Search Results - "CHETTA, M."

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    A Copernican revolution of multigenic analysis: A retrospective study on clinical exome sequencing in unclear genetic disorders by Chetta, M., Tarsitano, M., Rivieccio, M., Oro, M., Cammarota, A.L., De Marco, M., Marzullo, L., Rosati, A., Bukvic, N.

    “…Despite the inevitable shift in medical practice towards a deeper understanding of disease etiology and progression through multigenic analysis, the profound…”
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    Journal Article
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    Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A by Bafunno, V., Santacroce, R., Chetta, M., Peyvandi, F., Sessa, F., Chinni, E., Longo, V., Margaglione, M.

    “…Summary Development of inhibitory antibodies is perhaps the most serious complication of FVIII replacement therapy, precluding efficient clinical management of…”
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    A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome by Chiofalo, M. G., Sparaneo, A., Chetta, M., Franco, R., Baorda, F., Cinque, L., Granatiero, M., D’Agruma, L., Pezzullo, L., Scillitani, A., Guarnieri, V.

    Published in Cellular oncology (Dordrecht) (01-08-2014)
    “…Purpose The CDC73 gene, encoding parafibromin, has been identified as a tumour suppressor gene both in hyperparathyroidism-jaw tumour (HPT-JT) syndrome and in…”
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    Journal Article
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    Severe outbreaks of polyarthritis in kids caused by Mycoplasma mycoides subspecies capri in Sicily by Agnello, S., Chetta, M., Vicari, D., Mancuso, R., Manno, C., Puleio, R., Console, A., Nicholas, R. A. J., Loria, G. R.

    Published in Veterinary record (01-04-2012)
    “…Mycoplasmas isolated were from the all joints and milk on farm A and from the joints, ears, lung, brain, kidney, spleen and liver on farm B. The organisms were…”
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    Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH by Bukvic, N., Carri, V. Delli, Di Cosola, M. L., Pustorino, G., Cesarano, C., Chetta, M., Santacroce, R., Sarno, M., Sessa, F., Longo, V., Novelli, A., Gentile, M., Margaglione, M.

    “…X;Y translocation is a relatively rare event in humans. Analyzed cytogenetically, the majority of these aberrations have breakpoints at Xp22 and Yq11. Females…”
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    Spirocerca lupi isolated from gastric lesions in foxes (Vulpes vulpes) in Sicily (Italy) by Ferrantelli, V, Riili, S, Vicari, D, Percipalle, M, Chetta, M, Monteverde, V, Gaglio, G, Giardina, G, Usai, F, Poglayen, G

    Published in Polish journal of veterinary sciences (01-01-2010)
    “…Spirocerca lupi (Rudolphi 1809) is a cosmopolitan nematode of dogs and wild carnivores. In the past it has been reported in Italy, mainly in southern regions…”
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    Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization by Chetta, M, Drmanac, A, Santacroce, R, Grandone, E, Surrey, S, Fortina, P, Margaglione, M

    Published in Indian journal of human genetics (01-05-2008)
    “…Standard methods of mutation detection are time consuming in Hemophilia A (HA) rendering their application unavailable in some analysis such as prenatal…”
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    A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin by D'Andrea, Giovanna, D'Ambrosio, Rosa Lucia, Di Perna, Pasquale, Chetta, Massimiliano, Santacroce, Rosa, Brancaccio, Vincenzo, Grandone, Elvira, Margaglione, Maurizio

    Published in Blood (15-01-2005)
    “…Patients require different warfarin dosages to achieve the target therapeutic anticoagulation. The variability is largely genetically determined, and it can be…”
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    Porous EH and EH-PEG Scaffolds as Gene Delivery Vehicles to Skeletal Muscle by Falco, Erin E., Wang, Martha O., Thompson, Joshua A., Chetta, Joshua M., Yoon, Diana M., Li, Erik Z., Kulkami, Mangesh M., Shah, Sameer, Pandit, Abhay, Roth, J. Scott, Fisher, John P.

    Published in Pharmaceutical research (01-06-2011)
    “…ABSTRACT Purpose Synthetic biomaterials are widely used in an attempt to control the cellular behavior of regenerative tissues. This can be done by altering…”
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    Gene polymorphisms and sport attitude in Italian athletes by Sessa, Francesco, Chetta, Massimiliano, Petito, Annamaria, Franzetti, Mauro, Bafunno, Valeria, Pisanelli, Daniela, Sarno, Michelina, Iuso, Salvatore, Margaglione, Maurizio

    Published in Genetic testing and molecular biomarkers (01-04-2011)
    “…The aim of this study was to evaluate whether the distribution of polymorphisms in the ACE, ACTN3, NOS3, UCP2, and UCP3 genes, which has been reported to be…”
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    Polymorphic mi RNA ‐mediated gene contribution to inhibitor development in haemophilia A by Bafunno, V., Santacroce, R., Chetta, M., Peyvandi, F., Sessa, F., Chinni, E., Longo, V., Margaglione, M.

    “…Development of inhibitory antibodies is perhaps the most serious complication of FVIII replacement therapy, precluding efficient clinical management of…”
    Get full text
    Journal Article
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    Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin by D'Ambrosio, RL, D'Andrea, G, Cappucci, F, Chetta, M, Di Perna, P, Brancaccio, V, Grandone, E, Margaglione, M

    Published in Haematologica (Roma) (01-12-2004)
    “…Istituto di Genetica Medica, Dipartimento di Scienze Biomediche, Universita di Foggia, Italy. BACKGROUND AND OBJECTIVES: There is very considerable…”
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