Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: PELO[original query] |
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Fundus phenotype in retinitis pigmentosa associated with EYS mutations. Ophthalmic genetics 2018 8 39 (5): 589-602. Mucciolo Dario Pasquale, Sodi Andrea, Passerini Ilaria, Murro Vittoria, Cipollini Francesca, Borg Isabella, Pelo Elisabetta, Contini Elisa, Virgili Gianni, Rizzo Stanisl |
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease. Ophthalmic genetics 2018 Oct 1-7. Sodi Andrea, Passerini Ilaria, Bacherini Daniela, Boni Luca, Palchetti Simona, Murro Vittoria, Caporossi Orsola, Mucciolo Dario Pasquale, Franco Fabrizio, Vannozzi Lorenzo, Torricelli Francesca, Pelo Elisabetta, Rizzo Stanislao, Virgili Gian |
S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy. Italian journal of pediatrics 2018 1 44 (1): 2. Terlizzi Vito, Di Lullo Antonella Miriam, Comegna Marika, Centrone Claudia, Pelo Elisabetta, Castaldo Giuseppe, Raia Valeria, Braggion Cesa |
Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes.
Diabetes 2021 Dec . O'Connor Mark J, Schroeder Philip, Huerta-Chagoya Alicia, Cortés-Sánchez Paula, Bonàs-Guarch Silvía, Guindo-Martínez Marta, Cole Joanne B, Kaur Varinderpal, Torrents David, Veerapen Kumar, Grarup Niels, Kurki Mitja, Rundsten Carsten F, Pedersen Oluf, Brandslund Ivan, Linneberg Allan, Hansen Torben, Leong Aaron, Florez Jose C, Mercader Josep |
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy. Scientific reports 2022 12 12 (1): 20815. Karali Marianthi, Testa Francesco, Di Iorio Valentina, Torella Annalaura, Zeuli Roberta, Scarpato Margherita, Romano Francesca, Onore Maria Elena, Pizzo Mariateresa, Melillo Paolo, Brunetti-Pierri Raffaella, Passerini Ilaria, Pelo Elisabetta, Cremers Frans P M, Esposito Gabriella, Nigro Vincenzo, Simonelli Francesca, Banfi Sand |
X-linked retinoschisis: mutation spectrum and genotype-phenotype relationship in an Italian pediatric cohort. Ophthalmic genetics 2022 11 44 (1): 35-42. Fortunato P, Pagliazzi A, Bargiacchi S, Marziali E, Sodi A, Caputo R, Passerini I, Pelo E, Bacci G |
Genetic analysis of suicide: a sample study in Tuscany (Central Italy). Forensic sciences research 2023 2 7 (4): 790-797. Focardi Martina, Gualco Barbara, Pinchi Vilma, Gian-Aristide Norelli, Rensi Regina, Pelo Elisabetta, Carboni Ilaria, Ricci U |
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- Page last updated:Apr 16, 2024
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