Risultati della ricerca - Simona Portaro

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  1. 1
    Finite element analysis of sagittal balance in different morphotype: Forces and resulting strain in pelvis and spine

    Finite element analysis of sagittal balance in different morphotype: Forces and resulting strain in pelvis and spine di Filardi, Vincenzo, Simona, Portaro, Cacciola, Giorgio, Bertino, Salvatore, Soliera, Luigi, Barbanera, Andrea, Pisani, Alessandro, Milardi, Demetrio, Alessia, Bramanti

    Pubblicazione 2017
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  2. 2
    Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

    Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype di Emma Matthews, Simona Portaro, Ke Qian, Richa Sud, A. Haworth, Mary B. Davis, Robert C. Griggs, Michael G. Hanna

    Pubblicazione 2011
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  3. 3
    Diagnosis and Treatment of Bilateral Respiratory Epithelial Adenomatoid Hamartomas With and Without Sinonasal Polyposis

    Diagnosis and Treatment of Bilateral Respiratory Epithelial Adenomatoid Hamartomas With and Without Sinonasal Polyposis di Filippo Cascio, Giorgio Carmelo Basile, Andrè Wady Debes Felippu, Alexandre Felippu, David Militi, Simona Portaro, Salvatore Poma, Felice Cascio

    Pubblicazione 2019
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  4. 4
    A dental implant dislocated in the ethmoidal sinus: A case report

    A dental implant dislocated in the ethmoidal sinus: A case report di Filippo Cascio, Gianpaolo Antonio Basile, Alexandre Felippu, Andrè Wady Debes Felippu, Fabio Trimarchi, David Militi, Simona Portaro, Alessia Bramanti

    Pubblicazione 2020
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  5. 5
    Walking to your right music: a randomized controlled trial on the novel use of treadmill plus music in Parkinson’s disease

    Walking to your right music: a randomized controlled trial on the novel use of treadmill plus music in Parkinson’s disease di Rocco Salvatore Calabrò, Antonino Naro, Serena Filoni, Massimo Pullia, Luana Billeri, Provvidenza Tomasello, Simona Portaro, Giuseppe Di Lorenzo, Concetta M. Tomaino, Placido Bramanti

    Pubblicazione 2019
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  6. 6
    Efficacy of neuromodulation and rehabilitation approaches on pain relief in patients with spinal cord injury: a systematic review and meta-analysis

    Efficacy of neuromodulation and rehabilitation approaches on pain relief in patients with spinal cord injury: a systematic review and meta-analysis di Simona Portaro, Angelo Alito, Giulia C. Leonardi, Nicola Marotta, Adriana Tisano, Daniele Bruschetta, Umile Giuseppe Longo, Antonio Ammendolia, Demetrio Milardi, Alessandro de Sire

    Pubblicazione 2025
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  7. 7
    Prevalence study of genetically defined skeletal muscle channelopathies in England

    Prevalence study of genetically defined skeletal muscle channelopathies in England di Alejandro Horga, D.L. Raja Rayan, Emma Matthews, Richa Sud, Doreen Fialho, S. Durran, J. Burge, Simona Portaro, Mary B. Davis, Andrea Haworth, Michael G. Hanna

    Pubblicazione 2013
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  8. 8
    In Vivo Computed Tomography Direct Volume Rendering of the Anterior Ethmoidal Artery: A Descriptive Anatomical Study

    In Vivo Computed Tomography Direct Volume Rendering of the Anterior Ethmoidal Artery: A Descriptive Anatomical Study di Filippo Cascio, Alberto Cacciola, Simona Portaro, Gianpaolo Antonio Basile, Giuseppina Rizzo, Andrè Wady Debes Felippu, Alexandre Felippu, Antongiulio Bruschetta, Carmelo Anfuso, Felice Cascio, Demetrio Milardi, Alessia Bramanti

    Pubblicazione 2020
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  9. 9
    Genetic counselling in ALS: facts, uncertainties and clinical suggestions

    Genetic counselling in ALS: facts, uncertainties and clinical suggestions di Adriano Chió, Stefania Battistini, Andrea Calvo, Claudia Caponnetto, F. L. Conforti, Massimo Corbo, F. Giannini, Jessica Mandrioli, Gabriele Mora, Mario Sabatelli, Maria Rosaria Monsurrò, Gioacchino Tedeschi, Amelia Conte, Marco Luigetti, Serena Lattante, Giuseppe Marangi, Paolo Volanti, Kalliopi Marinou, Laura Papetti, Christian Lunetta, Giampaolo Pintor, Fabrizio Salvi, Ilaria Bartolomei, Aldo Quattrone, Antonio Gambardella, Giancarlo Logroscino, Isabella Laura Simone, Fabrizio Pisano, Rossella Spataro, Vincenzo La Bella, Tiziana Colletti, Gianluigi Mancardi, Paola Origone, Víctor Pérez, Giuseppe Borghero, Francesco Marrosu, Maria Giovanna Marrosu, Maria Rita Murru, Gianluca Floris, Antonino Cannas, Valeria Piras, E Costantino, Carla Pani, Maria Alessandra Sotgiu, Maura Pugliatti, Leslie D. Parish, P Cossu, Anna Ticca, Carmelo Rodolico, Simona Portaro, Claudia Ricci, Cristina Moglia, Irene Ossola, Maura Brunetti, Marco Barberis, Antonio Canosa, Stefania Cammarosano, Davide Bertuzzo, Giuseppe Fuda, Antonio Ilardi, Umberto Manera, Ida Pastore, William Sproviero, Francesco Logullo, Raffaella Tanel, Clara Ajmone, Enza Mastro, Debora Pain, Paola Mandich, Silvana Penco, Gabriella Restagno, Marcella Zollino, Antonella Surbone

