Torthaí cuardaigh - Serenella Servidei

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  1. 1
    Impairment of skeletal muscle adenosine triphosphate–sensitive K+ channels in patients with hypokalemic periodic paralysis

    Impairment of skeletal muscle adenosine triphosphate–sensitive K+ channels in patients with hypokalemic periodic paralysis de réir Domenico Tricarico, Serenella Servidei, P. Tonali, Karin Jurkat‐Rott, Diana Conte Camerino

    Foilsithe / Cruthaithe 1999
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  2. 2
    Vitamin D in Neurological Diseases

    Vitamin D in Neurological Diseases de réir Domenico Plantone, Guido Primiano, Carlo Manco, Sara Locci, Serenella Servidei, Nicola De Stefano

    Foilsithe / Cruthaithe 2022
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  3. 3
    MHC class I, MHC class II and intercellular adhesion molecule-1 (ICAM-1) expression in inflammatory myopathies

    MHC class I, MHC class II and intercellular adhesion molecule-1 (ICAM-1) expression in inflammatory myopathies de réir Emanuela Bartoccioni, Stefania Gallucci, Flavia Scuderi, Enzo Ricci, Serenella Servidei, Aldobrando Broccolini, P. Tonali

    Foilsithe / Cruthaithe 1994
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  4. 4
    Focal status epilepticus as unique clinical feature of COVID-19: A case report

    Focal status epilepticus as unique clinical feature of COVID-19: A case report de réir Catello Vollono, Eleonora Rollo, Marina Romozzi, Giovanni Frisullo, Serenella Servidei, Alberto Borghetti, Paolo Calabresi

    Foilsithe / Cruthaithe 2020
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  5. 5
    Acute myopathic quadriplegia in patients with COVID-19 in the intensive care unit

    Acute myopathic quadriplegia in patients with COVID-19 in the intensive care unit de réir Francesca Madia, Barbara Merico, Guido Primiano, Salvatore Lucio Cutuli, Gennaro De Pascale, Serenella Servidei

    Foilsithe / Cruthaithe 2020
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  6. 6
    Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.

    Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency. de réir Ronald G. Haller, S. F. Lewis, R.W. Estabrook, S. DiMauro, Serenella Servidei, Daniel W. Foster

    Foilsithe / Cruthaithe 1989
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  7. 7
    Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients

    Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients de réir Valerio De Stefano, Patrizia Chiusolo, Katia Paciaroni, Ida Casorelli, Elena Rossi, Marco Molinari, Serenella Servidei, Pietro Tonali, Giuseppe Leone

    Foilsithe / Cruthaithe 1998
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  8. 8
    γ1- and γ2-Syntrophins, Two Novel Dystrophin-binding Proteins Localized in Neuronal Cells

    γ1- and γ2-Syntrophins, Two Novel Dystrophin-binding Proteins Localized in Neuronal Cells de réir Giulio Piluso, Massimiliano Mirabella, Enzo Ricci, Angela Belsito, Ciro Abbondanza, Serenella Servidei, Annibale Alessandro Puca, P. Tonali, Giovanni Alfredo Puca, Vincenzo Nigro

    Foilsithe / Cruthaithe 2000
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  9. 9
    Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

    Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases de réir Michelangelo Mancuso, C. Angelini, Enrico Bertini, Valério Carelli, Giacomo P. Comi, Carlo Minetti, Maurizio Moggio, Tiziana Mongini, Serenella Servidei, Paola Tonin, António Toscano, Graziella Uziel, Massimo Zeviani, Gabriele Siciliano

    Foilsithe / Cruthaithe 2012
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  10. 10
    Impaired Skin Fibroblast Carnitine Uptake in Primary Systemic Carnitine Deficiency Manifested by Childhood Carnitine-Responsive Cardiomyopathy

    Impaired Skin Fibroblast Carnitine Uptake in Primary Systemic Carnitine Deficiency Manifested by Childhood Carnitine-Responsive Cardiomyopathy de réir Ingrid Tein, Darryl C. De Vivo, F Z Bierman, P Pulver, Linda J. De Meirleir, Ljerka Cvitanović-Šojat, Roberta A Pagon, Enrico Bertini, Carlo Dionisi‐Vici, Serenella Servidei, S. DiMauro

    Foilsithe / Cruthaithe 1990
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  11. 11
    Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1

    Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 de réir Jianping Zhou, Marcel Tawk, Francesco Danilo Tiziano, Julien Veillet, Mónica Bayés, Flora Nolent, Virginie Garcia, Serenella Servidei, Enrico Bertini, Francesc Castro-Giner, Yavuz Renda, Stéphane Carpentier, Nathalie Andrieu‐Abadie, Marta Gut, Thierry Levade, Haluk Topaloğlu, Judith Melki

    Foilsithe / Cruthaithe 2012
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  12. 12
    Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their Analogs

    Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their Analogs de réir Vincenzo Tragni, Guido Primiano, Albina Tummolo, Lucas Cafferati Beltrame, Gianluigi La Piana, Maria Noemi Sgobba, Maria Maddalena Cavalluzzi, Giulia Paterno, Ruggiero Gorgoglione, Mariateresa Volpicella, Lorenzo Guerra, Domenico Marzulli, Serenella Servidei, Anna Grassi, Giuseppe Petrosillo, Giovanni Lentini, Ciro Leonardo Pierri

    Foilsithe / Cruthaithe 2022
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  13. 13
    Macrophages excite muscle spindles with glutamate to bolster locomotion

    Macrophages excite muscle spindles with glutamate to bolster locomotion de réir Yuyang Yan, Nuria Antolin, Luming Zhou, Luyang Xu, Irene Lisa Vargas, Carlos Gómez, Guiping Kong, Ilaria Palmisano, Yi Yang, Jessica Chadwick, Franziska Mueller, Anthony M. J. Bull, Cristina Lo Celso, Guido Primiano, Serenella Servidei, Jean‐Françóis Perrier, Carmelo Bellardita, Simone Di Giovanni

