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Titolo Data di pubblicazione Autore(i) File
Neurons other than motor neurons in motor neuron disease 1-gen-2017 Ruffoli, R; Biagioni, F; Busceti, Cl; Gaglione, A; Ryskalin, L; Gambardella, S; Frati, A; Fornai, F
The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity 1-gen-2017 Gambardella, S; Ferese, R; Biagioni, F; Busceti, Cl; Campopiano, R; Griguoli, Amp; Limanaqi, F; Novelli, G; Storto, M; Fornai, F
Rapamycin promotes differentiation increasing beta III-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells 1-gen-2017 Ferrucci, M; Biagioni, F; Lenzi, P; Gambardella, S; Ferese, R; Calierno, Mt; Falleni, A; Grimaldi, A; Frati, A; Esposito, V; Limatola, C; Fornai, F
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 1-gen-2017 Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, L T; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E
Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion 1-gen-2017 De Cinque, Marianna; Palumbo, Orazio; Mazzucco, Ermelinda; Simone, Antonella; Palumbo, Pietro; Ciavatta, Renata; Maria, Giuliana; Ferese, Rosangela; Gambardella, Stefano; Angiolillo, Antonella; Carella, Massimo; Garofalo, Silvio
Next Generation Sequencing and ALS: known genes, different phenotyphes 1-gen-2017 Campopiano, Rosa; Ryskalin, Larisa; Giardina, Emiliano; Zampatti, Stefania; Busceti, Carla L; Biagioni, Francesca; Ferese, Rosangela; Storto, Marianna; Gambardella, Stefano; Fornai, Francesco
Revisiting the gamma loop in ALS 1-gen-2017 Limanaqi, Fiona; Gambardella, Stefano; Lazzeri, Gloria; Ferrucci, Michela; Ruggieri, Stefano; Fornai, Francesco
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 1-gen-2016 Cascella, R; Strafella, C; Gambardella, S; Longo, G; Borgiani, P; Sangiuolo, F; Novelli, G; Giardina, E
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 1-gen-2016 Ferese, R; Zampatti, S; Griguoli, Amp; Fornai, F; Giardina, E; Barrano, G; Albano, V; Campopiano, R; Scala, S; Novelli, G; Gambardella, S
The Autophagoproteasome a Novel Cell Clearing Organelle in Baseline and Stimulated Conditions 1-gen-2016 Lenzi, P; Lazzeri, G; Biagioni, F; Busceti, Cl; Gambardella, S; Salvetti, A; Fornai, F
Vacuolar Protein Sorting Genes in Parkinson's Disease: A Re-appraisal of Mutations Detection Rate and Neurobiology of Disease 1-gen-2016 Gambardella, S; Biagioni, F; Ferese, R; Busceti, Cl; Frati, A; Novelli, G; R, ; Fornai, F
Four copies of SNCA responsible of autosomal dominant Parkinson's disease in two Italian siblings 1-gen-2015 Modugno, N; Ferese, R; Campopiano, R; Zampatti, S; Giardina, E; Santilli, M; Nardone, A; Postorivo, D; Ruggieri, S; Fornai, F; Novelli, G; Gambardella, S
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 1-gen-2015 Cascella, R; Strafella, C; Ragazzo, M; Zampatti, S; Borgiani, P; Gambardella, S; Pirazzoli, A; Novelli, G; Giardina, E
Four Copies of SNCA Responsible for Autosomal Dominant Parkinson's Disease in Two Italian Siblings 1-gen-2015 Ferese, R; Modugno, N; Campopiano, R; Santilli, M; Zampatti, S; Giardina, E; Nardone, A; Postorivo, D; Fornai, F; Novelli, G; Romoli, E; Ruggieri, S; Gambardella, S
The Etiology of Acute Recurrent Pancreatitis in Children A Challenge for Pediatricians 1-gen-2011 Lucidi, V; Alghisi, F; Dall'Oglio, L; D'Apice, Mr; Monti, L; De Angelis, P; Gambardella, S; Angioni, A; Novelli, G
Novel mutations of TCOF1 gene in European patients with treacher Collins syndrome 1-gen-2011 Conte, C; D'Apice, Mr; Rinaldi, F; Gambardella, S; Sangiuolo, F; Novelli, G
Bone marrow and umbilical cord blood human mesenchymal stem cells: state of the art 1-gen-2010 Malgieri, A; Kantzari, E; Patrizi, Mp; Gambardella, S
New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis? 1-gen-2010 Corleto, Vd; Gambardella, S; Gullotta, F; D'Apice, Mr; Piciucchi, M; Galli, E; Lucidi, V; Novelli, G; Delle Fave, G
Variations of Inflammatory Mediators and alpha(1)-Antitrypsin Levels after Lung Volume Reduction Surgery for Emphysema 1-gen-2010 Mineo, D; Ambrogi, V; Cufari, Me; Gambardella, S; Pignotti, L; Pompeo, E; Mineo, Tc
Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal Abnormalities 1-gen-2010 Gambardella, S; Ciabattoni, E; Motta, F; Stoico, G; Gullotta, F; Biancolella, M; Nardone, Am; Novelli, A; Brunetti, E; Bernardini, L; Novelli, G
Mostrati risultati da 41 a 60 di 78
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