Search Results - Renieri, Alessandra
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COVID-19: a challenge and an opportunity by Renieri, Alessandra
Published 2022Text -
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First Identification of a Triple Corneal Dystrophy Association: Keratoconus, Epithelial Basement Membrane Corneal Dystrophy and Fuchs’ Endothelial Corneal Dystrophy by Mazzotta, Cosimo, Traversi, Claudio, Raiskup, Frederik, Rizzo, Caterina Lo, Renieri, Alessandra
Published 2014Text -
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The role of surgical lung biopsy in the management of interstitial lung disease: experience from a single institution in the UK by Blackhall, Vivienne, Asif, Mohammed, Renieri, Alessandra, Civitelli, Serenella, Kirk, Alan, Jilaihawi, Ali, Granato, Felice
Published 2013Text -
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In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in Euro... by Isidori, Andrea M., Marcelli, Marco, Castagna, Maria Grazia, Baldassarri, Margherita, Fava, Francesca, Renieri, Alessandra
Published 2021Text -
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Identification of a Novel SHANK2 Pathogenic Variant in a Patient with a Neurodevelopmental Disorder by Doddato, Gabriella, Fabbiani, Alessandra, Scandurra, Valeria, Canitano, Roberto, Mencarelli, Maria Antonietta, Renieri, Alessandra, Ariani, Francesca
Published 2022Text -
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Reduced expression of MECP2 affects cell commitment and maintenance in neurons by triggering senescence: new perspective for Rett syndrome by Squillaro, Tiziana, Alessio, Nicola, Cipollaro, Marilena, Melone, Mariarosa Anna Beatrice, Hayek, Giuseppe, Renieri, Alessandra, Giordano, Antonio, Galderisi, Umberto
Published 2012Text -
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Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams–Beuren Region by Comparative Genomics by Cupaioli, Francesca Anna, Fallerini, Chiara, Mencarelli, Maria Antonietta, Perticaroli, Valentina, Filippini, Virginia, Mari, Francesca, Renieri, Alessandra, Mezzelani, Alessandra
Published 2021Text -
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Nosological and Theranostic Approach to Vascular Malformation through cfDNA NGS Liquid Biopsy by Serio, Viola Bianca, Palmieri, Maria, Loberti, Lorenzo, Granata, Stefania, Fallerini, Chiara, Vaghi, Massimo, Renieri, Alessandra, Pinto, Anna Maria
Published 2022Text -
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Prognostic Value of Glomerular Collagen IV Immunofluorescence Studies in Male Patients with X-Linked Alport Syndrome by Massella, Laura, Gangemi, Concetta, Giannakakis, Kostas, Crisafi, Antonella, Faraggiana, Tullio, Fallerini, Chiara, Renieri, Alessandra, Muda, Andrea Onetti, Emma, Francesco
Published 2013Text -
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Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress by Imperatore, Valentina, Mencarelli, Maria Antonietta, Fallerini, Chiara, Bianciardi, Laura, Ariani, Francesca, Furini, Simone, Renieri, Alessandra, Mari, Francesca, Frullanti, Elisa
Published 2016Text -
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Functional Connectivity and Genetic Profile of a “Double-Cortex”-Like Malformation by Sprugnoli, Giulia, Vatti, Giampaolo, Rossi, Simone, Cerase, Alfonso, Renieri, Alessandra, Mencarelli, Maria A., Zara, Federico, Rossi, Alessandro, Santarnecchi, Emiliano
Published 2018Text -
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X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases by Mastrangelo, Antonio, Giani, Marisa, Groppali, Elena, Castorina, Pierangela, Soldà, Giulia, Robusto, Michela, Fallerini, Chiara, Bruttini, Mirella, Renieri, Alessandra, Montini, Giovanni
Published 2020Text -
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The effect of angiotensin-converting enzyme levels on COVID-19 susceptibility and severity: a Mendelian randomization study by Butler-Laporte, Guillaume, Nakanishi, Tomoko, Mooser, Vincent, Renieri, Alessandra, Amitrano, Sara, Zhou, Sirui, Chen, Yiheng, Forgetta, Vincenzo, Richards, J Brent
Published 2020Text -
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A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier by Petrosyan, Astgik, Cravedi, Paolo, Villani, Valentina, Angeletti, Andrea, Manrique, Joaquin, Renieri, Alessandra, De Filippo, Roger E., Perin, Laura, Da Sacco, Stefano
Published 2019Text -
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Author Correction: A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier by Petrosyan, Astgik, Cravedi, Paolo, Villani, Valentina, Angeletti, Andrea, Manrique, Joaquin, Renieri, Alessandra, De Filippo, Roger E., Perin, Laura, Da Sacco, Stefano
Published 2019Text -
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A Mutation in the Rett Syndrome Gene, MECP2, Causes X-Linked Mental Retardation and Progressive Spasticity in Males by Meloni, Ilaria, Bruttini, Mirella, Longo, Ilaria, Mari, Francesca, Rizzolio, Flavio, D’Adamo, Patrizia, Denvriendt, Koenraad, Fryns, Jean-Pierre, Toniolo, Daniela, Renieri, Alessandra
Published 2000Text -
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Capping of the N-terminus of PSD-95 by calmodulin triggers its postsynaptic release by Zhang, Yonghong, Matt, Lucas, Patriarchi, Tommaso, Malik, Zulfiqar A, Chowdhury, Dhrubajyoti, Park, Deborah K, Renieri, Alessandra, Ames, James B, Hell, Johannes W
Published 2014Text