檢索結果 - Sergio Cocozza
- Showing 1 - 11 results of 11
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Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARγ pathway as a therapeutic target in Friedreich’s ataxia 由 Giovanni Coppola, Daniele Marmolino, Daning Lu, Qing Wang, Miriam Cnop, Myriam Rai, Fabio Acquaviva, Sergio Cocozza, Massimo Pandolfo, Daniel H. Geschwind
出版 2009Artigo -
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Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease 由 Giorgio Casari, Maurizio De Fusco, Sonia Ciarmatori, Massimo Zeviani, Marina Mora, Patricio Fernández‐Silva, Giuseppe De Michele, Alessandro Filla, Sergio Cocozza, R. Marconi, A. Dürr, Bertrand Fontaine, Andrea Ballabio
出版 1998Artigo -
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Friedreich's ataxia: clinical and molecular study of 25 Brazilian cases 由 Lílian Maria José Albano, Mayana Zatz, Chong Ae Kim, Débora Romeo Bertola, Sofia M. M. Sugayama, Maria Joaquina Marques‐Dias, Fernando Kok, Ivan Ferraretto, Sérgio Rosemberg, Sergio Cocozza, Antonella Monticelli
出版 2001Artigo -
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A Combined Nucleic Acid and Protein Analysis in Friedreich Ataxia: Implications for Diagnosis, Pathogenesis and Clinical Trial Design 由 Francesco Saccà, Giorgia Puorro, Antonella Antenora, Angela Marsili, Alessandra Denaro, Raffaele Piro, Pierpaolo Sorrentino, Chiara Pane, Alessandra Tessa, Vincenzo Brescia Morra, Sergio Cocozza, Giuseppe De Michele, Filippo M. Santorelli, Alessandro Filla
出版 2011Artigo -
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Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder 由 Lorena Coretti, Claudia Cristiano, Ermanno Florio, Giovanni Scala, Adriano Lama, Simona Keller, Mariella Cuomo, Roberto Russo, Raffaela Pero, Orlando Paciello, Giuseppina Mattace Raso, Rosaria Meli, Sergio Cocozza, Antonio Calignano, Lorenzo Chiariotti, Francesca Lembo
出版 2017Artigo
相關主題
Biology
Genetics
Gene
Medicine
Ataxia
Neuroscience
Internal medicine
Allele
Frataxin
Iron-binding proteins
Phenotype
Psychiatry
Cell biology
Cerebral palsy
DNA
DNA damage
Disease
Endocrinology
Gene expression
Hereditary spastic paraplegia
Immunology
Mutation
Paraplegia
Pathology
Pediatrics
Spastic
Spinal cord
8-Hydroxy-2'-deoxyguanosine
Age of onset
Anticipation (artificial intelligence)