Хайлтын үр дүнгүүд - Denise Cassandrini
- 5-н 1 - 5 үр дүнгүүдийг харуулж байна
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Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients -н E. Pennisi, Marcello Arca, Enrico Bertini, Claudio Bruno, Denise Cassandrini, Adele D’Amico, Matteo Garibaldi, F. Gragnani, Lorenzo Maggi, Roberto Massa, Sara Missaglia, Lucia Morandi, Olimpia Musumeci, Elena Pegoraro, Emanuele Rastelli, Filippo M. Santorelli, Elisabetta Tasca, Daniela Tavian, António Toscano, C. Angelini
Хэвлэсэн 2017Artigo -
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Next-generation sequencing approach to hyperCKemia -н Anna Rubegni, Alessandro Malandrini, Claudia Dosi, Guja Astrea, Jacopo Baldacci, Carla Battisti, Giulia Bertocci, Maria Alice Donati, Maria Teresa Dotti, Antonio Federico, Fabio Giannini, Salvatore Grosso, Renzo Guerrini, Sara Lenzi, Maria Antonietta Maioli, Federico Melani, Eugenio Mercuri, Michele Sacchini, Simona Salvatore, Gabriele Siciliano, Deborah Tolomeo, Paola Tonin, Nila Volpi, Filippo M. Santorelli, Denise Cassandrini
Хэвлэсэн 2019Artigo -
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MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients -н Chiara Fiorillo, Guja Astrea, Marco Savarese, Denise Cassandrini, Giacomo Brisca, Federica Trucco, Marina Pedemonte, Rosanna Trovato, Lucia Ruggiero, Liliana Vercelli, Adele D’Amico, Giorgio Tasca, Marika Pane, Francesco Mari, Luca Bello, Paolo Broda, Olimpia Musumeci, Carmelo Rodolico, Sonia Messina, Gian Luca Vita, Maria Sframeli, Sara Gibertini, Lucia Morandi, Marina Mora, Lorenzo Maggi, Antonio Petrucci, Roberto Massa, Marina Grandis, Arianna Toscano, Elena Pegoraro, Eugenio Mercuri, Enrico Bertini, Tiziana Mongini, Lucio Santoro, Vincenzo Nigro, Carlo Minetti, Filippo M. Santorelli, Claudio Bruno
Хэвлэсэн 2016Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Internal medicine
Medicine
Biology
Pediatrics
Gene
Genetics
Pathology
Bioinformatics
Biopsy
Cohort
Environmental health
Muscle biopsy
Myopathy
Population
Weakness
Age of onset
Anatomy
Asymptomatic
Cardiology
Cohort study
Congenital myopathy
Creatine kinase
Disease
Genetic diagnosis
Genetic heterogeneity
Genetic testing
Genotype
Human genetics
Hypotonia
MYH7