    Foilsithe / Cruthaithe 2024
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  14. 14
    Genotype-phenotype correlation in Pompe disease, a step forward

    Genotype-phenotype correlation in Pompe disease, a step forward de réir Paola De Filippi, Kolsoum Saeidi, Sabrina Ravaglia, Andrea Dardis, C. Angelini, Tiziana Mongini, Lucia Morandi, Maurizio Moggio, Antonio Di Muzio, Massimiliano Filosto, Bruno Bembi, Fabio Giannini, Giovanni Marrosu, Miriam Rigoldi, Paola Tonin, Serenella Servidei, Gabriele Siciliano, Annalisa Carlucci, Claudia Scotti, Mario Comelli, António Toscano, Cesare Danesino

    Foilsithe / Cruthaithe 2014
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  15. 15
    Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years

    Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years de réir C. Angelini, Claudio Semplicini, Sabrina Ravaglia, Bruno Bembi, Serenella Servidei, Elena Pegoraro, Maurizio Moggio, Massimiliano Filosto, Elisabetta Sette, Grazia Crescimanno, Paola Tonin, Rossella Parini, Lucia Morandi, Maria Giovanna Marrosu, Giuseppe Greco, Olimpia Musumeci, Giuseppe Di Iorio, Gabriele Siciliano, Maria Alice Donati, Francesca Carubbi, Mario Ermani, Tiziana Mongini, António Toscano

    Foilsithe / Cruthaithe 2011
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  16. 16
    The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

    The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway de réir Hsien-Yang Lee, Ying Xu, Yong Huang, Andrew H. Ahn, Georg Auburger, Massimo Pandolfo, Hubert Kwieciński, David A. Grimes, Anthony E. Lang, Jørgen E. Nielsen, Yuri Averyanov, Serenella Servidei, Andrzej Friedman, Patrick Van Bogaert, Marc Abramowicz, Michiko Kimura Bruno, Beatrice F. Sorensen, Ling Tang, Ying‐Hui Fu, Louis J. Ptáček

    Foilsithe / Cruthaithe 2004
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  17. 17
    Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes

    Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes de réir Chiara Pizzamiglio, Hallgeir Jonvik, Stefen Brady, Patrick F. Chinnery, Lucía Galán, Gráinne S. Gorman, Alejandro Horga, Rita Horváth, Mirian C. H. Janssen, Albert Lim, Michelangelo Mancuso, Robert McFarland, Mária Judit Molnár, Olimpia Musumeci, Victoria Nesbitt, Wladimir, Guido Primiano, Ernestina Santos, Serenella Servidei, Rhys H. Thomas, Michael G. Hanna, Pedro Machado, Robert D. S. Pitceathly

    Foilsithe / Cruthaithe 2021
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  18. 18
    Factors associated with the severity of <scp>COVID</scp>‐19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular <scp>COVID</scp>‐19 Registry

    Factors associated with the severity of <scp>COVID</scp>‐19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular <scp>COVID</scp>‐19 Registry... de réir Chiara Pizzamiglio, Robert D. S. Pitceathly, Michael P. Lunn, Stefen Brady, Fabiola De Marchi, Lucía Galán, Jeannine M. Heckmann, Alejandro Horga, Mária Judit Molnár, Acary Sousa Bulle Oliveira, Wladimir Bocca Vieira de Rezende Pinto, Guido Primiano, Ernestina Santos, Benedikt Schoser, Serenella Servidei, Paulo Victor Sgobbi de Souza, Venugopalan Y. Vishnu, Michael G. Hanna, Mazen M. Dimachkie, Pedro Machado

    Foilsithe / Cruthaithe 2022
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  19. 19
    Management of seizures in patients with primary mitochondrial diseases: consensus statement from the <scp>InterERNs</scp> Mitochondrial Working Group

    Management of seizures in patients with primary mitochondrial diseases: consensus statement from the <scp>InterERNs</scp> Mitochondrial Working Group de réir Michelangelo Mancuso, Maria Papadopoulou, Yi Shiau Ng, Anna Ardissone, Marcello Bellusci, Enrico Bertini, Lidia Di Vito, Teresinha Evangelista, Carmen Fons, Omar Hikmat, Rita Horváth, Thomas Klopstock, Cornelia Kornblum, Costanza Lamperti, Laura Licchetta, Mária Judit Molnár, Kristin N. Varhaug, Mar O’Callaghan, Ronit Pressler, Manuel Schiff, Serenella Servidei, Nora Szabó, Gráinne S. Gorman, J. Helen Cross, Shamima Rahman

    Foilsithe / Cruthaithe 2024
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  20. 20
    Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration

    Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration de réir Valentina Muto, Elisabetta Flex, Zachary A Kupchinsky, Guido Primiano, Hamid Galehdari, Mohammadreza Dehghani, Serena Cecchetti, Giovanna Carpentieri, Teresa Rizza, Neda Mazaheri, Alireza Sedaghat, Mohammad Yahya Vahidi Mehrjardi, Alice Traversa, Michela Di Nottia, Maria Kousi, Yalda Jamshidi, Andrea Ciolfi, Viviana Caputo, Reza Azizi Malamiri, Francesca Pantaleoni, Simone Martinelli, Aaron R. Jeffries, Jawaher Zeighami, Amir Sherafat, Daniela Di Giuda, Gholamreza Shariati, Rosalba Carrozzo, Nicholas Katsanis, Reza Maroofian, Serenella Servidei, Marco Tartaglia

    Foilsithe / Cruthaithe 2018
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