Editorial: The genetics of inherited retinal diseases in understudied ethnic groups: Novel associations, challenges, and perspectives

por El Shamieh, Said, Maltese, Paolo Enrico
Publicado 2022

Molecular foundations of chiropractic therapy

por Maltese, Paolo Enrico, Michelini, Sandro, Baronio, Manuela, Bertelli, Matteo
Publicado 2019

BRUCH MEMBRANE RUPTURE AND CHOROIDAL NEOVASCULARIZATION COMPLICATING EXTENSIVE MACULAR ATROPHY WITH PSEUDODRUSEN-LIKE APPEARANCE: A CASE REPORT

por Romano, Dario, Colombo, Leonardo, Maltese, Paolo, Bertelli, Matteo, Rossetti, Luca M.
Publicado 2023

Genetic testing for autonomic dysfunction or dysautonomias

por Maltese, Paolo Enrico, Manara, Elena, Beccari, Tommaso, Dundar, Munis, Capodicasa, Natale, Bertelli, Matteo
Publicado 2020

Imbalance between Expression of FOXC2 and Its lncRNA in Lymphedema-Distichiasis Caused by Frameshift Mutations

por Missaglia, Sara, Tavian, Daniela, Michelini, Sandro, Maltese, Paolo Enrico, Bonanomi, Andrea, Bertelli, Matteo
Publicado 2021

FOXC2 Disease Mutations Identified in Lymphedema Distichiasis Patients Impair Transcriptional Activity and Cell Proliferation

por Tavian, Daniela, Missaglia, Sara, Michelini, Sandro, Maltese, Paolo Enrico, Manara, Elena, Mordente, Alvaro, Bertelli, Matteo
Publicado 2020

Comparison of 5-year progression of retinitis pigmentosa involving the posterior pole among siblings by means of SD-OCT: a retrospective study

por Colombo, Leonardo, Montesano, Giovanni, Sala, Barbara, Patelli, Fabio, Maltese, Paolo, Abeshi, Andi, Bertelli, Matteo, Rossetti, Luca
Publicado 2018

Neurobiological basis of chiropractic manipulative treatment of the spine in the care of major depression

por Kiani, Aysha Karim, Maltese, Paolo Enrico, Dautaj, Astrit, Paolacci, Stefano, Kurti, Danjela, Picotti, Pietro Maria, Bertelli, Matteo
Publicado 2020

Sudden unexplained death due to cardiac arrest

por Precone, Vincenza, Guerri, Giulia, Krasi, Geraldo, Lupi, Laura, Papa, Ilaria, Beccari, Tommaso, Maltese, Paolo Enrico, Manara, Elena, Bertelli, Matteo
Publicado 2019

FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function

por Tavian, Daniela, Missaglia, Sara, Maltese, Paolo E., Michelini, Sandro, Fiorentino, Alessandro, Ricci, Maurizio, Serrani, Roberta, Walter, Michael A., Bertelli, Matteo
Publicado 2016

Impaired Ca(2+) Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells

por Marino, Valerio, Dal Cortivo, Giuditta, Maltese, Paolo Enrico, Placidi, Giorgio, De Siena, Elisa, Falsini, Benedetto, Bertelli, Matteo, Dell’Orco, Daniele
Publicado 2021

Blue Cone Monochromatism with Foveal Hypoplasia Caused by the Concomitant Effect of Variants in OPN1LW/OPN1MW and GPR143 Genes

por Iarossi, Giancarlo, Coppè, Andrea Maria, Passarelli, Chiara, Maltese, Paolo Enrico, Sinibaldi, Lorenzo, Cappelli, Alessandro, Cetola, Sarah, Novelli, Antonio, Buzzonetti, Luca
Publicado 2021

A Novel GUCA1A Variant Associated with Cone Dystrophy Alters cGMP Signaling in Photoreceptors by Strongly Interacting with and Hyperactivating Retinal Guanylate Cyclase

por Biasi, Amedeo, Marino, Valerio, Dal Cortivo, Giuditta, Maltese, Paolo Enrico, Modarelli, Antonio Mattia, Bertelli, Matteo, Colombo, Leonardo, Dell’Orco, Daniele
Publicado 2021

Recessive multiple epiphyseal dysplasia and Stargardt disease in two sisters

por Gatticchi, Leonardo, Vešelényiová, Dominika, Miertus, Jan, Enrico Maltese, Paolo, Manara, Elena, Costantini, Alisia, Benedetti, Sabrina, Ďurovčíková, Darina, Krajcovic, Juraj, Bertelli, Matteo
Publicado 2021

Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy

por Iarossi, Giancarlo, Bertelli, Matteo, Maltese, Paolo Enrico, Gusson, Elena, Marchini, Giorgio, Bruson, Alice, Benedetti, Sabrina, Volpetti, Sabrina, Catena, Gino, Buzzonetti, Luca, Ziccardi, Lucia
Publicado 2017

Corrigendum to “Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy”

por Iarossi, Giancarlo, Bertelli, Matteo, Maltese, Paolo Enrico, Gusson, Elena, Marchini, Giorgio, Bruson, Alice, Benedetti, Sabrina, Volpetti, Sabrina, Catena, Gino, Buzzonetti, Luca, Ziccardi, Lucia
Publicado 2017

Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report

por Minnella, Angelo Maria, Pagliei, Valeria, Savastano, Maria Cristina, Federici, Matteo, Bertelli, Matteo, Maltese, Paolo Enrico, Placidi, Giorgio, Corbo, Giovanni, Falsini, Benedetto, Caporossi, Aldo
Publicado 2018

Resistance to Thyroid Hormones: A Case-Series Study

por Cannarella, Rossella, Musmeci, Marco, Garofalo, Vincenzo, Timpanaro, Tiziana A., Leone, Guido, Caruso, Manuela, Maltese, Paolo E., Condorelli, Rosita A., La Vignera, Sandro, Calogero, Aldo E.
Publicado 2022

Bacteriophages presence in nature and their role in the natural selection of bacterial populations

por Naureen, Zakira, Dautaj, Astrit, Anpilogov, Kyrylo, Camilleri, Giorgio, Dhuli, Kristjana, Tanzi, Benedetta, Maltese, Paolo Enrico, Cristofoli, Francesca, De Antoni, Luca, Beccari, Tommaso, Dundar, Munis, Bertelli, Matteo
Publicado 2020

Low Efficacy of Genetic Tests for the Diagnosis of Primary Lymphedema Prompts Novel Insights into the Underlying Molecular Pathways

por Bonetti, Gabriele, Paolacci, Stefano, Samaja, Michele, Maltese, Paolo Enrico, Michelini, Sandro, Michelini, Serena, Michelini, Silvia, Ricci, Maurizio, Cestari, Marina, Dautaj, Astrit, Medori, Maria Chiara, Bertelli, Matteo
Publicado 2022