Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome von 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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Dysbiosis in intestinal microbiome linked to fecal blood determined by direct hybridization von 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

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Post-operative interventional radiotherapy (brachytherapy) in advanced ocular surface and eyelid tumors as an alternative to surgical retreatment von 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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Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid von Sangiorgi, Eugenio, Giannuzzi, Federico, Molinario, Clelia, Rapari, Giulia, Riccio, Melania, Cuffaro, Giovanni, Castri, Federica, Benvenuto, Roberta, Genuardi, Maurizio, Massi, Daniela, Savino, Gustavo

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Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization von 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

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

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Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects von 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

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Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects von 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

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Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization von 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

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

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