Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population by Maria Rachele Ceccarini, Maria Rachele Ceccarini, Simona Fittipaldi, Cinzia Ciccacci, Erika Granese, Federica Centofanti, Laura Dalla Ragione, Matteo Bertelli, Matteo Bertelli, Tommaso Beccari, Tommaso Beccari, Annalisa Botta

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Imbalance between Expression of FOXC2 and Its lncRNA in Lymphedema-Distichiasis Caused by Frameshift Mutations by Sara Missaglia, Daniela Tavian, Sandro Michelini, Paolo Enrico Maltese, Andrea Bonanomi, Matteo Bertelli

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<i>FOXC2</i> Disease Mutations Identified in Lymphedema Distichiasis Patients Impair Transcriptional Activity and Cell Proliferation by Daniela Tavian, Sara Missaglia, Sandro Michelini, Paolo Enrico Maltese, Elena Manara, Alvaro Mordente, Matteo Bertelli

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Paraneoplastic Neurological Syndromes: Study of Prevalence in a Province of the Lombardy Region, Italy by Lorenzo Lorusso, Vincenza Precone, Daniela Ferrari, Gaelle K. Ngonga, Antonio Giampiero Russo, Stefano Paolacci, Matteo Bertelli

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Comparison of 5-year progression of retinitis pigmentosa involving the posterior pole among siblings by means of SD-OCT: a retrospective study by Leonardo Colombo, Giovanni Montesano, Barbara Sala, Fabio Patelli, Paolo Maltese, Andi Abeshi, Matteo Bertelli, Luca Rossetti

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Breakdown of Symbiosis in Radiation-Induced Oral Mucositis by Gianluca Ingrosso, Simonetta Saldi, Simona Marani, Alicia Y. W. Wong, Matteo Bertelli, Cynthia Aristei, Teresa Zelante

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Multimodal Study of <i>PRPH2</i> Gene-Related Retinal Phenotypes by Giulio Antonelli, Mariacristina Parravano, Lucilla Barbano, Eliana Costanzo, Matteo Bertelli, Maria Chiara Medori, Vincenzo Parisi, Lucia Ziccardi

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Complete Androgen Insensitivity Syndrome: From the Relevance of an Accurate Genetic Diagnosis to the Challenge of Clinical Management. A Case Report by Federica Barbagallo, Rossella Cannarella, Matteo Bertelli, Andrea Crafa, Sandro La Vignera, Rosita A. Condorelli, Aldo E. Calogero

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Analysis of 29 Targeted Genes for Non-Obstructive Azoospermia: The Relationship between Genetic Testing and Testicular Histology by Rossella Cannarella, Matteo Bertelli, Rosita A. Condorelli, Marija Vilaj, Sandro La Vignera, Davor Jezek, Aldo E. Calogero

Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals by Paolo Enrico Maltese, Leonardo Colombo, Salvatore Martella, Luca Rossetti, Said El Shamieh, Lorenzo Sinibaldi, Lorenzo Sinibaldi, Chiara Passarelli, Andrea Maria Coppè, Luca Buzzonetti, Benedetto Falsini, Benedetto Falsini, Pietro Chiurazzi, Giorgio Placidi, Benedetta Tanzi, Matteo Bertelli, Matteo Bertelli, Giancarlo Iarossi

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Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure by Rossella Cannarella, Rosita A Condorelli, Stefano Paolacci, Federica Barbagallo, Giulia Guerri, Matteo Bertelli, Sandro La Vignera, Aldo E Calogero

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Impaired Ca²⁺ Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells by Valerio Marino, Giuditta Dal Cortivo, Paolo Enrico Maltese, Giorgio Placidi, Elisa De Siena, Benedetto Falsini, Matteo Bertelli, Daniele Dell’Orco

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A Novel <i>GUCA1A</i> Variant Associated with Cone Dystrophy Alters cGMP Signaling in Photoreceptors by Strongly Interacting with and Hyperactivating Retinal Guanylate Cyclase by Amedeo Biasi, Valerio Marino, Giuditta Dal Cortivo, Paolo Enrico Maltese, Antonio Mattia Modarelli, Matteo Bertelli, Leonardo Colombo, Daniele Dell’Orco

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Ultrastructural Sperm Flagellum Defects in a Patient With CCDC39 Compound Heterozygous Mutations and Primary Ciliary Dyskinesia/Situs Viscerum Inversus by Rossella Cannarella, Eugenia Tiziana Maniscalchi, Rosita Angela Condorelli, Marina Scalia, Giulia Guerri, Sandro La Vignera, Matteo Bertelli, Aldo Eugenio Calogero

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Recessive multiple epiphyseal dysplasia and Stargardt disease in two sisters by Leonardo Gatticchi, Dominika Vešelényiová, Jan Miertus, Paolo Enrico Maltese, Elena Manara, Alisia Costantini, Sabrina Benedetti, Darina Ďurovčíková, Juraj Krajcovic, Matteo Bertelli

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Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment by Stefano Paolacci, Aysha Karim Kiani, Elena Manara, Tommaso Beccari, Maria Rachele Ceccarini, Liborio Stuppia, Pietro Chiurazzi, Laura Dalla Ragione, Matteo Bertelli

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Development of Salmon Sperm DNA/Regenerated Silk Bio-Based Films for Biomedical Studies on Human Keratinocyte HaCaT Cells under Solar Spectrum by Maria Rachele Ceccarini, Francesca Ripanti, Veronica Raggi, Alessandro Paciaroni, Caterina Petrillo, Lucia Comez, Kevin Donato, Matteo Bertelli, Tommaso Beccari, Luca Valentini

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Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations by Stefano Paolacci, Raul Ettore Mattassi, Giuseppe Marceddu, Elena Manara, Alessandra Zulian, Giulia Guerri, Luca De Antoni, Carlo Arduino, Daniela Cavalca, Matteo Bertelli

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Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report by Angelo Maria Minnella, Valeria Pagliei, Maria Cristina Savastano, Matteo Federici, Matteo Bertelli, Paolo Enrico Maltese, Giorgio Placidi, Giovanni Corbo, Benedetto Falsini, Aldo Caporossi

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Investigation on the role of biallelic variants in VEGF‐C found in a patient affected by Milroy‐like lymphedema by Sylvain Mukenge, Sawan K. Jha, Marco Catena, Elena Manara, Veli‐Matti Leppänen, Elisa Lenti, Daniela Negrini, Matteo Bertelli, Andrea Brendolan, Michael Jeltsch, Luca Aldrighetti

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