    Pubblicazione 2013
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  10. 10
    Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

    Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants di Caroline Neuray, Reza Maroofian, Marcello Scala, Tipu Sultan, G. Shashidhar Pai, Majid Mojarrad, Heba El Khashab, Leigh deHoll, Wyatt W. Yue, Hessa S. Alsaif, M. Natalia Zanetti, Oscar D. Bello, Richard Person, Atieh Eslahi, Zaynab Khazaei, Masoumeh Heidari Feizabadi, Stéphanie Efthymiou, Stanislav Groppa, Blagovesta Marinova Karashova, Wolfgang Nachbauer, Sylvia Boesch, Larissa Arning, Dagmar Timmann, Bru Cormand, Belén Pérez‐Dueñas, Gabriella Di Rosa, Jatinder S. Goraya, Tipu Sultan, Jun Mine, Daniela Avdjieva, Hadil Kathom, Radka Tincheva, Selina Banu, Mercedes Pineda-Marfa, Pierangelo Veggiotti, Michel D. Ferrari, Alberto Verrotti, Gian Luigi Marseglia, Salvatore Savasta, Mayte García-Silva, Alfons Macaya Ruiz, Barbara Garavaglia, Eugenia Borgione, Simona Portaro, Benigno Monteagudo Sanchez, Richard G. Boles, Savvas Papacostas, Michail Vikelis, Eleni Zamba Papanicolaou, Efthimios Dardiotis, Shazia Maqbool, Shahnaz Ibrahim, Salman Kirmani, Nuzhat Rana, Osama Atawneh, Georgios Koutsis, Marianthi Breza, Salvatore Mangano, Carmela Scuderi, Eugenia Borgione, Giovanna Morello, Tanya Stojkovic, Massimi Zollo, Gali Heimer, Yves Dauvilliers, Pasquale Striano, Issam Al-Khawaja, Fuad Al-Mutairi, Sherifa A. Hamed, Hala T. El‐Bassyouni, Doaa Soliman, S. Tekeş, Leyla Özer, Volkan Baltacı, Suliman Khan, Christian Beetz, Khalda Amr, Vincenzo Salpietro, Yalda Jamshidi, Fowzan S. Alkuraya, Henry Houlden

    Pubblicazione 2020
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  11. 11
    Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment

    Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment di Vincenzo Salpietro, Nancy T. Malintan, Isabel Llano‐Rivas, Christine G. Spaeth, Stéphanie Efthymiou, Pasquale Striano, Jana Vandrovcová, Maria Concetta Cutrupi, Roberto Chimenz, Emanuele David, Gabriella Di Rosa, Anna Marcé‐Grau, Miquel Raspall‐Chaure, Elena Martín‐Hernández, Federico Zara, Carlo Minetti, Oscar D. Bello, Rita De Zorzi, Sara Fortuna, Andrew Dauber, Mariam Alkhawaja, Tipu Sultan, Kshitij Mankad, Antonio Vitobello, Quentin Thomas, Frédéric Tran Mau‐Them, Laurence Faivre, Francisco Martínez‐Azorín, Carlos E. Prada, Alfons Macaya, Dimitri M. Kullmann, James E. Rothman, Shyam S. Krishnakumar, Henry Houlden, Vincenzo Salpietro, Stéphanie Efthymiou, Yamna Kriouile, M. El Khorassani, M. Aguennouz, Blagovesta Marinova Karashova, Daniela Avdjieva, Hadil Kathom, Radka Tincheva, Lionel Van Maldergem, Wolfgang Nachbauer, Sylvia Boesch, Larissa Arning, Dagmar Timmann, Bru Cormand, Belén Pérez‐Dueñas, Gabriella Di Rosa, Erica Pironti, Jatinder S. Goraya, Tipu Sultan, Salman Kirmani, Shahnaz Ibrahim, Farida Jan, Jun Mine, Selina Banu, Pierangelo Veggiotti, Michel D. Ferrari, Alberto Verrotti, Gian Luigi Marseglia, Salvatore Savasta, Barbara Garavaglia, Carmela Scuderi, Eugenia Borgione, Valeria Dipasquale, Maria Concetta Cutrupi, Simona Portaro, Benigno Monteagudo Sanchez, Mercedes Pineda-Marfa, Francina Munell, Alfons Macaya, Richard G. Boles, Gali Heimer, Savvas Papacostas, Andreea Manole, Nancy T. Malintan, M. Natalia Zanetti, Michael G. Hanna, James E. Rothman, Dimitri M. Kullmann, Henry Houlden

