Search Results - "Carducci, C"

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  1. 1

    Uncertainty evaluation of the Unified Method for thermo-electric module characterization by D’Aucelli, G.M., Giaquinto, N., Guarnieri Caló Carducci, C., Spadavecchia, M., Trotta, A.

    “…•Uncertainty of the Unified Method for TEMs characterization is carried out.•The uncertainty is Evaluated by means of a Monte Carlo Simulation.•A sensitivity…”
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    Post-traumatic stress disorder (PTSD) in parents of children with type 1 diabetes during Covid-19 pandemic by Carducci, C, Rapini, N, Deodati, A, Pampanini, V, Cianfarani, S, Schiaffini, R

    Published in Italian journal of pediatrics (26-08-2021)
    “…Abstract Introduction The Post-traumatic Stress Disorder (PTSD) is a group of persistent psychological and physiological symptoms due to a traumatic, severe,…”
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    Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency by Leuzzi, V, Carducci, Ca, Carducci, Cl, Pozzessere, S, Burlina, A, Cerone, R, Concolino, D, Donati, MA, Fiori, L, Meli, C, Ponzone, A, Porta, F, Strisciuglio, P, Antonozzi, I, Blau, N

    Published in Clinical genetics (01-03-2010)
    “…Leuzzi V, Carducci Ca, Carducci Cl, Pozzessere S, Burlina A, Cerone R, Concolino D, Donati MA, Fiori L, Meli C, Ponzone A, Porta F, Strisciuglio P, Antonozzi…”
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    Comparison of two advanced hybrid closed loop in a pediatric population with type 1 diabetes: a real-life observational study by Schiaffini, R., Deodati, A., Nicoletti, M. C., Carducci, C., Ciampalini, P., Lorubbio, A., Matteoli, M. C., Pampanini, V., Patera, I. P., Rapini, N., Cianfarani, S.

    Published in Acta diabetologica (01-07-2022)
    “…Objective The Advanced Hybrid Closed Loop (AHCL) systems have provided the potential to ameliorate glucose control in children with Type 1 Diabetes. The aim of…”
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    PNKP deficiency mimicking a benign hereditary chorea: The misleading presentation of a neurodegenerative disorder by Caputi, C., Tolve, M., Galosi, S., Inghilleri, M., Carducci, C., Angeloni, A., Leuzzi, V.

    Published in Parkinsonism & related disorders (01-07-2019)
    “…PNKP gene encodes for a kinase/phosphatase involved in DNA damage response, controlled and stabilized by ATM phosphorylation. PNKP deficiency, thus far…”
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    Impact of long-term use of eHealth systems in adolescents with type 1 diabetes treated with sensor-augmented pump therapy by Schiaffini, R, Tagliente, I, Carducci, C, Ullmann, N, Ciampalini, P, Lorubbio, A, Cappa, M

    Published in Journal of telemedicine and telecare (01-07-2016)
    “…Telemedicine in diabetes includes telemonitoring and transmission of important data (self monitoring of blood glucose data, insulin therapy, pump setting,…”
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    Validation of the Italian Quality of Life in Short Stature Youth (QoLISSY) questionnaire by Quitmann, J., Giammarco, A., Maghnie, M., Napoli, F., Di Giovanni, I., Carducci, C., Mohn, A., Bullinger, M., Sommer, R.

    Published in Journal of endocrinological investigation (01-10-2017)
    “…Purpose The Quality of Life in Short Stature Youth (QoLISSY) questionnaire is a disease-specific instrument developed to assess health-related quality of life…”
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    Pregnancy in a Methylmalonic Acidemia Patient With Kidney Transplantation: A Case Report by Lubrano, R., Bellelli, E., Gentile, I., Paoli, S., Carducci, C., Carducci, C., Santagata, S., Pérez, B., Ugarte, M., Labriola, D., Elli, M.

    Published in American journal of transplantation (01-07-2013)
    “…Presently pregnancy is no more exceptional in women with metabolic diseases. However, it still poses significant medical problems both before and after…”
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    The spectrum of phenylalanine variations under tetrahydrobiopterin load in subjects affected by phenylalanine hydroxylase deficiency by Leuzzi, V., Carducci, C., Carducci, C., Chiarotti, F., Artiola, C., Giovanniello, T., Antonozzi, I.

    Published in Journal of inherited metabolic disease (01-02-2006)
    “…Summary A fall in blood phenylalanine (Phe) after tetrahydrobiopterin (BH4) administration is a common trait in phenylalanine hydroxylase (PAH, EC 1.14.16.1)…”
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    A link between lead and cadmium kinetic speciation in seawater and accumulation by the green alga Ulva lactuca by Muse, J.O., Carducci, C.N., Stripeikis, J.D., Tudino, M.B., Fernández, F.M.

    Published in Environmental pollution (1987) (01-05-2006)
    “…In this work, studies on the bioaccumulation of Cd and Pb by Ulva lactuca at different sites of Gulf San Jorge (Patagonia, Argentina) are presented. Higher…”
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    Brain creatine depletion : Guanidinoacetate methyltransferase deficiency (improving with creatine supplementation) by LEUZZI, V, BIANCHI, M. C, TOSETTI, M, CARDUCCI, C, CERQUIGLINI, A, CIONI, G, ANTONOZZI, I

    Published in Neurology (14-11-2000)
    “…The authors describe an Italian child with guanidinoacetate methyltransferase deficiency, neurologic regression, movement disorders, and epilepsy during the…”
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    Gypsum effects on the spatial distribution of coffee roots and the pores system in oxidic Brazilian Latosol by Carducci, C.E., Oliveira, G.C., Curi, N., Heck, R.J., Rossoni, D.F., de Carvalho, T.S., Costa, A.L.

    Published in Soil & tillage research (01-01-2015)
    “…The aim of this study was to jointly evaluate the root system and soil pore distribution in depth and their relation to the development of the coffee crop…”
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    Simultaneous determination of free and conjugated bile acids in serum by cyclodextrin-modified micellar electrokinetic chromatography by Tripodi, V.P., Lucangioli, S.E., Scioscia, S.L., Carducci, C.N.

    “…A simultaneous determination of 15 free and most conjugated forms of bile acids (BA) in serum using capillary electrophoresis is described. The optimized and…”
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    Biochemical features of mtDNA 14484 (ND6/m64V) point mutation associated with Leber's hereditary optic neuropathy by Carelli, V., Ghelli, A., Bucchi, L., Montagna, P., De Negri, A., Leuzzi, V., Carducci, C., Lenaz, G., Lugaresi, E., Degli Esposti, M.

    Published in Annals of neurology (01-03-1999)
    “…We report the effect on complex I function of the 14484 Leber's hereditary optic neuropathy (LHON) mutation affecting the ND6 subunit gene. The same gene was…”
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    Analysis of cis– trans isomers and enantiomers of sertraline by cyclodextrin-modified micellar electrokinetic chromatography by Lucangioli, S.E., Hermida, L.G., Tripodi, V.P., Rodrı́guez, V.G., López, E.E., Rouge, P.D., Carducci, C.N.

    Published in Journal of Chromatography A (25-02-2000)
    “…In this work development, optimization and validation of a cyclodextrin-modified micellar electrokinetic chromatography (CD-modified MEKC) method is proposed…”
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