Search Results - "Calvo Malvar, Nahúm"

Phantom, clinical, and texture indices evaluation and optimization of a penalized‐likelihood image reconstruction method (Q.Clear) on a BGO PET/CT scanner by Reynés‐Llompart, Gabriel, Gámez‐Cenzano, Cristina, Vercher‐Conejero, José Luis, Sabaté‐Llobera, Aida, Calvo‐Malvar, Nahúm, Martí‐Climent, Josep M

“…Introduction The aim of this study was to evaluate the behavior of a penalized‐likelihood image reconstruction method (Q.Clear) under different count…”
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Evaluation of Dysphagia in Motor Neuron Disease. Review of Available Diagnostic Tools and New Perspectives by Romero-Gangonells, Elisabet, Virgili-Casas, M. Núria, Dominguez-Rubio, Raúl, Povedano, Mònica, Pérez-Saborit, Núria, Calvo-Malvar, Nahum, Barceló, Maria A.

“…Oropharyngeal dysphagia (OD) is highly prevalent (up to 80%) in patients with motor neuron disease (MND), influencing the prognosis of the disease. The…”
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Phantom, clinical, and texture indices evaluation and optimization of a penalized-likelihood image reconstruction method (Q.Clear) on a BGO PET/CT scanner by Reynés-Llompart, Gabriel, Gámez Cenzano, Cristina, Vercher Conejero, José Luís, Sabaté Llobera, Aida, Calvo Malvar, Nahúm, Martí Climent, Josep M

“…INTRODUCTION: The aim of this study was to evaluate the behavior of a penalized-likelihood image reconstruction method (Q.Clear) under different count…”
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Efficacy and safety clinical trial with efavirenz in patients diagnosed with adult Niemann-pick type C with cognitive impairment by Gascón-Bayarri, Jordi, Simon, Petru Cristian, Llop, Roser, Carnaval, Thiago, Ledesma, María Dolores, Rico, Imma, Sánchez-Castañeda, Cristina, Campdelacreu-Fumadó, Jaume, Calvo-Malvar, Nahum, Cos, Mònica, de Lama, Eugenia, Cortés-Romera, Montserrat, Rodríguez-Bel, Laura, Pérez-Sousa, Celia, Cerdán Sánchez, María, Muelas, Nuria, Sevillano, María Dolores, Mir, Pablo, López de Munain, Adolfo, Ferrer, Anna, Videla, Sebastián

“…Niemann-Pick disease Type C (NPC) is a genetic, incurable, neurodegenerative disorder. This orphan disease is most frequently caused by mutations in the NPC1…”
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