    Pubblicazione 2019
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  12. 12
    Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification

    Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification di Lucía Schottlaender, Rosella Abeti, Zane Jaunmuktane, Carol Macmillan, Viorica Chelban, Benjamin O’Callaghan, John McKinley, Reza Maroofian, Stéphanie Efthymiou, Alkyoni Athanasiou‐Fragkouli, Raeburn Forbes, Marc P. M. Soutar, John H. Livingston, Bernardett Kalmar, Orlando Swayne, Gary Hotton, Alan Pittman, João Ricardo Mendes de Oliveira, Maria De Grandis, Angela Richard-Loendt, Francesca Launchbury, Juri Althonayan, Gavin McDonnell, Aisling Carr, Suliman Khan, Christian Beetz, Atıl Bişgin, Sevcan Tuğ Bozdoğan, Amber Begtrup, Erin Torti, Linda Greensmith, Paola Giunti, Patrick J. Morrison, Sebastian Brandner, Michel Aurrand‐Lions, Henry Houlden, Stanislav Groppa, Blagovesta Marinova Karashova, Wolfgang Nachbauer, Sylvia Boesch, Larissa Arning, Dagmar Timmann, Bru Cormand, Belén Pérez‐Dueñas, Gabriella Di Rosa, Jatinder S. Goraya, Tipu Sultan, Jun Mine, Daniela Avdjieva, Hadil Kathom, Radka Tincheva, Selina Banu, Mercedes Pineda-Marfa, Pierangelo Veggiotti, Michel D. Ferrari, Alberto Verrotti, Gian Luigi Marseglia, Salvatore Savasta, Mayte García-Silva, Alfons Macaya Ruiz, Barbara Garavaglia, Eugenia Borgione, Simona Portaro, Benigno Monteagudo Sanchez, Richard G. Boles, Savvas Papacostas, Michail Vikelis, Eleni Zamba Papanicolaou, Efthimios Dardiotis, Shazia Maqbool, Shahnaz Ibrahim, Salman Kirmani, Nuzhat Rana, Osama Atawneh, Georgios Koutsis, Marianthi Breza, Salvatore Mangano, Carmela Scuderi, Eugenia Borgione, Giovanna Morello, Tanya Stojkovic, Massimi Zollo, Gali Heimer, Yves Dauvilliers, Pasquale Striano, Issam Al-Khawaja, Fuad Al-Mutairi, Sherifa A. Hamed

    Pubblicazione 2020
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  13. 13
    Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination

    Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination di Stéphanie Efthymiou, Vincenzo Salpietro, Nancy T. Malintan, Mallory Poncelet, Yamna Kriouile, Sara Fortuna, Rita De Zorzi, Katelyn Payne, Lindsay B. Henderson, Andrea Cortese, Sateesh Maddirevula, Nadia Alhashmi, Sarah Wiethoff, Mina Ryten, Juan A. Botía, Vincenzo Provitera, Markus Schuelke, Jana Vandrovcová, Stanislav Groppa, Blagovesta Marinova Karashova, Wolfgang Nachbauer, Sylvia Boesch, Larissa Arning, Dagmar Timmann, Bru Cormand, Belén Pérez‐Dueñas, Jatinder S. Goraya, Tipu Sultan, Jun Mine, Daniela Avdjieva, Hadil Kathom, Radka Tincheva, Selina Banu, Mercedes Pineda-Marfa, Pierangelo Veggiotti, Michel D. Ferrari, Arn M. J. M. van den Maagdenberg, Alberto Verrotti, Gian Luigi Marseglia, Salvatore Savasta, Mayte García-Silva, Alfons Macaya Ruiz, Barbara Garavaglia, Eugenia Borgione, Simona Portaro, Benigno Monteagudo Sanchez, Richard G. Boles, Savvas Papacostas, Michail Vikelis, James E. Rothman, Dimitri M. Kullmann, Eleni Zamba Papanicolaou, Efthimios Dardiotis, Shazia Maqbool, Shahnaz Ibrahim, Salman Kirmani, Nuzhat Rana, Osama Atawneh, Shen‐Yang Lim, Mohd. Farooq Shaikh, Georgios Koutsis, Marianthi Breza, Salvatore Mangano, Carmela Scuderi, Eugenia Borgione, Giovanna Morello, Tanya Stojkovic, Massimo Zollo, Gali Heimer, Yves Dauvilliers, Carlo Minetti, Issam Al-Khawaja, Fuad Al-Mutairi, Sherifa A. Hamed, Menelaos Pipis, Conceição Bettencourt, Simon Rinaldi, Laurence E. Walsh, Erin Torti, Valeria Iodice, Maryam Najafi, Ehsan Ghayoor Karimiani, Reza Maroofian, Karine Siquier-Pernet, Nathalie Boddaert, Pascale de Lonlay, Vincent Cantagrel, M. Aguennouz, M. El Khorassani, Miriam Schmidts, Fowzan S. Alkuraya, Simon Edvardson, Maria Nolano, Jérôme Devaux, Henry Houlden

    Pubblicazione 2019
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