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