, Magis, D, Bolla, M, Casali, C, Santorelli, F M, Schoenen, J

    Published in Neurology (05-05-2009)
    “…In migraine, an interictal reduction of mitochondrial energy metabolism and a preventive effect of high-dose riboflavin were reported. To explore the relation…”
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    Do the Four Clades of the mtDNA Haplogroup L2 Evolve at Different Rates? by Torroni, Antonio, Rengo, Chiara, Guida, Valentina, Cruciani, Fulvio, Sellitto, Daniele, Coppa, Alfredo, Calderon, Fernando Luna, Simionati, Barbara, Valle, Giorgio, Richards, Martin, Macaulay, Vincent, Scozzari, Rosaria

    Published in American journal of human genetics (01-12-2001)
    “…Forty-seven mtDNAs collected in the Dominican Republic and belonging to the African-specific haplogroup L2 were studied by high-resolution RFLP and…”
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    Journal Article
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    The wolframin His611Arg polymorphism influences medication overuse headache by Di Lorenzo, C., Sances, G., Di Lorenzo, G., Rengo, C., Ghiotto, N., Guaschino, E., Perrotta, A., Santorelli, F.M., Grieco, G.S., Troisi, A., Siracusano, A., Pierelli, F., Nappi, G., Casali, C.

    Published in Neuroscience letters (13-09-2007)
    “…Homozygosis for wolframin ( WFS1) mutations determines Wolfram syndrome (WS), and common polymorphisms of WFS1 are associated with psychiatric illnesses and…”
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    Journal Article
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    Identification of Native American Founder mtDNAs Through the Analysis of Complete mtDNA Sequences: Some Caveats by Bandelt, H.‐J., Herrnstadt, C., Yao, Y.‐G., Kong, Q.‐P., Kivisild, T., Rengo, C., Scozzari, R., Richards, M., Villems, R., Macaulay, V., Howell, N., Torroni, A., Zhang, Y.‐P.

    Published in Annals of human genetics (01-11-2003)
    “…Summary In this study, a detailed analysis of both previously published and new data was performed to determine whether complete, or almost complete, mtDNA…”
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    Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop by Cricchi, F, Di Lorenzo, C, Grieco, G.S, Rengo, C, Cardinale, A, Racaniello, M, Santorelli, F.M, Nappi, G, Pierelli, F, Casali, C

    Published in Journal of the neurological sciences (15-03-2007)
    “…Abstract Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with…”
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    Journal Article
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    The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype by Valentino, M L, Barboni, P, Rengo, C, Achilli, A, Torroni, A, Lodi, R, Tonon, C, Barbiroli, B, Fortuna, F, Montagna, P, Baruzzi, A, Carelli, V

    Published in Journal of medical genetics (01-07-2006)
    “…Background: Overlapping phenotypes including LHON, MELAS, and Leigh syndrome have recently been associated with numerous mtDNA point mutations in the ND5 gene…”
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    Journal Article
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    Phylogeography of the human mitochondrial haplogroup L3e: a snapshot of African prehistory and Atlantic slave trade by BANDELT, H.‐J., ALVES‐SILVA, J., GUIMARÃES, P. E. M., SANTOS, M. S., BREHM, A., PEREIRA, L., COPPA, A., LARRUGA, J. M., RENGO, C., SCOZZARI, R., TORRONI, A., PRATA, M. J., AMORIM, A., PRADO, V. F., PENA, S. D. J.

    Published in Annals of human genetics (01-11-2001)
    “…The mtDNA haplogroup L3e, which is identified by the restriction site +2349 MboI within the Afro‐Eurasian superhaplogroup L3 (−3592 HpaI), is omnipresent in…”
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    The ND1 gene of complex I is a mutational hot spot for Leber’s hereditary optic neuropathy by Valentino, M.L., Barboni, P., Ghelli, A., Bucchi, L., Rengo, C., Achilli, A., Torroni, A., Lugaresi, A., Lodi, R., Barbiroli, B., Dotti, M., Federico, A., Baruzzi, A., Carelli, V.

    Published in American journal of ophthalmology (01-02-2005)
    “…A novel mitochondrial DNA (mtDNA) transition (3733G--> A) inducing the E143 K amino acid change at a very conserved site of the NADH dehydrogenase subunit 1…”
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    Intervertebral disc lesions in diffuse idiopathic skeletal hyperostosis (DISH) by DI GIROLAMO, C, PAPPONE, N, RENGO, C, MINIERO, E, CRISCI, C, OLIVIERI, I

    Published in Clinical and experimental rheumatology (01-05-2001)
    “…In order to evaluate the relationships between DISH and vertebral osteochondrosis (degenerative disc disease), the radiographs of the spine of 69 DISH patients…”
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    Journal Article
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    Systemic sclerosis could mask the presentation of psoriasis in a patient with symptomatic and bilateral sacroiliitis by di Girolamo, C., Rengo, C., Ferrucci, M.G., Miniero, E., Cuomo, G., Crisci, C., Valentini, G.

    Published in Scandinavian journal of rheumatology (01-05-2003)
    “…Psoriasis is rarely associated with systemic sclerosis (SSc), and sacroiliitis associated to Connective Tissue Diseases is also rather rare. In this report we…”
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    Journal Article
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