Search Results - Molinario, Clelia

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  1. 1
    Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome

    Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome by Sangiorgi, Eugenio, Azzarà, Alessia, Molinario, Clelia, Pietrobono, Roberta, Rigante, Donato, Verrecchia, Elena, Sicignano, Ludovico Luca, Genuardi, Maurizio, Gurrieri, Fiorella, Manna, Raffaele

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  2. 2
    Dysbiosis in intestinal microbiome linked to fecal blood determined by direct hybridization

    Dysbiosis in intestinal microbiome linked to fecal blood determined by direct hybridization by Cafiero, Concetta, Re, Agnese, Pisconti, Salvatore, Trombetti, Marina, Perri, Mariarita, Colosimo, Manuela, D’Amato, Gerardo, Gallelli, Luca, Cannataro, Roberto, Molinario, Clelia, Fazio, Alessia, Caroleo, Maria Cristina, Cione, Erika

    Published in 3 Biotech
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  3. 3
    Post-operative interventional radiotherapy (brachytherapy) in advanced ocular surface and eyelid tumors as an alternative to surgical retreatment

    Post-operative interventional radiotherapy (brachytherapy) in advanced ocular surface and eyelid tumors as an alternative to surgical retreatment by Cuffaro, Giovanni, Fionda, Bruno, Piccinni, Fabrizio, Pagliara, Monica Maria, Sammarco, Maria Grazia, Blasi, Maria Antonietta, Molinario, Clelia, Castri, Federica, Tagliaferri, Luca, Massi, Daniela, Savino, Gustavo

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  4. 4
    Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid

    Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid by Sangiorgi, Eugenio, Giannuzzi, Federico, Molinario, Clelia, Rapari, Giulia, Riccio, Melania, Cuffaro, Giovanni, Castri, Federica, Benvenuto, Roberta, Genuardi, Maurizio, Massi, Daniela, Savino, Gustavo

    Published in Genes
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  5. 5
    Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization

    Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization by Tabolacci, Elisabetta, Molinario, Clelia, Marangi, Giuseppe, Nobile, Veronica, Arena, Vincenzo, Mendes, Marisa I., Smith, Desiree E. C., Salomons, Gajja S., Tana, Milena, Costa, Simonetta, Vento, Giovanni, Genuardi, Maurizio

    Published in Clinical genetics
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  6. 6
    Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura

    Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura by Milillo, Annamaria, Molinario, Clelia, Costanzi, Stefano, Vischini, Gisella, La Carpia, Francesca, La Greca, Francesco, Rigante, Donato, Gambaro, Giovanni, Gurrieri, Fiorella, Sangiorgi, Eugenio

    Published in Journal of nephrology
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  7. 7
    Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects

    Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects by Francesca, La Carpia, Claudia, Rendeli, Molinario, Clelia, Annamaria, Milillo, Chiara, Farroni, Natalia, Cannelli, Emanuele, Ausili, Valentina, Paolucci, Giovanni, Neri, Costantino, Romagnoli, Eugenio, Sangiorgi, Fiorella, Gurrieri

    Published in Child's nervous system
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  8. 8
    Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects

    Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects by La Carpia, Francesca, Rendeli, Claudia, Molinario, Clelia, Milillo, Annamaria, Farroni, Chiara, Cannelli, Natalia, Ausili, Emanuele, Paolucci, Valentina, Neri, Giovanni, Romagnoli, Costantino, Sangiorgi, Eugenio, Gurrieri, Fiorella

    Published in Child's nervous system
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  9. 9
    Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization

    Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization by Tabolacci, Elisabetta, Molinario, Clelia, Marangi, Giuseppe, Nobile, Veronica, Arena, Vincenzo, Mendes, Marisa I, Smith, Desiree E C, Salomons, Gajja S, Tana, Milena, Costa, Simonetta, Vento, Giovanni, Genuardi, Maurizio

    Published in Clinical genetics
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  10. 10
    Dysbiosis in intestinal microbiome linked to fecal blood determined by direct hybridization

    Dysbiosis in intestinal microbiome linked to fecal blood determined by direct hybridization by Cafiero, Concetta, Re, Agnese, Pisconti, Salvatore, Trombetti, Marina, Perri, Mariarita, Colosimo, Manuela, D'Amato, Gerardo, Gallelli, Luca, Cannataro, Roberto, Molinario, Clelia, Fazio, Alessia, Caroleo, Maria Cristina, Cione, Erika

    Published in 3 Biotech
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